Acknowledgments The Disability Advocacy and Access Team, FaHCSIA would like to thank the many people who contributed to the development of this Toolkit. The process for developing the Toolkit included: A review of the previous NDAP Quality Improvement Toolkit, the Quality Strategy Toolkit for Disability Employment and Rehabilitation Services, and research of existing and relevant advocacy sector, state and Commonwealth resources; Consultation with key stakeholders including disability advocacy agencies, Certification Body and audit personnel, the Disability Advocacy Network Australia (DANA) Limited, and FaHCSIA State and National Office staff; and A workshop to road test the draft Toolkit with key stakeholders. We would like to acknowledge the following organisations for their contribution to this process. Advocacy Law Alliance Inc (Disability Advocacy NSW and Mid North Coast Community Legal Centre) Advocacy Tasmania Inc Disability Advocacy Network Australia (DANA) Ltd E-QUAL (Enhancing Quality) Joint Accreditation System of Australia and New Zealand (JAS -ANZ) Newell Advocacy Inc North East Citizen Advocacy Inc Regional Information and Advocacy Council (RIAC) SAI-Global Villamanta Disability Rights Legal Service Inc We would also like to thank those disability advocacy agencies who allowed us to include relevant case studies and examples of their policies, procedures, tools and templates in this Toolkit. Parliamentary Secretary Foreword Over the last few years significant reforms for people with disability have been achieved. The signing of the United Nations Convention on the Rights of Persons with Disabilities by the Australian Government affirmed a commitment to safeguarding rights for people with disability. The introduction of the National Disability Agreement in 2009 paved the way for significant reform of the disability services system and in February 2011 the Council of Australian Governments endorsed the National Disability Strategy which outlines a ten-year national policy framework to improve the lives of people with disability, promote participation, and create a more inclusive society. The National Disability Strategy recognises the important role that disability advocacy will play to safeguard the rights of people with disability. Additionally the foundation work has commenced for a National Disability Insurance Scheme. This work will result in transformative reform of the disability service system. A well administered, quality assured disability advocacy sector will be crucial to support Australia’s human rights framework and the achievement of broader disability reforms outlined in the National Disability Agreement, the National Disability Strategy, the United Nations Convention on the Rights of Persons with Disabilities and a National Disability Insurance Scheme. The Government is committed to supporting the advocacy sector to meet these potential future demands. A new Quality Assurance system to be introduced from 1 July 2012 for disability advocacy agencies funded by the Australian Government features a third-party certification process, independent from government, to assess the compliance of disability advocacy agencies against a tailored set of Disability Advocacy Standards. It builds on the strengths of the previous Quality Assurance system but provides greater assurances about the quality of disability advocacy support being provided and increased guidance for advocacy services to improve service quality. This National Disability Advocacy Program Quality Toolkit provides key resources for agencies to meet the requirements under the new Quality Assurance system and to foster a commitment to continuous improvement. It is our vision that reforms being progressed, and the introduction of a new Quality Assurance system will ensure quality disability advocacy support that is easy to access, responds flexibly to the changing environment and provides people with disability access to advocacy that promotes, protects and ensures their full and equal enjoyment of all human rights, enabling full community participation. SENATOR THE HON JAN MCLUCAS Parliamentary Secretary to the Prime Minister and Parliamentary Secretary for Disabilities and Carers Feedback form We welcome your feedback about how useful you find this Toolkit, including your suggestions for additional resources or information for future inclusion. Name: Organisation: Mailing Address: Email address: Contact telephone number: I wish to: Submit an additional resource to be considered for inclusion in the Toolkit (attach resource) Provide feedback about Toolkit’s tools or resources I have found useful Provide general feedback about the Toolkit Other Feedback (please attach additional pages if required) Please send to: Post Advocacy and Access Team, PO Box 7576, Canberra Mail Centre, ACT 2610 Email disabilityadvocacy@fahcsia.gov.au Contents Section 1: Purpose of the NDAP Quality Toolkit ............................................... 1 Section 2: Overview of the Quality Strategy for the NDAP ................................ 2 2.1 Description of the NDAP…………………………………………………………….2 2.2 Purpose of the NDAP Quality Strategy…………………………………………….4 2.3 Key features and components of the NDAP Quality Strategy…………………...5 2.4 Information about the Disability Advocacy Standards, key performance indicators and examples of evidence…………………………………………………..7 2.5 Overview of the third party certification process………………………………….8 2.6 Responsibilities of stakeholders……………………………………………………9 Section 3: Quality assurance and a step by step guide to certification ......... 10 3.1 Key points about the QA system…………………………………………………..10 3.2 Step by step guide to Disability Advocacy Standards certification…………….12 Step 1: Start the process early .............................................................................. 12 Step 2: Choose your Certification Body ................................................................. 13 Step 3: Notify FaHCSIA ......................................................................................... 15 Step 4: Conduct your self-assessment .................................................................. 15 Step 5: Prepare for your certification audit ............................................................ 18 Step 6: Participate in your certification audit ......................................................... 25 Step 7: Audit team assessment report and follow up ............................................ 27 Step 8: Start three year audit cycle ....................................................................... 28 3.3 Summary of the step by step guide to Disability Advocacy Standards certification……………………………………………………………………………….31 3.4 Comprehensive step by step guide to Disability Advocacy Standards certification……………………………………………………………………………….33 Section 4: Disability Advocacy Standards, examples of evidence and selfassessment worksheets ..................................................................................... 37 4.1 Disability Advocacy Standards, KPIs and evidence examples………………...39 Standard 1: Accessing advocacy .......................................................................... 39 Standard 2: Individual needs ................................................................................. 43 Standard 3: Decision making and choice .............................................................. 48 Standard 4: Privacy, dignity and confidentiality ..................................................... 53 Standard 5: Participation and integration .............................................................. 57 Standard 6: Valued status ..................................................................................... 61 Standard 7: Complaints and disputes .................................................................... 64 Standard 8: Agency management ......................................................................... 68 Standard 9: Staff, recruitment, employment and training ...................................... 71 Standard 10: Protection of human rights and freedom from abuse ....................... 74 4.2 Self-assessments…………………………………………………………………...78 4.3 Self-Assessment Worksheets ……………………………………………………..80 Section 5: Continuous Improvement ................................................................. 90 5.1 Sample policies, procedures, templates and tools………………………………92 Standard 1: Accessing advocacy ........................................................................ 92 Standard 2: Individual needs ............................................................................. 102 Standard 3: Decision making and choice .......................................................... 108 Standard 4: Privacy, dignity and confidentiality ................................................. 124 Standard 5: Participation and integration .......................................................... 131 Standard 6: Valued status ................................................................................. 134 Standard 7: Complaints and disputes ................................................................ 139 Standard 8: Agency management ..................................................................... 159 Standard 9: Staff, recruitment, employment and training .................................. 197 Standard 10: Protection of human rights and freedom from abuse .................. 217 5.2 Case studies……………………………………………………………………….224 Standard 1: Accessing advocacy ........................................................................ 224 Standard 2: Individual needs ............................................................................... 228 Standard 3: Decision making and choice ............................................................ 231 Standard 4: Privacy, dignity and confidentiality ................................................... 235 Standard 5: Participation and integration ............................................................ 237 Standard 6: Valued status ................................................................................... 239 Standard 7: Complaints and disputes .................................................................. 241 Standard 8: Agency management ....................................................................... 243 Standard 9: Staff, recruitment, employment and training .................................... 249 Standard 10: Protection of human rights and freedom from abuse ..................... 252 5.3 Links to other resources…………………………………………………………..256 Standard 1: Accessing advocacy ........................................................................ 256 Standard 2: Individual needs ............................................................................... 256 Standard 3: Decision making and choice ............................................................ 256 Standard 4: Privacy, dignity and confidentiality ................................................... 257 Standard 5: Participation and integration ............................................................ 258 Standard 6: Valued status ................................................................................... 258 Standard 7: Complaints and disputes .................................................................. 258 Standard 8: Agency management ....................................................................... 259 Standard 9: Staff, recruitment, employment and training .................................... 259 Standard 10: Protection of human rights and freedom from abuse .................. 260 Section 6: Complaints handling mechanisms ................................................ 261 6.1 Complaints associated with the NDAP Quality Strategy………………………261 6.2 External referrals…………………………………………………………………..263 Section 7: Key contacts .................................................................................... 267 Section 8: Glossary ........................................................................................... 272 Attachment 1 - JAS-ANZ Procedure 29 ........................................................... 280 Attachment 2 - Consent for the Release of Information................................. 306 Attachment 3 - Disability Advocacy Standards, key performance indicators and examples of evidence ................................................................................ 308 Section 1: Purpose of the NDAP Quality Toolkit Following a review of the NDAP and consultations with the sector in 2007/8, it was decided that a strategy to improve the quality of disability advocacy support was needed to provide assurances to people with disability, the disability advocacy sector and Government. The NDAP Quality Strategy includes: 1. A Quality Assurance (QA) system that commenced on 1 July 2012. A key aspect of the new QA system is continuous improvement for disability advocacy agencies to achieve better outcomes for people with disability. 2. A range of tools and supports to assist the sector to meet the requirements of the new QA system, including this Toolkit, training, and mentoring. 3. Ensuring the quality of advocacy support by assisting disability advocacy agencies to meet their requirements under their funding agreements. This Toolkit has been developed as a resource for NDAP funded disability advocacy agencies, and certification/accreditation personnel who will be involved in conducting assessments of the quality of disability advocacy being provided. It is designed to help you by providing a step by step guide to the QA certification process, as well as case studies, and sample policies and procedures you may wish to apply or adapt, or that may otherwise inspire your quality improvement. You can use, adapt and copy the material in this Toolkit however you like. Please remember that implementing the tools in this Toolkit does not automatically result in compliance with the Disability Advocacy Standards or your certification. The tools are designed to help you build on your existing systems and bring them together cohesively. 1 Section 2: Overview of the Quality Strategy for the NDAP 2.1 Description of the NDAP The NDAP provides people with disability access to effective disability advocacy that promotes, protects and ensures their full and equal enjoyment of all human rights enabling community participation. The NDAP is funded and administered by the Australian Government Department of Families, Housing, Community Services and Indigenous Affairs (FaHCSIA). The target group for advocacy support provided by NDAP agencies, as required under section 8 of the Disability Services Act 1986 (Commonwealth), consists of people with disability that: a. ‘is attributable to an intellectual, psychiatric, sensory or physical impairment or a combination of such impairments; b. is permanent or likely to be permanent; and c. results in: i. a substantially reduced capacity of the person for communication, learning or mobility; and ii. the need for ongoing support services. Definition of disability advocacy The Disability Services Act 1986 (Commonwealth) requires that disability advocacy agencies support people with disability to exercise their rights and freedoms, being rights and freedoms recognised by the Convention on the Rights of Persons with Disabilities (Disabilities Convention). Approaches to disability advocacy can be categorised into two broad approaches being individual advocacy and systemic advocacy. Advocacy for individuals supports people with disability to exercise their rights and freedoms through either one-to-support, or by supporting people to advocate for themselves individually, through a third party, or on a group basis. Models of advocacy support for individuals include: Individual advocacy Citizen advocacy Family advocacy Legal advocacy 2 Self advocacy Individual advocacy – seeks to uphold the rights and interests of people with all types of disabilities on a one-to-one basis by addressing instances of discrimination, abuse and neglect. Individual advocates work with people with disability on either a short-term or issue-specific basis. Individual advocates: Work with people with disability requiring one-to-one advocacy support; Develop a plan of action (sometimes called an individual advocacy plan) in partnership with the person with a disability that maps out clearly defined goals; Educate people with disability about their rights; and Work through the individual advocacy plan in partnership with the person with a disability. Citizen advocacy seeks to support people with a disability (also called protégés) by matching them with volunteers. Some of the matches made may last for life. Through citizen advocacy: People with disability who are vulnerable, isolated and may have no family or community supports or networks are sought out; Citizen advocates (who are volunteers) are encouraged to represent the interests of a person with a disability as if they were their own and be free from conflict of interest; and Citizen advocates are recruited, trained and supported by a coordinator who manages the work of the citizen advocacy agency. Family advocacy works with parents and family members to enable them to act as advocates with and on behalf of a family member with disability. Family advocates work with parents and family members on either a short-term or an issue-specific basis. Family advocates work within the fundamental principle that the rights and interests of the person with disability are upheld at all times. Through family advocacy: Family members are provided with advice and support; The person with disability is assisted via the family member being directly supported by the agency to advocate on their behalf. Legal advocacy seeks to uphold the rights and interests of people with all types of disabilities on a one-to-one basis by addressing legal aspects of instances of discrimination, abuse and neglect. Legal advocates may: 3 Provide legal representation for people with disability as they come into contact with the justice system; Pursue positive changes to legislation for people with disability; and Assist people with disability to understand their legal rights. Self advocacy supports people with disability to advocate on their own behalf, to the extent possible, on a one-to-one or group basis. Through self advocacy: Advocates work with people with disability to develop their personal skills and self-confidence to enable them to advocate on their own behalf; and People with disability are educated about their rights. Systemic advocacy seeks to introduce and influence long-term changes to ensure that the rights and freedoms of persons with disabilities, being rights and freedoms recognised or declared by the Disabilities Convention, are attained and upheld so as to positively affect the quality of their lives. The systemic advocacy agency: Pursues positive changes to legislation, policy and service practices in partnership with groups of people with disability, advocacy agencies and other relevant organisations; and Seeks to address barriers and discriminatory practices to produce long-term positive changes. 2.2 Purpose of the NDAP Quality Strategy The goal of the NDAP Quality Strategy is to introduce an effective performance framework for Australian Government funded disability advocacy agencies that will: Provide people with disability, the disability advocacy sector and government with assurances about the quality of disability advocacy support being delivered; Introduce a set of measurable performance requirements via the introduction of the Disability Advocacy Standards and key performance indicators (KPIs); Introduce mechanisms independent from government to assess the compliance of advocacy agencies against the Disability Advocacy Standards and KPIs; and Support disability advocacy agencies to continuously improve. Quality should be seen as a right of people with disability receiving advocacy support from a disability advocacy agency, and a collective responsibility of agency staff, management and Boards or equivalents. A ‘quality culture’ is central to the delivery of high quality advocacy support. 4 The values and commitment of a disability advocacy agency, combined with the agency’s systems and processes work towards enhancing quality, which then drives outcomes for people with disability.1 2.3 Key features and components of the NDAP Quality Strategy The components of the Quality Strategy The NDAP Quality Strategy is based on a quality management approach and comprises the new QA system which includes continuous improvement, the provision of tools and other support and assistance for agencies to meet the requirements under their funding agreements. QA system: Key features of the QA system include: A set of 10 Disability Advocacy Standards and 25 KPIs, (which build on the Disability Services Standards which have been in place since 1992); Certification of advocacy agencies’ compliance with the Standards and KPIs on the basis of assessments undertaken by independent, accredited Certification Bodies; and Accreditation of Certification Bodies by the Joint Accreditation System of Australia and New Zealand (JAS-ANZ). Accreditation requirements are contained in JAS-ANZ Procedure 29 at Attachment 1. QA provides confidence that a particular standard of quality for a service or product has been met and maintained. QA incorporates: Standards against which internal and/or external assessment is undertaken; and Processes to control components of the quality system e.g. plans, policies, procedures, guidelines. Continuous improvement: With a quality management approach, continuous improvement systems incorporate a quality cycle of continuous improvement. Quality management is seen as an ongoing journey of continuous improvement. Continuous improvement involves: 1 Progressively increasing the value of advocacy support through changes designed to better address the needs and preferences of people with disability; Enhancing performance against the Standards; and Commitment to identifying needs and opportunities for improvement in a systematic and planned way. Quality Framework Handbook, Department of Human Services, Victoria 5 Quality systems Quality management practice should be deployed through a quality system. This ensures that a cyclical, consistent and coordinated approach to measuring, monitoring and improving disability advocacy support is ensured. A quality system framework includes formalisation of the disability advocacy agency’s plans, policies and procedures, as well as documentation of processes and practices such as position descriptions, meeting minutes and system controls. Compliance with legislative and statutory requirements is integral to a disability advocacy agency’s quality system. A ‘systems approach’ to management is a way of thinking that helps to link continuous improvement of all internal processes or activities. In each stage of a system there will be processes which require monitoring for opportunities for improvement. A robust quality system aims to establish a consistent level of quality against agreed Standards and achieve a culture of quality and continuous improvement. Disability advocacy agencies that have integrated a quality system into how they work can achieve better outcomes for people with disability, the organisation, and ultimately, the broader community. Some of the benefits include2: For people with disability: More likely to get the support they need and want, and achieve better outcomes; Greater confidence that the agency is well run; More opportunities to have a say and be involved in decision making about the agency. For disability advocacy agency staff: Greater job satisfaction; Greater efficiency and effectiveness; Greater sense of involvement and empowerment in their work; Opportunities to learn new skills and a more interesting learning environment. For Boards or equivalent: Greater confidence that the disability advocacy agency is achieving its mission and purpose; Development of a culture of ongoing learning and continuous improvement; Opportunities to promote the values of the disability advocacy agency and demonstrate these to the community. For managers: 2 Development of a culture of ongoing learning and continuous improvement; More efficient and effective work processes; More time and resources spent on planning rather than reacting to problems; Opportunities to promote the values of the disability advocacy agency and demonstrate these to the community. Adapted from Quality Systems, A Resource Package for Disability Services, Disability Services Commission, WA 6 2.4 Information about the Disability Advocacy Standards, key performance indicators and examples of evidence Disability Advocacy Standards The 10 Disability Advocacy Standards and 25 associated key performance indicators (KPIs) are central to the NDAP QA system. The Standards define the elements of quality advocacy support for people with disability. The KPIs describe a measurable element of practice that may be used to assess whether the practice meets a particular Standard. To achieve certification, disability advocacy agencies need to comply with, and demonstrate continuous improvement against all the Disability Advocacy Standards and KPIs. A complete set of the Standards and KPIs appears in Section 4, and is available on the ComLaw website. The Disability Advocacy Standards apply to all disability advocacy agencies across the range of advocacy models funded under the NDAP. However, the inherent differences between the six different models of advocacy are recognised under the QA system. The examples of evidence provided in Section 4 describe the different types and examples of evidence applicable to the different models of advocacy. Examples of evidence Examples of evidence are tools to help you gather and develop evidence to: Demonstrate to a Certification Body what your disability advocacy agency is doing to meet the Disability Advocacy Standards; Use internally to assess your disability advocacy agency's performance against the Disability Advocacy Standards; and Use internally to help your disability advocacy agency find ways to continually improve and innovate. The examples of evidence are not an all-inclusive checklist. You may have different examples of evidence than those in the guidelines for demonstrating compliance with the KPIs for each Standard. Other Standards Some NDAP disability advocacy agencies may also be required to meet other Standards through certification schemes accredited by JAS-ANZ, for example State Government disability services certification schemes. If this applies to you, then your disability advocacy agency can have the extent of any common criteria considered during the certification process to avoid audit duplication. This could include co-scheduling of audits, where practicable. For more information, see Section 3. 7 2.5 Overview of the third party certification process Audits against the Disability Advocacy Standards will be conducted by independent third party Certification Bodies. These Certification Bodies will be accredited to perform audits against the Disability Advocacy Standards by JASANZ (see Diagram 1). Diagram 1: Hierarchy of the QA system Certification Bodies Report QA audit results Certification FaHCSIA: the funding body for certified NDAP disability advocacy agencies that administers the QA system Accreditation JAS-ANZ (accreditation body) Disability Advocacy Agencies Certification Certification is recognition by a third party that a disability advocacy agency conforms to the requirements of the Disability Advocacy Standards. Disability advocacy agencies that achieve certification will receive a certificate that will be recognised by the Australian Government as proof that the agency is delivering services in line with the Standards. Certification will be at the level of the disability advocacy organisation – this means that all outlets and all advocacy models provided by the organisation must be compliant with the Disability Advocacy Standards for it to achieve certification. Accreditation Accreditation is the process by which JAS-ANZ formally recognises that a Certification Body is competent to carry out specific tasks — in this case to undertake assessments and offer certification against the Disability Advocacy Standards, according to a formal JAS-ANZ accreditation assessment. 8 2.6 Responsibilities of stakeholders The role of FaHCSIA FaHCSIA is responsible for administering the Quality Strategy for disability advocacy agencies. In the new QA system FaHCSIA will remain independent of the assessment and certification decision making process. FaHCSIA will work closely with the NDAP sector to support NDAP disability advocacy agencies to gain certification, to facilitate continuous improvement and assist them to meet the requirements of their funding agreements. The role of JAS-ANZ JAS-ANZ is responsible for accrediting the Certification Bodies that audit disability advocacy agencies against the Disability Advocacy Standards. The criteria for accreditation of Certification Bodies are set out in JAS-ANZ Procedure 29 Requirements for Bodies Providing Audit and Certification of Advocacy Agencies under the National Disability Advocacy Program. Procedure 29 contains requirements for Certification Bodies, not disability advocacy agencies. It covers requirements governing the impartiality, confidentiality and competence of the Certification Body. Procedure 29 also sets out guidance for how certification processes are to be conducted. Procedure 29 is included in Attachment 1. More information about JAS-ANZ, including all JAS-ANZ Procedures, is available on the JAS-ANZ website. The role of Certification Bodies Certification Bodies are third party accredited entities that independently audit disability advocacy agencies funded by FaHCSIA against the Disability Advocacy Standards. Audit teams include competent personnel identified by a Certification Body as meeting required team competencies as set down in JASANZ Procedure 29. The audit team will generally include a Lead Auditor and a Consumer Technical Expert (CTE). Procedure 29 requires a person with a disability to be included in the team either as a Leader Auditor or as a CTE. Certification Bodies rate the performance of disability advocacy agencies against the 10 Disability Advocacy Standards and 25 KPIs, using a scale of 0 (major nonconformity), 1 (nonconformity) and 2 (conformity). These results are reported to the disability advocacy agency and FaHCSIA in the form of an audit report. 9 Section 3: Quality assurance and a step by step guide to certification 3.1 Key points about the QA system 1. The QA system applies to all NDAP funded disability advocacy agencies. 2. It involves independent assessments to certify that they comply with the 10 Disability Advocacy Standards. Quality is specified through 25 KPIs across the Standards. 3. Third party Certification Bodies undertake the certification audits. 4. Certification Bodies are accredited by the JAS-ANZ. Accreditation requirements are contained in JAS-ANZ Procedure 29. JAS-ANZ accredits Certification Bodies as competent and impartial for undertaking audits against the Disability Advocacy Standards. 5. The QA system has been designed to ensure that people with disability are involved with all aspects and stages of the process. 6. Under the QA system, the role of FaHCSIA is to develop policy and provide support and resources to help disability advocacy agencies gain certification and pursue continuous improvement. 7. The QA system was formally implemented from 1 July 2012, with disability advocacy agencies currently funded under the NDAP required to achieve certification by 7 November 2013. 8. Those advocacy agencies that do not meet the 7 November 2013 deadline will no longer be eligible for funding. 9. It is important to prepare for certification well in advance of the certification deadline, to allow for the availability of Certification Body audit teams, as well as to close out any nonconformities. 10. If disability advocacy agencies receive nonconformities against any of the Disability Advocacy Standards, they have three months to take corrective action for major nonconformities, and six months to take corrective action for nonconformities. 11. Certified disability advocacy agencies receive a certificate of compliance that is recognised by the Australian Government as proof that they are delivering services in line with all of the Disability Advocacy Standards and KPIs. 12. If a disability advocacy agency has been audited to another set of Standards by a JAS-ANZ accredited Certification Body, then common criteria can be considered during the NDAP QA process to avoid audit duplication. 13. The timing of audits is important for continued funding. At 12 and 24 months of certification, certified disability advocacy agencies participate in a surveillance audit conducted by their chosen Certification Body. The first surveillance audit must occur not more than 12 months after the last day of the certification audit – the second surveillance must occur not more than 13 months after the last day of the first surveillance audit. Prior to 36 months of certification, disability advocacy agencies participate in a full recertification audit. 10 Diagram 2 below shows the steps involved in the certification process. Diagram 2: The certification process 11 3.2 Step by step guide to Disability Advocacy Standards certification Step 1: Start the process early The first step in preparing for the audit process is to gather and review background information about your disability advocacy agency. This may include information about its structure, the models of advocacy used and any documented policies and procedures. Your disability advocacy agency will also need to consider its contractual requirements – including the advocacy models and target group which form part of the FaHCSIA funding agreement. This helps you assess exactly what you will need to consider for your certification audit. This scoping exercise is a preliminary process before the more detailed self-assessment your disability advocacy agency will need to undertake later as part of your preparation – see Step 4. It is highly recommended that disability advocacy agencies start this process as soon as possible. Disability advocacy agencies need to think carefully about the deadline for certification, which is 7 November 2013, and work back from this date in planning for the audit. Although three months is allowed to correct any identified major nonconformities, and six months for nonconformities, they must be closed out before 7 November 2013 – irrespective of when the audit was conducted. Also, there may be issues around the availability of Certification Bodies for assessment in ‘peak’ times close to the deadline, so getting the process happening earlier is a wise move. For these reasons, and in order to allow the maximum time to address any major/nonconformities identified, the audit should be conducted before the second half of 2013. FaHCSIA will encourage disability advocacy agencies that have ratings of nonconformity in the Self-assessment completed in February 2012, to nominate for an audit soon after the implementation of the QA system in July 2012. This will ensure that those agencies that may require additional support to achieve certification will have a longer period of time to access that support and make the necessary improvements to their systems and operations to meet the 7 November 2013 deadline. 12 Step 1: Checklist Check that you have considered: Is our disability advocacy agency familiar with the Disability Advocacy Standards, KPIs and relevant examples of evidence? What are the contractual responsibilities in our Funding Agreement/Contract? Who will be involved in our audit process? Consider: Management and staff People with disability Family members/carers/interpreters/others Board members and management Community members External stakeholders How will we arrange and actively encourage the involvement of people with disability? Do we have documented policies and procedures? Where are they? When were they last updated? How do they reflect all of the Disability Advocacy Standards? Does our disability advocacy agency operate any other QA systems? Could these systems contribute any evidence for our certification audits? Have we spoken to our FaHCSIA Contract Manager to discuss the process? Have we thought through the timeframe for certification, and when we would need to get started to ensure compliance before the deadline? HINTS: Reviewing policies, procedures and documentation: Develop a matrix to match your disability advocacy agency’s policies against the Disability Advocacy Standards; Link/hyperlink policies and procedures to the Standards; Use this as an opportunity to provide training in quality management for advocacy staff.3 Step 2: Choose your Certification Body When choosing a Certification Body, remember that you will be working together into the future, usually for at least three years. It is a good idea to 'shop around' until you find a Certification Body that can work well with your disability advocacy agency. 3 Final Report, Evaluation of the Trial of the NDAP QA System, December 2010 p. 31 13 HINTS: Selecting a Certification Body Consider: The scope of QA services provided by the Certification Body i.e. ensure that the Certification Body has been accredited by JAS-ANZ to undertake certification assessments of disability advocacy agencies; The experience the Certification Body has in assessment of disability advocacy agencies, disability services, and its understanding of disability advocacy; The experience of their audit team, particularly in working with people with disability, for example, their strategies and approaches to communicating with people with disability; The gender composition of the audit team – sometimes a mix of male/female auditor/CTE may be appropriate to consider the specific needs of people with disability; Speaking to other disability agencies/services which the Certification Body has assessed; Asking to meet the audit team, including the CTE (Note: auditors typically only get two days per month in the office, and are auditing the rest of the time, so this may take time to arrange); Putting the same effort into contracting your Certification Body, as if you were recruiting a member of your management team; The cost of the Certification Body's services – you should compare the quotes from at least two Certification Bodies; Whether the Certification Body conducts audits for other disability advocacy agencies/organisations in your area and could organise for sharing of travel/accommodation costs by co- scheduling of audits (of particular relevance for agencies in remote or rural locations); If you are already audited to another set of Standards by a JAS-ANZ accredited Certification Body (e.g. Queensland Disability Standards, Employment Standards, ISO 9001), whether the audits could be combined to minimise audit duplication, as well as cost; The consistency of the audit team throughout the audit cycle, and how the Certification Body can review and change the team if your agency has problems/issues with a team member(s); The availability of the Certification Bodies for conducting audits, and the lead time you would need to provide them with to ensure that they are available for conducting your audit at a suitable time. To find a Certification Body, you can use the register provided on the JAS-ANZ website. In the ‘Program’ field select ‘Product Certification’, and then select ‘National Disability Advocacy Program’ from the ‘Scheme’ drop down options. 14 Step 2: Checklist Check that you have considered: Is the Certification Body formally accredited by JAS-ANZ to assess services against the Disability Advocacy Standards? JAS-ANZ can confirm accreditation status. Is the Certification Body experienced at auditing disability advocacy agencies similar to ours? Can it provide references? Is it possible to meet with the audit team prior to the audit (may not be feasible in rural and remote areas)? The extent to which the Certification Body will avoid audit duplication where a disability advocacy agency holds a current accredited certification to service standards containing common or significantly similar criteria. Can the audit team provide examples of past (de-identified) audit reports? Are these reports of good quality? What approaches does the Certification Body have to engaging people with disability in the audit process? What is the likely composition of the audit team, and will this be consistent throughout the audit cycle? How does the quote from the Certification Body compare to other Certification Bodies? Remember to compare ‘apples with apples’ and double check what the quote includes/excludes. Step 3: Notify FaHCSIA As soon as you have engaged a Certification Body to conduct your quality assurance certification audit you need to provide the details to your FaHCSIA Contract Manager. This should include the name of the Certification Body and, if scheduled, the dates of the Stage 1 and Stage 2 audits. Contact details for FaHCSIA appear in Section 7. Step 3: Checklist Check that you have considered: Have we provided FaHCSIA with details of our Certification Body and, if scheduled, the dates of the Stage 1 and Stage 2 audit? Step 4: Conduct your self-assessment Self-assessment is the opportunity for your disability advocacy agency to identify how it is currently travelling in relation to the Disability Advocacy Standards. Self-assessment involves the review of your policies, procedures and system documentation to confirm compliance with the Disability Advocacy Standards. Certification Bodies will require you to submit a copy of: Your latest self-assessment; Your documented policies and procedures relating to your management system; 15 Your current funding agreement with FaHCSIA, and details of the models of advocacy delivered and location(s) of the disability advocacy agencies. The Certification Body will use this information to decide whether to proceed with a certification audit. This is why it is important that you conduct a selfassessment in plenty of time before the official certification assessment is scheduled. This will give you time to address any major issues identified by the Certification Body prior to the audit. The self-assessment process identifies areas of practice that are currently working well and meeting the Standards, and thought can be given to how to maintain and improve these systems and processes to ensure an ongoing level of quality in advocacy support. Self-assessment is an initial analysis (or snapshot) of quality in your agency. The results of your self- assessment should lead to an improvement process which is assessed over the three year cycle. Self-assessment should be conducted annually in the lead up to the external annual surveillance or three yearly reassessment audits. Involving stakeholders The self-assessment process provides an excellent opportunity to involve people at all levels of your disability advocacy agency. Promoting high levels of participation in the self-assessment process will increase the long term sustainability of your quality system, as more people within your disability advocacy agency develop an understanding and ownership of not only the process but the outcomes of the process as well. This Toolkit contains some resources and tools that can help you with conducting self-assessments including: Disability Advocacy Standards, KPIs and examples of evidence (see Section 4) Self-assessment worksheets against each Standard (see Section 4) Continuous improvement resources that your disability advocacy agency can use for each Standard as part of ongoing improvement actions (see Section 5) Step 4: Checklist Check that you have considered Have we involved the governing board, staff, management, people with disability and other key stakeholders in the self-assessment process (see next section)? Have we allowed enough time before the certification assessment is scheduled, so that there is time to address any gaps? Have we developed and communicated a strategy to key stakeholders about how the self-assessment will take place? Have we taken action to address gaps identified by the selfassessment process using some of the continuous improvement 16 Check that you have considered resources in Section 5? Do we have the self-assessment materials ready to show the audit team? HINT: How to involve people with disability in the self-assessment process Although the involvement of people with disability in the self- assessment process is not mandatory, it is highly recommended and will provide valuable feedback. There are various ways you can involve people with disability in the self- assessment process. These could include: Feedback forms or questionnaires Telephone interviews Face-to-face or group interviews Use of ‘Skype’ technology A suggestion box Focus groups Remember that the purpose is to find out about people’s perceptions of the disability advocacy agency in relation to the Standards and KPIs. A range of Easy Read and Standard Read NDAP QA information for people with disability which will be useful resources are available on the FaHCSIA website. To encourage people with disability to participate in the assessment processes consider: Explaining to them why their contribution is important and how it will have an effect on your disability advocacy agency’s operations; Integrating feedback gathering for a self-assessment into other activities your agency currently does; Linking the internal feedback to an event such as an afternoon tea to show appreciation of the contribution people with disability make; Keeping the costs of participation down by: o utilising some written surveys and reply paid envelopes as part of the feedback process; and/or o arranging meetings at venues on good public transport routes; Including independent support people or advocates. The experience of previous certification assessments involving people with disability suggests that face to face feedback usually provides more valuable feedback than written surveys. Involving people with disability in the self-assessment process makes sense on a number of levels, and in particular demonstrates to a Certification Body how your disability advocacy agency puts into practice Standard 3 (Decision making and choice). 17 Step 5: Prepare for your certification audit Once the self- assessment has been completed your disability advocacy agency will need to forward the required documentation to the chosen Certification Body. The audit is then conducted in 2 stages (Stage 1 and Stage 2). At the Stage 1 audit the Certification Body: Reviews your system documentation (policies, procedures, perhaps samples some records); Reviews your self- assessment results and decides if your disability advocacy agency is ready for the Stage 2 audit. Note: Conducting the selfassessment early in the process provides time for your disability advocacy agency to address any major issues prior to the audit; Confirms staff numbers, consumer numbers, types of advocacy models provided, other logistical needs; Discusses consumer participation methods for the Stage 2 audit (e.g. what is going to work for your disability advocacy agency, how will consumers be selected, what interview methods will work best for your consumer group etc.); Plans the Stage 2 audit (e.g. determining/confirming dates, developing a draft plan). This is also an opportunity to advise the Certification Body of any other set of Standards that your disability advocacy agency has already been certified against by a JAS-ANZ accredited Certification Body, for example ISO 9001, or State Government Disability Services Certification Schemes. In these cases the Certification Body will consider the extent of demonstrated conformances for any common criteria, and may co-schedule audit activities for multiple certifications, to avoid audit duplication. To reduce travel costs, the Stage 1 audit may be conducted remotely. Normally the Stage 1 audit is conducted on site. Once the Certification Body has assessed that your disability advocacy agency is ready to participate in the Stage 2 audit, they will: Prepare an assessment/audit plan; Advise details of the audit team to the disability advocacy agency; Make plans for consultation with people with disability as early as possible. The Certification Body’s CTE will have discussions with your disability advocacy agency about the support needs and sensitivities of selected people with disability; Advise how the different models will be audited (if more than one advocacy model is provided); Advise how any other JAS-ANZ accredited certification held by your disability advocacy agency will be used to avoid duplication. 18 At this stage, your disability advocacy agency will: Liaise with the Certification Body about audit activities; Schedule meetings and activities; Prepare any necessary further material for the audit; Prepare people with disability for involvement in the audit, and plan for providing a list of willing participants to the Certification Body; Advise the Certification Body audit team in advance of specific consumer issues (e.g. behavioural) that they need to be aware of. Remember that what is normal for disability advocacy agency staff may not necessarily be normal for the auditor or CTE. For example, if the consumer wants to greet the audit team with a hug, then it is useful for the audit team to be forewarned about this. It is also useful for the audit team to know of ‘signs’ that may indicate an interview should be concluded (e.g. fidgeting, or other personal behaviours that indicate the consumer is ready to leave, or may be getting upset). Key things to know about preparing for the certification audit How are different advocacy models included in the audit? Where a disability advocacy agency provides multiple advocacy models, the Certification Body is required to assess every advocacy model, and to sample people with disability and/or key stakeholders from every advocacy model. JASANZ Procedure 29 requires that the time spent auditing the different advocacy models, and therefore the number of people with disability/stakeholders sampled per model, is proportional to the level of funding provided for each model. How will people with disability and other key stakeholders be involved in the certification audit? JAS-ANZ Procedure 29 requires that ‘consumer’ feedback is a key element of the audit process. For individual advocacy this means people with disability who have received individual advocacy support within the last three months from the individual disability advocacy agency being audited. In the case of family advocacy, ‘consumers’ to be involved and interviewed should include parents and/or family members. For citizen advocacy, the citizen advocate is also considered a ‘consumer’. For systemic advocacy this means people with disability who are associated with the systemic advocacy work of the agency through stakeholder committees and groups. Where such ‘consumers’ are not available, other external stakeholders connected with the advocacy work will be sampled, including nongovernment, and government agencies. The Certification Body will also sample whatever documents or records are available to cross-check information gathered in interviews with external stakeholders. Certification Bodies shall ensure that wherever possible, people with disability have been offered the opportunity to participate in the audit process. It is not usually practicable for all consumers to provide direct feedback, and this is why a sampling approach is used. 19 How does consumer sampling work? The strategy for sampling people with disability should be developed by the disability advocacy agency, and negotiated with the Certification Body, taking into account the needs of the consumer group. Consideration should be given to the individual context of each advocacy agency, for example, a disability advocacy agency with a small number of people with disability would not need an extensive consultation mechanism around sampling. Ideally the disability advocacy agency needs to contact people with disability in advance about the audit process, and ask who may be interested in providing feedback to the audit team. The disability advocacy agency then provides a list of willing participants to the Certification Body, which in turn selects the sample of people with disability to be interviewed. The Certification Body aims to select a sample that represents the demographics of the advocacy agency consumers. These include: Disability type; Gender; Age; Cultural or language differences; Complexity and variety of advocacy issues; Length of tenure with the agency (including those exited). Only those people with disability who have received advocacy support of an ongoing nature should be included in the consumer group. Those who have received information of a one-off nature only from the disability advocacy agency (e.g. phone calls or requests for information) are not considered to have received ‘ongoing’ support. Consumer file sampling will aim to cross check information gathered from people with disability selected in the sample, and to confirm outcomes for those people with disability. JAS-ANZ Procedure 29 requires that the minimum number of consumers to be sampled for an audit of a disability advocacy agency for initial and recertification audits is: The square root of the number of consumers receiving advocacy support over the last three months. The minimum number of consumers to be sampled for an audit of a disability advocacy agency for surveillance audits is: 0.6 times the square root of the number of consumers receiving advocacy support over the last three months. How should communication with consumers take place during the audit? The Certification Body should maintain a flexible approach to consumer involvement methods, ensuring that priority is given to methods involving direct 20 communication where possible. JAS-ANZ Procedure 29 provides examples of the types of methods which could be used, e.g. face-to-face interview, focus groups, telephone survey, mail survey. However it is important to negotiate what will work best for your consumer group with the Certification Body when planning the audit. Based on the findings of the trial of the NDAP QA process, the following methods are suggested as useful options: Before each interview, providing the audit team with background information on the person they will be speaking to; Using a specialist independent support person known to many of the consumers to facilitate a group meeting; Allowing a minimum of 1.5 hours for conducting the group interviews; Using Skype technology to conduct audit interviews with advocacy consumers living in remote locations; Conducting consumer workshops before the audit to raise awareness of the Standards; Considering the cultural needs of consumers, for example female Indigenous consumers may not be comfortable being interviewed by a male CTE; Spending unstructured time observing, listening and having informal conversations with protégés (citizen advocacy); Reading events and outcomes of protégé-advocate relationships in files (citizen advocacy); Using consumer feedback forms that may be completed during the year; Providing a range of meeting/appointment times; Meeting with people in a place of their choosing. Step 5: Checklist Check that you have considered: Have we collated our disability advocacy agency’s policies, procedures and self-assessment documents, and forwarded these to the Certification Body? Have we provided general information to the Certification Body about our consumers and the disability advocacy models we deliver? Note: All advocacy models provided by your disability advocacy agency will be assessed during the audit process and a sample of your sites. JAS-ANZ Procedure 29 provides further guidance on this. Have we taken action to address any issues identified by the Certification Body in the Stage 1 audit? Have we liaised with our Certification Body to discuss how the certification audit will proceed including the details to be covered by the audit, such as the: Sample of people with disability that they require? Inclusion of all advocacy models provided? Inclusion of all demographics (e.g. age, disability type, 21 Check that you have considered: gender, cultural or language differences, complexity and variety of advocacy issues, length of tenure with our disability advocacy agency)? Consideration, where appropriate, of any other JAS-ANZ accredited certification our disability advocacy agency already has? Have we invited people with disability to participate in the audit? In turn the Certification Body will select from a list of willing participants (see the following Hints regarding how you can encourage and support people with disability to participate, plus Easy Read and Standard Read NDAP QA information for people with disability). The Certification Body will negotiate the proposed sample numbers and sampling approach, including methods of communication and sampling methods (face-to-face interviews, focus groups, telephone survey, mail survey, visits) with the advocacy agency during this planning phase. Note: JAS-ANZ Procedure 29 specifies the process and formula for determining consumer sample size. Have we arranged consent forms and consent for access to files for participating consumers (for models of advocacy where the person with disability or a member of their family is a consumer of the disability advocacy agency) plus citizen advocates (in the case of citizen advocacy)? See Attachment 2 for a sample consent form. Have we organised appropriate support for participating consumers? Have we coordinated audit activities in line with our Certification Body's requirements, including: • Preparing the formal entry and exit meetings (e.g. arranging a room and alerting attendees); • Scheduling interviews with staff, management, governing body, people with disability, external stakeholders. HINT: How to encourage people with disability and other disability advocacy agency consumers to participate in certification audits In certification audits, the Certification Body should aim to have a flexible approach to consumer involvement methods, ensuring that priority is given to methods using direct communication. Your disability advocacy agency is responsible for ensuring that people with disability, and any other agency consumers, are able to provide feedback and be involved in the audit. Depending on the nature of the advocacy your agency undertakes, they may or may not be direct consumers. Feedback obtained from consultation with people with disability and other agency consumers should be related to the systems and processes your disability advocacy agency has in place to meet the Disability Advocacy Standards, and what can be done to maintain and/or improve these. Broader 22 feedback may also be used to develop and improve opportunities for people with disability to participate in the activities of your agency. Consultation is not intended to provide general feedback or personalised complaints – although where this occurs, your agency will need to address the concern. Considering the needs of people with disability In involving people with disability and other disability advocacy agency consumers in the audit process, your agency will need to consider: The needs of people with disability and other agency consumers The necessary supports required The time required How to consult with people with disability and other agency consumers in planning the approach How to ensure feedback on the specific Standards and KPIs How to protect the confidentiality of those involved How to document and report findings How to take action for improvement based on findings How to provide feedback to people with disability and other agency consumers on the findings and actions your agency has undertaken Communication needs To engage people with disability in the audit process your disability advocacy agency will need to consider whether, or what specific, communication assistance may be needed to enable their full participation. Your agency will need to make the information used easy to understand, for example, providing information about the NDAP QA process for people with disability in Easy Read and/or Standard Read format. It may mean involving a family member or carer to support the person with disability, or where this is not possible or appropriate, involving an independent support person. Interpreters might be needed for oneon-one or group interviews. Level of participation The level of participation of people with disability will vary according to a range of factors, such as their disability type, their level of interest, their relationship to your disability advocacy agency, and the processes your agency chooses to use. People with disability may be actively involved in all aspects of the process. Your agency might consult with them to obtain feedback and keep them informed of the process and how their feedback has been used, or where the person/ people with disability have a limited capacity to contribute feedback, they may be supported by a family member/ carer/ advocate. Your agency will need to tailor methods of involving consumers to meet different needs. Confidentiality To ensure participants’ confidentiality, your disability advocacy agency should aim to get their informed consent, where possible. Where this is not possible, an 23 independent support person should be involved to determine the capacity of the person to provide consent and to support an appropriate level of involvement by the person. It is preferable to obtain consent in writing. Building trust In arranging consultation mechanisms, it is important to keep in mind that this is not a one-off activity, but a recurring process. Trust will build over time, and by informing people how their feedback is used and demonstrating the effects on agency practice, your disability advocacy agency will be demonstrating that feedback is valued and useful. Where a person/ people with disability are reluctant to participate, your agency should respect this, but inform them that their role is important to the process. Preparing people with disability In certification audits, the Certification Body aims for direct communication where possible with people with disability. To ensure that this happens, your disability advocacy agency will need to prepare individuals to participate where possible. It is important for people with disability to understand that the audit is not a check or ‘test’ of them, but is a way of checking how your agency is providing advocacy support. The Easy Read and Standard Read NDAP QA information available on the FaHCSIA website are useful resources for preparing consumers for the audit. Key questions for this stage In planning, consider the following questions: What is your disability advocacy agency hoping to achieve from consultation with people with disability? How do people with disability want to participate and provide feedback? What consultation strategies will suit the people with disability who will be involved? Who does your disability advocacy agency need to include? What processes for participation does your agency already use, and can they be used in the audit process? Who else will need to be involved? (e.g. family members/ carers, advocates, facilitators, interpreters) What resources will be needed? What time is best to hold the consultations? Is it necessary to provide an option for anonymous feedback? What tools are needed for the consultation? (e.g. a survey, a meeting agenda) What support is needed for people with disability to fully participate? What information do people with disability need to participate? 24 How will your disability advocacy agency record and use the feedback, and then inform people with disability of the outcomes? Step 6: Participate in your certification audit Who conducts certification audits? Audits are conducted by a team nominated by the Certification Body, which always includes an Auditor and a Consumer Technical Expert. Lead Auditor - a person who has knowledge of disability advocacy and quality management practices and skills in collecting and analysing data, as well as leadership experience. They are responsible for organising and directing the activities of the audit team, as well as participating in general auditing activities. Auditor - a person who has knowledge of disability advocacy and quality management practices, and skills in collecting and analysing data. Auditors collect and analyse evidence from a range of sources and have input into audit ratings. Consumer Technical Expert (CTE) - a person with disability, engaged for his/her specialist knowledge and abilities (e.g. empathy with the life experience of people with disability) and ability to plan and facilitate the effective input of people with disability in an audit process. They must themselves have been a service recipient of a State or Commonwealth funded disability organisation in Australia. Witness auditors - additional auditors may participate in your audit. Called witness auditors, they are appointed by JAS-ANZ and are there to observe how your Certification Body conducts the audit. Witness auditors are part of JAS-ANZ's system for ensuring that organisations receive a quality certification audit. Certification Bodies also use witness audits or ‘verifications’ as part of their training and ongoing auditor monitoring programs where another auditor will come along to ‘verify’ that the audit team is competent and following the right processes and procedures. What does a certification audit involve? Certification audits involve a range of activities designed to collect evidence to demonstrate that a disability advocacy agency is complying with the Disability Advocacy Standards and KPIs. These include interviewing the governing body, agency management, staff, people with disability and other agency consumers, and reviewing files. It may also include observing the environment/physical layout, as well as interactions between staff/management/people with disability. The time needed for the on-site assessment will vary depending on your agency size, number/type of models, and the communication abilities and support needs of people with disability. JAS-ANZ Procedure 29 provides guidance on audit duration. 25 The Stage 2 audit (on-site assessment) will typically include: A formal entry meeting - when the audit team must formally explain the scope and objectives of the audit, the timetable and planned audit activities, as well as allow adequate time for your questions. Evidence gathering - most of which involves observations, sighting documents, forms, and records and conducting interviews with the governing body, management and staff. When gathering evidence, many auditors work on the basis of “Show me”. A specific component of the evidence gathering involves consultation with people with disability and other agency consumers. Certification Bodies are required to have developed a consultation plan for people with disability before the on-site assessment, and to communicate with you about sample size, selection and consultation methods. An audit review meeting - when the audit team discusses findings and develops its assessment decisions. Most audit teams work on the principle of “no surprises” so the agency is kept informed throughout the audit of any compliance issues. The audit team will assess each agency as either compliant or noncompliant with the Disability Advocacy Standards. The assessment is based on the ratings scale in JAS-ANZ Procedure 29 and outlined next in Step 7. The audit team will explain the process if there are nonconformities, including how to close these out, and the specific timeframes which must be met. Remember that a nonconformity is not a failure – it just means that it will take more time for your disability advocacy agency to become certified. A formal exit meeting - when the audit team presents its findings, including compliance with each of the 10 Disability Advocacy Standards and 25 KPIs. If a disability advocacy agency has any questions about the audit team’s assessment of their agency, they should take this opportunity to ask questions. If the agency feels they have been unfairly assessed, they are able to make an appeal. See Section 6 of this Toolkit for further information. Step 6: Checklist Check that you have considered: Have we prepared the venue for the formal entry meeting and ensured that it is an empowering environment for all individuals present? Have we taken the opportunity to ask any questions we need to about the audit process at the formal entry meeting? Have we assisted our Certification Body to gather evidence and observe activities? Have we ensured that staff and people with disability and other agency consumers, Board/management members are present for scheduled interviews or feedback sessions? Have we prepared the venue for the formal exit meeting and ensured 26 Check that you have considered: that it is an empowering environment for all individuals present? Have we taken the opportunity to comment on the findings of the audit team at the formal exit meeting? Step 7: Audit team assessment report and follow up After your certification audit, you will receive a draft audit report from the Certification Body within 10 working days of completing the on-site audit for a single site agency (or 20 working days for multiple site agencies). Audit Reports You will receive a draft report from your Certification Body with ratings against each Standard and KPI, based on the following rating system: Major nonconformity (you have three months to correct) Nonconformity (you have six months to correct) Conformity The KPI with the lowest rating under each Standard determines the overall rating for each Standard. If your disability advocacy agency delivers more than one model of advocacy support, you will receive one overall report, with one overall rating provided for each KPI. If your agency has a number of outlets, the organisation as a whole will be assessed, outlets sampled, and one overall report provided. The report will identify nonconformities at on-site audit completion even if your agency has addressed nonconformities before the report is finalised. JAS-ANZ Procedure 29 provides details of what will be included in audit reports. Reports may also include 'observations' which could include positive feedback or notes about opportunities for improvement. Such observations do not prevent certification but you should carefully consider them, to make sure that the issue does not create a nonconformity in the future. Your agency has 10 working days from receiving the draft written report in which to provide a response to the Certification Body. The Certification Body will consider any responses provided by your disability advocacy agency, and the final certification decision is made by Certification Body personnel not involved in the actual audit itself. The final audit report is then provided to FaHCSIA and your agency within a further seven working days. Step 7: Checklist Check that you have considered: Have we provided feedback from the draft report to people with disability and other relevant stakeholders, staff/management, and the 27 Check that you have considered: governing body? Have we provided responses back to the Certification Body within 10 working days? If you have received a 0 - major nonconformity rating: Have we sent a corrective action plan to the Certification Body within five working days? Have we taken corrective action within three months? Have we participated in a follow-up visit by our Certification Body to assess the corrective action within three months? If your Certification Body thinks that corrective action has been partly successful, the 0 rating may be upgraded to a 1. This will give you an additional three months to correct the nonconformity. If you have received a 1 - nonconformity rating: Have we taken corrective action within six months? Has our Certification Body verified the corrective action we have taken within six months? HINT: Achieving certification Your disability advocacy agency cannot be granted certification until all major nonconformities and nonconformities have been corrected, and that correction has been verified by the Certification Body. It is advisable for all disability advocacy agencies to plan their certification activity early within the transition period, so that audits can be organised and booked in advance, and there is sufficient time to correct any nonconformities or major nonconformities. Step 8: Start three year audit cycle Once your disability advocacy agency has achieved certification, you begin a three year audit cycle involving annual self-assessments, surveillance audits and recertification audits. Internal audits are also a very practical tool to utilise each year as part of continuous improvement activity (see Section 5 for further information about internal audits). Self-Assessment The self-assessment should take place annually as per the suggestions in Step 4. The self-assessment will provide valuable information about areas for improvement which can be addressed in the lead up to the surveillance and recertification audits. Surveillance and recertification audits Surveillance audits happen once a year to check that your disability advocacy agency continues to comply with the Disability Advocacy Standards. The first surveillance audit must take place within 12 months from the date of the last 28 day of the on-site certification audit. The second surveillance audit must take place within 13 months from the last day of the first surveillance audit. Disability advocacy agencies should plan for and book in their surveillance audit at least two months prior to the deadline. Surveillance audits typically cover: 1. Interviews with relevant management and a sample of consumers; 2. An assessment of Standards 2, 7, 8, and 10 and other selected Standards; 3. Your procedures for periodically evaluating and reviewing your compliance with relevant legislation and regulations; 4. Progress of planned activities aimed at continuous improvement; and 5. Follow-up action taken on nonconformities identified during the last audit. Recertification audits happen every three years. The first recertification audit must be undertaken within three years of the issue of the certificate of compliance. The purpose is to verify the continuing overall effectiveness of your disability advocacy agency and to examine the commitment and actions towards continuous improvement. Recertification audits review past performance over the three year certification period. Recertification audits generally take as long as, and involve a similar level of consultation with people with disability and other key stakeholders, as the initial certification audit. Step 8: Audit cycle checklist During the first year after certification: Have we ensured that there are methods in place to continuously improve against the Disability Advocacy Standards? Have we undertaken a self-assessment prior to the surveillance audit? Have we made arrangements for our surveillance audit, has it been conducted and have we checked the areas for improvement or action items and included them on our improvement plan? During the second year after certification: Have we undertaken a self-assessment prior to the surveillance audit? Have we ensured that we have methods in place (e.g. internal audits) to continuously improve against the Disability Advocacy Standards? Have we made arrangements for our surveillance audit, has it been conducted and have we checked the areas for improvement or action items and included them on our improvement plan? .During the third year after certification: Have we undertaken a self-assessment prior to the recertification audit? Have we ensured that we have methods in place (e.g. internal audits) to continuously improve against the Disability Advocacy Standards? Have we re-negotiated our contract with our current Certification Body or negotiated a contract with a new Certification Body with sufficient time to ensure the audit takes place before the end of the third year? Refer to Step 2 for what to consider in choosing a Certification Body. Additional considerations include: How professionally, fairly and efficiently you feel the audit team conducted certification and surveillance audits in the last cycle 29 During the first year after certification: Quality and quantity of feedback provided at audits Quality of the audit report. Have we prepared for our recertification audit? Checklist for your consideration: Where is our last audit report? What comments did the audit team make? Are there any priority issues we can identify for this audit cycle? What did we learn from the last audit cycle? What strategies could we use to overcome barriers we identified? Has our disability advocacy agency substantially changed since our last audit cycle (e.g. staff or structural changes)? How will this impact our agency’s performance against the Disability Advocacy Standards? 30 3.3 Summary of the step by step guide to Disability Advocacy Standards certification This is an overall summary of the steps involved, timeframes and actions required for achieving initial certification and entering into the three year audit cycle. Step Milestones/Notes 1. Start the process Pre-audit 2. Select a Certification Body 3. Notify FaHCSIA 4. Conduct selfassessment 5. Prepare for certification audit/Stage 1 audit Review your disability advocacy agency’s structure and documented policies and procedures Consider who will be involved in the audit – staff, management, people with disability, board members, other stakeholders Become familiar with the tools available in this Toolkit Consider how your disability advocacy agency will arrange and encourage consumer participation Choose an accredited Certification Body that best suits your disability advocacy agency Negotiate your contract with the Certification Body Advise FaHCSIA of your chosen Certification Body Conduct an assessment of your disability advocacy agency’s performance against the Standards and KPIs Identify any gaps your agency will need to work on before the audit Take action to address gaps identified by the self-assessment process Submit materials relating to selfassessment, including policies and procedures relevant to the Standards, to the Certification Body prior to the official audit Liaise with your Certification Body to discuss the audit plan Provide general information to your Certification Body about consumers etc. Actively encourage consumers to be involved in the audit Your certification body reviews your disability advocacy agency’s documentation (Stage 1) and decides if they are ready for the audit Your certification body will nominate an audit team and prepare an audit plan 31 Step Milestones/Notes 3 yearly cycle Assessment and Decision 6. Participate in certification audit/Stage 2 audit 7. Audit team assessment report and follow up 8. Start three year cycle a)Prepare for first surveillance audit b) Prepare for second surveillance audit c) Re-negotiate contract with Certification Body d)Prepare for recertification audit Liaise with your Certification Body about preparations, in particular strategies for consumer consultation An audit team from the Certification Body will visit your disability advocacy agency on site Your agency will be expected to help organise audit activities Assist your Certification Body to gather evidence and observe activities The audit team prepares a draft audit report including an assessment of your disability advocacy agency’s compliance and provides verbal feedback Your agency takes the opportunity to comment on the findings of audit team Your agency receives the draft report and provides response The audit team finalises the report and provides a copy to your agency and FaHCSIA Certification Body personnel independent of the audit team reviews the audit report and makes a decision regarding certification A certificate of compliance is issued to your agency by your Certification Body who provide a copy to FaHCSIA NB: All nonconformities need to be addressed before a certificate of compliance can be issued Ongoing continuous improvement and corrective action Review your Certification Body’s cost and quality of work Document continuous improvement 32 3.4 Comprehensive step by step guide to Disability Advocacy Standards certification This is a more comprehensive guide for steps involved in the certification process. Step 1 – Start the process Date Notes Has your disability advocacy agency collated the documentation that describes the advocacy work of your agency? What model/s of advocacy does the agency undertake? Has your disability advocacy agency collated policies and procedures Does your agency have written policies and procedures? Where are they and when were they last updated? Do they reflect all of the Disability Advocacy Standards? Collate documentation for other quality systems Does your organisation operate any other quality systems? Could these systems contribute any evidence for the NDAP certification audits and avoid audit duplication? Has your disability advocacy agency developed a plan for involving all relevant stakeholders? Who should be involved in the audit process? Regardless of whether people with disability are consumers of your agency, they will need to be involved in the audit process. Your disability advocacy agency will need to consider involving: staff/ volunteers people with disability/consumers family members/carers Board members and management. Step 2 – Select a Certification Body Date Notes Has your disability advocacy agency investigated the options What requirements are important to your agency in selecting a Certification Body? Is the Certification Body experienced in auditing similar agencies? Can they provide references? What are the costs of the Certification Body? Has your disability advocacy agency submitted an application form to the chosen Certification Body, following any requirements they have outlined. Has your agency negotiated a contract with a Certification Body? 33 Step 3 – Notify FaHCSIA Date Note Step 4 – Conduct a self-assessment Date Notes Has your disability advocacy agency completed the following steps? Has your agency involved consumers and people with disability and stakeholders (where people with disability are not the consumers of the agency, they will still need to be involved)? Has your agency conducted a self-assessment against the Disability Advocacy Standards? Has your agency taken action to address gaps identified by the self-assessment process? Has your agency documented self-assessment findings? Step 5 – Prepare for the certification audit Date Notes Notify FaHCSIA of your chosen Certification Body Has your disability advocacy agency completed the following steps? Has your agency collated the agency’s policies and procedures and self-assessment findings? Has your agency sent the relevant documents to your Certification Body? Has your agency provided general information to your Certification Body about the consumers and the model/s of advocacy undertaken? If the Certification Body identified any issues in their Stage 1 Audit, has your agency taken action to address these? Has your agency liaised with your Certification Body to discuss how the certification audit will proceed, for example, the sample of consumers or people with disability who will need to be involved in the audit and how your agency will include representatives of all demographics (e.g. gender, age, cultural, or language differences, complexity of support needs including communication, and length of tenure with the agency, including those exited)? NOTE: If your agency offers more than one model of advocacy or operates from more than one site, the sample will include representation from each model of advocacy and each site selected by the Certification Body for the audit. JAS-ANZ Procedure 29 provides further details about this sampling Has your agency prepared the sample of consumers and/or people with disability to provide feedback and organised support, where necessary? Has your agency actively encouraged consumers and 34 people with disability to participate and arranged their involvement and organised support, where necessary? Has your agency arranged consent forms and consent for access to files of participating consumers (for models of advocacy where the person with disability or a member of their family is a consumer of the advocacy agency)? See Attachment 2 for a sample consent form. Has your agency prepared for audit activities in line with your Certification Body’s requirements, including: preparation for the formal entry and exit meeting e.g. schedule, arrange a room and alert attendees? organised interviews with consumers and people with disability? Step 6 – Participate in the certification audit Date Notes Has your disability advocacy agency prepared the venue for the formal entry meeting and ensured that it is an empowering environment for all individuals present? Has your agency taken the opportunity to ask any questions about the audit process at the formal entry meeting? Has your agency assisted your Certification Body to gather evidence and observe activities? Has your agency ensured that staff, volunteers, consumers and people with disability are present for scheduled interviews or feedback sessions? Has your agency taken the opportunity to comment on findings of the audit team? Step 7 – Audit team assessment report and follow up Date Notes Has your disability advocacy agency prepared the venue for the formal exit meeting and ensured that it is an empowering environment for all individuals present? Has your agency taken the opportunity to comment on findings of the audit team at the formal exit meeting? Has your agency reviewed the draft report when received? Has your agency provided a response on the draft report to Certification Body? Has your agency provided feedback about the audit results to: consumers/ people with disability? staff, volunteers and management of the agency? the Board of the agency? Has your agency addressed suggested improvements Did the Certification Body suggest any improvements to your agency’s operations? How will your agency address suggestions? 35 Has your agency addressed nonconformities Did your agency receive a major nonconformity or nonconformity assessment against any of the Standards or KPIs? Does your agency feel the assessment is fair? (If not, you can lodge an appeal – please see the complaints resolution information in Section 6) If your agency is not appealing the decision, what corrective action will be taken to address the nonconformity? Did your agency gain certification? Celebrate! Step 8 – Start 3 year cycle Date Notes Has your disability advocacy agency put in place an ongoing system for continuous improvement and corrective action? 1) Has your agency prepared for and participated in the first surveillance audit: Conducted annual self-assessment? Implemented continuous improvement activities? Participated in a surveillance audit before the end of the first year? 2) Has your agency prepared for and participated in the second surveillance audit: Conducted annual self-assessment? Conducted continuous improvement activities? Participated in a surveillance audit before 13 months after the last surveillance audit? 3) Has your agency re-negotiated/negotiated a contract with a Certification Body: Considered the professionalism of the audit team during the last three years, the quality and quantity of feedback at audits, and the quality of the audit reports? 4) Has your agency prepared for and participated in a recertification audit? Check that you have considered: o Undertaking a new self-assessment; o What did we learn from the last audit cycle? o Are there any priority issues we can audit for this audit cycle? o What strategies could we use to overcome barriers we identified? o Has our organisation substantially changed since our last audit cycle? 36 Section 4: Disability Advocacy Standards, examples of evidence and self-assessment worksheets In this section, you will find the Disability Advocacy Standards with policy and program context, and examples of evidence for each Standard. This information will be essential during the self-assessment process. You will also find recommended self-assessment worksheets, which allow you to rate your own agency against each of the Disability Advocacy Standards. Disability Advocacy Standards The 10 Disability Advocacy Standards and 25 KPIs define the elements of quality advocacy support for people with disability. The Standards form the basis for QA and continuous improvement processes. To be certified, disability advocacy agencies must comply with and demonstrate continuous improvement against the Disability Advocacy Standards. A complete set of the Standards and KPIs appears in the following pages in this Section, and can be found on the ComLaw website. The Disability Advocacy Standards have the same intent across all advocacy models, but may require different kinds of evidence to demonstrate compliance and continuous improvement. Disability advocacy agencies undertaking different advocacy models will demonstrate conformity with the Disability Advocacy Standards in different ways and with different forms of evidence. Auditors are required to have a clear understanding of the different models of advocacy and what this means for demonstrating compliance and reporting requirements. Policy and program context for Disability Advocacy Standards Each Standard contains a statement about the policy and program context of the Standard for disability advocacy agencies. This statement is intended to highlight the strategic intent and key features of the Standard. Over time these statements may be updated to reflect new policy or program initiatives or changed stakeholder expectations. Where compliance with the Standard will be different depending on the approach to advocacy, this has been indicated. Examples of evidence Examples of evidence have been developed for all of the Disability Advocacy Standards and are provided in this Toolkit to assist disability advocacy agencies in preparing for the certification process. A complete set of the Standards, KPIs and examples of evidence is included in Attachment 3. The core examples of evidence are a resource that your disability advocacy agency can use to reflect on what may constitute evidence of compliance with a 37 Disability Advocacy Standard. Your agency can use this resource to help gather and develop evidence to: Use internally to assess your agency’s performance against the Disability Advocacy Standards (for example, through the self-assessment); Demonstrate to a Certification Body’s audit team what your agency is doing to meet the Disability Advocacy Standards; and Use internally to help your agency find ways to continually improve and innovate. Examples of evidence have been developed for each Standard, and the related KPIs, to guide disability advocacy agencies on the types of evidence that might be appropriate to demonstrate compliance. There are some forms of evidence that will be applicable to all models of advocacy and others specific to the model/s of advocacy undertaken. As the majority of disability advocacy agencies deliver advocacy through a range of models, they will demonstrate conformity with the Standards through the use of evidence appropriate to the various models of advocacy used. It is important to remember that the examples of evidence are not intended to be a compliance checklist. Rather they offer examples and guidance only. If you have different or additional evidence that shows how your disability advocacy agency has complied with, or continually improved against the Standards, you can present that evidence to your audit team. Think of evidence not in terms of what your agency does, but how your agency can demonstrate what it does. The strongest evidence is that which can be verified through three sources: interview, observation and documentation (sometimes referred to as ‘people, process and paper’).4 Your documentation, your staff’s understanding and compliance with it and people with disability and agency consumer’s confirmation of its application are key components for verification that your processes and systems comply with the requirements of the Disability Advocacy Standards. The focus of evidence for certification will be on practical observations (‘Show me’) of on-the-ground practices and consumer feedback that demonstrate that your disability advocacy agency has a systematic approach to meeting the Standards. Organisational checklist – evidence examples Check that you have considered: Have we become familiar with the examples of evidence for the relevant advocacy models we provide? Have we used the examples of evidence to develop material to show the audit team? Have we reviewed the examples of evidence internally to assess performance through self-assessments? Have we reviewed the examples of evidence internally to find ways to continually improve? 4 Disability Sector Quality System, Resources and Guide, Queensland Government 38 4.1 Disability Advocacy Standards, KPIs and evidence examples Standard 1: Accessing advocacy Each person with disability has opportunities to access advocacy on the basis of relative need and available resources. 1.1 The advocacy agency adopts, applies and promotes non-discriminatory policies in respect of age, gender, race, culture, religion, disability or living arrangements, consistent with the contractual obligations and purpose of the advocacy agency and the relative need and available resources. 1.2 The advocacy agency has processes to determine how the individuals or issues supported are chosen and prioritised based on relative need and available resources. 1.3 Each person with disability is informed about how decisions are made in relation to access and advocacy issues. Policy and program context This Standard covers the policies, procedures and practices used by disability advocacy agencies to ensure people with disability have opportunities to access advocacy – where an individual or group directly seek advocacy; where the agency seeks to provide opportunities for individuals and groups to access advocacy; and where the agency supports and facilitates advocacy undertaken by families, citizens or the person with disability. In terms of entry processes in relation to Standard 1, disability advocacy agencies should consider: Target group – the group of people whose needs the agency is designed or funded to meet, potentially specifying characteristics, such as age, geographical location, the type of needs which can be met, or type of disability; Eligibility criteria – the criteria for determining whether a person is part of the agency’s target group and therefore eligible for advocacy; Entry processes – the basis for deciding between applicants when there are more people wanting to access advocacy than there are vacancies available; and Exit processes. Every disability advocacy agency must be able to demonstrate that its entry processes are non-discriminatory in respect of age, gender, race, culture or disability. The agency’s eligibility criteria must not contain any restrictions on entry, other than those defined by its target group and FaHCSIA’s contractual 39 obligations. Similarly, the agency’s process for allocating priority between eligible applicants should only be based on FaHCSIA’s contractual requirements, the relative needs of applicants and its available resources. In terms of exit processes, the disability advocacy agency should consider: The circumstances in which people with disability can voluntarily leave the agency, for example, when their needs have changed; The agency’s contractual requirements in relation to exits; The circumstances in which people with disability can be required to leave the agency and the basis on which such decisions may be made, for example, when the agency can no longer meet their needs; The agency’s approach to referrals to other advocacy agencies, either when the agency does not have the capacity to accommodate a new consumer or when they can no longer meet a current consumer’s needs; What happens to personal information about a consumer when he or she leaves the agency; and Consumer involvement in decision making about the exit process in any of the above instances. Disability advocacy agencies undertaking family advocacy should outline in their purpose statement, policies and practices that the focus of the advocacy is on the person with disability. As disability advocacy agencies undertaking systemic advocacy do not undertake advocacy on an individual basis, they will need to outline and make clear in their purpose statement, policies and practices that they do not work with individual people with disability. In this context, systemic advocacy agencies should demonstrate opportunities given for people with disability to contribute to/ participate in the prioritising of processes that determine which systemic issues receive attention. Things to consider: Accessing advocacy All disability advocacy agencies We clearly communicate with people with disability, who our agency works with to promote, protect and defend the welfare of and justice for people with disability Disability advocacy agencies with individual consumers Our eligibility criteria and entry procedures are non-discriminatory, consistent with the contractual obligations and purpose of our agency Our entry procedure is documented and consistently applied by staff. Procedure specifies the catchment area/ target population of our agency and other relevant eligibility criteria We use proactive strategies to reach those who are unable or unlikely to access advocacy for various reasons 40 Exit procedure is documented and consistently applied by staff Referral policy is documented and used when the demand for advocacy is greater than our agency’s capacity, or our agency cannot meet an applicant’s needs System for determining priority of access to advocacy is documented and consistently applied. System is fair, equitable and takes account of relative need and available resources Our consumers are informed about and understand how decisions regarding access and prioritisation of resources are made Information about our agency is accessible to people with disability including those from Culturally and Linguistically Diverse (CALD) backgrounds Systemic We inform people with disability about the systemic advocacy issues our agency pursues The following table contains some examples of evidence an agency may want to use to demonstrate their compliance with Standard 1. 41 Disability Advocacy Standards, KPIs and Examples of Evidence 2012 Standard Key Performance Indicator Examples of Evidence Standard 1: Accessing advocacy 1.1 The advocacy agency adopts, applies and promotes nondiscriminatory policies in respect of age, gender, race, culture, religion, disability or living arrangements, consistent with the contractual obligations and purpose of the agency and the relative need and available resources. All agencies Purpose statement that makes it clear who the agency works with to promote, protect and defend the welfare of and justice for people with disability. Evidence of staff participation in anti-discrimination and cultural awareness training and/or evidence of links with relevant specialist agencies as appropriate, such as MOUs or participation in joint projects with multicultural or indigenous advocacy agencies. Evidence that the organisation is aware of demographic information/ABS statistics and match of this to the profile of people with disability who receive advocacy support. Documented and implemented non-discriminatory practices and policies for identifying and/or responding to requests for information, referral and/or advocacy support. Each person with disability has opportunities to access advocacy on the basis of relative need and available resources. 1.2 The advocacy agency has processes to determine how the individuals or issues supported are chosen and prioritised based on relative need and available resources. 1.3 Each person with disability is informed about how decisions are made in relation to access and advocacy issues. Agencies undertaking individual advocacy/ legal advocacy Documented and implemented entry and exit policies and procedures highlighting non-discriminatory practice, which may include ongoing access for people with disability who receive advocacy support after their issue/case is closed. Agencies undertaking systemic advocacy Documented and implemented practices and/or policies for deciding and communicating which systemic issues the agency will work on. Documented and implemented practices and policies showing how people with disabilities influence/contribute to the prioritising processes that determine which issues receive attention. Agencies undertaking citizen advocacy Annual protégé recruitment plan that reflects diversity and level of vulnerability of people with disability. Consistent practice of “seek-out” recruitment of people with a disability who need advocacy, but who would not ordinarily come to the attention of the agency if it relied solely on (self- or other-initiated) referrals. Established Advisory Support Group (e.g. Sub-Committee), which can assist in the implementation of the appropriate Protégé entry and exit policies and procedures. 42 Standard 2: Individual needs Each person with disability receives advocacy that is designed to meet their individual needs and interests. 2.1 The advocacy agency has a process for determining and documenting the advocacy objectives that reflect the wishes, needs or interests of each person with disability. 2.2 Advocacy activities are directed to meeting the advocacy objectives of each person with disability. 2.3 Each person with disability engaged in determining advocacy objectives is provided with opportunities to involve a support person of their choice. 2.4 In meeting the needs of a person with disability, the advocacy agency avoids, where possible, any conflict of interest or the perception of any conflict of interest in relation to the conduct of its advocacy work, and deals with any conflict or perceived conflict transparently. 2.5 The advocacy agency helps to empower people to advocate for themselves or their family or others with appropriate strategies (e.g. information, training, mentoring, support.) Policy and program context Disability advocacy agencies must ensure support is provided in a manner sensitive to the age, sex, and the cultural, linguistic and religious background of each person with disability. In the context of Standard 2, where applicable to the programs and activities they undertake, agencies are expected to ensure that: Advocacy objectives are established to reflect the needs of people with disability; Individual’s objectives and plans do not have any unnecessary restrictions or constraints; The social and cultural values, beliefs and practices of people with disability are respected; People with disability are adequately involved in the development and review of advocacy objectives and plans; and People are empowered to advocate for themselves or family or others. Standard 2 refers to ‘individual need’ in terms of both the needs of an individual person that may be met through individual advocacy provided to the person with disability, and the collective needs of people with disability that may be met through systemic advocacy. For those disability advocacy agencies that provide advocacy on an individual basis, people with disability are entitled to receive advocacy that is tailored to their individual needs and interests. In these cases, they should ensure people with disability have: individual advocacy objectives; and an individual advocacy plan that outlines strategies to be used. 43 In the context of systemic advocacy, where disability advocacy agencies do not have individual consumers, or develop individual advocacy plans, they should demonstrate that people with disability have been consulted prior to systemic advocacy actions being undertaken on their behalf; or, in reactive cases, that people with disability have been informed of the actions being undertaken on their behalf. Disability advocacy agencies undertaking family advocacy do not provide direct support to the individual with disability. In this context, they should demonstrate how the best interests and needs of the person with disability are determined when advocates work directly with family members of the person with disability. It is expected that self advocacy agencies will have established practices and policies for developing the capacity of people with disability to self advocate. In the case of individual and citizen advocacy, the agency may not provide specific self advocacy training, but in the course of their work with the person with disability, may empower individuals to do as much as possible for themselves, and show effective advocacy processes so they could self advocate in the future. Things to consider: Individual needs All disability advocacy agencies We ensure people with disability are actively involved in establishing advocacy objectives (on an individual or collective basis, as appropriate to the purpose of our agency) We avoid where possible, conflict of interest arising in relation to advocacy work We involve people with disability in regular reviews of advocacy activities to ensure their continued relevance (on an individual or collective basis, as appropriate to the purpose of our agency) People with disability are satisfied with the way we work with them to determine their needs People with disability are satisfied with the way we respond to their needs People with disability are informed of the advocacy activities being undertaken (on an individual or collective basis, as appropriate to the purpose of our agency) Where people with disability are the direct consumers of the disability advocacy agency We ensure that consumers understand and, where appropriate, sign-off on advocacy activities undertaken 44 We ensure that people with disability are empowered to advocate for themselves or family or others with appropriate strategies Family advocacy We consider the needs of the person with disability as the priority in planning advocacy that supports their family member The following table contains some evidence examples that an agency might consider using to show how they comply with Standard 2. 45 Disability Advocacy Standards, KPIs and Examples of Evidence 2012 Standard Standard 2: Individual needs Each person with disability receives advocacy that is designed to meet their individual needs and interests. Key Performance Indicator Examples of Evidence 2.1 The advocacy agency has a process for determining and documenting the advocacy objectives that reflect the wishes, needs or interests of each person with disability. 2.2 Advocacy activities are directed to meeting the advocacy objectives of each person with disability. 2.3 Each person with disability engaged in determining advocacy objectives is provided with opportunities to involve a support person of their choice. 2.4 In meeting the needs of a person with disability, the advocacy agency avoids, where possible, any conflict of interest or the perception of any conflict of interest in relation to the conduct of its advocacy work, and deals with any conflict or perceived conflict transparently. 2.5 The advocacy agency helps to empower people to advocate for themselves or their family or others with appropriate strategies (e.g. information, training, mentoring, support) All agencies Evidence of practice of supporting/educating people with disabilities to advocate for themselves and/or of supporting/educating families to advocate on their behalf. Examples of how the agency has taken into account the specific needs of people from Indigenous and CALD backgrounds, people with specific disabilities such as hearing impairment, people with literacy difficulties. Interpreters are provided where requested or where a need is identified. Agency promotional material that makes it clear the extent, if at all, the agency provides training and support. Documented and implemented policies and practice of responding to the information needs of people with disabilities/families and providing referrals as appropriate. Agency policy on conflict of interest. Documented and implemented practices and policies for identifying and transparently dealing with conflicts of interest that arise for the organisation, Board and staff, for example, a Conflict of Interest register maintained for staff and Boards of Management, or evidence in minutes of a standing agenda item that flags the need to declare any conflict of interest. Management, staff and volunteer training in recognising and dealing with conflicts of interest. Agencies undertaking individual advocacy/ legal advocacy Documented and implemented policies and practices for developing and implementing individual advocacy plans in partnership with people with disability and/or their families/guardians (as appropriate). Evidence of collecting and reviewing feedback about the extent to which the needs of the person with a disability are met. 46 Agencies undertaking self advocacy Observations of people with disabilities receiving support to develop advocacy action plans to address their wishes, needs or goals. Agencies undertaking systemic advocacy Documented and implemented practices and policies showing how people with disabilities influence the choice of advocacy objective. Evidence of reporting of outcomes / review of advocacy process. Evidence of advocacy plan, actions taken and people/agencies involved, or file notes detailing progress or justification for not having a plan in place. Policies and procedures to address how the agency selects and prioritises the systemic issues it addresses. Agencies undertaking citizen advocacy Documented and implemented practices and policies for developing confidential individual written profiles detailing ‘need’ and seeking advocates based on their skills in relation to these needs. Observations of individual being given opportunity to discuss their advocacy needs and advocate role. Details of completed relationships, and/or those being rematched or awaiting rematching. Documented and implemented practices and policies for reviewing the extent to which the needs of the person with a disability are being met. Practice of one-to-one (or near one-to-one) matching of people with a disability with advocates to ensure that the individual needs of the person with the disability remains the focus of the advocacy relationship. Practice of recruiting advocates whose role is strictly voluntary, thereby avoiding any conflicts of interest arising from receipt of monetary and/or inkind payments. 47 Standard 3: Decision making and choice Each person with disability has the opportunity to participate as fully as possible in making decisions about the advocacy activities undertaken. 3.1 The advocacy agency’s policies support each person with disability to direct, within the limits of their capacity or interest, the advocacy activities undertaken to meet their advocacy objectives. 3.2 In all circumstances the advocacy activity is informed by ethical guidelines. Policy and program context The intent of this Standard is to ensure that disability advocacy agencies: Ensure people with disability are supported to direct within the limits of their capacity and interest, the advocacy activities undertaken to meet their personal objectives; Provide opportunities for people with disability to make informed decisions and choices according to their individual needs; Incorporate flexible options to facilitate informed decision making; and Are informed by ethical guidelines and apply the principles of duty of care and least restrictive alternative. This Standard recognises that advocacy outcomes are best achieved where people with disability have input into the decisions and choices about the advocacy they receive. Primarily, people with disability will have input into the day-to-day decisions and choices made in relation to their advocacy planning, but input will also extend into the broader planning for the agency. This Standard recognises that some people with disability may not always make the decisions, but that they are supported to direct within the limits of their capacity and/or interest the advocacy activities undertaken. Emphasis is put on their involvement to improve the quality of decision and choices, and that people with disability are informed at all stages in the decision making process. People with disability may contribute to decision making in the following areas: Planning the advocacy they receive as an individual (e.g. individual advocacy plans); Planning the overall priorities and direction of the advocacy agency (e.g. corporate, business and advocacy planning, where appropriate); and QA and continuous improvement processes (e.g. participation in consumer consultations as part of an internal or certification audit). Within each of these areas, disability advocacy agencies are expected to: Ensure appropriate access to information about opportunities for participation of people with disability; 48 Ensure that people with disability are encouraged and supported to access these opportunities; and Act upon the outcomes of people with disability’s contribution and influence. Specifically, disability advocacy agencies are expected to: Develop suitable processes for communicating with and educating all people with disability about the audit process and the quality system; Promote and implement opportunities that support the contribution of people with disability in the consultation activities of certification assessments with particular consideration given to supporting the participation of ‘difficult to reach’ groups; and Develop suitable mechanisms for facilitating people with disability’s representation in audit preparation activities (e.g. self-assessments) and certification assessment and reporting processes. For systemic advocacy agencies, where people with disability are not the direct consumers of the agency, the agency should, where appropriate and possible, involve people with disability in decision making about the systemic advocacy actions the agency will pursue on their behalf. For family advocacy agencies, where the family member is the direct consumer of the agency rather than the person with disability, agencies should demonstrate that the person with disability has been consulted about the advocacy activities undertaken on their behalf. Things to consider – Decision making and choice All disability advocacy agencies We give consumers/ people with disability the information they need to make choices that are genuinely informed The information our agency provides to consumers/ people with disability is in accessible formats We ensure consumers/ people with disability have the opportunity to participate in decision making and choice at the management/ corporate level of our agency We support consumers/ people with disability to take on roles on Board/ management committees in our agency We ensure the choices/ preferences/ suggestions of consumers/ people with disability are taken into account at an organisational level We have systems for ensuring that the choices of consumers/ people with disability are acted upon (where reasonable) 49 We ensure that people with disability are encouraged to be involved in our agency’s QA activities In all circumstances the advocacy activity is informed by ethical guidelines Where people with disability are the direct consumers of the disability advocacy agency We obtain valid informed consent, where this is possible We ensure consumers/ people with disability have the opportunity to participate in decision making and choice at a personal/ individual level The following table contains some examples of evidence an agency may want to use to demonstrate their compliance with Standard 3. 50 Disability Advocacy Standards, KPIs and Examples of Evidence 2012 Standard Standard 3: Decision making and choice Each person with disability has the opportunity to participate as fully as possible in making decisions about the advocacy activities undertaken. KPI 3.1 3.2 Examples of Evidence The advocacy agency’s policies support each person with disability to direct, within the limits of their capacity or interest, the advocacy activities undertaken to meet their advocacy objectives. In all circumstances the advocacy activity is informed by ethical guidelines. All agencies Observations of the way advocates interact with people with disability in making decisions about advocacy activities. Evidence of the involvement of people with disability in agency decision-making (e.g. representation on the Board, participation in consultations that feed into agency’s strategic plan or lead to improve practices, involvement in surveys that inform agency policies and procedures). Evidence of the involvement of people with disability in the agency’s QA activities. Observation of information, strategies and ideas presented to people with disabilities and families in ways that they can understand. Agencies undertaking individual advocacy/legal advocacy Ethics guidelines for supporting people with disability in making decisions about advocacy activities. Procedures are established and implemented for the regular review of advocacy actions and these require review of the extent to which the agency promotes the person’s choices and decisions. Feedback is sought from people with disability on the extent to which the agency promotes choice and decision making. Documented and implemented practices and policies for determining a decision on behalf of a person who has impaired decision making capacity e.g. consultation with them, documenting factors taken into account including knowledge gathered over time. 51 Agencies undertaking citizen advocacy Evidence of induction and or training that orientates advocates to the need to support people with a disability, where appropriate, to make decisions and choices. Practice of supporting advocates to facilitate the process, where appropriate, of decisions and choices made by people with a disability. Evidence of feedback gained from people with disability about how they are supported to make their choices. Agencies undertaking systemic advocacy Documented and implemented practices and policies that demonstrates that people with disabilities influence decision making about advocacy activities. Observations of individual people with disability and/or their families becoming involved in systemic advocacy activities of their choice. Ethical guidelines inform systemic advocacy policy and practice. Agencies undertaking family advocacy Documented and implemented practices and policies for encouraging families to include the views of the person with disability in advocacy efforts where appropriate. 52 Standard 4: Privacy, dignity and confidentiality The right of each person with disability to privacy, dignity and confidentiality is recognised and respected. 4.1 The advocacy agency complies with the Information Privacy Principles of the Privacy Act 1988 in order to protect and respect the rights of each person with disability. 4.2 The advocacy agency promotes privacy, dignity and respect for each person with disability. Policy and program context In the context of Standard 4, disability advocacy agencies are expected to: Comply with the privacy principles contained within relevant legislation; Ensure that people with disability are treated with dignity and respect in all aspects of their lives; and Maintain the confidentiality of all personal information relating to people with disability. This Standard refers to the promotion of tolerance and respect for people with disability’s personal needs and circumstances. It relates not just to the disability advocacy agency’s legal and contractual obligations in the area of privacy, but more fundamentally to the values demonstrated by it in interacting and communicating with people with disability. This includes: Use of language and terminology within the agency; How staff communicate with people with disability; How staff work with people with disability (for example, where physical assistance is required, it is provided in such a way as to respect and promote the individual’s dignity, or where challenging behaviours are displayed, these are dealt with well); and How people with disability collaborate in advocacy planning and delivery (see Standard 3). In terms of legal compliance, people with disability have a right to privacy and confidentiality consistent with the Information Privacy Principles contained in the Privacy Amendment Act (Private Sector) 2000 and the Privacy Act 1988. Agencies should be familiar with the Information Privacy Principles which cover, among other things, requirements in relation to: Collection – the disability advocacy agency should only collect personal information if that information is necessary for one or more of its functions or activities. It must take reasonable steps to ensure that the individual is aware of the fact that he or she is able to gain access to the information and the purposes for which the information is collected Use or disclosure – the disability advocacy agency must not use or disclose personal information about an individual for a purpose other than 53 the primary purpose of collection unless the individual has consented to the use or disclosure Data quality – the disability advocacy agency must take reasonable steps to make sure that the personal information it uses or discloses is accurate, complete and up-to-date Data security – the disability advocacy agency must take reasonable steps to protect the personal information it holds from misuse and loss and from unauthorised access, modification or disclosure Openness – the disability advocacy agency must set out in a document, clearly expressed policies on its management of personal information Disposal – the disability advocacy agency must destroy or permanently deidentify personal information if it is no longer needed for any purpose for which it was collected. Destruction of personal information must be conducted under secure conditions. Disability advocacy agencies should demonstrate documented procedures consistent with the privacy principles. These may include: Storing files in locked filing cabinets; Ensuring consumer consent forms are signed; and Ensuring staff and volunteers sign confidentiality agreements. For further information in relation to the collection of information about individuals, please refer to the Office of the Australian Information Commissioner website. Every disability advocacy agency and its staff should demonstrate respect for the privacy and dignity of people with disability in terms of the way they interact with and refer to people with disability. As systemic advocacy agencies do not undertake advocacy on a one-to-one basis they are less likely to collect information on individuals. However, where information on individuals is collected as part of a systemic advocacy action, agencies will need to adhere to the above requirements. Although people with disability are not the direct consumers of family advocacy agencies, it likely that personal information about the person with disability will be collected while supporting the person’s family member. This information should be treated in the same way as other agencies are expected to deal with their consumers’ information. Things to consider – Privacy, dignity and confidentiality All disability advocacy agencies We have documented privacy and confidentiality policies and procedures, in line with the relevant requirements of the Privacy Act 1988 We ensure consistent implementation of our privacy and confidentiality policies and procedures 54 We provide staff/ volunteer training that includes privacy, dignity and confidentiality Policies for this Standard may cover: record keeping; access policy for confidential information, record disposal, confidentiality and privacy Staff, management and volunteers demonstrate their commitment to tolerance and respect We have proactive strategies to promote tolerance and respect both for individual needs and circumstances, and cultural, ethnic and religious sensitivity People with disability are satisfied with the tolerance and respect demonstrated by our agency We have practices in place that ensure staff have the right mix of skills to treat people with disability with dignity We have secure storage for both our paper and electronic files We ensure that our privacy policies and procedures are updated, when needed as technology changes Our premises have a private space for use that has two exits We have practices in place that ensure our privacy and safety obligations are met Where people with disability are the direct consumers of the disability advocacy agency We use, and make sure consumers understand, information release/consent forms that consumers sign when a third party wants to access their information We inform and ensure that people with disability understand how we will use their information The following table contains examples of evidence a disability advocacy agency may consider using to demonstrate their compliance with Standard 4. 55 Disability Advocacy Standards, KPIs and Examples of Evidence 2012 Standard KPI Standard 4: Privacy, dignity and confidentiality 4.1 The advocacy agency complies with the Information Privacy Principles of the Privacy Act 1988 in order to protect and respect the rights of each person with disability. 4.2 The advocacy agency promotes privacy, dignity and respect for each person with disability. The right of each person with disability to privacy, dignity and confidentiality is recognised and respected. Examples of Evidence All agencies Observations of the way advocates and agency staff talk and write about people with a disability. Clear privacy policy ensuring compliance with relevant State/Territory and Federal legislation. Documented and implemented practices and policies for obtaining consent where relevant and possible, examples could include consent to use photographs for publicity or to share information. Confidential information safely stored e.g. locked filing cabinets. Staff [and volunteers and contractors] sign confidentiality agreements. Evidence that information about right to privacy is provided to people with disabilities and their families when they receive advocacy support. Evidence that the feedback from people with disability who receive advocacy support is used to influence the development of policies, procedures and practice of the agency. Feedback from people with disability who receive advocacy support about the attitude of agency staff to people with a disability. Feedback from external observers on the attitudes of the advocacy agency to people with disability. Agencies undertaking citizen advocacy Feedback from people with disability who receive advocacy support about the attitude of agency staff to people with disability. Feedback from people with disability who receive advocacy support on the attitudes of the advocacy agency to people with disability. Feedback from people with disability who receive advocacy support. Content and practice of orienting advocates to the importance of recognising and respecting the right of people with disability to privacy, dignity and confidentiality. Agencies undertaking family advocacy Documented and implemented practices and policies for encouraging families to obtain the approval of the person with disability before sharing information about the person with disability in the pursuit of advocacy efforts, where appropriate. 56 Standard 5: Participation and integration Each person with disability is supported and encouraged to participate and be involved in the community. 5.1 Through advocacy, opportunities for participation and involvement in the community are promoted. 5.2 Where appropriate, the advocacy agency takes action to introduce, influence or produce positive systemic change in the community. Policy and program context The Australian Government recognises that the quality and sustainability of advocacy outcomes for people with disability are enhanced by physical and social integration into the life of the wider community. The intent of Standard 5 is to provide advocacy that facilitates the inclusion of people with disability into the life of the community. The capacity of disability advocacy agencies to facilitate such integration will vary according to several factors, including the nature of the advocacy they undertake, FaHCSIA contractual obligations, the purpose of the agency and other factors outside of their control. However, all disability advocacy agencies have a responsibility to respond to barriers that limit opportunities for participation and involvement in the community. Disability advocacy agencies may engage in community education programs to create awareness in the community of the need for change. A holistic approach to advocacy recognises the importance of both immediate outcomes for the individual consumer/ person with disability, and the barriers that limit the participation and involvement of people with disability in the community. In practice, the ways in which disability advocacy agencies address this Standard will vary according to the nature of the advocacy undertaken. For example, systemic advocacy agencies will be able to demonstrate the systemic issues the agency has selected to pursue. However, systemic changes may take a significant amount of time to influence and it is important to remember that agencies cannot control all outside factors, so it is expected that agencies will only demonstrate the steps taken towards this goal. Disability advocacy agencies that undertake advocacy on an individual basis may demonstrate steps taken towards systemic change by identifying systemic issues occurring for their consumers, and referring these to systemic advocacy agencies to pursue. Referred cases should have appropriate follow-up and support. Where individual advocacy planning occurs, consideration should be given not only to immediate needs and goals, but to the sustainability of these opportunities. Advocacy plans should be reviewed regularly to ensure people 57 with disability are supported in making informed choices about either continuing current advocacy strategies, or pursuing alternative opportunities which offer greater physical and social integration with the wider community. The community participation activities or programs should be meaningful and varied and, where applicable to the model of advocacy being undertaken, tailored to the individual’s community participation goals. Additionally, people with disability must have access to appropriate information about the scope of opportunities that an agency is able to offer so they can make informed decisions about whether it will meet their needs. Disability advocacy agencies undertaking individual advocacy may demonstrate activities or programs they have engaged in that support participation in community life. File notes may demonstrate the strategies and goals for addressing barriers to community participation. Citizen advocacy agencies will demonstrate the activities undertaken that promote the involvement of people with disability in the community, recognising that decisions about the advocacy activities undertaken made by the citizen advocate and person with disability are outside the control of the agency. Family advocacy agencies will not directly undertake advocacy activities with the individual with disability but, where appropriate, will be able to demonstrate that through supporting their family member, the person with disability’s opportunities for participation in the community are enhanced. Self advocacy agencies will work with individuals to build their skills and abilities to advocate on their own behalf, which in turn increases their ability to participate in wider community life. Things to consider – Participation and integration All disability advocacy agencies We provide information in accessible formats to help people with disability to participate in the community We provide support for people with disability to participate in the community (may be on an individual or collective basis) We develop networks within the community to promote and support the participation of people with disability We create an inclusive and ‘non-threatening’ atmosphere within our agency environment to make all consumers/ people with disability and their families feel comfortable and welcome We network and liaise with relevant ethnic organisations to facilitate the participation and integration of consumers/ people with disability in their own communities 58 We have practices to ensure that proposed advocacy activities are not in conflict with the cultural and religious beliefs and practices of consumers/ people with disability We gather current information about the ethnic background of residents in our agency’s local area Where people with disability are the direct consumers of the disability advocacy agency We align the ethnic profile of applicants and our agency’s current consumer groups to more closely reflect the demographics of the local area We investigate referral rates when there is a low or nil response from local ethnic communities to assess what steps need to be taken to improve our agency We gather and make available resources pertaining to ethnic communities (e.g. appropriate service directories, reference books, statistical information) We promote our agency to all potential consumers (e.g. through ethnic radio and in ethnic newspapers and newsletters) Systemic advocacy We take action to introduce, influence or produce positive systemic change in the community The following table contain examples of evidence an agency may consider using to demonstrate their compliance with Standard 5. 59 Disability Advocacy Standards, KPIs and Examples of Evidence 2012 Standard KPI Standard 5: Participation and integration 5.1 Through advocacy, opportunities for participation and involvement in the community are promoted. 5.2 Where appropriate, the advocacy agency takes action to introduce, influence or produce positive systemic change in the community. Each person with disability is supported and encouraged to participate and be involved in the community. Examples of Evidence All agencies Purpose statement that makes it clear that the agency seeks to promote participation and inclusion. Examples of barriers to community participation being raised with other agencies and authorities for the purpose of promoting change. People with disability connected to the organisation report that they feel valued and accepted by agency staff. Agencies undertaking individual advocacy/legal advocacy Evidence of advocacy taken on behalf of individual people with disabilities aimed at increasing their participation and inclusion in the community. Agencies undertaking citizen advocacy Examples of activities people with disability who receive advocacy support and advocates are involved in – while recognising that the citizen advocates and the person with a disability make their own decisions outside of the control of the funded agency. Observation that community participation is covered in citizen advocate orientation. Practice of recruiting advocates who—by virtue of being non-service, “ordinary” members of the community—can facilitate the participation and integration of people with a disability. Content and practice of orienting advocates to their potential role in facilitating the participation and integration of people with a disability. Agencies undertaking family advocacy /systemic advocacy/ self advocacy Examples of events /activities hosted or engaged in which promote the inclusion of people with disabilities as valued and contributing members of community. Examples of evaluation forms from events or activities hosted by the organisation. 60 Standard 6: Valued status The intrinsic value of each person with disability is recognised and each person is supported and encouraged to enhance their valued status in the community. 6.1 Through advocacy, the aspirations and strengths of each person with disability is promoted. 6.2 The advocacy agency promotes the intrinsic value and the valued status of each person with disability in all its activities. Policy and program context Advocacy activities are undertaken on the basis that they support and enhance the valued status of people with disability, whether on an individual or collective basis. Disability advocacy agencies recognise that a person’s self-worth can be affected by how well they fit into roles that are valued in the community. It may be appropriate for agencies’ mission and vision statements to include reference to valued status. Disability advocacy agencies are required to undertake advocacy in a way that enables people with disability, as far as possible, to live and work in ways that are valued by the community. Agencies may undertake activities in the community to promote the intrinsic value of people with disability. Depending on the model/s of advocacy the agency undertakes, this may include community education, media and communications that positively promote people with disability, or speaking at public conferences and lectures. Disability advocacy agencies are expected to promote a positive image of people with disability both within the community and within the advocacy agency itself. For all agencies, promoting the valued status of people with disability will involve the way in which people with disability are referred to by the agency and staff, for example, in promotional material. In cases where agency staff or volunteers undertake advocacy on a one-to-one or near one-to-one basis, activities should promote the person’s valued status and enhance their abilities, skills and/or opportunities to make valued contributions to the community. For example, the person with disability may be supported to undertake activities that enhance their confidence and skills, and encouraged to participate according to their abilities. Although systemic advocacy agencies will not directly support people with disability to develop skills to enhance their valued status in the community, the systemic actions pursued by the agency should, where appropriate, aim to enhance the valued status of people with disability. In the case of citizen advocacy, it is recognised that decisions about the advocacy activities undertaken made by the citizen advocate and person with disability are outside the control of the agency. 61 Family advocacy agencies will not directly undertake advocacy activities with the individual with disability but, where appropriate, will be able to demonstrate that through supporting their family member, the person with disability’s valued status is promoted. In the context of Standard 6, it is recognised that ‘status’ and ‘value’ are subjective terms and that people will have different understandings of what constitutes valued roles and status, as will different cultures. Where applicable, consideration should be given to what the person with disability accessing the agency considers as valued status. Things to consider – Valued status All disability advocacy agencies Our agency’s mission statement refers to supporting the valued status and intrinsic value of people with disability Our staff relate to consumers/ people with disability in a way that supports their valued status Staff/ volunteers do not demonstrate any of the following behaviours/ attitudes which can undermine valued status: o disrespectful or patronising manner of speech to consumers/ people with disability o use of words that devalue a person’s adult status or draw attention to the disability first , rather than the person o lack of attention to the recognition people deserve Our agency management, Board, staff and volunteers believe and know that people with disability have the ability to fulfill valued roles in the community Our marketing and promotional material supports the valued status of people with disability We network within the community and/ or use community events to promote valued status of people with disability The following table contains some evidence examples that a disability advocacy agency might consider using to show how they comply with Standard 6. 62 Disability Advocacy Standards, KPIs and Examples of Evidence 2012 Standard KPI Standard 6: Valued status 6.1 Through advocacy, the aspirations and strengths of each person with disability is promoted. 6.2 The advocacy agency promotes the intrinsic value and the valued status of each person with disability in all its activities. The intrinsic value of each person with disability is recognised and each person is supported and encouraged to enhance their valued status in the community. Examples of Evidence All agencies The valued status of people with disability is promoted in reports and promotional material. Details of public speaking at conferences, lectures and professional gatherings to promote a positive image of people with disabilities. Examples of issues raised or referrals made to systemic advocacy agencies and/or other agencies and authorities. Examples of activities and issues that the agency engages in that supports the valued status of people with a disability. Agencies undertaking citizen advocacy Examples of activities people with disability who receive advocacy support and advocates are involved in that promote the intrinsic value and the valued status of people with disability– while recognising that the citizen advocates and the person with a disability make their own decisions outside of the control of the funded agency. Citizen advocacy orientation documentation includes information about valued status and what this means in practice. 63 Standard 7: Complaints and disputes Each person with disability, who has a complaint or dispute with the advocacy agency, is encouraged to raise it, and have it resolved without threat of retribution. 7.1 The advocacy agency informs each person with disability about how to raise a complaint or initiate a dispute about any areas of dissatisfaction with the advocacy agency, without threat of retribution. 7.2 The advocacy agency seeks to resolve complaints or disputes raised or initiated by a person with disability, with access to both internal complaints resolution mechanisms and external complaints resolution mechanisms. Policy and program context All disability advocacy agencies are expected to: Encourage the raising of complaints regarding any area of dissatisfaction with the advocacy agency, without any fear of retribution; Create an atmosphere whereby complaints are viewed proactively as an opportunity for improvement; Provide an accessible, accountable and transparent process for the management of complaints; Enable people with disability to access independent support as needed throughout a complaints process; and Ensure the satisfactory closure of the complaint through an open and transparent process. It is the responsibility of disability advocacy agencies to provide an accessible and effective complaint process for people with disability, taking into consideration that people with disability may feel less empowered to make a complaint. Disability advocacy agencies should have an internal complaint/ feedback mechanism that provides: Commitment at all levels of the agency to resolving the complaint at the local level. This can be demonstrated through effective dissemination of policies and procedures, that recognise the positive and important role of complaints to increase the satisfaction of consumers/ people with disability, and provide insights to continuously improve the agency Fairness to all concerned, including the complainant, the agency and the person complained about. This would include availability of support or appropriate referral to another to provide support to ensure that the complainant can make the complaint effectively and does not suffer retribution or intimidation as a result 64 Accessible information about the process in a variety of appropriate formats (including plain English and other languages where appropriate) that is promoted both internally and externally. There should be flexible methods of making complaints, with assistance available to complainants as necessary. This element is particularly important, as people with disability may not feel empowered to make a complaint A responsive process, including full, impartial and timely investigation of all aspects of the complaint and fair and reasonable remedies where warranted An effective mechanism that addresses individual complaints and uses the information collected to improve overall delivery of advocacy and address systemic and recurring problems. The disability advocacy agency’s complaints/ feedback mechanism should be reviewed regularly to ensure that it is meeting the needs of people with disability. The system should also demonstrate: Openness and accountability – so people with disability can judge for themselves whether the system is working effectively Privacy, dignity and confidentiality, as outlined in Standard 4 External referral where a complaint cannot be resolved by the internal process. This may involve an alternative dispute resolution procedure such as mediation, or referral to another appropriate avenue for resolving the complaint, such as an appeal procedure or other legal remedy Cooperation with external complaint resolution agencies where a person with disability has approached such an agency, in the investigation of complaints. External complaints mechanisms can include the Complaints Resolution and Referral Agency (CRRS), the National Abuse and Neglect Hotline, the Australian Human Rights Commission, the Privacy Commissioner or other advocacy agencies. Disability advocacy agencies are expected to refer people with disability to other advocacy agencies for support during the complaints process, if this support is requested. Things to consider – Complaints and disputes All disability advocacy agencies We have a clearly documented complaints policy and procedure We have an escalation process if a complaint is not resolved in the first instance (documented in our complaints procedure) Our escalation process states how external referrals will be used, when necessary 65 Our complaints process is made available and explained to people with disability so that they understand their right to make a complaint and how they can do this We inform people with disability they can have a support person with them during the complaints process and we assist them to access a support person We publicise the Complaints Resolution and Referral Service (CRRS) in our office(s) and inform people with disability of the role of the CRRS We have a documented complaints handling register, which includes who is handling the complaint, timeframe for resolution, the resolution and the complainant’s satisfaction/ dissatisfaction We review the complaints register regularly to ensure timeliness of, and satisfaction with, complaints handling and resolution We ensure that we do not breach confidentiality in the way that we handle complaints We have a procedure in place to appropriately deal with complaints that involve a serious allegation or a potential crime We use information (de-identified) from our complaints handling to inform continuous improvement The following table contains some evidence examples that an agency might consider using to show how they comply with Standard 7. 66 Disability Advocacy Standards, KPIs and Examples of Evidence 2012 Standard Standard 7: Complaints and disputes Each person with disability, who has a complaint or dispute with the advocacy agency, is encouraged to raise it, and have it resolved without threat of retribution. KPI Examples of Evidence 7.1 The advocacy agency informs each person with disability about how to raise a complaint or initiate a dispute about any areas of dissatisfaction with the advocacy agency, without threat of retribution. 7.2 The advocacy agency seeks to resolve complaints or disputes raised or initiated by a person with disability, with access to both internal complaints resolution mechanisms and external complaints resolution mechanisms. All agencies Documented complaints policy and procedures. Documented and implemented practices and policies for investigating and resolving complaints – cover both internal and external complaints resolution mechanisms, including the Complaints Resolution and Referral Service (CRRS). File review demonstrates that the agency completes complaints investigations in accordance with its complaints procedures. People with disability who access the advocacy agency are provided with information about the agency’s complaints policy and procedures. The agency reviews its complaints policy, procedures, processes and practices to ensure implementation is appropriate to complainants. Service user feedback about the complaints mechanism. Complaints register. 67 Standard 8: Agency management Each advocacy agency adopts quality management systems and practices that optimise the effectiveness of advocacy for each person with disability and facilitates continuous improvement. 8.1 The advocacy agency has clearly stated aims and objectives that communicate to each person with disability and other relevant stakeholders the scope and limitations of the advocacy agency. 8.2 The advocacy agency has governance and management systems in place that facilitate quality management practices and continuous improvement. 8.3 The advocacy agency operates independently and is structured in such a way that it is as free as possible from conflicts with other service provision and the interests of each person with disability. Policy and program context This Standard recognises that effective and efficient management of the disability advocacy agency is essential for optimising the effectiveness of advocacy for people with disability. It is expected that disability advocacy agencies will have a positive organisational culture and through strong and effective governance and robust management be responsive to the needs of people with a disability, meet their compliance and reporting obligations and embed a culture of continuous improvement by implementing quality management systems. The disability advocacy agency’s management system encompasses all the things an agency does to establish the outcomes it wants to achieve and the policies and procedures it uses to ensure these outcomes are attained. However, the type and complexity of the management systems used by agencies are expected to vary greatly, depending on the size of the organisation and the models of advocacy undertaken. Clearly, a small rural agency is not expected to have the same management system as a large multisite agency. In addition, where an agency is part of a larger organisation, it will need to consider what management systems are needed at the local level and how they link to management systems across the organisation as a whole. Audit teams will take into account the relative size of agencies, and the budgets and funding they have available to them. In all cases, what is important is that every disability advocacy agency has a management system that best enables it to optimise the effectiveness of advocacy for people with disability. For all agencies, a quality management system involves: A clear organisational structure and corporate governance arrangements that provide confidence for people with disability in the probity and accountability for the management of the agency. These governance 68 arrangements should include skilled and qualified Board/management members; Processes for setting and working towards business priorities and outcomes for people with disability (e.g. corporate or business planning processes); Continuous improvement processes for identifying agency strengths and weaknesses and working towards improvements; Documented policies and procedures relevant to the Disability Advocacy Standards; and Internal controls to comply with relevant Standards and other legislation and funding requirements. Things to consider – Agency management All disability advocacy agencies We have clearly stated aims and objectives that are communicated to stakeholders We have a clear identification and understanding of the powers, roles, responsibilities and accountabilities between the Board, the Chief Executive Officer and management Responsibilities are clearly communicated to key stakeholders The Board has appropriate decision making processes. There is clear distinction between what decisions should be made by the Board and those decisions that should be made by our agency’s management We have skilled and qualified Board and management members We have a quality management system that facilitates quality management practices and continuous improvement We have processes governing policy development, implementation and review, which involve input from stakeholders We have written policies and associated processes which reflect relevant legislation, standards, and funding requirements We have a risk management plan that is supported by risk management strategies and reviewed regularly We have practices in place to ensure the agency is structured and operates independently and is as free as possible from conflict with other service provision and the interests of people with disability The following table contains some evidence examples that an agency might consider using to show how they comply with Standard 8. 69 Disability Advocacy Standards, KPIs and Examples of Evidence 2012 Standard KPI Standard 8: Agency management 8.1 The advocacy agency has clearly stated aims and objectives that communicate to each person with disability and other relevant stakeholders the scope and limitations of the agency. 8.2 The advocacy agency has governance and management systems in place that facilitate quality management practices and continuous improvement. 8.3 The advocacy agency operates independently and is structured in such a way that it is as free as possible from conflicts with other service provision and the interests of each person with disability. Each advocacy agency adopts quality management systems and practices that optimise the effectiveness of advocacy for each person with disability and facilitates continuous improvement. Examples of Evidence All agencies Documented agency aims and objectives. Documented and implemented practices and policies for promotion and communication of agency aims and objectives with people with disability who receive advocacy support and stakeholders. Reviews of agency management systems involving service users (e.g. people with disability who receive advocacy support, family members, citizen advocates) – including documented annual self-assessments and continuous improvement plans. Clear governance arrangements. Documented and implemented policies and practices for performance and risk management are undertaken. Documented policy on agency independence. Agency management and staff can provide practical examples of how they operate to ensure they are as free as possible from things that conflict with the best interests of people with disability. Policies and procedures include referral to another agency if required to prevent a conflict of interest. Evidence of the involvement of people with disability in the agency’s QA activities. Minutes of management committee meetings. Documented roles and responsibilities of management committee office bearers. 70 Standard 9: Staff, recruitment, employment and training Each person who has an employment or volunteer relationship with the advocacy agency has appropriate skills and competencies. 9.1 The advocacy agency ensures that its staff have relevant skills and competencies. 9.2 The advocacy agency provides opportunities for the appropriate and continuing training and skills development for each staff member. Policy and program context This Standard recognises that having staff with appropriate skills and competencies, and providing opportunities for professional development, training and organisational learning, are critical to achieving the best advocacy outcomes for people with disability. Crucial to an effectively managed organisation is a skilled workforce with the right values and attitudes. Having staff without appropriate skills and competencies should be considered an unacceptable management practice due to the vulnerable nature of people with disability accessing disability advocacy agencies. The staff of disability advocacy agencies require skills in areas such as communication, respect and dignity, confidentiality, effective supports, appropriate conduct, positive attitudes, behavioural support and responding to individual needs. In agencies that are contracted to provide advocacy for people with a specific type of disability, some specialist knowledge and skills may also be required. Disability advocacy agencies will need to identify and document the skills and competencies needed for positions within the agency in role descriptions. Established practices and policies for recruitment and induction should ensure paid and unpaid staff have the necessary skills and competencies for their position, including relevant qualifications (where appropriate). Agencies should outline the methods for assessing these skills and competencies, and addressing any gaps through staff training and/or recruitment. The disability advocacy agency’s management should also have strategies to support agency-wide learning that acknowledges the changing needs of the agency and its staff and continues to develop responses to new challenges. Recruitment practices should meet probity requirements and disability advocacy agencies should be committed to training and equipping staff and unpaid staff to meet the needs of the people they support and to maximise positive outcomes. Planning for future workforce needs is essential. In this Standard, ‘staff’ refers to both paid and unpaid staff of the agency. However, in citizen advocacy and family advocacy, the advocates do not have an employment relationship with the advocacy agency – for these models, ‘staff’ refers to staff of the advocacy agency employed either to support and 71 recruit volunteer citizen advocates or to support family members of people with disability. Things to consider – Staff, recruitment, employment and training All disability advocacy agencies Our agency has detailed job descriptions for all roles, including responsibilities Job descriptions are maintained and updated as necessary We have an induction process for all new staff/ volunteers and Board members We have processes in place to ensure staff/ volunteers understand the skill/ competency requirements of their job We encourage appropriately skilled and qualified people with disability (along with people from other disadvantaged groups) to apply for positions We have clear policies and procedures regarding the roles, responsibilities and treatment of volunteers. Volunteers are made aware of and understand these We ensure recruitment based on qualifications and skill, and the competency requirements of the role Conditions of employment are agreed and evidenced through a signed Contract of Employment We ensure our staff have the relevant skills and competencies Staff and Board members’ performance is periodically reviewed Staff have input regarding their own development and training needs Staff are given opportunities to access appropriate training and development activities to enable them to perform their work The following table contains some evidence examples that an agency might consider using to show how they comply with Standard 9. 72 Disability Advocacy Standards, KPIs and Examples of Evidence 2012 Standard KPI Examples of Evidence Standard 9: Staff, recruitment, employment and training 9.1 The advocacy agency ensures that its staff have relevant skills and competencies. Each person who has an employment or volunteer relationship with the advocacy agency has appropriate skills and competencies. 9.2 The advocacy agency provides opportunities for the appropriate and continuing training and skills development for each staff member. All agencies Current list of all people who have an employment relationship with the advocacy agency. Position descriptions of all paid and unpaid staff that describe skills and competencies needed for their role. Documented and implemented practices and policies for recruitment & induction that ensure paid and unpaid staff have the necessary skills and competencies for their position, including relevant qualification (where appropriate). Staff appraisals conducted at least annually. Training and development plans for all staff. Agencies undertaking citizen advocacy Independent evaluations of practices for developing the capacity of citizen advocates to assist people with disability meet their advocacy objectives. Regular opportunities for the staff and board of management to avail themselves of Citizen Advocacy-related training, including participation in the independent evaluation of other Citizen Advocacy agencies, as a means to enhance conceptual and practical knowledge. 73 Standard 10: Protection of human rights and freedom from abuse The advocacy agency acts to prevent abuse and neglect and to uphold the legal and human rights of each person with disability. 10.1 The advocacy agency takes all practical and appropriate steps to prevent abuse, neglect and discrimination of each person with disability. 10.2 The advocacy agency upholds and promotes the legal and human rights of each person with disability. Policy and program context Standard 10 requires disability advocacy agencies to uphold the legal and human rights of people with disability. Agencies are expected to advocate to prevent abuse and neglect and, where people with disability are supported on an individual basis, to empower and support them to exercise their human rights. Australia is party to a number of international agreements and conventions that require the upholding of the basic legal and human rights of all Australians, including people with disability. Australia ratified the United Nations Convention on the Rights of People with Disabilities (CRPD) in July 2008 as part of a global effort to promote the equal and active participation of people with disabilities. The CRPD’s guiding principles on fairness and human rights include: Respect for human dignity and freedom Equality before the law Privacy Protection against discrimination Equal opportunity in employment Disability advocacy agencies are expected to be proactive in preventing abuse and neglect of people with disability, where consistent with contractual obligations and the purpose of the agency. In comparison with the general population, people with disability are more likely to experience abuse and neglect. There are many forms of abuse, including: Physical, sexual, psychological or emotional abuse Constraint and restrictive practices Neglect and deprivation Some forms of abuse may be intentional while others are more likely to result from system failures or poor practice. Every disability advocacy agency should have prevention strategies in place within their own agency. Some considerations include: 74 The agency’s workplace culture supports valued attitudes Staff have basic competencies/ skills in abuse prevention Human resource planning, including monitoring indicators and risks related to abuse occurs Policy guidelines related to abuse prevention are developed Although all disability advocacy agencies have a commitment to uphold the legal and human rights of people with disability and endeavour to prevent abuse and neglect, they will undertake different activities. For agencies that undertake advocacy on an individual basis, a proactive strategy for preventing abuse could involve proactive outreach to consumers who may be vulnerable, isolated, or otherwise unlikely to access an advocacy agency. Agencies undertaking legal advocacy, may pursue legal activities that uphold the legal and human rights of people with disability. Those agencies undertaking family advocacy will demonstrate how providing support to family members of people with disability will uphold the rights of people with disability and prevent abuse and neglect. For agencies undertaking systemic advocacy, preventing abuse and neglect or upholding the legal rights of people with disability will involve pursuing positive systemic changes for people with disability. The National Disability Abuse and Neglect Hotline was established for reporting allegations of abuse and neglect against people with disability. Agencies are expected to actively promote the existence of the Hotline to people with disability (see Section 7 for contact details of the Hotline). Things to consider – Protection of human rights and freedom from abuse All disability advocacy agencies We have clearly documented policies and procedures for preventing and responding to abuse and neglect Management, staff and volunteers have been informed of, and trained in, the policy and procedures relevant to abuse and neglect Our procedures reflect the best interests of the person alleged to have been abused Our documented reporting procedures include roles, responsibilities and identification of when and how to report to the police or other relevant bodies 75 We provide/ make available appropriate support to alleged victims, families and staff/ volunteers around allegations of abuse and neglect We have an incident reporting process which includes: o Nature of incident o Names of people involved o Outcomes o Response to person making allegation o Records which are dated and signed Our register of incidents and complaints files are kept secure The following table contains some evidence examples that an agency might consider using to show how they comply with Standard 10. 76 Disability Advocacy Standards, KPIs and Examples of Evidence 2012 Standard KPI Standard 10: Protection of human rights and freedom from abuse 10.1 The advocacy agency takes all practical and appropriate steps to prevent abuse, neglect and discrimination of each person with disability. 10.2 The advocacy agency upholds and promotes the legal and human rights of each person with disability. The advocacy agency acts to prevent abuse and neglect and to uphold the legal and human rights of each person with disability. Examples of Evidence All agencies Staff knowledge and skills in recognising and reporting criminal activities, abuse and neglect. Evidence of staff knowledge/learning about human and legal rights. Agency management and staff can provide practical examples of how they act to prevent abuse and neglect – (e.g. an outreach program which seeks out people with disability who are abused or neglected and who would not normally come to the attention of other agencies; community education to raise awareness about abuse of people with disabilities and strategies to prevent and respond to it, etc.). Documented and implemented policies and procedures around responding to/reporting in situations of abuse and neglect. Examples could include a flow chart on who to notify and/or stages of reporting sequence/steps. Documented and implemented policies and procedures reflect prevention of abuse that could occur internal to the agency and external to the agency. Evidence of advocacy agency activities to promote and uphold the legal and human rights of people with disabilities on either an individual or systemic basis. Agencies undertaking citizen advocacy Practice of recruiting advocates for people with a disability who are isolated and otherwise vulnerable, in order to ensure their protection of human rights and freedom from abuse, consistent with the mission of Citizen Advocacy. Content and practice of orientating advocates to their role in ensuring the protection of the human rights, and prevention from abuse, of peoples with a disability. Practice of supporting advocates in their role of ensuring the protection of the human rights, and prevention from abuse, of people with a disability. 77 4.2 Self-assessments Self-assessments are a key part of the NDAP QA system. Self-assessment is the opportunity for your disability advocacy agency to assess how your quality management system (including your policies, procedures, practices) meets the requirements of the Disability Advocacy Standards. Self-assessments are an ideal platform from which to then plan continuous improvement activities. As part of the initial certification process, the Certification Body will use this information to decide whether to proceed with a certification audit (refer Section 3). The self-assessment process is of great value in implementing a quality management philosophy and creating an internal culture which encourages excellence. Principles of quality management suggest that high levels of participation lead to the establishment of a more sustainable quality system through increased staff commitment and ‘ownership’ of any planned changes. There should be input from governance, management, staff, people with disability and other relevant stakeholders. Note: input from people with disability is not mandatory in NDAP self-assessments, though is highly recommended as a measure of how people with disability participate in agency decision making (Standard 3), and agency management (Standard 8). The Easy Read and Standard Read NDAP QA information for people with disability, provided on the FaHCSIA website will be useful for this process. What methods can be used to do the self-assessment? There is no set formula for conducting self-assessments, as it will vary in part due to the size and type of the advocacy agency. Some useful methods include: Feedback from staff, people with disability, relevant stakeholders – either through interviews, or a survey; A review of policies and procedures; Workshops to discuss where your agency is working well and where there are gaps in systems; Staff meetings discussing the self-assessment as a training/staff development exercise. To assess current performance, you could use the compliance/non-compliance rating scale consistent with audit assessments: Rating of 0: Major nonconformity – that means that you have not met the requirements of a KPI, or the outcomes are ineffective. Rating of 1: Nonconformity – this means that you have not fully met the requirements of a KPI or the outcomes are only partially effective. Several related nonconformities may also constitute a major nonconformity. Rating of 2: Conformity – this means you have met the requirements of a KPI. 78 HINT: What is the difference between self-assessment and internal audit? Self-assessment and internal audit are not synonymous. Self-assessments check the extent to which documents in the management system meet the requirements of the Disability Advocacy Standards. Internal Audits do this, as well as check to see if those procedures are implemented and followed. The NDAP QA certification process does not specifically require disability advocacy agencies to have an internal audit process. However, internal audits are an important tool in ensuring an effective quality management system, and are highly recommended to check that procedures are in place and are being followed (see Section 5, Standard 8, for more information). It would be desirable (though not mandatory) for agencies to aim to implement an internal audit process by the end of the first three year certification cycle. HINT: Can peer assessments be used in place of self-assessments? An increasing number of NDAP agencies are now undertaking peer assessments against the Disability Advocacy Standards as part of their continuous improvement processes. JAS-ANZ Procedure 29 provides that the results of peer assessments can be used in place of self-assessments. Where this occurs, it would be desirable for your agency to also have in place its own internal audit process to provide a backup of internal controls. HINT: What format does NDAP disability advocacy agencies need to use for completion of the self-assessment? A template is provided (see next page) however this template is not mandatory. It is mandatory that self-assessment is against the Disability Advocacy Standards. The National Association of Community Legal Centre’s QA process provides an on-line self-assessment process (which maps relevant Standards to evidence against other related Standards). It is understood that the Disability Advocacy Standards will be integrated into this system by the NACLC during 2012. If NDAP agencies wish to utilise this system, the outcomes of the self-assessment process should be made available to the Certification Body for consideration during the Stage 1 audit. 79 4.3 Self-Assessment Worksheets Self-Assessment Worksheet – Disability Advocacy Standards Date of Self-Assessment: Name of Disability Advocacy Agency: Standard 1: Accessing advocacy Each person with disability has opportunities to access advocacy on the basis of relative need and available resources. KPI Key Performance Indicator 1.1 The advocacy agency adopts, applies and promotes non-discriminatory policies in respect of age, gender, race, culture, religion, disability or living arrangements, consistent with the contractual obligations and purpose of the advocacy agency and the relative need and available resources. 1.2 The advocacy agency has processes to determine how the individuals or issues supported are chosen and prioritised based on relative need and available resources. 1.3 Each person with disability is informed about how decisions are made in relation to access and advocacy issues. Assessment of current performance (rating = 0, 1 or 2) Examples of Evidence Improvement action 80 Self-Assessment Worksheet – Disability Advocacy Standards Date of Self-Assessment: Name of Disability Advocacy Agency: Standard 2: Individual needs Each person with disability receives advocacy that is designed to meet their individual needs and interests. KPI Key Performance Indicator 2.1 The advocacy agency has a process for determining and documenting the advocacy objectives that reflect the wishes, needs or interests of each person with disability. 2.2 Advocacy activities are directed to meeting the advocacy objectives of each person with disability. 2.3 Each person with disability engaged in determining advocacy objectives is provided with opportunities to involve a support person of their choice. 2.4 In meeting the needs of a person with disability, the advocacy agency avoids, where possible, any conflict of interest or the perception of any conflict in relation to the conduct of its advocacy work, and deals with any conflict or perceived conflict transparently. 2.5 The advocacy agency helps to empower people to advocate for themselves or their family or others with appropriate strategies (e.g. information, training, mentoring, support). Assessment of current performance (rating = 0, 1 or 2) Examples of Evidence Improvement action 81 Self-Assessment Worksheet – Disability Advocacy Standards Date of Self-Assessment: Name of Disability Advocacy Agency: Standard 3: Decision making and choice Each person with disability has the opportunity to participate as fully as possible in making decisions about the advocacy activities undertaken. KPI Key Performance Indicator 3.1 The advocacy agency’s policies support each person with disability to direct, within the limits of their capacity or interest, the advocacy activities undertaken to meet their advocacy objectives. 3.2 In all circumstances the advocacy activity is informed by ethical guidelines. Assessment of current performance (rating = 0, 1 or 2) Examples of Evidence Improvement action 82 Self-Assessment Worksheet – Disability Advocacy Standards Date of Self-Assessment: Name of Disability Advocacy Agency: Standard 4: Privacy, dignity and confidentiality The right of each person with disability to privacy, dignity and confidentiality is recognised and respected. KPI Key Performance Indicator 4.1 The advocacy agency complies with the Information Privacy Principles of the Privacy Act 1988 in order to protect and respect the rights of each person with disability. 4.2 The advocacy agency promotes privacy, dignity and respect for each person with disability. Assessment of current performance (rating = 0, 1 or 2) Examples of Evidence Improvement action 83 Self-Assessment Worksheet – Disability Advocacy Standards Date of Self-Assessment: Name of Disability Advocacy Agency: Standard 5: Participation and integration Each person with disability is supported and encouraged to participate and be involved in the community. KPI Key Performance Indicator 5.1 Through advocacy, opportunities for participation and involvement in the community are promoted. 5.2 Where appropriate, the advocacy agency takes action to introduce, influence or produce positive systemic change in the community. Assessment of current performance (rating = 0, 1 or 2) Examples of Evidence Improvement action 84 Self-Assessment Worksheet – Disability Advocacy Standards Date of Self-Assessment: Name of Disability Advocacy Agency: Standard 6: Valued status The intrinsic value of each person with disability is recognised and each person is supported and encouraged to enhance their valued status in the community. KPI Key Performance Indicator 6.1 Through advocacy, the aspirations and strengths of each person with disability is promoted. 6.2 The advocacy agency promotes the intrinsic value and the valued status of each person with disability in all its activities. Assessment of current performance (rating = 0, 1 or 2) Examples of Evidence Improvement action 85 Self-Assessment Worksheet – Disability Advocacy Standards Date of Self-Assessment: Name of Disability Advocacy Agency: Standard 7: Complaints and disputes Each person with disability, who has a complaint or dispute with the advocacy agency, is encouraged to raise it, and have it resolved without threat of retribution. KPI Key Performance Indicator 7.1 The advocacy agency informs each person with disability about how to raise a complaint or initiate a dispute about any areas of dissatisfaction with the advocacy agency, without threat of retribution. 7.2 The advocacy agency seeks to resolve complaints or disputes raised or initiated by a person with disability, with access to both internal complaints resolution mechanisms and external complaints resolution mechanisms. Assessment of current performance (rating = 0, 1 or 2) Examples of Evidence Improvement action 86 Self-Assessment Worksheet – Disability Advocacy Standards Date of Self-Assessment: Name of Disability Advocacy Agency: Standard 8: Agency management Each advocacy agency adopts quality management systems and practices that optimise the effectiveness of advocacy for each person with disability and facilitates continuous improvement. KPI Key Performance Indicator 8.1 The advocacy agency has clearly stated aims and objectives that communicate to each person with disability and other relevant stakeholders the scope and limitations of the advocacy agency. 8.2 The advocacy agency has governance and management systems in place that facilitate quality management practices and continuous improvement. 8.3 The advocacy agency operates independently and is structured in such a way that it is as free as possible from conflicts with other service provision and the interests of each person with disability. Assessment of current performance (rating = 0, 1 or 2) Examples of Evidence Improvement action 87 Self-Assessment Worksheet – Disability Advocacy Standards Date of Self-Assessment: Name of Disability Advocacy Agency: Standard 9: Staff, recruitment, employment and training Each person who has an employment or volunteer relationship with the advocacy agency has appropriate skills and competencies. KPI Key Performance Indicator 9.1 The advocacy agency ensures that its staff have relevant skills and competencies. 9.2 The advocacy agency provides opportunities for the appropriate and continuing training and skills development for each staff member. Assessment of current performance (rating = 0, 1 or 2) Examples of Evidence Improvement action 88 Self-Assessment Worksheet – Disability Advocacy Standards Date of Self-Assessment: Name of Disability Advocacy Agency: Standard 10: Protection of human rights and freedom from abuse The advocacy agency acts to prevent abuse and neglect and to uphold the legal and human rights of each person with disability. KPI Key Performance Indicator 10.1 The advocacy agency takes all practical and appropriate steps to prevent abuse, neglect and discrimination of each person with disability. 10.2 The advocacy agency upholds and promotes the legal and human rights of each person with disability. Assessment of current performance (rating = 0, 1 or 2) Examples of Evidence Improvement action 89 Section 5: Continuous Improvement Continuous improvement is an integral component of the NDAP Quality Strategy and the associated QA system of certification. Continuous improvement allows disability advocacy agencies to constantly review performance against the Disability Advocacy Standards and plan ongoing improvements. To be certified and receive Australian Government funding, your disability advocacy agency must be able to demonstrate the quality of your continuous improvement processes and outcomes. As part of your certification audit, an independent Certification Body assesses your continuous improvement processes and outcomes against Disability Advocacy Standard 8 (Agency management). However, the real value of continuous improvement as part of the overall quality system is to create stronger, more sustainable support that better meets the advocacy needs of people with disability. A quality improvement culture helps disability advocacy agencies accommodate changes, such as government reforms, variations in the economy and the needs of consumers, and continually develop a high quality agency to meet the needs of people with disability. Quality agencies are agencies which generally show: Strong customer focus; Clear direction and accountability; Continuous learning and innovation; Valuing people and diversity; Collaborative work practices; Evidence based decision making Social and ethical responsibility. 5 The intent of continuous improvement is to lay solid foundations to underpin agency delivery outputs, outcomes and impacts – that is, to: Improve efficiency (to do things right) Improve effectiveness (to do the right thing) Improve consumer outcomes/outcomes for people with disability. 6 Continuous improvement operates at both an individual agency level and a sector level. Ideally, improvement actions at the two levels are related so that information 5 South Australian Department of Families and Communities, Benefits of a Quality System, Service Excellence Program: http://www.dfc.sa.gov.au/pub/tabid/267/itemid/755/Benefits-of-a-Qualty-System.aspx Disability Service Queensland, Introduction to Quality Management: https://www.disabiltiy.qld.gov.au/keyprojects/quality/documents/section-26 90 about successful innovations is shared across the sector, and areas of need are identified so that training and support can be provided. Effective continuous improvement is integrated into the day-to-day life of organisations. It should be part of your disability advocacy agency’s core functions. Implementing quality improvement processes has a range of benefits for consumers, staff, Board and other stakeholders. How your disability advocacy agency can continually improve This section contains information about how your agency can continually improve against the Disability Advocacy Standards. The information is practically based and is intended to be referred to in conjunction with your certification progress. The selfassessment process is an ideal place to review your agency’s performance and further your improvement opportunities. How to use information in this section Each Disability Advocacy Standard is provided with a range of resources, including: Sample policies, procedures, templates and tools; Case studies; Links to other resources. These resources will support you in planning quality improvement actions arising from your self-assessment, and as part of ongoing continuous improvement activities. The resources are not prescriptive, and you can adapt them based on your disability advocacy agency’s purpose and practices. Your agency is not expected to adopt all policies or practices or use all resources provided. Some of the resources will be relevant to all agencies, while others will only apply to particular models of advocacy. The sections are numbered as per the sequencing of the Disability Advocacy Standards, however, it is not essential to work through them in this order. The results of your self-assessment will identify those Standards and KPIs that require improvement actions, and you may wish to refer directly to those sections. Another useful option is to commence with Standard 8: Agency management. This Standard is about the overall management system of disability advocacy agencies, and it connects all of the other Disability Advocacy Standards. Experience of other QA systems has shown that conformance with Standard 8 requirements is essential for overall conformity with the other Standards. DISCLAIMER: This section contains ideas and practice related to the Disability Advocacy Standards which have been used by disability advocacy agencies, disability services, and a range of government and non-government organisations. The resources are not intended to be prescriptive, but may help you think of ideas to improve the quality of advocacy support within your agency. Using these resources does not guarantee certification. The resources also need to be considered in the context of compliance with relevant Commonwealth and State/Territory legislation. 91 5.1 Sample policies, procedures, templates and tools Standard 1: Accessing advocacy 1.1 Sample policies and procedures Sample Policy: Entry, Non-Discrimination, Referral, Exit and Accessibility7 Entry criteria The definition of disability as per the Disability Discrimination Act 1992, is: (a) total or partial loss of a person’s bodily or mental functions; or (b) total or partial loss of a part of the body; or (c) the presence in the body of organisms causing disease or illness; or (d) the presence in the body of organisms capable of causing disease or illness; or (e) the malfunction, malformation or disfigurement of a part of the person’s body; or (f) a disorder or malfunction that results in the person learning differently from a person without the disorder or malfunction; or (g) a disorder, illness or disease that affects a person’s thought processes, perception of reality, emotions or judgment or that results in disturbed behaviour; and includes a disability that: (h) presently exists; or (i) previously existed but no longer exists; or (j) may exist in the future; or (k) is imputed to a person. Consistent with the contractual obligations and purpose of the agency, our agency will advocate for people with disability as defined above, as well as for the families and carers of those people (note that in the case of systemic and family advocacy agencies, people with disability are not consumers of the agency). All consumers of our agency must also live, work, or have close links to [insert region/ area]. Non-discrimination policy When deciding on eligibility for entry into our agency, we will adopt, apply and promote non-discriminatory entry rules in respect of age, gender, race, culture, religion or disability, consistent with the contractual obligations and purpose of our agency. Where people with disability are not consumers of the advocacy agency, the mechanisms for involving people with disability with our agency are nondiscriminatory in respect of age, gender, race, culture, religion or disability, consistent with the contractual obligations and purpose of our agency. 7 National Disability Advocacy Program Quality Improvement Toolkit 2009 FaHCSIA 92 Entry procedure Where people with disability and/or the carers and family of people with disability are consumers of the advocacy agency, our agency will assess the eligibility of consumers who: Contact our agency directly; Are referred to our agency; Are identified through any recruitment and promotional activities of our agency. To ensure that our agency addresses the needs of Culturally and Linguistically Diverse (CALD) and Indigenous consumers at the point of entry, our agency will: Ensure that appropriate translating or interpreting services are provided, if required, to assist the consumer during the assessment of eligibility and entry process; Ensure that any recruitment or promotional activities of our agency are targeted so as to be accessible to those of CALD or Indigenous background. This may include the provision of information in languages other than English, particularly for languages spoken widely in the catchment area. Where possible, our agency will periodically compare consumer data with available demographic data for the catchment area to assess whether the needs of minority groups are being met by our agency. Once entry eligibility has been established, our agency will: Describe to the person what our agency does and how advocacy will be undertaken; Describe to the person any relevant specific agency or program information, and provide written material relating to relevant specific advocacy activities or programs; Discuss our agency’s privacy, dignity and confidentiality policy; and Provide a consent form for signing if appropriate. If resources are currently unavailable, our agency will: Offer a place on the waiting list Inform the person of the approximate waiting period Place the person on the mailing list for the newsletters and other relevant information Provide interim information and/or referral, as appropriate. If the person is not eligible, our agency will: Provide the person with the reason Document the reason Provide information and/or referral as appropriate Provide information about complaints and disputes. Priority of advocacy provision Where people with disability and/or their families and carers are consumers of the advocacy agency, when our agency assesses applications, priority will be given to the following: The actual or potential seriousness of the problem the person or group is facing The lack of alternative assistance to resolve the problem 93 The probability of successful outcome for the person in relation to: (a) our agency’s limited resources and (b) other high priority advocacy matters. Highest priority will be given to advocacy requests where there is an urgent and serious risk of harm – including physical or psychological harm to the individual and exposure to a harmful situation, such as jail or homelessness. Our agency will also take into account ethical issues, especially potential conflicts of interest. Where people with disability are consumers of the advocacy agency, when our agency assesses applications, priority will also be given to the seriousness of the person's disability in terms of the way it affects his or her ability to deal with the problem they are facing. Referral Where people with disability and/or their families and carers are consumers of the advocacy agency and our agency is unable to accommodate a potential consumer, it will arrange for a referral. Our agency will develop and maintain up-to-date networks and information with a comprehensive range of agencies and services within the region to ensure appropriate referrals can be made (note where the agency is located in a regional area the potential for referral may be limited). When making a referral, our agency will: Provide the person with information to facilitate informed choice and decision making regarding referrals Provide collaboration and seek permission before referral is made (when possible) contact the referral agency with the person present (if this is not possible) provide a referral form including full contact details, including a contact name Provide a privacy, dignity and confidentiality form for signing, if appropriate support referrals if necessary Note all referrals on the person’s file. Consumer exits Where people with disability and/or their families and carers are consumers of the advocacy agency, consumer exits will occur: At any time when the consumer makes an informed decision that they will no longer continue to require advocacy; or When the problem/ issue for which advocacy was sought has been resolved; or When our agency can no longer assist the consumer, because: o The consumer displays unsafe or unacceptable behaviour and all steps have been taken to address the effects of this behaviour o Our agency reasonably believes that our agency, in its capacity to advocate for other consumers, or the consumer, will be negatively impacted if the advocacy is pursued o Due to changes in the consumer’s mental capacity they are no longer able to instruct our agency o All reasonable avenues of complaint and appeal in relation to the advocacy matter are exhausted and further effort is futile or unwarranted on the 94 evidence available. When the consumer or advocate is moving to another area. Where a consumer is moving to another area, our agency will investigate referral options on behalf of the consumer. Accessibility of information on our advocacy agency Our agency will ensure that written and audio materials about our activities (and eligibility and entry requirements, where people with disability and/ or their families or carers are consumers of the advocacy agency) are available to people with disability, their families and carers. These materials will be: Written in a style that will be easily comprehensible for people with disability, for example, plain English Provided for Culturally and Linguistically Diverse (CALD) populations. The agency will use available demographic information to assess which CALD population groups should be targeted. Sample procedure: Steps in the Enquiry Process8 1. Enquiry Initial contact for information, referral and/or advocacy Complete (yellow) Advocacy Enquiry Form and forward to Coordinator. The provision of the information is voluntary, but if this information is not provided, Rights In Action Inc. may be unable to process the enquiry. Coordinator identifies immediate action required and/or refers to regular “Status Review Meeting”. Forward to Administration to register on consumer database, send an “Initial Advocacy” letter (if applicable) and file. 2. Request for advocacy Discuss at “Status Review Meeting”. Prioritise based on vulnerability. Nominate an Advocate to address the follow up action. This may include: arranging an initial meeting to identify the advocacy issue, refer to another service, provide information to support self advocacy, notify the individual they have been placed on a waiting list or arrange an appointment to commence advocacy effort. If declined document reason, notify and file accordingly See following pages for Rights In Action Inc’s Advocacy enquiry flowchart and spectrum of vulnerability. 8 Rights in Action Inc 95 96 SPECTRUM OF VULNERABILITY HIGH Risk of Suicide No Income No Food Homeless MEDIUM Risk of Institutionalisation LOW Poor Literacy and Numeracy No Natural Support System (Family, Friends) No Valid Activities/ Lifestyle (Social/ Abusive Situation Impaired capacity/ Decision making Difficulties (may have or Living in Segregated Setting (Nursing Communication Difficulties (Sensory/ Home/ Hospital/ Institution/ Supported Accommodation) Indigenous or CALD need Adult Guardian/ Public Trustee) Cogitative/ Speech Impairment) Recreational/ vocational) Unemployed & looking for work Poor Social Setting (Live in Caravan Park / Boarding house) Rural and Remote Mobility Impairment Aging or Young Carers Justice/ Health order (treatment order, parole/ probation) Requiring Personal Support (lack of support/ funding) 97 1.2 Sample templates Template: Assessment Information Checklist9 Giving this checklist of information to consumers at the time of initial assessment is one way that you can demonstrate the information you provide. Asking the consumer to sign the form verifies they received the information. You can adapt the checklist based on your agency’s practices or the type of advocacy you provide. I have explained the following information to: ………………………..Date: ……… Signed by assessment officer: …………………………….…………………………. 1. Eligibility criteria for entry to our agency, and procedures for prioritising access Yes/No 2. Consumer’s right to access a support person of their choice to assist them when entering or exiting our agency, and in developing their personalised plan Yes/No 3. How our agency works with the consumer to develop a personalised plan to assist them to achieve their goals, and in what format the copy of the plan will be provided Yes/No 4. What support will be provided, what support will not be provided, how the support will be delivered, and how frequently the personalised plan will be reviewed Yes/No 5. Procedures for minimising risks to the consumer without unduly limiting their choices Yes/No 6. The consumer’s rights in relation to privacy and confidentiality of personal information, and how they may access information held about them Yes/No 7. Procedures for release of personal information to another party and the requirement for informed consent Yes/No 8. The processes for raising a complaint or concern, and our agency’s policies for resolving issues causing dissatisfaction Yes/No 9. How the consumer can participate in decision-making processes to assist our agency to improve Yes/No 9 Resource adapted from Disability Services Queensland, Introduction to Quality Management: https://www.disability.qld.gov.au/key-products/quality/docuents/section-2-intro.pdf 98 Template: Referrals Register10 You can use a document register, like the example provided below, to provide evidence of the consistency and fairness of your entry and exit procedures, decisions on relative need, non-discriminatory access, and referrals made to alternative agencies/ services. You may want to adapt this format based on your agency’s practice. Date Consumer name/ of contact details referral Nominated support person contact details Date of assessment Priority entry rating Date of entry Referrals made Outcome of referrals 10 Adapted from Disability Services Queensland , Introduction to Quality Management: https://www.disability.qld.gov.au/key-products/quality/docuents/section-2-intro.pdf 99 1.3 Tools Tool: Information for consumers on entry and exit policy and procedures11 Entry to the service GDAI provides an individual advocacy service to people with disability, as well as carers and family members of people with disability. When you ask for a service from the GDAI we will: Do all we can to make you feel welcome and treat you with dignity and respect at all times Clearly explain to you the details of the individual advocacy service and advise you on what the GDAI can offer you Deliver an individual advocacy service to you in a way that best empowers you. Prepare an individual advocacy plan with your input Ensure that all people seeking an advocacy service will be treated fairly. However, when a number of requests are received at the same time priority will be given to those deemed to be at risk or in the most need. Exiting the service The service will cease When you no longer need the service The problem has been resolved You agree that after discussing all available options with your advocate that the outcome you want is not realistically achievable When GDAI has referred you on to a more appropriate service that is better equipped to assist you and you do not need or want your progress monitored by GDAI. Your individual advocacy plan can be destroyed at your request when you no longer require an advocacy service from GDAI. 11 Extract from Gippsland Disability Advocacy Client Information Handbook (Plain English) 100 Tool: Checklist for culturally competent disability advocacy access12 Culturally competent disability advocacy support Things to consider for accessing advocacy: Do we provide information about our services in formats that are accessible to all identifiable groups within our service area? For example, do we provide, promote and distribute material in languages other than English, or in audio formats? Do we have established practices that give equity of access to people with disability from a CALD or Indigenous background? What evidence of this could we gather? Do our intake processes take note of special requirements relating to a person’s culture, language or religion? Are all new consumers provided with important information about user rights and responsibilities in a manner that is appropriate to their needs? For example, is information provided via an interpreter and in written and/or audio format in the consumer’s preferred language? Things to consider for service exit: Do our exit policies ensure that people from a CALD or Indigenous background are fully aware of available options for their future needs? Do we have an established referral policy that informs the referral agency of any cultural and linguistic factors that they will need to consider in meeting the consumer’s needs? Do we liaise and network with ethnic or Indigenous organisations services that may help someone who is exiting our service make the transition to another agency? 12 Adapted from MDAA document, Building Cultural Competency in the Disability Services, 2003 NSW: https://www.mdaa.org.au 101 Standard 2: Individual needs 2.1 Sample policies and procedures Sample Policy: Individual Needs for Disability Advocacy13 Where people with disability are the consumers of the advocacy agency, when a consumer enters our agency, our agency will create an individual profile tailored to the needs of that consumer. The individual profile will: Include any relevant details of the consumer’s personal history, as well as details of age, sex, and cultural, linguistic and religious backgrounds. The agency will ensure that the consumer is treated appropriately according to any cultural or linguistic needs identified in this process Identify the goals and needs of the consumer Where relevant and appropriate, work with the family, carers and friends of the consumer to identify the consumer’s needs. The individual profile will be periodically reviewed by our agency in consultation with the person with disability to take account of their changing circumstances and needs. Our agency will, as much as possible, take into account the specific needs and issues identified in the consumer profile when providing planning and undertaking advocacy with and on behalf of the consumer. Where people with disability are not the agency’s consumers (systemic and family advocacy), in planning and undertaking advocacy, our agency will consult people with disability to identify their needs. This will be on an individual or collective basis, as appropriate to the advocacy approach. Supporting individual needs Where people with disability are the consumers of the advocacy agency, the advocacy process will be: Sensitive to each consumer's age, sex, cultural and religious background As much as possible, planned around the preferred advocacy objectives of the consumer. Our agency will: Inform consumers about how their needs will be met Where possible, inform consumers of timeframes for actions undertaken with and on their behalf Use the information from the individual profile to appropriately match advocates to consumers. 13 National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA, 2009 102 Our agency will ensure that Culturally and Linguistically Diverse (CALD) and Indigenous consumers are provided with culturally appropriate services and are adequately supported through the advocacy process. Where people with disability are not the agency’s consumers (systemic and family advocacy), our agency will aim to undertake advocacy activities to reflect and supports their needs. 103 2.2 Sample templates Tool: Personalised Plan Format14 Where people with disability are the direct consumers of your agency, it is likely you will develop and document individual plans for each consumer. Recently established agencies may find this sample template useful as a starting point for developing your agency’s individual plan formats. Individual Program Plan for__________________________________________________________________________ For the period_______________________________________________________________________ __________ Agency name: Support worker: Nominated advocate/ support person: Plan developed in consultation with: Review date for individual program plan: Plan authorised by: _____________________________ (Signature of consumer/ nominated support person) Copy of plan provided to consumer/ support person: Preferred format: _______________________________ (enter date) Identified skills/ knowledge/ attributes:__________________________________________________________________ Health and wellbeing needs:_________________________________________________________________________ Behavioural support needs:__________________________________________________________________________ Physical support needs/ aids:_________________________________________________________________________ 14 Adapted from Disability Services Queensland, Introduction to Quality Management: https://www.disability.qld.gov.au/key8-projects/quality/documents/section-2-intro.pdf 104 Psycho-social support needs:________________________________________________________________________ Communication needs:______________________________________________________________________________ Cultural needs:____________________________________________________________________________________ Who will provide the required support: For what length of time:___________________________ At what time: Under what conditions:___________________________ What risks are involved in implementing the plan:_________________________________________________________ How will risks be managed___________________________________________________________________________ Consumer’s vision statement:________________________________________________________________________ Long-term goals: 1._______________________________________________________________________________________________ 2.______________________________________________________________________________________________ 3.______________________________________________________________________________________________ Short-term goals: 1.1 1.2___________________________________________ 2.1 2.2___________________________________________ 3.1 3.2___________________________________________ 4.1 4.2___________________________________________ 105 RESPONSES: Our agency will address progression towards achieving these goals in the following manner: Long-term goals: 1. Measuring device:____________________________________________________________________________________ 2. Measuring device:____________________________________________________________________________________ 3. Measuring device: ___________________________________________________________________________________ 4. Measuring device: ___________________________________________________________________________________ 5. Program content details for: ___________________________________________________________________________ 6. Date/s: _____________________________Days:_____________________ Date Action Review date Date for next review: 106 Tool: Personalised Plan Review Schedule15 To continue to meet the needs of people with disability, where they are the consumers of your agency, you will need to regularly review consumers’ individual plans. Your staff or volunteer advocates may want to use a document similar to the template below to record the planned schedule for review of individual plans for the consumers who he/she is supporting. Consumer’s name Date of last plan review Date next quarterly review due Appointment made with consumer Goal attainment reviewed and new activities planned 15 Adapted from Disability Services Queensland, Introduction to Quality Management: https://www.disability.qld.gov.au/key8-projects/quality/documents/section-2-intro.pdf 107 Standard 3: Decision making and choice 3.1 Sample policies and procedures Sample Policy: Decision Making and Choice for Disability Advocacy16 Our agency will ensure that people with disability are provided with the opportunity and the necessary support to participate as fully as possible in making decisions about steps in the advocacy process and in the way in which our agency operates. Our agency will encourage and support people with disability to make informed choices about advocacy activities our agency pursues with and on their behalf. However, in some circumstances, this must be balanced against our agency’s responsibility not to act on decisions by a person/ people with disability that might pose a significant and foreseeable risk to their safety or interests, our agency’s ability to assist other people with disability and the safety of our agency’s staff and volunteers. People with disability – decision-making about advocacy Our agency will respect and promote the right of people with disability to selfdetermination and assist them to identify and clarify their needs and goals – this may be on an individual or collective basis, based on our agency’s approach to advocacy. Where people with disability are the consumers of the advocacy agency, our agency will work with the individual consumer to ensure informed decisionmaking and, where possible and appropriate, act upon the consumer’s choices. Where people with disability are not the consumers of the advocacy agency, effort will be made to discuss advocacy activities with the relevant person/ people with disability prior to deciding on and undertaking the advocacy activities. Where this is not possible, for example, we will endeavour to inform people with disability of actions being undertaken. Agencies may limit a person/ people with disabilities right to self-determination when, in their judgment, the person’s actions or potential actions pose a serious, foreseeable, and imminent risk to themselves or others. Informed consent Where people with disability are the consumers of the agency, advocacy will be provided to consumers only in the context of valid informed consent, where this is possible. Our agency will use clear and understandable language to inform consumers of the purpose of the advocacy activities, risks related to the 16 (National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA 2009 108 advocacy activities, limits to advocacy activities because of our agency’s contractual obligations to FaHCSIA, relevant costs, reasonable alternatives, consumers' right to refuse or withdraw consent, and the time frame covered by the consent. Consumers should be given an opportunity to ask questions. If consumers are not literate or have difficulty understanding English, our agency should take steps to ensure consumers' comprehension. This may include providing consumers with a detailed verbal explanation or arranging for a qualified interpreter or translator whenever possible. Where consumers have impaired decision-making abilities, our agency will use ethical guidelines in determining the actions pursued (Refer to following section on Consumers who Lack Decision-Making Capacity). Duty of care Where people with disability are the consumers of the agency, our agency has a duty of care to these consumers. A duty of care exists where a consumer is reasonably likely to be affected by what our agency does or doesn’t do, that is, what information our agency provides or fails to provide in response to an inquiry; what actions our agency takes or fails to take in response to a request requiring advocacy support and what information our agency provides in advocacy development activities. Duty of care is part of the law of negligence. To establish that our agency has been negligent in providing advocacy, a consumer must be able to show that: • • • Our agency owed a duty of care to the consumer; and Our agency breached that duty: our agency should reasonably have known that its action/ advice (or its failure to act/ provide information or advice) would harm the consumer, but our agency failed to take reasonable steps to prevent that harm; and The consumer has actually suffered harm as a result of our agency’s action/ information/ advice/ failure to act. In advising consumers before they make a decision/ choice, agency staff and volunteers should use the duty of care checklist and: • • • • Assess the likelihood and extent of any foreseeable harm Assess the likelihood and extent of the foreseeable benefit Look for ways to minimise the risk of harm without sacrificing the benefit, and Balance the foreseeable harm against the benefit. Consumers who lack decision-making capacity In instances when consumers lack the capacity to provide informed consent, where possible, our agency will protect consumers' interests by seeking permission from an appropriate third party recognised by the law (e.g. guardian, 109 parent, person responsible), informing consumers consistent with the consumers' level of understanding. In such instances, our agency will seek to ensure that the third party acts in a manner consistent with consumers' wishes and interests. Advocates should take reasonable steps to enhance such consumers' ability to give informed consent. If there is no alternative decision maker for the consumer our agency will, in the first instance, support relevant agencies or people to make application to the Guardianship Tribunal. Our agency will take this avenue in the first instance to allow the advocate more freedom to support the consumer through the Guardianship Tribunal process if necessary. However, in circumstances where our agency is particularly concerned about a consumer’s welfare and there are no alternative applicants it may seek to make an application for an alternative decision maker itself. If there is no alternative decision maker or the decision maker appears to be acting against the consumer’s wishes or interests, the advocate should take reasonable steps to safeguard the interests and rights of the consumer. In doing so, ethical guidelines should be used. The following principles will help to guide the advocate’s actions: Take the least restrictive option: the intervention by the advocate will be the least restrictive option in relation to the freedom of the consumer Consider the consumer’s wishes: the advocate will take into account the consumer’s present and past wishes and feelings so far as they can be ascertained Consult with relevant others: the advocate will seek and take into account the views of relevant people who are close to the consumer or who may know the consumer well. In weighing up the views of relevant others the advocate will consider issues such as conflict of interest Encourage and support consumer to use whatever skills he/ she has: the advocate will encourage their consumer to exercise whatever skills that he or she may have to participate in decision making about their welfare and where practicable help the consumer develop new skills. Advocacy process procedure Where the advocate has an employment relationship with the agency advocates will ensure that consumers, if they so wish, participate in decision making during the advocacy process and will follow a procedure with each consumer or group of consumers to ensure that this happens. The following procedures should be undertaken as soon as possible after the consumer has contacted our agency: Clarify with the consumer what their preferred objective is regarding the issues they have raised and plan the advocacy process around this preferred objective Clarify with the consumer any foreseeable consequences of actions that may achieve their preferred outcome. This may involve suggesting a range of actions along with providing alternative information sources 110 Inform the consumer about options for participating in the advocacy process, based on the approach/es to advocacy we deliver Does the consumer understand the options before them, or would the advocacy process be improved if the consumer was supported by a family member, friend etc. who knew the consumer well Inform the consumer about our agency's policy relating to consent if the consumer wishes information to be disclosed to people outside our agency during the advocacy process. Decision making in the management of our agency Consumers, people with disability, advocates, volunteer advocates, families and interested members of the public are encouraged to give feedback and have input into our agency. Our agency will encourage consumers and people with disability to participate in our agency’s operations. People with disability will be encouraged to be involved in governance of our agency and be provided with the necessary support, by Committee members, staff and volunteers, to ensure their representation is as active as possible. All stakeholders of our agency, including people with disability, their families, carers and advocates, will be invited to participate in policy development and evaluation of our agency. 111 Sample Policy: Consumer/ people with disability – Participation17 Policy statement: In developing its services, Service Excellence will involve customers through consultation and active participation in decision making. Contents 1. 2. 3. 4. 5. 6. Purpose Scope Links to other documents Aims Principles Review 1. Purpose To consult with consumers/ people with disability or have consumers/ people with disability participate in decisions that may affect them or will shape the future of our agency. In addressing quality, continuous improvement, learning and development – we are committed to the belief that by involving consumers/ people with disability our advocacy delivery will more relevant to their needs. We are committed to achieving real outcomes for consumers/ people with disability. Consumers’/ people with disability’s participation is seen as fundamental to meeting current objectives, achieving positive outcomes for consumers/ people with disability and developing meaningful advocacy delivery into the future. 2. Scope The term “consultation” refers to our agency having dialog with consumers/ people with disability for the purpose of gaining their opinions and views. The term “participation” refers to our agency actively involving consumers/ people with disability in the decision making process. The principles of consumers’/ people with disability’s participation are detailed in Section 5 of this Policy. 3. Links to other documents 4. Aims The Policy aims to outline the principles relating to consumers’/ people with disability’s participation. Fundamental to our approach to consumers’/ people with disability’s participation is a commitment to: 17 South Australian Department of Families and Communities, Benefits of a Quality System, Service Excellence Program http://www.familiesandcommunities.sa.gov.au/DesktopModules/SAHT_DNN2_Documents/Download/633 652959205440320/SE%20CustomerParticipationPolicy.pdf 112 Consumers’/ people with disabilities' needs being central to all that we do Consumers’/ people with disability’s involvement being an integral part of continuous improvement Consumers/ people with disability being involved in decision making through either consultation or participation Working collaboratively with consumers/ people with disability to reach our objectives. 5. Principles To operationalise the vision for consumers’/ people with disabilities' participation, the Board and agency management will ensure the following principles are adhered to: • Consumers/ people with disability will have a voice • Consumers/ people with disability will be involved in the planning and development of advocacy activities that may affect them • Consumers’/ people with disability’s participation includes a two-way sharing responsibility involving consumers/ people with disability and all staff • Our agency accepts that as a result of customer participation our advocacy activities may evolve differently to that originally envisaged • Consumers’/ people with disability’s participation will be a continuing processes and a culture – it will not be a one-off event • Consumers’/ people with disability’s participation strategies will, in general, include: o Providing accurate information o Seeking views though consultation o Active participation in decision making processes. Specific participation strategies our agency will use to involve consumers/ people with disability will include: o Participation in planning processes o Consultation on the development of resources, policies and procedures o Consultation on issues relating to advocacy activities. Our agency will be open and honest with consumers/ people with disability about where there is scope for choices to be made and where there is not. Consumers/ people with disability will be involved early in planning and decision making processes, not later when directions are already set. When they have been involved, consumers/ people with disability will be given prompt feedback regarding the actions that resulted from their input. 6. Review Our agency is committed to continually working to improve its consumers’/ people with disability’s participation. In keeping with this commitment, the Board will ensure that this Policy is reviewed initially after one year from its introduction and on a triennial basis thereafter. 113 Sample Policy: Board Members with intellectual disability policy and procedure18 Citizen Advocacy South Australia Inc. (CASA) strives to ensure that any person with intellectual disability acting in any Board of Management (BoM) capacity understands, to the best of their ability, the consequences of any decision being made within the organisation, and that through proper mentoring and support, people with intellectual disability can grow and develop into their role. Policy CASA endorses the view of the funding body that people with intellectual disability should have opportunities to be mentored to participate at an organisational level within CASA. All BoM Members have voting rights and their opinions are valued. CASA recognises that many of the decisions and procedures used within the organisation are complex and take time to understand. This reality, combined with CASA’s awareness of not wishing to place any person in a position where they could be made to feel inadequate, or seen as tokenistic, the following procedure has been written. Procedure BoM members with intellectual disability may require a variety of supports from another member when motions are moved or seconded or voted upon at Board meetings. 18 Citizen Advocacy South Australia (CASA) 114 3.2 Tools Tool: How to conduct focus groups for consumers'/ people with disabilities' feedback19 Focus groups are an informal way of obtaining feedback from consumers/ people with disability in a friendly, non-threatening atmosphere. This sample process takes you through steps for organising and conducting focus groups, and using and distributing the information generated. This process is one way that consumers/ people with disability can have an input into agency management and make decisions and choices about advocacy. The process can also be used as a feedback mechanism for complaints about your agency’s systems and processes, and gathering information to continually improve. 1. Select a topic Ideas for a useful focus group topic can come from many sources: • • • From issues identified by consumers/ people with disability From staff meetings From management needs. Once you have selected a topic, define a series of key questions relating to the topic (not more than 10, in the interests of clarity). Example: In the process of developing your corporate plan, you may seek feedback on the topic of ‘The Corporate Plan and Advocacy Agency Satisfaction’, specifically: The Mission Statement Goals of your agency Quality of advocacy delivery What advocacy is provided How your agency should be marketed What consumers/ people with disability liked or disliked What was missing from support Suggested changes or areas of improvement. 19 Based on the process used by Personnel Employment, SA, a Disability Employment Network service, Quality Strategy Toolkit for Disability Employment and Rehabilitation Services, FaHCSIA 115 2. Arrange a convenor So that consumers/ people with disability are able to communicate their views frankly, it is useful for the focus group convenor to be someone from your agency who is not directly involved in advocacy delivery to those consumers/ people with disability. Make sure the independent convenor you select is adequately briefed on relevant background relating to the focus group topic, your agency and your consumers/ people with disability. 3. Invite consumers/ people with disability Invite consumers/ people with disability to attend. Using groups of less than 10 consumers/ people with disability are recommended. You could encourage participation by integrating the focus group with another event, like a lunch or morning tea. Encourage consumers/ people with disability of different ages, genders, backgrounds, to participate so that your group is more representative of your agency as a whole. Consider at this point whether any of the attending consumers/ people with disability will require support to participate in the focus group, and how you can arrange support for them. 4. Convenor conducts the meeting The convenor will then facilitate the focus group. The convenor should establish some ground rules to emphasise that all participants should listen to one another’s views, take turns to express their opinion and respect the views of others. The convenor will find it useful to tape record the focus group, but should check first that the participants consent to be taped and complete consent forms. Advise all participants that their comments will be kept anonymous. 5. Convenor writes-up results The convenor should then write-up the results of the focus group into a summary report, using the views expressed by the participants. The write-up should not identify any participants, either by name or other identifying details. 6. Convenor circulates write-up to focus group members The convenor should circulate the summary report to focus group participants only. The focus group members should confirm that: 116 They have not been inadvertently identified in the write-up The write-up is accurate. During the focus group the convenor should establish how participants would like to be contacted to review the summary report and whether they will require any support to review the summary report. The convenor should make changes to the report as required by the participants. 7. Distribute findings When the participants have reviewed and confirmed the write-up, distribute the summary report to the areas in your agency where the information could have an impact. Depending on the focus group topic, these might include: The management and CEO The Board Continuous improvement committee or other form of quality committee A person responsible for organising/administering training programs. 8. Follow-up If the summary report suggested any specific changes, you may wish to followup with the relevant area of your agency to see whether any changes have been made based on the focus group feedback. You could do this as an automatic process, three months after every focus group. You should document any changes or responses, and keep the records alongside the focus group summary report. This documentation may be able to be used as evidence of continuous improvement processes. Guide to Engagement20 Engagement is a term used to describe the range of interactions between people (consumers/ people with disability, staff, and management). It is an ongoing process that can influence people’s interest, expectations and motivation to participate. It can include a variety of approaches, such as informal communication or information exchange, active listening, and relationship management. Engagement is an active process that allows: 20 Adapted from Disability Services Queensland Service User Participation Snapshot and Guide, www.disability.qld.gov.au/quality 117 The establishment and maintenance of relationships information sharing An increased awareness of the value of consumers/ people with disability participation. Why is effective engagement so important? For consumers/ people with disability, effective engagement demonstrates that their needs, experiences and feedback can directly influence the way that advocacy is delivered, and that they have roles that contribute to your agency’s planning, development and delivery. To feel motivated to participate, the potential benefits of doing so need to be outlined to consumers/ people with disability. It is through the later participation in your agency’s processes (activities) that the benefits are reinforced. Effective engagement enables your agency to build a relationship with consumers/ people with disability that is based on the value of consumers’/ people with disabilities' feedback driving advocacy delivery, and enables a greater understanding of consumers’/ people with disabilities' needs and what investment is required to facilitate their participation. Goals of engagement Create a foundation for participation in your agency activities. Identify ways to work together according to each other’s capacity and capability. Identify, plan and resource supports required to enable participation. How does engagement occur? Engagement occurs each and every day in your agency: from a consumer’s first day at (during their orientation or initial meeting), in the information you make available about your agency (through pamphlets or websites) and in the way you respond to consumers/ people with disability on an ongoing basis (such as acting on a parent’s suggestion or complaint). All of these are examples of engagement activities. They involve the establishment of relationships, a sharing of information, and a raising of awareness that consumers’/ people with disabilities’ participation is valued. How does engagement enable participation? Through engaging consumers/ people with disability, you are able to demonstrate to them that they are valued and are the focus of your agency. Effective participation will be dependent to a large extent on whether consumers/ people with disability feel valued and respected as vital contributors by both staff/ volunteers and management. 118 Trust, respect, support, openness – these are key components in building rapport and relationships with consumers/ people with disability and their families. Furthermore, it is through establishing strong relationships that consumers/ people with disability, staff and agencies are able to communicate more effectively and gain information about how consumers/ people with disability can participate in agency processes such as planning, development and delivery. The diagram below represents how an environment for participation is supported by ongoing engagement activities (i.e. investment, communication): Environment for participation Example: Your agency is holding a planning day (the participation activity) and would like to have consumers/ people with disability contribute to providing direction and decision making (their role). By using your agency newsletter (the communication method), you can inform them (raise awareness) of their potential role in the activity and how you will use their contribution (your intent). You can determine what resources (the investment) are required to support their participation in the activity based on the information you collect through your day-to-day interactions. Results from your annual satisfaction survey (feedback mechanism) can also be used to indirectly contribute to the planning day and assist in measuring (evaluation) the success of the participation activity. This activity, developed by Disability Services Queensland, asks you to reflect on the way you engage people with disability in your agency and their participation in planning, development and delivery. 119 Engagement Engagement is the foundation for participation, and supports consumers/ people with disability in choosing to actively participate in your agency processes of planning, development and delivery. A number of key elements (domains) will contribute to the achievement of these goals and inform the development of your engagement strategies and activities: Roles: In identifying opportunities for participation in your agency processes (planning, development and delivery), potential roles will need to be identified and agreed on by consumers/ people with disability and agencies. These roles may be contributing to agency planning or informing the results of improvements or consulting on staff recruitment. Some roles, such as a consumers/ people with disability representative on the Board of management, may be formally recognised in your constitution. Communication: Communication allows greater awareness (information sharing) of each other’s needs and potential. By maintaining open communication mechanisms (informal and formal) you can continue to exchange information – as consumers’/ people with disabilities' needs and interests change or your agency’s capacity and capability to respond to those needs changes. The communication you establish during engagement can then be utilised when needed according to the participation activity (planning, development and delivery). Investment: During engagement, there are two parts to investment. The first is a commitment to providing opportunities for participation. Then, after having determined potential roles and the supports required to enable participation, you can begin to identify the investment required in terms of funds, time, skills development, staff, resources, support aids and so on. Engagement strategies and activities can be subtle and informal, e.g. in day-today consumers/ people with disability and staff interactions. There are also formal processes for engagement, including: Mission and vision statements – which could articulate your commitment to participation Brochures or posters – which can raise awareness of the potential benefits of participation Consumer assessment – which increases your understanding of their needs, interests and motivations in order to plan your participation support and activities Newsletters – which could outline how consumers/ people with disability can choose to participate in decision-making processes. Advocacy planning Engagement is a precursor to participation in agency processes like agency planning. So, after considering and reflecting on ways you engage with service users, the next step is to consider how you have involved (or plan to involve) 120 them in your planning. This might include formal processes e.g. forums, consultations, surveys or questionnaires, focus groups, small working groups or individual interviews. You may also establish advisory committees or reference groups, facilitate planning or evaluation meetings, or include consumers/ people with disability representatives on your board of management. Using information from your complaints register is an indirect form of consumers’/ people with disability’s participation in your planning processes. Consider the different levels of planning – strategic, operational and individual – at which people with disability can participate. Advocacy development and delivery The next step in the exercise asks you to consider consumers’/ people with disability’s involvement in advocacy development and delivery. Consider how consumers/ people with disability are involved in these activities and whether the degree of involvement is appropriate to consumers’/ people with disability’s capacity and the nature of the task. Agency development includes developing policies, procedures, systems and programs and all the things your agency does to make improve. Advocacy delivery includes (but is not limited to) the activities that link directly to providing access, support, care, advocacy etc. Advocacy delivery may include structured processes or activities, such as how a consumer accesses your agency or how development of individual plans occurs. Now consider the questions in the following table and complete your agency’s snapshot of consumer/ people with disability participation. Once the table is complete you may use this information to identify specific areas where you could improve participation link and link these to continuous improvement activities. 121 Consumer/ people with disability participation Engagement Advocacy Planning Investment (support and capability) Describe how you have invested in the following areas to enable participation: * Skill development for staff or people with disability * Communication support * Time * Financial assistance * Family support Roles (potential) Have you identified with people with disability ways to work together? If so how? Activity Outline the opportunities that exist for participation in advocacy planning activities. From this, what are the potential roles involved in working together? What contributions do people with disability make to planning? Communication/Information (range) Outline the range of communication methods used to raise awareness of participation opportunities. Communication/Information (actual) Which communication methods do you use to raise awareness of planning activities and results? What information is exchanged between you and your people with disability to enable participation? What communication supports do people with disability access in order to be actively involved in planning? Describe how this impacts on your relationship with people with disability. How has working together changed your relationship? Goals for participation What are you hoping to achieve by involving people with disability in your agency? Evaluation Have you evaluated the level of participation in planning activities? Is there shared understanding between you and people with disability about what you can achieve through participation? If yes, did the activities contribute towards your reaching your goals for participation? Roles (actual) Describe the specific roles around advocacy planning activities. Advocacy development and delivery Activity Outline the opportunities that exist for participation in advocacy development and delivery activities. Roles (actual) Describe the specific roles around advocacy development and delivery activities? What contributions do people with disability make to service development and delivery? Communication/Information (actual) Which communication methods do you use to raise awareness of advocacy development and delivery activities and results? What communication supports do people with disability access in order to be actively involved in advocacy development and delivery? How has working together changed your relationship? Evaluation Have you evaluated the level of participation in advocacy development and delivery activities? If yes, did the activities contribute towards your reaching your goals for participation? 122 Engagement Investment (support and capability) Advocacy Planning Activity Advocacy development and delivery Activity Roles (potential) Roles (actual) Roles (actual) Communication/Information (range) Communication/Information (actual) Communication/Information (actual) Goals for participation Evaluation Evaluation 123 Standard 4: Privacy, dignity and confidentiality 4.1 Sample policies and procedures Sample Policy: Collection and Use of Information21 Collecting Consumer Information 1. Any information obtained by our agency about consumers, both past and present, will be regarded as confidential and must not be used for any purpose other than that for which it is given. 2. A consumer will be advised and made aware of what information is kept about him/her, why it is kept and who has access to it. 3. Our agency will only collect consumer information that is directly relevant to effective advocacy assistance. 4. All staff, volunteers and Management Committee members of our agency will sign a confidentiality declaration indicating that they understand the confidentiality and privacy requirements to which their work is subject. Information Disclosure and Consent 1. Each consumer has the right to access any information that our agency keeps about him/her. Any person except an advocate, approved student advocate, approved volunteer advocate must obtain consent from the consumer before obtaining access to the consumer's file. 2. Before any identifying information is disclosed to any individual or organisation other than authorised advocate of our agency, consent must be obtained from the consumer. If information of a sensitive nature must be disclosed in order to reach the outcome requested by the consumer, then written consent must be obtained from the consumer (e.g. a consumer wishes information about their case to be provided to the media). 3. If another organisation wishes to make contact with a consumer, our agency may either invite the consumer to contact the organisation or obtain consent from the consumer to provide relevant information. 4. Identifying information in a consumer's file must not be used for the purpose of research without written consent from the consumer. Exceptions to confidentiality Statistical Information Statistics may be gathered about consumers who use our agency for the purposes of agency planning, accountability and systemic advocacy. However, this information will be used sensitively and in a manner that does not identify individuals. Case studies used for the purpose of community education will not contain information which will cause a consumer to be identified (i.e. identifying information may be altered to protect the privacy of the consumer). If there is 21 National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA 2009 124 any concern that such information might identify an individual, our agency should seek the consumer's consent. Supervision From time to time, an advocate may need to seek independent professional supervision or consultation to assist consumers in achieving the outcome they wish. Identifying information should not generally be given to the professional supervisor. However, if providing such information is essential, advocates/ volunteer advocates should seek the consent of the consumer. A professional supervisor should be given a copy of this policy and agree to abide by it. Subpoena If a consumer's file is ordered by a subpoena, the consumer will be notified as soon as possible. Only information ordered by subpoena will be released. In this instance, the information may be photocopied. Necessity There may be an exception to confidentiality where our agency reasonably believes that the use of disclosure is necessary to prevent a serious and imminent threat to the individual’s life, health or safety or, a serious threat to public health or safety. A decision to disclose information to seek help or protect the consumer will pay due regard to the particular consumer’s capacity to make decisions. Any need to disclose consumer information on the basis of necessity should be discussed with senior staff wherever possible. Complaints processes Should a complaint occur about the operation of our agency, a delegated member of the Management Committee may have access to the nominated consumer’s file in order that the Management Committee member can participate in the resolution of the complaint. Mandatory reporting requirements Our agency’s staff/ volunteers may be required by legislation to disclose relevant consumer information to the Department of Community Services (or any equivalent body as specified by legislation) if that paid staff member has reasonable grounds to suspect that a child is at risk of harm and that those grounds arise during the course of or from that person’s work. Funding Body’s Access Our agency is required to make files available to the government funding body for auditing purposes if the funding contract stipulates this. Our agency will 125 ensure that government funding body obtain permission from individual consumers before making any files available. File management Treatment of files A file will be created for each new person being assisted by our agency Files will not be duplicated, except where sections of a file have been requested by subpoena Files remain the property of our agency. However, copy can be made of any or all information for the consumer on request. A consumer's file will be placed into secure storage upon the consumer ending their association with our agency. Such files will be destroyed after five years. Maintenance of files Documentation should contain objective information. Care should be taken with the choice of language used. Consumer files should contain the originals of incoming documents and copies of any outgoing correspondence. All incoming and outgoing correspondence must be dated. File security Consumer files will be filed in lockable cabinets. Information kept on computer should be kept in a secure fashion. Only our agency’s advocates (or the citizen advocate associated with a particular consumer) may have access to consumer files. General volunteers or students on placement may access specific files under supervision of advocates. A consumer file should not be removed from the office unless special circumstances prevail and permission is first sought from our agency’s Coordinator. Personal privacy and dignity In all decisions and dealings of our agency, our agency will ensure that people with disability are treated with dignity and respect. Where people with disability and/or their family members are consumers of the agency, our agency will respect consumer’s rights to personal privacy (e.g. in personal hygiene tasks). 126 4.2 Tools Tool: The National Privacy Principles and Information Privacy Principles – Protecting Privacy throughout the information cycle22 Note: The National Privacy Principles (NPP) are the base line privacy standards which some private sector organisations need to comply with in relation to personal information they hold. The Information Privacy Principles (IPP) are the base line privacy principles which Commonwealth government agencies need to comply with in relation to personal information kept in their records. 23 It is a condition of the current NDAP funding agreement, and a requirement of Standard 4 of the Disability Advocacy Standards, that NDAP funded disability advocacy agencies must comply with the IPPs contained within the Privacy Act 1988. 22 Quality Strategy Toolkit for Disability Employment and Rehabilitation Services, FaHCSIA: https://www.fahcsia.gov.au/sa/disability/pubs/employers/Documents/quality_strategy_toolkit 23 See Office of the Privacy Commissioner, www.privacy.gov.au 127 The National Privacy Principles and Information Privacy Principles – protecting privacy throughout the information cycle. 128 Tool: Sample Privacy Statement for Consumers24 Gippsland Disability Advocacy Inc. (“GDAI”) is committed to meeting the requirements of the Information Privacy Act (2000) and the Health Records Act (2001). These two pieces of legislation govern the way we handle your information from collection through to disposal. More detailed information on the rights and responsibilities of both consumers and the GDAI is available in GDAI’s Privacy Policy. A copy of GDAI’s Privacy Policy can be made available upon request. The Gippsland Disability Advocacy Inc will: identify the main purpose for the collection of information from you collect only the information required for this purpose* not share this information without your consent* let you see your file on request correct file information if it is established that file content is inaccurate provide you with access to your file, if you require it* keep your file in a secure place destroy your file in accordance with our statutory requirements. We reserve the right given to us under both Acts to restrict your access to information in your file because that access may: unreasonably affect the privacy of other individuals pose a serious threat to the life or health of any person expose information given in confidence by a third party be unlawful because other legislation requires our agency to withhold information prejudice a law enforcement function by a law enforcement agency. I acknowledge that I have read this statement and agree to my file being held and disposed of in accordance with statutory requirements without being notified at the end of the statutory holding period. Consumer (Please print full name)________________________________________ Signed Date_____________________ Advocate (Please print full name)________________________________________ Signed Date_____________________ *Statistical information will be collected to meet relevant funding body requirements and for research and analysis purposes as allowed for under both Acts. Importantly this information is maintained in a manner which ensures that it cannot be identified with you or your file. 24 Gippsland Disability Advocacy Inc. 129 Tool: Sample Confidentiality Agreement25 CONFIDENTIALITY AGREEMENT This agreement is to be read and signed by each member of the Board and all staff members This will also be a requirement for advocates, volunteers, contractors, consultants and business partners who work with CASA and have, or are likely to have access to information used by CASA. CASA has a significant responsibility to protect the information it holds and encounters in relation to its services, the work it undertakes and its stakeholders. The undersigned recognises the importance of using information appropriately and safeguarding information from unauthorised disclosure or use, whether this information is directly related or incidental to their involvement with CASA. The undersigned agrees to: Ensure that confidential information which is acquired in connection with Citizen Advocacy will not be disclosed to any person or organisation, unless authorised to do so or legally required to do so in which case the Board shall be notified within twenty-four hours. Take careful and reasonable measures to secure and maintain the confidentiality of all information at all times. This standard of care relates to all forms of information (e.g. verbal, written, and electronic). Return all information in your possession promptly to CASA if requested to do so, including all copies of information, and notes of meetings and conversations. Comply with these requirements even after ceasing to be involved with or transact with CASA. Seek advice from the Program Manager or their delegate, or in their absence the Chair of the Board, where any uncertainty exists in relation to the use, storage, distribution or security of information. This agreement is made between CASA Inc. and the undersigned. Signatory’s Name: (Please Print Name in Full) Signature CASA Delegate: Signature: Date: 25 Citizen Advocacy South Australia 130 Standard 5: Participation and integration 5.1 Sample policies and procedures Sample Policy: Participation and Integration26 Our advocacy agency will: Educate staff regarding: o The importance of ending the discrimination, segregation and neglect of people with disability in the community o The importance of participation by people with disability in regular activities in the community Encourage staff, volunteers and advocates to develop links between our agency and people and groups that will benefit people with disability Where possible and appropriate, participate in community education or activities to promote greater understanding and awareness of disabilities. To enable effective integration and participation, our agency will maintain and develop relationships with the local community, as well as coordinating with other agencies to be an effective community partner. Where people with disability are the consumers of the agency, our agency will: Provide information about resources, activities and opportunities for consumer participation and inclusion in local community events/ activities. Information will be filed and updated regularly, and made available for consumers’ use Provide consumers with information about general community facilities and services and how to use them Support people with disability to form and maintain a variety of appropriate ties, connections and involvements in the community. Systemic change policy Where the agency does not undertake systemic advocacy, our agency will: Document the issues consumers of our agency identify Identify trends and any ongoing systemic issues Refer any systemic issues to a systemic advocacy agency and ensure follow up with the agency. Where the agency undertakes systemic advocacy, our agency will: Where possible, consult with people with disability about the systemic actions that should be pursued. Where this is not possible, for example, in reactive cases, inform people with disability about the actions being pursued Follow up systemic issues referred by other advocacy agencies. 26 National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA, 2009 131 Sample Policy – Participation and Integration27 Gippsland Disability Advocacy Incorporated recognises the valuable contribution people with disability can make to the communities in which they live. The Council encourages and supports each person with a disability to participate and be involved in the life of the community. Participation in community activities The GDAI will facilitate the integration of people with disability in community life by actively encouraging and supporting their participation in or use of: Community based Advocacy and Self Advocacy Groups, Committees of Management, Steering and Advisory committees (e.g. Access Committees). Forums, workshops and seminars offered within the community. Community based recreation and leisure facilities and facilitate access to other social options and activities. Public transport to maximise independent travel. Community based services and facilities available to all members of the community. Information regarding general community services and facilities, and how to use them, will be available upon request from the GDAI. This information will be available in alternate format to suit the needs of the person making the request. Community education and advocacy GDAI will further the opportunity for participation and integration of people with disability in community activities by effective advocacy, and community education programs, which include: 27 Extensive media coverage highlighting the abilities of people with "disabilities", the implication of disability and disability issues. Conducting disability awareness programs in schools and tertiary institutions (e.g. TAFE Colleges), and guest-speaking at Service Clubs and Community Groups. Conducting Community Awareness forums and workshops available to the public. Supporting regional self advocacy groups within local communities. Identifying and resolving issues, which are preventing or hindering further participation of people with disability in community life, through effective systemic advocacy by Community self advocacy groups. Advocating for improvements to physical access within the community. Gippsland Disability Advocacy Inc. 132 Advocating for changes to general services and facilities so they have the capacity to cater for the extra needs of people with disability. Availability of policy The Policy Manual, including the Participation and Integration Policy, is available to all consumers and potential consumers in a suitable format. Review of policy The Participation and Integration Policy will be reviewed at least every 12 months, more often if necessary. This policy will be reviewed by staff, members of the Committee of Management and consumers, in General Meetings or Special General Meetings or consultation by mail or telephone. 133 Standard 6: Valued status 6.1 Sample policies and procedures Sample policy: Valued status28 Our advocacy agency will: Support people with disability to obtain the same rights as other citizens through the advocacy process (whether on a collective or individual basis) Operate from a physical environment which encourages participation of people with disability and their family members/ carers (fully accessible premises in local community areas) Ensure that venues for meetings, conferences, workshops, etc. are accessible Involve people with disability in the management, planning or operations of our agency, where possible and appropriate Identify and respond to the needs and ideas for developing sustainable connections and networks in the community, which will support people with disability’s valued status Work with the community and in the community to foster opportunities for people with disability to participate in ways which will be valued. Where people with disability are the consumers of the advocacy agency, our agency will: Provide consumers with real opportunities to maintain and develop skills and capacities which will support their aspirations and strengths Be responsive to the individual needs of people with disability wishing to develop and maintain valued roles in the community Support each person with disability to have the opportunity to develop and maintain skills, capacities and lifestyles that are valued in the community Where possible and appropriate, support consumers to participate as agency members at conferences and brief them about the purpose of the meeting and their role as a participant. Promoting ‘valued status’ in the community Our agency's community education/ awareness strategy will promote the abilities and competencies of people with disability. Our agency recognises and promotes the inherent value of all people with disability and values the contributions and skills of people with disability and their family members/ carers. Any publications or promotional material produced by our agency will: 28 National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA, 2009 134 Promote the abilities, skills and contributions to the community of people with disability, by: o using language that puts the person first i.e. ‘people with disability’ o referring to adults with disability as adults, not children o describing a person’s needs (if necessary) by using terms such as ‘low support needs’, ‘high support needs’ o advocating that labels such as ‘disabled’, ‘spastic’, ‘handicapped’, ‘retarded’, ‘mental’ and patronising terms are not used Not use the term ‘disability’ in a negative way to attract support, financial or otherwise Present the concerns of people with disability and their carers positively to the media, in publications, conferences etc. Provide the best quality information available to people from an Aboriginal or Torres Strait Islander or Culturally and Linguistically Diverse background with disability and their carers in a culturally appropriate way. Within our scope and available resources, our agency will develop and/or implement programs and activities in and with the community to promote valued status. 135 Sample Policy: Valued status -Gippsland Disability Advocacy GDAI recognises, upholds and promotes the valued status, abilities, competencies, and contributions of people with disability by: Creating a level of membership within the association, namely Full Membership, which gives people with disability and/or carers voting rights; Including a rule in the Articles of Incorporation which ensures Committee of Management is made up only of Full Members of the Association; Facilitating the participation and management of regional advocacy groups and support groups by people with disability; Respecting and upholding the consumer and human rights of people with disability; Providing services in the least restrictive and most empowering way; Constantly consulting with people with disability; Providing service within a fully accessible generic location with high quality facilities; Ensuring services are provided by carefully selected and appropriately trained staff. GDAI will support and encourage people with disability to develop and maintain the necessary skills and capacities, to enable them to attain a valued role in the community by: providing information about, and referral to, educational and skill enhancement services; providing or arranging support for people with disability to enable them to access educational and training services. Availability of policy The Policy Manual, including the Valued Status Policy, is available to all consumers and potential consumers in a suitable format. Review of policy The Valued Status Policy will be reviewed at least every 12 months, more often if necessary. This policy will be reviewed by staff, members of the Committee of Management and consumers, in General Meetings or Special General Meetings or consultation by mail or telephone. 136 Sample Policy: Valued status - Sunshine Coast Citizen Advocacy29 SunshineCoast Citizen Advocacy will: Support people with disability to obtain the same rights as other citizens through supporting People with disability to achieve ‘Valued Status’ Sunshine Coast Citizen Advocacy will: Support people with disability to obtain the same rights as other citizens through the advocacy process. Operate from a physical environment which encourages participation of people with disability and their family members/ carers (fully accessible premises in local community areas) Ensure that venues for meetings, conferences, workshops etc. are accessible Involve people with disability in the management, planning or operations of Sunshine Coast Citizen Advocacy, where possible and appropriate. Identify and respond to the needs and ideas for developing sustainable connections and networks in the community, which will support people with disability’s valued status. Work with the community and in the community to foster opportunities for people with disability to participate in ways which will be valued. Sunshine Coast Citizen Advocacy will support and encourage citizen advocates to: Provide protégés with real opportunities to maintain and develop skills and capacities which will support their aspirations and strengths Be responsive to the individual needs of protégés wishing to develop and maintain valued roles in the community Support protégés to have the opportunity to develop and maintain skills, capacities and lifestyles that are valued in the community Where possible and appropriate, support protégés to participate at conferences and brief them about the purpose of the meeting and their role as a participant. Promoting ‘Valued Status’ in the community Sunshine Coast Citizen Advocacy’s community education/ awareness strategy will promote the abilities and competencies of people with disability. Sunshine Coast Citizen Advocacy recognises and promotes the inherent value of all people with disability and values the contributions and skills of people with disability and their family members/ carers. Any publications or promotional material produced by Sunshine Coast Citizen Advocacy will: Promote the abilities, skills and contributions to the community of people with disability, by using language which is image enhancing and which will promote valued social status of people with disability. 29 http://www.citizenadvocacy.com/policies/policies-and-procedures/valued-status/ 137 Not use the term ‘disability’ in a negative way to attract support, financial or otherwise. Present the concerns of people with disability positively to the media, in publications, conferences etc. Provide the best quality information available to people from an Aboriginal or Torres Strait Islander or Culturally and Linguistically Diverse background with disability and their carers in a culturally appropriate way. Within our scope and available resources, Sunshine Coast Citizen Advocacy will develop and/or implement programs and activities in and with the community to promote valued status. 138 Standard 7: Complaints and disputes 7.1 Sample policies and procedures Sample Policy: Complaints and disputes30 Principles Our agency supports the right of people with disability, or of the carers and families of people with disability, to make a complaint without retribution. Our agency will take all reasonable steps to ensure that anyone involved in making a complaint is not victimised, and will inform complainants of how they will do this. Our agency’s complaints and disputes policy and procedure will be accessible to consumers and people with disability. Copies of the complaints and disputes mechanisms will be available, written in clearly understandable language. Provisions will also be made for people from a Culturally and Linguistically Diverse (CALD) background with disability to have access to material relating to complaints and disputes policy and procedures where required. The material explaining the complaints and disputes system will make explicit that there will be no retribution against anyone who makes a complaint against our agency. Sample Procedure Step One In the first instance, the person with disability is encouraged to discuss the matter with the person perceived to be responsible for the grievance. If the person with disability feels unable to discuss the matter directly with the person involved, for instance because the allegation is a serious one such as sexual harassment, the matter should be referred directly to the Management Committee of our agency. Confidentiality and privacy should be respected as much as possible. Step Two If the matter is not resolved by discussion with the involved parties, the grievance should be referred to the Management Committee. The Management Committee will form a sub-committee to address grievances. This subcommittee will discuss with the complainant whether the complainant requires a support person to assist them through the dispute resolution process. Step Three 30 National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA, 2009 139 Where the dispute cannot be resolved at Committee level, the Committee will appoint, with the complainant’s approval, an independent conciliator to assess the grievance. The conciliator will report on the outcome to the Committee and the consumer. Step Four Disputes that are still unresolved after this stage should be referred to an external body. Sexual harassment Sexual harassment is unwelcome sexual attention or uninvited sexual advances that result in you feeling embarrassed, humiliated or intimidated. Sexual harassment may be explicit or implicit. It may be a single incident or occur over a period of time. Examples of behaviours that may be considered sexual harassment include: Sexual jokes, lewd suggestions, whistling, foul language, leering, obscene gestures Belittling comments about a person’s anatomy or based on sex-role stereotypes Persistent demands for participation in social activities or repeated requests for dates Asking about a person’s private or sex life, explicit sexual suggestions in return for ‘reward’ Unwanted physical contact of a sexual nature including touching, brushing or kissing Display of pornographic and/or sexually suggestive pictures, screen savers, jokes etc. and/or sexual objects Sexually offensive written, telephone or electronic communications Indecent exposure Trying to force another person to have sex. Our agency will: Treat all complaints of sexual harassment seriously and will deal with them promptly, impartially and confidentially Take steps necessary to ensure that sexual harassment does not continue, that complainants and witnesses are not victimised in any way and that, where possible, a fair and appropriate resolution of the problem is reached Discipline any staff found harassing others. Complaints about sexual harassment within our agency should use the normal system of complaint/ dispute resolution outlined in our agency’s complaints and disputes policy. However, the complainant may wish to omit Step One if they are uncomfortable discussing the matter directly with the other person. 140 Staff misconduct and discipline Definitions Misconduct is failure by an employee to fulfil their duties. Misconduct includes the following actions carried out at agencies or during the course of an employee’s duties: Theft Physical assault Sexual harassment Psychological and emotional abuse (e.g. bullying) Intoxication Use of illegal drugs (unless prescribed by a recognised medical practitioner) Gross negligence Serious breach of policies/ procedures Serious breach of safety procedures Illegal or fraudulent acts while on agency business Wilful or malicious damage Wilfully disregarding/ disobeying a reasonable instruction Inefficiency/ incompetence Negligence/ carelessness in carrying out duties Engaging in improper conduct Engaging in patronage, favouritism or discrimination in the discharge of duties Supplying incorrect/ misleading information in relation to their employment. There are two possible responses to misconduct by employees: counselling/ warning or dismissal. Staff members/ volunteers involved in misconduct or discipline procedures have the right to notify an accredited representative of their Union or other support person/ advocate of their choice, to organise a meeting with the appropriate program manager and to accompany the employee at any time during these procedures. Allegations of misconduct should be referred to a member of the Management Committee. Procedures (From Employer’s First Guidelines) The 4 step procedure outlined next, aims to get an employee [defined as any person who has an employment relationship with agency] who has not been performing or behaving satisfactorily ‘back on track’. The steps are designed to ensure that the employee is treated fairly. Step 1. Counselling and Oral Warning The employee’s supervisor or a member of the Management Committee will initiate a discussion with the employee about their performance or behaviour. 141 The purpose is to bring the unsatisfactory performance or behaviour to the employee’s attention. Before the discussion the supervisor or committee member will: Check the matter thoroughly and gather all the facts including any previous performance reviews Ensure the employee has received any training they should have been given to perform the job satisfactorily Remove any genuine obstacles to the employee performing the job properly Prepare an outline of main points to be covered. During the discussion the employee’s supervisor or committee member will: State the specific problem Give the employee a chance to explain their point of view Consider their response and, if not satisfied, tell the employee the changes they expect and warn that if the employee does not improve further disciplinary action will be taken. After the discussion, the employee’s supervisor or committee member will: Record in a file note the date and place of the meeting, who was present and what was said, particularly the wording of the warning Seek advice from Employer’s First before proceeding to Step 2. Step 2. Counselling and Written Warning Before the discussion the employee’s supervisor or committee member will follow the procedures in Step 1. In addition, the employee’s supervisor or committee member will: Tell the employee that they may have a friend or other support person present during the discussion Organise a program manager, the employee’s supervisor or other senior employee to be present during the discussion to observe and assist. During the discussion, the employee’s supervisor or committee member will: Review the previous discussion Discuss the employee’s performance or behaviour during the review period Give the employee a chance to respond and explain Tell the employee the specific changes s/he requires Ask the employee to confirm they understand what is expected of them Tell the employee they will receive a written warning after the discussion and that failure to change may put their job at risk Seek advice from Employer’s First before proceeding to Step 3. After the discussion, the employee’s supervisor or committee member will: Give the employee a written warning which contains o The dates of the first and second discussions 142 o o o Details of the problem/s A statement of the changes s/he requires A statement saying that if they fail to change or improve they may jeopardise their employment and will be subject to further disciplinary action Record these details in a file note and attach a copy of the written statement to the employee to the file. Step 3. Counselling and Final Written Warning The committee member will: Follow the same procedure as in Step 2 Give the employee a letter which states clearly that because of their failure to improve satisfactorily following Steps 1 and 2, this final warning is now being given and their employment will be terminated if they fail to make necessary improvements Ask the employee to sign the letter, acknowledging receipt, keep copies on file and re-state to the employee that this is their final warning Seek advice from Employer’s First before proceeding to Step 4. Step 4. Dismissal Before the dismissal, the Committee member will: Discuss the employee’s performance or behaviour with other management and senior people involved before taking action Review all supporting documents on file, leave records, performance reviews Prepare an outline of the points to be covered Consider responses to possible questions from the employee Organise a program manager or the employee’s supervisor to be present during the dismissal. During the dismissal, the Committee member will: Have someone else from senior management present Ask the employee to come to her/his office or another private area, and allow them to bring a support person Tell the employee s/he is considering terminating their employment Put the allegation specifically to the employee in enough detail to allow them a fair opportunity to respond Ask for, and answer, any question the employee has and give the employee a chance to put their position Listen to the employee’s explanation and assess whether it changes her/his views about termination Take a short break to consider the employee’s explanation and if s/he considers termination is still appropriate, prepare a letter of termination stating reasons and any entitlements owing, including notice or payment in lieu, then resume the meeting Tell the employee that the explanation has not been satisfactory and s/he is terminating their employment, outlining the reasons with reference to previous steps taken 143 Give the employee a dismissal letter Give the employee any information they need about payment, superannuation entitlements etc. Explain whether the employee is to leave with notice or with pay in lieu of notice If the employee is to leave immediately consider whether, for security reasons, it is desirable for a senior manager to escort the employee to their office and then from the premises. After the dismissal the Committee member will: Write down what was said and what happened during the meeting. Instant Dismissal This will only be considered if an employee does the following activities at work: Theft Physical assault Sexual harassment Intoxication Use of illegal drugs (unless prescribed by a recognised medical practitioner) Gross negligence Illegal or fraudulent acts while on MDAA business Wilful or malicious damage. The Committee member will: Inform the employee promptly of the specific allegation/s against them Inform the employee that s/he will investigate the allegation/s promptly and that they will have an opportunity to respond Inform the employee that they can have a friend or other support person present when s/he discusses the allegation/s Undertake the investigation as soon as s/he is aware of the allegation/s and speak to anyone who can shed light on them Consider the facts carefully after the investigation Discuss the allegation/s with the employee with a witness present and take notes or record what is said Give the employee an opportunity to respond to the allegation/s Take time to consider the facts after the employee had responded Only terminate the employee’s employment if s/he is satisfied that the major points of the allegation/s did take place and that the reason for termination justifies instant dismissal from an objective point of view Write down what happened and what was said in the dismissal procedure and put any notes made during or immediately after the termination in the employee’s file Give the employee a letter confirming their dismissal and stating the reasons. 144 Sample Complaints Policy and Procedure - Rights in Action Inc.31 Policy RIA acknowledges that all people seeking advocacy have the right to be heard on issues of concern, undertakes to address all concerns and complaints made, and to quickly work towards an outcome satisfactory to all parties. This will be done without fear of retribution and in an equitable way. RIA believes that queries, concerns and complaints provide valuable feedback about how the organisation can improve its service. People seeking advocacy have the right to: Have complaint pursued confidentially, objectively and with an aim towards permanent resolution and elimination of the chance of repetition wherever possible; Be told what avenues are open to them to resolve the complaint; and Have another person, friend or family member present to support them. RIA Advocates have a responsibility to maintain complete confidentiality if they provide information during the investigation of a complaint. Spreading gossip or rumours could expose people to defamation action. It is the responsibility of RIA staff to inform people seeking advocacy of this policy. All people seeking advocacy will have access to the Complaints Policy. Procedure The following procedure ensures the efficient and accountable actions of RIA staff and the Management Committee when responding to complaints (see figure on following page): In the first instance, the person advocated for should try to address the staff member with whom they have a complaint to negotiate a resolution. Where this is not appropriate or is unresolved, the person advocated for can arrange to talk to the Service Coordinator. This contact may be made in writing, by telephone or in person. The person advocated for can bring a friend or family member to support them in this discussion. Written statements will be disclosed to all parties. Within two working days, the Coordinator will arrange an interview with the person. Details of the complaint and response will be documented and documents signed by all parties If the complaint is still unresolved, the Coordinator will arrange a meeting between those concerned to facilitate resolution. This should occur within 10 working days. If this is unsuccessful, or at the request of either party, the Coordinator may either elect to involve a third, independent person to act as mediator or refer the complaint to the President of the Management Committee. 31 Excerpt from Rights In Action Inc. Policy and Procedures Manual, Section 6: The Rights and Responsibilities of People Seeking/Receiving Advocacy 145 The person advocated for may elect to refer their complaint direct to the President of the Management Committee. The President will take the complaint to a sub-committee (consisting of one independent person and representatives of the Management Committee), which will interview those concerned separately and privately within 10 days of the complaint being made. The complaint and response will be documented. If this is unsuccessful, the sub-committee may elect to involve a third, independent service to act as mediator. The referral for mediation must take place within two working days. At any stage throughout the complaint process, the person advocated for may seek external support and assistance (e.g. Complaints Resolution and Referral Service, Anti-discrimination Commission Queensland, or a community mediation service) to resolve his/her complaint. Similarly, the Coordinator and/or Management Committee may request assistance or advice from external parties. (See following page for Complaint Procedure Time Frame Flow Chart) Confidential records Confidential records are kept of the complaint process. The documentation must be stored securely so that the privacy of the person advocated for is protected. People seeking advocacy may view documentation related to their own complaint. Extending timeframes Timeframes for achieving stages of this procedure may be extended if there is reasonable justification for doing so. Reasons for doing so must be clearly documented. Complaints Resolution and Referral Service If the person advocated for is not happy with the way RIA addressed his/her complaint, he/she should be encouraged to contact the Complaints Resolution and Referral Service (CRRS) on 1800 880 052. CRRS is a service that helps people with disability sort out complaints about advocacy services funded by the Australian Department of Families, Housing, Community Services and Indigenous Affairs. CRRS helps deal with complaints when a service is not meeting the National Disability Services Standards or Disability Advocacy Standards. When looking at a complaint, CRRS: • Will talk to the person who makes the complaint; • Will get the other side of the story; • Will write a letter to the service; • May investigate the complaint; and/or • May hold a special conciliation meeting. If the complaint is not solved, CRRS will inform the Department of Families, Housing, Community Services and Indigenous Affairs. It is RIA’s responsibility to inform the person advocated for that this service exists. 146 Complaint procedure time frame flow chart 147 7.2 Tools Tool: Resources Complaints Handling – Guiding Principles based on the Australian Standard on Complaint Handling (AS 4269 – 1995)32 1. VISIBILITY Information about how and where to complain should be wellpublicised to customers, personnel and other interested parties. 2. ACCESSIBILITY The complaints handling process should be easily accessible to all complainants. This includes readily accessible information about the process, flexibility in the methods of making complaints and special arrangements and/or support for complainants with specific needs (including interpreters). 3. RESPONSIVENESS Receipt of each complaint should be acknowledged to the complainant immediately. Complaints should be addressed promptly; complainants should be treated courteously and kept informed of the progress of their complaint through the complaints handling process. 4. OBJECTIVITY Each complaint should be addressed in an equitable, objective and unbiased manner through the complaints handling process. 5. CHARGES Access to the complaints handling process should be free of charge to the complainant. 6. CONFIDENTIALITY Personally identifiable information concerning the complainant should be available where needed, but only for the purposes of addressing the complaint within the agency and should be actively protected from disclosure, unless the customer or complainant expressly consents to its disclosure. 7. INVESTIGATION OF COMPLAINTS Every reasonable effort should be made to investigate all the relevant circumstances and information surrounding a complaint. 8. CUSTOMER-FOCUSED APPROACH The agency should adopt a customer-focused approach, be open to feedback including complaints, and should show commitment to resolving complaints by its actions. Paraphrased from the Australian Standards Customer satisfaction – Guidelines for complaints handling in organizations (AS ISO 10002-2006), Disability Services Commission Consumer Liaison Service February 2007, www.disability.wa.gov.au/dscwr/_assets/main/guidelines/documents/doc/australian_standards_guiding_principles.doc 32 148 9. RESOLUTION OF COMPLAINT Following an appropriate investigation, the agency should offer a response, for example, correct the problem and prevent it happening in the future. The decision or action taken regarding the complaint should be communicated to the complainant as soon as the decision or action is taken. 10. ACCOUNTABILITY The agency should ensure that accountability for and reporting on the actions and decisions of the organisation with respect to complaints handling is clearly established. 11. CONTINUAL IMPROVEMENT The continual improvement of the complaints handling process and the quality of services should be a permanent objective of the agency. 149 Tool: Setting up an Effective Complaints System33 1. Set up a group Ask your staff/ volunteers and consumers/ people with disability and their families about how they think the complaints system should work. You should use this group as a resource throughout the development of your complaints policies and procedures. 2. Show management support You need a clear statement from the management of your agency about why the complaints process is being set up. Outline the benefits for your agency and for consumers. You should include this in a policy statement for your agency. 3. Accept all complaints There should be channels for people to complain about anything in your agency that they think does not work or is unfair. Just by listening actively and using good communication skills you can resolve many complaints on the spot. If you have a complaints form, ensure that it is simple and easy to use for both supported employees and staff. 4. Three levels of complaint handling Informal – for simple straightforward complaints. Make clear your staff authority to resolve such complaints as far as possible. Formal – for more complex or serious matters which need to be referred to a designated complaints person, a supervisor or manager. External – for when complaints cannot be resolved internally. Consumers/ people with disability should have the opportunity to use external systems at any time in your complaints process. For disability advocacy agencies and employment services, the external complaints body is the National Disability Complaints Resolution and Referral Service (CRRS). 5. Make it easy for consumers/ people with disability and others to complain You need to think about the accessibility of your complaints and resolution procedures – Easy English, Auslan, interpreter, Braille, tape. Are your procedures widely available and documented? 6. Record received complaints and comments You should have a system for recording complaints, comments and suggestions. This is an excellent tool for continuous improvement and helps you keep a handle on what’s happening in your agency. It’s good to keep positive feedback and distribute to your agency for morale. 7. Staff/ volunteer training NSW Community Services Commission ‘An Easy To Follow Guide To Good Complaints Handling’, in Quality Strategy Toolkit for Disability Employment and Rehabilitation Services, FaHCSIA 33 150 You should have a policy document that outlines your complaints system – both the process and the philosophy. You need to ensure that your message is getting across through staff meetings, newsletters, posters, training, induction training, employment contracts and agreements. 8. Train your consumers/ people with disability Your system is useless if your consumers/ people with disability, their families and other members of the public don’t know about it. How can you best communicate your complaints policy? Is it in a poster, a pamphlet, a newsletter? Are the formats you are communicating in appropriate for the target group? 9. Use your feedback to keep improving your agency Monitor your complaints system – is it working? If you are not receiving complaints, what does this mean? What are the complaints you are receiving telling you about your agency’s operation? 151 Tool: Accessible complaints policy checklist34 Easy English. Policy is explained in easy-to-understand English, with clear and short sentences, and in other formats appropriate to specific disability as required (e.g. Braille). If a complex word or term is used, an easy English definition is also provided. Responsive and timely. Complaint is handled quickly and timeframes are short and clear. Process is clearly explained and easy to follow (e.g. Step 1, Step 2…). Demonstrated commitment to resolution is in line with our agency’s vision, aims and objectives. Assistance is offered to consumers to lodge complaints. Follow up. Complainant is kept informed of progress. There is a good use of pictures that are age-specific and not childlike. Referral and contact details are provided for external services where complaint is unresolved or complainant chooses to go elsewhere. Advocacy and other supports are encouraged throughout the process and referral details provided if required Flexible. Complaints can be received in a range of formats including verbally. Complainants are encouraged to try and resolve issue at the most local level. Policy has a statement about no retribution and that complaints are welcomed, will be taken seriously and will be handled honestly, fairly and without bias. Confidential. Privacy of complainant and details of complaint is maintained. Permission is sought from complainant if it is necessary to discuss details with other stakeholders. Other opportunities for feedback, including anonymous feedback, are encouraged (e.g. suggestion box, focus groups, surveys). There is a commitment to use information from complaints for improvement. Policy is regularly reviewed and the review date included. Promotion. Policy is displayed and regular training is provided. Record keeping. Policy has a statement about keeping all records of the complaint, including file notes of discussions. 34 Quality Strategy Toolkit for Disability Employment and Rehabilitation Services, FaHCSIA 152 Tool: Local resolution meeting documents35 This document from the Complaints Resolution and Referral Service (CRRS) includes an agenda, agreement form and meeting guidelines that may assist your agency when you have a meeting to resolve a complaint. MEETING AGENDA Date:______________________________________________________ Venue: ____________________________________________________ Present:___________________________________________________ Purpose: To come together in an atmosphere of cooperation, trust and willingness to resolve the complaint. To listen to, and gain a better understanding of, each other’s views. What has happened in the past cannot be changed but what is worked out in the present and at this meeting will affect the future. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Welcome and Introductions Housekeeping egg: toilets, water, mobile phones Meeting Guidelines – Complete MEETING GUIDELINES sheet Key Discussion Points: Take turns to discuss each point and write down all agreements. _______________________________________________ _______________________________________________ _______________________________________________ _______________________________________________ Future Relationship and Communication – moving forward Follow up 35 Complaints Resolution and Referral Service (CRRS) http://www.crrs.org.au/publications.html 153 MEETING GUIDELINES Before the meeting: Check that the meeting room is private, quiet and accessible Allow enough time for the meeting. Clear your diary Enter the meeting in good faith and with a positive attitude During the meeting: Go through each point below and tick all agreed ones. Agree to switch off any mobile phones to avoid distractions Check time constraints. How much time do all parties have for the meeting? Acknowledge and thank everyone for coming and being committed to resolving the complaint Discuss and agree on the following guidelines: Agree to listen to the other person’s point of view or side of the story without interrupting or talking over. When talking about your side of the story remember to say how you felt and use ‘I’ statements Agree to be respectful when others are speaking and use respectful language Agree to respect each other’s privacy and confidentiality. That is, what is said in the meeting will not be talked about to others outside the meeting Agree to be open and honest Be objective; that is, put yourself in the other person’s shoes Anyone can request a break at any time Anyone can end the meeting at any time All parties to be given a copy of the agreement AGREEMENT 154 Date: ___/___/___ Parties to the Agreement: Complainant: _______________________________________________ Advocate: __________________________________________________ Support Person: _____________________________________________ Service Staff:_________________ Position:_______________________ Service Staff:________________ Position:________________________ Agreements: 1. _______________________________________________________ _______________________________________________________ _______________________________________________________ 2 _______________________________________________________ _______________________________________________________ _______________________________________________________ 3 _______________________________________________________ _______________________________________________________ _______________________________________________________ 4. _______________________________________________________ _______________________________________________________ _______________________________________________________ 5. _______________________________________________________ _______________________________________________________ _______________________________________________________ Signature:______________________________________ Signature:______________________________________ Signature: 155 Tool: Sample compliment/ complaints feedback form36 About you (if you want to make an anonymous complaint or compliment, go to the next section) Your details — please only provide the contact details that you are happy for our staff to use to contact you. Name: Mr/Mrs/Miss/Ms/Dr_________________________________________ Mailing address:________________________________________________ __________________________________________Postcode:___________ Email:___________________________ Mobile number:________________ Contact phone number during business hours:________________________ Do you have an advocate you would like us to discuss your complaint with? Yes Name of representative: __________________________________ Mailing Address: __________________________________________ Phone: __________________________________________________ Email: ___________________________________________________ No: _________ Please advise our office as soon as possible if any of your contact details change. About the respondent (who you are complimenting or complaining about) I am complimenting/complaining about: _____________________________________________________________ _____________________________________________________________ 36 Rights in Action Inc. 156 Have you raised this compliment or complaint before? If yes—what was the response, if any? _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ Your compliment or complaint Please give us details of your compliment or complaint: _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ Please tell us what you would like to see happen as a result of your compliment or complaint: _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ _______________________________________________________________ We undertake to respond to your compliment or complaint within one week of receiving it. If you have raised a complaint, the timeframe for resolving your complaint is explained in our complaints policy and procedure, which is attached for your information 157 Tool: Complaints Register37 Establishment of a complaints register enables your agency to monitor your internal processes to ensure complaints and concerns raised are addressed in accordance with the principles of natural justice. Where a significant issue/ concern is raised through informal channels (i.e. is not a formally documented complaint) an entry should still be made in the register, in order for you to evidence your practice. Where the action you take for resolution leads to a continuous improvement activity (e.g. a change in a policy or procedure), this should be noted in Action taken column with reference to the allocated CQI ID #. Complainant’s Contact name Details Date Issue/ complaint concern raised received Action taken Date action taken Date of resolution / closure Date of feedback 37 Disability Service Queensland, Introduction to Quality Management: https://www.disability.qld.gov.au/key-projects/quality/documents/section-2-intro.pdf 158 Standard 8: Agency management Each agency adopts quality management systems and practices that optimise the effectiveness of advocacy for each person with disability and facilitates continuous improvement. As Standard 8: Agency management is about the overall management system of the disability advocacy agency, it connects all of the other Disability Advocacy Standards. In this section of the Toolkit, the discussion of Standard 8 has been divided into six different subject areas: 8a: Corporate governance 8b: Quality management systems 8c: Continuous Improvement o Developing Quality Networks o Internal audits 8d: Policies and procedures 8e: Duty of care 8f: Conflict of interest In each of these areas you will find a discussion of overall considerations, resources and case studies. While these are important areas to consider under Standard 8, they are not necessarily exhaustive, and you will also need to refer to the KPIs and examples of evidence for this Standard. 8a: Corporate governance Corporate governance can be described as: The system by which companies are directed and managed. It influe nces how the objectives of the company are set and achieved, how risk is monitored and assessed, and how performance in optimised. Good corporate governance structures allow companies to create value...and provide accountability and control system commensurate with the risks involved. 38 The corporate governance framework should ensure the strategic guidance of the organisation, and the effective monitoring of management by the governing body which is accountable to the organisation and its stakeholders. Accountability includes how the organisation assesses itself against quality and financial targets. The members should be equipped with the appropriate knowledge, skills and training to fulfil their responsibilities, act in good faith with 38 ASX Corporate Governance Council, Principles of Good Corporate Governance and Best Practice Recommendations, March 2003 159 due diligence and care and in the best interest of the organisation and stakeholders.39 Features of good corporate governance40 There are some key features of good governance that should be central to an agency’s corporate governance framework and should be included in governance related documentation which may include organisational plans, business plans, marketing plans, policy and procedures manuals, risk management reviews and/or QA manuals. Features are described below. Strategy setting and planning Planning is a critical element of good governance. Overall strategy setting and planning for your agency must be clearly documented and communicated. Some points for good planning include: The Board should establish the goals for your agency, in conjunction with management, to provide the framework for planning The plan should be ‘owned’ by your agency Board members and management must be actively involved Consultation with: o Key stakeholders, including staff and consumers o Funding bodies and key community contacts Assistance from a specialist facilitator (this can have great benefits, but care must be taken to ensure that the role is kept to facilitation and that the plan does not become ‘owned’ by the facilitator). Good planning helps clearly set the objectives, strategies and actions for a period. It also provides a means to monitor your agency’s performance. Plans should be regularly reviewed and updated given changing circumstances. Risk management Risk management is an important concept in agency management. The Board should consider whether it has a clear risk management framework that covers your agency’s operations. Risk should be thought of in terms of what, and how, losses (or gains) may affect your agency through a wide range of sources. The Board is not directly responsible for risk management but is responsible for ensuring that managers and staff of your agency have an appropriate risk management framework in place to mitigate or reduce identified risks. 39 Standards in action: Practice requirements and guidelines for services funded under the Disability Services Act, NSW Family and Community Services, 2011 40 National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA 2009 160 You should have an ongoing process to identify risk, assess its impact, take treatment actions to address and/or monitor risk, and report this to the Board. If your agency has never undertaken a formal risk assessment of its operations or key aspects of its operations, it would be advisable to do so. Consultation Consultation with key stakeholders is an essential feature of good governance. It enables the stakeholders to understand your objectives and strategies and helps them to work with your agency in achieving those objectives. Stakeholders might include: Your funders Local community People with disability and their families/ carers Staff/ volunteers External stakeholders. Roles and responsibilities Board members need to clearly understand their role and responsibilities under relevant legislation and the rules of incorporation. Your agency should develop a documented policy describing the roles and responsibilities of the Board, of individual Board members and of management. The policy should be clearly communicated and understood by the Board, management, staff, consumers and members of your agency. Skills, independence and resources The Board should have the right mix of skills to manage your agency’s affairs. As an individual Board member it is difficult to have the expertise across all areas, but you should have experience or skills in at least one of the following: Business acumen/ expertise o Finance o Marketing o Management Other o Legal o Disability Your Board should include people who are independent of the agency to provide a balanced, objective representation on the Board. There should be a balance in the number of Board members between those who meet the criteria of independence and those who have a keen interest and advocacy background. The Board needs access to adequate and appropriate resources to ensure that it can fulfil its roles and responsibilities effectively. There should also be an 161 induction process for new members to the Board so they are aware of their role and responsibilities and understand your agency’s objectives and operations. Conduct and ethics In setting a standard that you expect people in your agency to work to, it is very important that a Code of Conduct be established, which covers the Board members, management and staff. The Code of Conduct should be developed with management and staff. Performance You should have a process for assessing the performance of Board members. As they are largely volunteers, the requirements should not be overly oppressive and onerous, but it is important to have some formal means of establishing an expected level of performance and to assess if it is being achieved. Means of performance measurement should be established based on the definition of the roles of each Board member. Succession planning At some point in the future a successor will be required to continue the management of your agency. If possible, the current manager should be responsible for grooming other senior staff as potential successors. However, if your agency does not have access to these resources, the Board should be aware of this risk and review it and act accordingly. The selection of a manager, whether internally or externally, should be based on specific selection criteria and their qualifications, experience and suitability for the role. If possible, the Board should develop the selection criteria in consultation with the previous manager. Financial and operational reporting Timely financial and operational reporting is important in ensuring that you are able to assess your agency’s performance and to assist in decision making. Reports should incorporate not just actual achievements, but projected or budgeted targets that should have been achieved. Reporting should be against key actions in the business plans and against other initiatives put in place by the Board. As a Board, you should establish an agreed format for reporting to ensure that all matters that should be reported are in fact reported. Reports need to be made available to you allowing sufficient time to enable you to properly consider them before Board meetings. Management should also be available to present their reports to the Board meetings. 162 Audit committees An audit committee’s role is to assist the Board in fulfilling its oversight responsibilities for the financial reporting process, the system of internal control over financial reporting, the audit process, and your agency’s process for monitoring compliance with laws and regulations. For larger agencies, an audit committee of non-executive (independent) Board members can be useful in considering audit related issues in more depth than would normally be undertaken by the full Board. However, the audit committee should not act as a barrier between the auditor and the full Board or presume to overtake the functions of the full Board. Small to medium sized agencies may not require an audit committee. 163 Tool: Better practice corporate governance—checklist41 You can use this checklist to review your agency's current features and help to identify any weaknesses that may require action. Better practice feature Assessment Board roles, responsibilities and skills Are the powers, roles, responsibilities and accountabilities of the Board, the CEO and management clearly identified? Are these responsibilities clearly communicated? Who are they communicated to (e.g. each other, key stakeholders)? Is there a good understanding of management’s responsibilities in relation to internal control? Is there a sound system of procedural and financial delegations approved by the Board? Does it promote efficiency as well as control? Are appropriate decision-making processes adopted by the Board? Is there a clear distinction between what decisions should be made by the Board and what decisions should be made by management? Are decisions that should be made by the Board, clearly documented and understood? Are there processes governing policy development, implementation and review, which ensure that the Board approves new policy? Is there a clear separation of roles and responsibilities between the Board, the CEO and management? Are appointments made to the Board with regard to the skill requirements of the Board? Are there adequate induction processes for new Board members? Does the Board have, collectively, a mix of appropriate skills, knowledge and experience covering: business acumen/expertise the industry within which the agency operates the services/products being provided by the agency policy development executive leadership skills finance 41 Adapted from Corporate Governance Handbook for Company Directors and Committee Members, FaHCSIA, 2nd edition, 2010. Available at: http://www.fahcsia.gov.au/sa/disability/pubs/general/CorporateGovernanceHandbook/Pages/Overview.a spx 164 marketing regulatory environment legal vocational training disabilities. Independence Is the majority of the Board independent of the CEO, management team and commercial dealings with the agency? Are there sufficient numbers on the Board to achieve independence, but not too many to become inefficient? Are there appropriate policies and procedures to identify any potential conflicts of interest? Are there adequate policies and procedures to deal with potential conflicts of interest, once identified? Board meetings Are regular Board meetings held and are financial reports tabled? Board resources Do Board members have access to independent professional advice to enable them to discharge their duties? For companies, is there a company secretary with the primary role of supporting the Board and chairperson? Code of conduct Is there a written code of conduct to be followed by the Board, CEO and staff? Is this code of conduct communicated and understood by the Board, CEO and staff? Are there clear guidelines in the code of conduct in relation to conflict of interest? Strategy setting and planning Is there an overall organisational plan, and is it supported by a business plan, budgets and marketing plan (if necessary)? Are there clearly defined performance measures (operational and financial) incorporated into the plans? Does the Board approve the budget set by management, including any budget revisions? Risk management Is there a risk management plan that is supported by risk management strategies? Does the Board regularly review the risk management strategies? 165 Are there any procedures for the Board to review the strategies and assess whether they are working effectively? Is the risk management plan reviewed regularly to ensure new risks are identified and risk management strategies are put into place? Financial and operational reporting Are there appropriate performance measures, financial and nonfinancial, which enable the efficiency and effectiveness of the agency to be assessed? Are reports tailored to particular levels of responsibility? Do reports efficiently and effectively communicate key financial data? Are the financial reports prepared on a full accruals basis as required under the Australian Accounting Standards (a requirement of the Department of Families, Housing, Community Services and Indigenous Affairs (FaHCSIA) Service Agreement)? Do financial reports show a comparison between year-to-date, budget, last year-to-date and full-year data? Are financial reports supported by explanations of significant variations? Are financial reports provided to the Board at least quarterly? Are financial reports provided to the CEO at least monthly? Are financial reports derived directly from the underlying accounting systems and is there a QA process over the compilation of the reports? Do adequate accounting systems and records support financial reports? Are financial reports provided to the Board in sufficient time to enable review before meetings? Do members of the management team brief the Board when financial reports are tabled? Does the management team include a person with appropriate financial management expertise and experience? Does that person have a direct reporting line to the Board? Board performance Are there mechanisms to monitor performance of the Board and individual Board members? Audit committee—for larger agencies Is there an audit committee? Is there a charter for the audit committee covering such responsibilities as: management and financial reporting compliance with laws and regulations maintenance of an effective audit function 166 suitable risk management and internal control frameworks membership frequency of meetings committee authority Board reporting obligations. Does the audit committee include a majority of independent (nonExecutive) Board members? Do members of the audit committee have adequate financial and accounting expertise? Does the audit committee have unlimited access to internal and external auditors and to senior management? Does the audit committee have direct access to the Chief Executive Officer, Chief Financial Officer and external auditor and internal audit? Does the audit committee meet at least quarterly? Does the audit committee review the status of all internal audit and external audit recommendations and their implementation? Do status reports summarise recommendations, officers responsible and implementation dates? Does the audit committee approve and monitor policies for risk management, reporting and internal control? Statutory accountability Is there a process that identifies all legislation relevant to the organisation, and monitors changes to the legislation and new legislation impacting on the organisation? Does financial and management reporting encompass reporting on critical legislative compliance obligations? Does the Board fully understand and continually assess its contractual requirements under the terms and conditions of service agreements with key stakeholders, including the Department of Families, Housing, Community Services and Indigenous Affairs (FaHCSIA) 167 Tool: Sample business planning process42 Appropriate governance related documentation should also include a business plan which is the product of a business plan process. A business plan should include the documented goals, the strengths, weaknesses, opportunities and threats and key objectives and strategies of your agency — all underpinned by budgets and, where necessary, a marketing plan. A business plan should support the overall governance related organisational plan. The following is a suggested business planning process: Establish team sub-committee of Board or portfolio director key management outside expertise define responsibilities for tasks Determine overall goals and stakeholders identify goals of agency by reference to objectives or corporate plan identify key stakeholders confirm goals and key stakeholders with Board Carry out research perform a SWOT (strengths, weaknesses, opportunities, threats) analysis perform market analysis and consider strategies undertake product or service research and development identify current operations, resources, infrastructure and personnel consult with stakeholders Undertake financial analysis compile historical financial data covering three years estimate income/ costs of new initiatives or ventures prepare financial forecasts for next three years identify funding needs assess viability of existing activities, new initiatives or ventures and identify those to be pursued Establish and monitor business plan identify key objectives and strategies identify key actions to achieve objectives and strategies allocate responsibility establish timeframe for actions review and update plan 42 Adapted from Corporate Governance Handbook for Company Directors and Committee Members, FaHCSIA, 2nd edition, 2010. Available at: http://www.fahcsia.gov.au/sa/disability/pubs/general/CorporateGovernanceHandbook/Pages/Overview.a spx 168 Tool: Draft code of conduct for the Board43 The following sample code of conduct may be a useful base to tailor for your agency, and is adapted from the code of conduct for members of the Australian Institute of Company Directors. Other useful sources include, for example, AS 8000:2003 Corporate Governance Standards and the ASX Corporate Governance Principles and Recommendations, 2nd edition 2007. Code of conduct A Board Member must act honestly, in good faith and in the best interests of the agency as a whole. A Board Member has a duty to use due care and diligence in fulfilling the functions of their office and exercising powers attached to that office. A Board Member must use the powers of their office for a proper purpose, in the best interests of the agency as a whole. A Board Member must recognise that the primary responsibility is to the agency as a whole but should, where appropriate, have regard to the interests of all stakeholders in the agency. A Board Member must not make improper use of information acquired as a Board member. A Board Member must not take advantage of being in the position of a Board member. A Board Member must not allow personal interests, or the interest of any associated person, to conflict with the interest of the agency. A Board Member has an obligation to be independent in judgment and actions and to take all reasonable steps to be satisfied as to the soundness of all decisions taken by the Board. Confidential information received as a Board Member in the course of exercising those duties remains the property of the agency from which it was obtained and it is improper to disclose it, or allow it to be disclosed, unless that disclosure has been authorised by that agency, or the person from whom the information is provided, or is required by law. A Board Member should not engage in conduct likely to bring discredit to the agency. A Board Member has an obligation, at all times, to comply with the spirit, as well as the letter, of the law 43 Adapted from Corporate Governance Handbook for Company Directors and Committee Members, FaHCSIA, 2nd edition, 2010. Available at: http://www.fahcsia.gov.au/sa/disability/pubs/general/CorporateGovernanceHandbook/Pages/Overview.a spx 169 8b: Quality management systems The NDAP QA system requires disability advocacy agencies to have a quality management system (QMS) in place as part of compliance with Standard 8. Quality assurance (QA) provides confidence that the Disability Advocacy Standards are being met and maintained. QA incorporates the basic components required of a quality system by ensuring internal (selfassessment) and external (certification) assessments are undertaken, together with the processes in place to control the components of the quality system. With a quality management approach, continuous improvement systems are added to QA by incorporating a quality cycle of continuous improvement. Unlike QA, where the goal is to meet the specified standards, quality management is seen as an ongoing journey of continuous improvement. A quality management system is designed to provide evidence that a specified standard of quality has been met and continuously improved. Quality management system44 Disability Sector Quality System, Partners in Quality – Resources and Guide, Queensland. Available at: http://www.communities.qld.gov.au/disability/key-projects/disability-sector-quality-system/publicationstools-and-resources/resources/partners-in-quality-resources-and-guide 44 170 The above diagram illustrates how QA (standards, documentation, standardisation of process, process control and planning and evaluation) combined with continuous improvement (leadership, consumer focus, participation, a culture that embraces change) lead to quality management. Quality management in agencies delivers outcomes for people with disability which are a measure of the quality of advocacy support. There is no set formula for a QMS for a disability advocacy agency. Factors including the size, type, location and maturity of the disability advocacy agency will influence the design and development of their QMS. Quality management principles One of the key principles of the International Standard 900045 for Quality Management Systems is that identifying, understanding and managing interrelated processes as a system contributes to the organisation's effectiveness and efficiency in achieving its objectives. Key benefits include integration and alignment of the processes that will best achieve the desired results, and providing confidence to interested parties as to the consistency, effectiveness and efficiency of the organisation. The driving principle is commonly accepted as customer or consumer satisfaction. Quality is not something that occurs as an independent activity — it needs to be designed into all elements and functions of the organisation, and then systematically controlled. Objective evidence of a quality system is provided through its documentation (which standardises processes and procedures), through monitoring of how personnel within the organisation implement and control those procedures, and from recorded feedback from service users. A quality management system therefore recognises the interrelatedness of the key components of paper, process and people in contributing to quality. Consumer satisfaction comes from agencies knowing what people with disability want, and developing systems and processes to incorporate responses to individual needs. Focusing on the consumer and identifying his/her wants and needs is essential to delivering effective quality services. Once we have documented our processes to standardise them, we then need to continually monitor their effectiveness. Where variation is identified, or a process is shown to be ineffective, an opportunity for improvement exists. Significant benefits accrue through organisation-wide involvement in the quality system, including an increased understanding of all systems of the organisation, and their interdependence. Participation provides opportunities for service 45 http://www.iso.org/iso/iso_catalogue/management_and_leadership_standards/quality_management/qmp/qmp-5.htm 171 users, staff and management to share knowledge, skills and experiences; to learn through review and improvement; and to share successes. This concept is equally true for both small and large agencies. It is important to recognise that, when you adopt a quality management approach, quality is not something you can put in place and just forget. It is not like an obsolete policy document on the shelf. Quality management is a journey, not a destination. Quality viewed as a destination is really QA, where you are aiming to meet a required standard, with no commitment to improvement. QA is more applicable when your output is a product. However, where your output is the delivery of support to people with disability, quality becomes an ongoing journey. The concept of quality improvement needs to be embedded in all levels of your agency. A good starting point is to include quality improvement as a standing agenda item on all management committee meetings and team meetings. Anecdotal evidence from the disability sector suggests that many providers believe they do provide quality support with a strong focus on consumers. However, some of what they do is not documented or formalised. The disadvantage of informal systems is their lack of sustainability. They are highly dependent on the knowledge of key individuals within the agency and this leaves your agency and its service users vulnerable. Small agencies typically rely on informal systems, presenting a significant risk that corporate knowledge will be lost in the event of the resignation of a key person. The establishment of formal systems reduces your disability advocacy agency’s exposure to risk. A quality system framework should include: Formalisation of your agency’s plans, policies and procedures; Documentation of processes and practices such as position descriptions, work instructions, forms, schedules, meeting minutes and system controls; A range of formats, such as videos, electronic systems, flowcharts etc.; and Compliance with legislative and statutory requirements, necessitating development of mechanisms to monitor regulatory changes to ensure that adjustments to policy and practices are made when appropriate. However, it is the processes adopted to implement the system which are of critical significance in ensuring that the quality initiative is effective and sustainable. The ‘systems approach’ A system can be defined as inter-related processes and their support structures (e.g. documentation, resources) put in place to achieve a specified purpose. A system is static. It IS. 172 Processes are the series of steps, and the resources needed, to complete a task. Processes ‘add value’, or transform the inputs of the system to create the desired output. They are goal-oriented, with the desired outcome directing the process. A process is dynamic. It DOES. Disability advocacy agencies have many systems, such as a system for accessing advocacy, individual needs and planning, information management, grievances and complaints, financial management, maintenance, and human resource management. Some will also have sub-systems. For example, your human resource management system will have sub-systems for recruitment, selection, orientation, staff training, performance management, grievances etc., each of which will have its own processes. Once you start thinking in terms of systems and processes, the interdependence of all sections of your agency become increasingly clear. The systems model encourages a planned (rather than an ad hoc) approach. It reminds us to set clear goals, plan what activities we need to undertake to accomplish those goals, monitor and evaluate the effectiveness of activities, and use evaluation findings to inform continuous improvement. A ‘systems approach’ to management is simply a way of thinking that helps us to link continuous improvement to all internal processes or activities. In each stage of a system there will be processes which require monitoring for opportunities for improvement. It is the combination of all of an organisation’s operational systems that form the overarching ‘quality system‘. While adoption of a quality system may necessitate considerable effort and organisational change, it is planned change that has purpose and direction. When the decision to adopt a quality management approach is related to perceived benefits in outcomes for people with disability, rather than a sense of external imposition, acceptance and involvement is likely to be higher. What we are aiming to do in applying principles of continuous improvement is to improve efficiency (by identifying critical points and controlling for variation) by maximising our use of resources, and to improve effectiveness (by identifying individual needs, and developing appropriate responses to achieve improved outcomes). Both may require changes to existing processes in order to gain the desired result. 173 Tool: Continuous Quality Improvement Register46 Use this template to record suggestions/ issues for improvement to your agency, who the issue was raised by and the improvement activities that will address the issue and when the activity is complete. Where an activity does not achieve intended results, plan and record a new activity. Use this form to keep a summary of, and track, improvements (while your continuous improvement plans will contain more details). Some examples are included in the sample below. CQI ID# Date Source Issue Improvement activity/ies Closure CQI 01 30/5/04 Consumer assessment Opportunities for consumer input into policy development Establish a monthly representative consumer forum, comprised of individuals nominated by other consumers Date of first forum meeting CQI 02 5/6/04 Complaint Dissatisfaction with staff member Review staff allocation rosters and replace the member allocated to that consumer Date of new roster CQI 02 18/6/04 WH&S Committee Audit of 15/6/04 identified that access to fire emergency exit door was blocked by stored equipment Clear impediments to emergency exits. Review fire safety requirements at team meeting of 20/6/04. To be reassessed during next WH&S audit Date of satisfactory audit Disability Sector Quality System, Partners in Quality – Resources and Guide Queensland. Available at: http://www.communities.qld.gov.au/disabiltiy/key-projects/disability-sector-quality-system/publications-tools-and-resources 46 174 Tool: Quality Monitoring Schedule47 This template can be used to record your planned annual schedule to enable you to evidence your commitment to quality control and ongoing quality improvement. Some examples of the major monitoring activities that require the planning and allocation of resources are included in the sample below. Review subject Process Planning e.g. Strategic Plan Annual management/ staff planning day Document review e.g. review of all policies and procedures for continuing applicability Performance e.g. staff performance reviews Suppliers e.g. quality monitoring of suppliers Assets management monitoring e.g. assets management and maintenance Review for effectiveness and currency and re-endorse during annual planning Records e.g. consumer records system Agency quality/ improvement Who When Committee and Staff Month due/ date Committee and staff Month due/ date CEO/ Manager CEO/ Manager Month due/ date Month due/ date Manager & treasurer Month due/ date (prior to AGM) Month due/date Performance appraisal process Contract review of requirements and performance Review of Assets Register and updating of warranty details and depreciation Audit of maintenance schedules for continuing effectiveness Random survey of 10% of consumer records against policystipulated content requirements, clarity of entries, security, currency/ archiving procedures a) Staff Satisfaction survey Manager Manager Month due/ date CEO/Manager Month due/ date Disability Sector Quality System, Partners in Quality – Resources and Guide Queensland. Available at: http://www.communities.qld.gov.au/disabiltiy/key-projects/disability-sector-quality-system/publications-tools-and-resources 47 175 e.g. Staff Satisfaction/ retention rates/ levels b) Review of retention rates/ reasons for leaving for CQI planning Consumer satisfaction a) Survey of consumers/ people with disability to assess awareness of their rights, satisfaction levels, and suggestions for improvements. b) consumers/ people with disability agency assessment process a) Review of Continuous Quality Improvement (CQI) Register (template available in this Toolkit), Quality Improvement Plan and minutes of meetings to ensure actions have been recorded b) consumers/ people with disability planning forums Program Managers Complaints Review Complaints Register for patterns/ trends emerging, and actions taken for continuous improvement CEO/ Manager Workplace Health and Safety e.g. staff/ consumers safety and regulatory compliance a) Standing agenda item for management meetings for review of accidents/ incidents b) Internal environmental safety compliance audits against documented procedures c) Fire safety environmental audits and inspection of equipment d) Electrical equipment checking and tagging a) Preparation and submission of reports against funding agreement requirements b) Annual acquittals and financial reporting to funding bodies Management Month due/ date WH&S officer Month due/ date Fire Department WH&S CEO/ Manager Month due/ date Month due/ date Month due/ date CEO/ Manager Month due/ date Continuous improvement Accountabilities/reporting e.g. reporting to funding bodies Month due/ date Month due/ date CEO/ Manager Month due/ date 176 Tool: Action Minutes Format for Meetings48 A format like the one below for recording minutes of meetings ensures that decisions made are recorded in a way that facilitates follow-up in matters arising from the previous minutes. Where an issue is raised requiring an improvement activity, it should then be transferred to your continuous improvement plan. Tasks not completed by the due date are referred to the following meeting, under the same identification number (ID#), until it is closed out. Name of meeting Date/ time Names of those present Apologies received Acceptance of minutes of last meeting Matters arising ID # Issue Action to be taken Person responsible Date for reporting back Person responsible Date for reporting back Task completed Correspondence in/ out Presentation and tabling of reports New business ID # Issue Action to be taken Disability Sector Quality System, Partners in Quality – Resources and Guide Queensland. Available at: http://www.communities.qld.gov.au/disabiltiy/key-projects/disability-sector-quality-system/publications-tools-and-resources 48 177 Tool: Document Control Register49 Use this template to control your agency’s key documents e.g. policies and procedures that are part of the management system – the register is used to record whether documents are up-to-date, where they are located and specifications for limited access. Disability Services Queensland suggest a good strategy for effective information management is to include in the footer of each document its electronic file path, the document control number, and the date of issue. A separate Records Register is suggested for records which are separate to documents, and include forms, consumer files, meeting minutes, financial records etc. A Records Register should show the type of record, its retention time, access controls, archived location and disposal method. ID # Policies, Procedur es Document title Name of document Access Any security access codes required, or specify limited access Electronic file pathway File location Date last reviewed Should be consistent with date in document footer Archived Location of archived documents Disposal method Disposal method, e.g. shredding Adapted from Disability Sector Quality System, Partners in Quality – Resources and Guide Queensland. Available at: http://www.communities.qld.gov.au/disabiltiy/key-projects/disability-sector-quality-system/publications-tools-and-resources 49 178 Tool: Risk Analysis Likelihood Matrix50 This risk analysis matrix enables you to analyse the potential risk of an activity/ event. By considering both the probability of an incident, and its likely consequence should it occur, you are able to allocate a risk rating. Where the risk is extreme or high, immediate action should be taken to mitigate the risk. Disability Sector Quality System, Partners in Quality – Resources and Guide Queensland. Available at: http://www.communities.qld.gov.au/disabiltiy/key-projects/disability-sector-quality-system/publications-tools-and-resources 50 179 8c: Continuous improvement considerations Continuous improvement model Continuous improvement operates at two levels: Individual agency levels—looking for improvements in your agency’s processes and practices Industry level—looking for improvements across the sector as a whole. Ideally, these are closely related so that information about successful innovations within one agency is shared across the sector, and areas of general underperformance are identified so that appropriate training and support can be provided. In this model (illustrated below), continuous improvement can be thought of as two interacting circles: an inner circle of continuous improvement applied in unique ways by individual agencies and another circle of sector-wide capacity building and support. Continuous improvement model The diagram above refers to the linkages between ‘good’ practice and benchmarking. The intent of ‘good practice’ is for agencies to gather insight and information via comparison with like agencies with a view to better, more 180 efficient and effective methods and approaches to identify and implement the good practice. Benchmarking is one aspect of good practice. Methods can include approaching like-minded agencies which have a similar operation, or to involve an industry group to form a task group to review an industry wide process. However, the transfer of good ideas and approaches has to be thoroughly tested, including the fit into the organisation culture. Another consideration is innovation. If everyone copies ‘good practice’ everyone may behave in the same way. Sometimes you may want to at least trial something that is different and innovative.51 Develop a quality network - planning for excellence In addition to planning continuous improvement activities in your disability advocacy agency relating to the Disability Advocacy Standards, your agency should also consider the wider context in which you can develop quality practices by developing a quality network. A quality network is a group of similar organisations that works together to continuously improve the quality of their advocacy support. Participating in a quality network can provide opportunities to: Discuss common problems Work together to find solutions Generate 'best practice' tools and ideas' Share the cost and administration of joint events, such as: o Training o Information sessions o Guest speakers 51 The rise and fall of the best practice method, Derek Stockley. Available at: http://derekstockley.com.au/newsletters-05/042-best-practice-consulting.html 181 Tool: Sample process for developing a quality network52 This sample process outlines the key steps to establishing a quality network, a group of local agencies who collaborate for reasons including developing quality management systems and addressing QA issues. The sample process outlines the elements your disability advocacy agency will need to consider from practical matters of where and when meetings will be held to issues such as the structure or purpose of the group. a. Determine the type of quality network that you want For example, what do you want to achieve? Do you want to: work on developing a quality management system? address QA issues? work with agencies with a similar work output etc.? Goals: _____________________________________________________________ _____________________________________________________________ _____________________________________________________________ _____________________________________________________________ b. Identify potential agencies Identify agencies that you would like to develop a quality network with. Name: Contact Information: If you do not know any appropriate agencies to develop a network with, contact: Department of Families, Housing, Community Services and Indigenous Affairs (FaHCSIA) NDS (National Disability Services): DANA (Disability Advocacy Network Australia): c. Decide on a structure For example, will the quality network be: 1. action based? 2. for information sharing? 3. for resource sharing? 52 Quality Strategy for Disability Employment and Rehabilitation Services, FaHCSIA. Available at: http://www.fahcsia.gov.au/sa/disability/pubs/Documents/quality_strategy_toolkit 182 Structure: _____________________________________________________________ _____________________________________________________________ _____________________________________________________________ ____________________________________________________________ d. Set up the network Here are some key elements to consider when developing a meeting system, with examples of what you might choose to do. Where: (For example, choose a mutually convenient venue, or if the agencies in your network operate near one another, each agency could take a turn hosting the meeting at their premises.) When: (For example, meet once every month for one day, or 4–5 hours, allowing for travel time.) Who is responsible: (For example, have each agency in turn be responsible for running the meeting and appointing a chairperson.) What will be done at each meeting: For example, for a quality network you could: have each monthly meeting focus on a particular quality theme. In this way, you will have achieved a complete review of the quality themes within a calendar year. identify which quality theme will be discussed at the meeting. Request that all attendees bring material for discussion relating to that quality theme, such as queries, barriers, obstacles, best practice examples and ideas for evidence gathering. Request the chairperson of the meeting (or another member of their agency) research and prepare an overview of the quality theme to present to the group). ____________________________________________________________ ____________________________________________________________ ____________________________________________________________ ____________________________________________________________ ____________________________________________________________ ____________________________________________________________ ____________________________________________________________ e. Conduct your meetings For example, for a quality network: 183 chairperson presents an overview of the quality theme to the group. group members discuss and share their practices and experiences relating to this quality theme. group members work through any tools or resources relating to the quality theme that agencies may have (including the Toolkit). identify any gaps in knowledge in the group. You may wish to seek outside help (for instance, a guest speaker, consultant or trainer) to help your network develop in this particular area. Agreed meeting structure: ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ f. Develop the network Review the progress of your network to adapt to changes in the aims and goals of network agencies. The focus of your network should change to reflect new directions and changing needs. Document future directions: ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ ______________________________________________________________ 184 Internal audits Continuous improvement is one of the key components of the Quality Strategy. Continuous improvement should be part of the day-to-day life of your agency. Although it is not mandatory, it is highly recommended that agencies implement a system of internal audits against the Disability Advocacy Standards. Internal audits are a means of checking that your agency’s systems processes and procedures are working as intended, reviewed regularly and amended as necessary. Internal audits are a strong demonstration of evidence of continuous improvement for Standard 8. Internal audit tips from a Certification Body The internal audit process does not need to be complex, and can be integrated into the operations of each disability advocacy agency, rather than as a one-off yearly activity. The ‘Things to Consider’ for each Standard in Section 4 are recommended as a useful checklist for internal audits. To check that processes are implemented, your agency could use the ‘Things to Consider’ checklist, obtain a sample of files, check to see that what is supposed to happen is actually happening, check that procedures are current and being followed, provide areas for improvement, and report to management. As files generally follow the entry to exit process for a consumer, it is far easier to follow the process flow rather than checking standard by standard (note that standard by standard is useful to check if documentation is in place). Process flows could be identified for a range of processes, e.g. consumer related processes, human resource processes, governance processes, finance/purchasing processes etc. Tool: Sample process for systematic internal audits53 This sample process describes one systematic way of conducting regular internal audits against the Disability Advocacy Standards. Month-by-month actions January: Arrange meeting process Assess your agency's performance against Standard 1: Advocacy access Convene an internal audit committee meeting with representation from consumers, staff, management and the Board of your agency. At the initial meeting you should: o determine a regular meeting date for each month o arrange for minutes to be taken for each meeting o arrange for outcomes to be reported to the Board with a list of actions to be addressed. 53 Quality Strategy Toolkit for Disability Employment and Rehabilitation Services, FaHCSIA. Available at: http://www.fahcsia.gov.au/sa/disabiltiy/pubs/employers/Documents/quality_strategy_toolkit 185 Assess your agency's compliance. Use the self-assessment worksheets (in Section 4) and the internal audit worksheet to assess your agency's compliance with and continuous improvement against the Standard. Other information you could use to assess your agency includes: o de-identified information from your complaints register o feedback from people with disability o issues identified by other meetings/committees in your agency (e.g. occupational health and safety (OH&S) committees, management committees) o observations contained in the report from your certification audit or annual surveillance audit. Develop a priority list of actions to be completed against the Standard. Document actions to be taken on a 'continuous improvement register', which should include the following information: o Action to be taken o Person responsible o Anticipated timeframe o Action completed? Appoint a designated person to be responsible for updating the register at each monthly meeting. February: Assess your agency's performance against Standard 2: Individual needs. Follow-up actions from the previous meeting o Convene an internal audit committee meeting. o Assess your agency's compliance with and continuous improvement against the Standard. o Develop a priority list of actions to be completed against the Standard and document them on the 'continuous improvement register' o Follow-up actions added to the register at the previous month's meeting. o Document the results of actions. March: Assess your agency's performance against Standard 3: Decision making and choice. Follow-up actions from the previous meeting. o Convene an internal audit committee meeting. o Assess your agency's compliance with and continuous improvement against the Standard. o Develop a priority list of actions to be completed against the Standard and document them on the 'continuous improvement register'. o Follow-up actions added to the register at the previous month's meeting. o Document the results of actions. April onwards: Continue to use this process throughout the year, assessing one Standard for each month and documenting and tracking actions taken against each Standard. 186 Internal audit worksheets You can print out these internal audit worksheets and use them as templates to plan and document continuous improvement activities for your agency under each KPI of the Disability Advocacy Standards. You may wish to distribute them among staff, management and people with disability/stakeholders. This task could be shared out, with individuals or work groups taking on the internal audit of specific Standards. You may wish to attach an extra page if you need more space for your response. It is important to think about documenting evidence of your actions towards each KPI. You may wish to refer to the name and/or number/date of relevant policies and procedures, or attach copies of these policies and procedures to your worksheets, which could then be provided to your Certification Body. Evidence should be in the form of actual outcomes and achievements. 187 Internal Audit Worksheets Standard: KPI: What are our planned actions for meeting the requirements of this KPI? Policies, procedures and management systems What improvements have we tried or made in the past 12 months? Things tried or done in the past 12 months Key learning/insights 188 What are our claims about our current performance in this area? Strengths (what we do well) Weaknesses (areas to improve) Do we comply with the requirements of this KPI? Evidence that demonstrates our compliance Areas where we need additional evidence or changes to our management systems What are our priorities for continuous improvement over the next 12 months? Planned actions Anticipated results 189 Standard: KPI: Using the activity of the previous page, document the continuous improvement actions your agency plans to take in relation to this KPI. Action to be taken Person responsible Timeline for action Date completed 190 8d: Policies and procedures As part of strong agency management, your disability advocacy agency should have written policies and procedures. These policies and procedures should relate specifically to the requirements of the Disability Advocacy Standards, as well as other relevant operations of your agency. Here are some considerations to help you to improve your agency's practices in this area Review: Do we have a set of written policies and procedures? Could we improve our policies and procedures? Do our policies and procedures reflect the content of the Disability Advocacy Standards? Who is responsible for reviewing our policies and procedures? How often are our policies and procedures reviewed? How frequently are staff and people with disability trained in the requirements of our policies and procedures? Do we review whether policies and procedures are implemented? 191 Sample Policy: Policy Format54 This is a sample policy format that can be used as a basis when developing your policies. Policy Number (as entered in Document Control Register): POLICY TITLE (N.B. Enter electronic file path and date of endorsement/ currency in the document footer and in the Document Control Register) POLICY STATEMENT The policy statement/ purpose provides the direction and rationale. SCOPE The scope may need to be specified to clarify applicability (e.g. are any program areas exempted from any clauses, where specific criteria may apply for their agency type — otherwise, delete this heading). PRINCIPLES Explicit values which drive this policy. They may link to agency values, constitutional objects, or principles of practice etc. REFERENCES Identify regulatory or situational references (e.g. QDSS, strategic plan, crossreferenced policies, legislation/ regulations, Australian standards). ATTACHMENTS Controlled forms mentioned in the procedures, which form part of this policy. Delete if not applicable. PROCEDURAL FRAMEWORK 1. Heading 1.1 Sub-heading if more than one element to this procedure Identification of clauses under this heading. Disability Sector Quality System, Partners in Quality – Resources and Guide, Queensland. Available at: http://www.communities.qld.gov.au/disability/key-projects/disability-sector-quality-system/publicationstools-and-resources/resources/partners-in-quality-resources-and-guide 54 192 8e: Duty of care Duty of care is a hot topic for disability agencies. Legally, we all have a duty to take reasonable care not to cause foreseeable harm to other people or their property. This is also known as the law of negligence.55 Key areas for consideration in relation to duty of care could include: 1. to whom do you have a duty of care? 2. what is your duty of care to everyone in, or associated with, your agency? 3. what would you as a reasonable person do/ not do to ensure that as far as possible there is no breach of duty of care, and that no one will suffer harm or loss because of your actions/inactions? 4. what regular, ongoing and documented training do you provide to ensure that individuals at all levels of your agency make informed decisions about things that could harm them? Simple framework for duty of care The framework above is a useful tool for thinking through, in a group, issues related to duty of care in your agency. The key is to balance the rights of all stakeholders with possible risks. Training is critical to help minimise risk to all stakeholders and to ensure all stakeholders are informed of the potential risks and benefits involved. It is important when considering duty of care to consult your own state or territory legislation. 55 National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA, 2009 193 8f: Conflict of interest Standard 8 requires that the disability advocacy agency is structured and operates independently in such a way as it is free as possible from conflicts with other service provision and the interests of people with disability. Sample Policy: Management Conflict of Interest56 Conflict of Interest Register: Our agency will maintain a conflict of interest register, where all staff, management Committee members and volunteers will declare any personal or professional interests that may give rise to a conflict. The conflict of interest register will be publicly available. To minimise conflict of interest, our agency will: Not provide direct disability services (e.g. day programs, recreation, accommodation, employment, equipment services etc.). The agency will, however, provide disability information as part of the advocacy process. The agency may undertake projects such as research and training, provided they do not compromise its ability to independently advocate for people with disability Ensure that Management Committee members serve as individual members and not as representatives of other agencies (e.g. direct disability service providers) If individual Committee members, staff members or volunteers are aware of associations or situations that may potentially cause a conflict of interest they must declare this interest and remove themselves from the decision-making process Ensure that individual advocacy matters are not taken to the Committee as a whole, nor are they discussed with individual Committee members unless a Committee member is providing supervision or professional advice with the consent of the consumer Management Committee members shall not be paid employees of our agency. If a Committee member wishes to apply for a paid position, he or she must first resign from the Committee. Generally, a Committee member will not be immediately replaced in this situation and is free to re-apply to be a Committee member if he or she is not employed Wherever possible Management Committee members shall not be active operational volunteers (e.g. volunteer advocates, office support volunteers) of our agency. However if this does occur, such Committee members should closely adhere to our agency’s conflict of interest policy and must declare this interest and remove themselves from the decision-making process People with disability and their carers are strongly encouraged to be Management Committee members. If a Committee member is also a consumer of our agency and they are involved in a complex personal 56 National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA, 2009 194 advocacy matter (i.e. a high level of conflict) a Committee member may stand down or resign from the Committee if there is a possible conflict of interest. A Committee member should discuss any such concerns with the Management Committee as a whole or with the President before making this decision. Disability Advocacy Policy: Consumer–Advocate Conflict of Interest Where a consumer–advocate conflict of interest arises: The affected consumer will be made aware of the potential for conflict of interest The affected consumer will be involved and consulted in any decisions about appropriate actions Our agency will offer the consumer a referral to an alternative agency or advocate. Where either the consumer or the advocate feels that advocacy activities will be compromised by the potential conflict of interest, the consumer should be referred to another agency or advocate. Once the consumer has been provided with the full information of the circumstances of the conflict of interest, the consumer can decide to continue using our agency with the existing advocate. Consumer – Consumer Conflict of Interest Our agency will sometimes encounter situations where there are dilemmas for advocates involved in assisting consumers with conflicting needs. To deal with this issue: Our agency will make a check of its consumer records to see if there is a conflict of interest before offering assistance If there is a conflict of interest our agency will normally assist the first person who has come to it for assistance Our agency will inform the other person why it cannot assist. The agency will then assist the person to find an alternative advocate. Conflict of Interest – Person with a Disability – Carers Our agency tries to assist both carers and individuals with a disability in the advocacy process. However, if there is a conflict of advice from the carer and person with disability, our agency will in general take the advice of the person with disability. Sexual Relationships with Consumers Staff (including volunteers) should under no circumstances engage in sexual activities or sexual contact with consumers whether such contact is consensual or not. Staff (including volunteers) should not engage in sexual activities or sexual contact with relatives of consumers or other individuals with whom consumers maintain a close personal relationship when there is a risk of exploitation or potential harm to the consumer. 195 Gifts and Other Benefits from Consumers Staff (including volunteers) should be conscious of the perception to others of accepting gifts and other benefits. Staff must not solicit or accept anything of value from a consumer or associate which might interfere with their independence and the conduct of their duties and responsibilities. The very acceptance of a gift may create the perception that staff member’s independence and integrity has been compromised. In general, gifts of any type should be politely declined. However, a token gift may be accepted if there are circumstances where it would cause offence or disrespect to the gift giver to refuse the gift or where it may jeopardise the positive working relationship with the person. An example of a token gift might be flowers, chocolates, home-made produce, and modest refreshments etc. with a value of no more than $50. If a staff member is unsure about the status of a particular gift he or she should discuss with the Coordinator. Staff (including volunteers) should not enter into any financial transactions or arrangements with consumers. Examples of a financial transaction with a consumer may be purchasing agency/ equipment or accepting a loan of money/ goods. If there is any doubt, the staff member should discuss the matter with our agency management. 196 Standard 9: training Staff, recruitment, employment and 9.1 Sample policies and procedures Sample Policy: Staff Recruitment, Employment and Training57 Equal Employment Opportunity Policy Our agency will encourage appropriately skilled and qualified people with disability (along with people from other disadvantaged groups) to apply for positions All reasonable accommodations will be made to ensure that employees with a disability are able to undertake the inherent requirements of their position Our agency will ensure the selection process is merit-based by developing selection criteria which are fair and reasonable and directly related to the skills required for the job and instructing the selection panel to select a job applicant based solely on these approved criteria. Job Descriptions Job descriptions for Management Committee members, volunteers and employees will be created and maintained/ updated by our agency. Job descriptions will include the main duties of the position as well as the skills/ competencies required of the staff member. The Management Committee will review these job descriptions as part of the regular staff appraisal and supervision process. This process will also ensure that staff understand the skill/ competency requirements of their jobs. Employment Process Principles Our agency will employ staff on the basis of their skills and not on any other basis. Staff will be recruited in accordance with equal employment opportunity legislation and all our recruitment based on the following principles: • Clear and accurate definition and description of the requirements of the position are provided to all applicants who request an information package • Selection is based on merit • Assessment of the applicant’s merit is measured against clear, predetermined selection criteria which have been supplied to all applicants who request an information package • Selection panel has relevant expertise and experience, and includes a person from outside our agency as well as a person with disability 57 National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA, 2009 197 • Confidentiality is maintained • Affirmative action principles apply. Advertising Our agency will provide an information package for applicants, including selection criteria, job description and information about our agency. Our agency will advertise all positions, internally and externally, through agency publications and appropriate newspapers. All advertising for positions vacant will indicate that our agency is an equal employment opportunity and affirmative action employer, encourages people with disability, including people from Culturally and Linguistically Diverse (CALD) backgrounds with disability, to apply. Selection To assess the applicants, a selection panel will be convened. The panel usually comprises three people and should include a member of the Management Committee and an independent person who is not employed by our agency. The third member is usually the manager or supervisor of the position for selection. The panel should have representation or input from a person with disability. The selection committee: 1. Considers all applications 2. Decides which applicants warrant an interview 3. Meets before the selection interviews to determine appropriate, nondiscriminatory questions to ask the applicants 4. Contacts applicants’ referees after the interviews. All unsuccessful applicants will be notified by mail and informed that their application will remain confidential. All unsuccessful applications are destroyed after six months. At the time of appointment, the successful applicant for a job is provided with a formal letter/ employment contract detailing: The position they are being offered The date of commencement The probationary period A job description which includes a statement of duties The conditions of appointment, including whether it is full-time, part-time, casual, permanent (subject to recurrent funding), temporary, fixed term or by negotiated contract; and including leave entitlements and notice of termination of employment The rate of pay, including details of the relevant industrial award and the position classification under that award. 198 Formal acceptance of the employment offer must be signed by the manager responsible for staff and the successful applicant. Orientation Our agency will provide reasonable adjustment to the work environment by supplying any aids/ equipment necessary to assist a person with disability to perform their duties and will ensure that access to training and career development opportunities is available on an equitable basis. Our agency will provide training sessions, induction materials to ensure that all staff/ volunteers are fully introduced to their new positions. Staff will be introduced to their roles and responsibilities, as well as to any administrative requirements of their jobs. Staff Appraisal Our agency will undertake a regular appraisal of staff skills/ competencies and performance (for example, annually) These appraisals will also include opportunities for staff members to discuss their goals for training and development within our agency These appraisals will be the responsibility of the immediate supervisor of each staff member, and the finished appraisals will be reported to the Management Committee. Staff Development and Training Our agency will budget for regular and appropriate forms of staff development Training and information will also be provided to staff and volunteers to ensure that they understand their roles, the administration of our agency and their accountability for their work related activities Staff training and skills development will be identified through the appraisal process and through forums such as staff meetings. Volunteers Volunteers will be oriented to our agency, as is a paid employee or Board member, and agree to the Charter of Volunteer Rights and Responsibilities and our agency’s Charter of Rights and Responsibilities in relation to volunteer workers. Charter of Volunteer’s Rights and Responsibilities The volunteer has the right: To be treated as a co-worker To know as much as possible about our agency – its policies, its people, its programs 199 To a suitable assignment – with consideration for personal preference, temperament, skills, abilities, education and employment background To a written Job Description and written Contract of Employment Conditions To refuse to do a task requested of them To determine the number of hours that they will volunteer and when these hours will be worked To refuse to contribute anything (e.g. money, resources, etc., other than their time, experience and skills in undertaking a job) To relevant training for the job, which is thoughtfully planned and effectively presented To continuing education on the job, as a follow-up to initial training, which provides information about new developments and other relevant matters To supervision by someone who is experienced, well informed and who has the time to invest in giving guidance To a safe working environment To promotion to greater responsibility as appropriate, and a variety of experiences To be heard and listened to – have a part in planning, to feel free to make suggestions, to be shown respect for an honest opinion, to have these acted upon when agreed to as valid statements, and to receive information back as to the outcomes of these suggestions To a fair and equitable Disputes Procedure if there is a problem with the standard of the work that the volunteer worker is doing To be free of discrimination or harassment because of racial, religious, sexual, marital, age and ability status To knowledge of existing or impending industrial disputes, presented in a balanced manner, to enable the volunteer workers to make informed choices of action To a fair and equitable Termination Procedure (which includes reasons for dismissal and an appeals process) To a written performance evaluation at the end of the contract. The volunteer has a responsibility to: Support the vision, objectives and underpinning values of our agency Be clear about what they will and will not do Accept and adhere to our agency’s policies and procedures Welcome supervision and seek direction as required Respect the rights of other volunteers, paid staff and members, including participant’s rights to privacy Take part in a workplace culture, which is free from sexual, racial, disability or any other harassment or vilification. Charter of our agency’s Rights and Responsibilities in relation to volunteers Our agency has the right: To employ or not employ any volunteer worker based on the needs of our agency, its consumers and people with disability To expect the volunteer to meet minimum standards as defined by our agency 200 To expect the highest level of dedication, commitment and effort that the volunteer can give, even on a short-term basis To expect conscientious acceptance of responsibilities as to promptness, reliability and good performance from the volunteer To expect enthusiasm and belief from the volunteer in the work that our agency is doing To make a decision as to where the volunteer would best fit within our agency, after negotiations with the volunteer To express constructive criticism to the volunteer in a diplomatic way, and suggest changes To expect loyalty to our agency and only constructive criticism from the volunteer To expect clear and open communication from the volunteer at all times To expect appropriate behaviour from the volunteer at all times To expect an effective and appropriate work productivity from volunteers in leadership positions To expect that volunteers will not discuss any consumer’s circumstances and details outside of our agency To expect the worker to bring any concerns about consumers and their circumstances to our agency for discussion To tell a volunteer worker that their services are no longer required, and the reasons for this decision. Our agency has a responsibility to: Have employment policies which also cover volunteers, for example, have: o Job descriptions o Job contracts o Insurance cover o Disputes procedure o Termination arrangements o Boundaries of levels of legal, professional liability and expertise of each job Properly meet and fulfil the Volunteer Worker Rights, and ensure that no volunteer is exploited Ensure that our agency and its paid staff address any concerns raised by volunteers, make decisions regarding those concerns, and report this back to the volunteers Ensure that no volunteer is discriminated against or harassed Ensure that volunteers work in conditions which comply with Occupational, Health and Safety standards for the job they are performing; and that volunteer workers receive ongoing Occupational, Health and Safety training so as to ensure their ongoing personal safety Ensure that volunteers are not employed in situations where an industrial dispute is in progress. Nor should volunteers be co-opted to be involved in such disputes 201 Ensure that volunteers receive initial and ongoing training, support and supervision Ensure that volunteers receive some form of recognition/ rewards (instead of money) Ensure that volunteers are able to participate in and have access to our annual agency review Ensure that volunteers have a current National Police Clearance. Training The main forms of training and support opportunities identified by advocacy agencies include: • • • External facilitator o Experienced leader (with experience of audits, understands the QI language) o Consultant on individual agency basis, to meet agency needs. Regional quality theme based workshops Seminars - more formal training for staff and Board. Other forms of training and support for quality that advocacy agencies identified include: • • • • • • • • Peer networks Purposive visits – visits to other advocacy programs Links to international networks Organisational learning – internal workshops Participating in external reviews Local advocacy development – request for mentoring from other more experienced advocacy agencies Mentoring for staff and Board Renewal/ time out – for agency to reflect on policies, procedures and practice. 202 9.2 Sample Templates Template: Competency-based job description template58 You can use the fields in this template to document the skills, knowledge and attributes required by the employee to fulfil their employment role. Name Job title Background Key responsibilities Job Skills, Knowledge and Attitudes Skills Must do 58 Knowledge Must know Attitudes/Attributes/Aptitudes Must be aware of http://www.communitydoor.org.au 203 Template: Job description questionnaire59 NAME JOB TITLE SUPERVISOR 1. In one paragraph describe the basic purpose of your job. 2. What are the key responsibilities of your job and what percentage of time do you spend on each? 3. What are the secondary responsibilities or tasks required of your position? 4. Who do you report to? • • • • • • Who assigns your work? How often is work assigned? How are the assignments given e.g. written, oral etc.? Who reviews and approves your work? What decisions are you required to make in the course of your work? What decisions must be referred to your supervisor/manager? 5. What records or reports are you accountable for? 6. For what purpose are the records and reports used. 7. Do you have any supervisory responsibilities? 8. If you were promoted what type of education, training, job related experience would your replacement need? 59 http://www.communitydoor.org.au 204 Template: Recruitment and Selection Checklist 60 You can use this sample template as a guide for the recruitment process and as a way of evidencing your quality practice. Process Who is responsible Date task due for completion Check box Human resource planning and analysis of skills/ competencies required Develop job specification of skills/ competencies/ knowledge required Develop position description that articulates duties to be undertaken Identify the key selection criteria from the core competencies required for the position Place advertisement, which includes the date for close of applications, and telephone contact for provision of an applicants’ information pack Distribute applicants’ information pack to those who inquire regarding the position. The pack should include clear instructions regarding addressing the key selection criteria in applications submitted Close application period Establish an interview panel Train the panel in interview techniques, EEO principles, ‘Merit’ principles, awareness of ‘familiarity bias’ (the tendency to favour candidates who are similar to the panel member), awareness of ‘primacy and recency’ effect (tendency to forget responses from candidates interviewed first when comparing candidates’ responses to questions) Evaluate applications according to the key selection criteria, using a scoring matrix Short-list the candidates Develop structured interview questions from the key selection criteria, and note your expected Disability Sector Quality System, Partners in Quality – Resources and Guide, Queensland. Available at: http://www.communities.qld.gov.au/disabilitiy/key-projects/disability-sector-quality-system/publications-tools-and-resources/resources/partners-in-quality-resources-and-guide 60 205 responses Weight key selection criteria to acknowledge the relative importance of each predictor Notify short-listed candidates and arrange interview appointments Notify unsuccessful candidates in writing Conduct structured interviews with short-listed candidates using standard questions and a scoring grid Panel members to compare their ratings/ scores, and make a decision on the successful applicant Telephone referees, and verify qualifications Notify successful candidate of offer of appointment, and confirm date appointment will take effect and date of commencement of induction Notify unsuccessful candidates in writing 206 Template: Applicant Short-listing Matrix 61 This sample template provides a guide for short-listing applicants, based on their responses to the key selection criteria (KSC) – you can add or delete columns based on the number of criteria. Each member of an interview panel allocates a score based on the ratings scale for each of the key selection criteria (KSC), and then the total score should then be calculated. NAME OF APPLICANT: ……………………………………………………………… DATE: ……..……………………………………… POSITION APPLIED FOR: ……………………………………………………………. PANEL MEMBER: ………………………………… Ratings scale Exceptional=10 High level = 9 or 8 Above Requirements= 7 or 6 Meets Requirements=5 Meets some Requirements=4 or 3 Limited= 2 or 1 Does not meet requirements=0 KSC1 KSC2 KSC3 KSC4 KSC5 KSC6 KSC7 KSC8 TOTAL SCORE: …………………………………….. COMMENTS: ………………………………………………………………………………………………………………………………………… Disability Sector Quality System, Partners in Quality – Resources and Guide, Queensland. Available at: http://www.communities.qld.gov.au/disabilitiy/key-projects/disability-sector-quality-system/publications-tools-and-resources/resources/partners-in-quality-resources-and-guide 61 207 Interview Scoring Grid This is a more complex interview scoring system. Each interview panel member makes an independent decision, based on the merit of each candidate’s response to questions related to the key selection criteria (KSC). Once the panel has decided whether any selection criteria are to be weighted (to acknowledge their relative importance), they allocate a ‘raw score’ out of a possible 10 (based on the rating scale). This score is then multiplied by the weighting given to determine the total score against each KSC. Name of applicant: ……………………………………………………………… Date of interview: ……………………………………. Position applied for: …………………………………………………………. Name of panel member: ……………………………... Key selection criteria KSC 1 – Weighting = KSC 2 – Weighting = KSC 3 – Weighting = KSC 4 – Weighting = KSC 5 – Weighting = KSC 6 – Weighting = RATING SCALE: 10 Exceptional SCORES: Application: 8–9 High level Raw score 6–7 Above requirements Interview: Total Comments 5 Meets requirements 3–4 Meets some requirements Referee check: 2–1 Limited 0 Does not meet requirements TOTAL SCORE: 208 Template: Staff/Volunteer Induction Checklist62 You can use this checklist as a reference for developing an induction process for new staff/ volunteers. Having the checklist complete and signed by the new staff member/ volunteer is a way of evidencing your good practice and ensuring all steps are complete. Personal information • Contract of employment • Position description • Performance monitoring/ appraisal processes • Code of ethics (accepted and signed) • Confidentiality agreement (accepted and signed) • Allocation of IT access code • Terms and conditions of employment/ Award conditions Documented essential practice guidelines • Review of agency policies and documented procedures • Quality monitoring and continuous improvement systems • The agency’s mission, vision and values • Consumer participation in agency management Workplace Health and Safety Instruction in safe work practice Duty of care Fire safety procedures Standard operating procedures Time sheets Leave requests/ Entitlements Training records/ Entitlements Disability Sector Quality System, Partners in Quality – Resources and Guide, Queensland. Available at: http://www.communities.qld.gov.au/disabilitiy/key-projects/disability-sector-quality-system/publications-tools-andresources/resources/partners-in-quality-resources-and-guide 62 209 Mandatory training Premises security Use of vehicles Schedule of staff meetings Internal communication mechanisms Advocacy delivery • Eligibility criteria for consumers, and processes for assessing prioritisation of need • Principles of operation in supporting consumers • Rights of consumers and their nominated supports • Advocacy delivery orientation period completed under supervision (“buddy” or supervisor) I confirm I have completed my formal induction process and have understood my responsibilities in relation to the information provided Signed: ………………………………………… Dated: …………… 210 Template: Staff Performance Appraisal and Professional Development Record63 This template could be used to help you develop a positive system for staff performance reviews that focuses on opportunities for further professional development. Staff members can complete this sample template themselves, identifying the skills, knowledge and abilities they need to undertake their duties proficiently, and rating themselves from not competent to highly competent in each area. Where they feel further knowledge would be of benefit, they identify professional development goals. This is then discussed with their supervisor, necessary amendments jointly negotiated, and timelines established for the goals to be achieved over the next twelve months. The targets met can be ticked off as they are completed. Assessment codes NC = Not competent C = Competent HC = Highly competent Duties from position description Skills, knowledge and competencies needed NC C HC Goals Targets met NC C HC Disability Sector Quality System, Partners in Quality – Resources and Guide, Queensland. Available at: http://www.communities.qld.gov.au/disabilitiy/key-projects/disability-sector-quality-system/publications-tools-and-resources/resources/partners-in-quality-resources-and-guide 63 211 Template: Staff Professional Development Log64 Keeping a professional development log for each staff member, like the template below, is a way of evidencing your agency’s commitment to staff development, and monitoring equitable distribution of professional development resources across staff. You might want to document only external activities, such as programs/ conferences in this form, and record internal activities in your annual agency training calendar. Each staff member is responsible for maintaining and updating his/ her own professional development log. One copy may be kept by the employee for his or her curriculum vitae, and one copy should be retained by the Executive Director in the personnel file. If the training completed has been at the cost of the staff member, note “AOE” (At Own Expense) in the “Cost” column. If the training program has been attended in the staff member’s own time, note “IOT” (In Own Time) in the “Hours” column when recording the hours involved. NAME: POSITION TITLE: DATE COMMENCED: Date Course/ conference attended Hours Cost Disability Sector Quality System, Partners in Quality – Resources and Guide, Queensland. Available at: http://www.communities.qld.gov.au/disabilitiy/key-projects/disability-sector-quality-system/publications-tools-and-resources/resources/partners-in-quality-resources-and-guide 64 212 9.3 Tools Tool: Step-by-step guide to good practice recruitment This guide to best practice in recruitment is based on a document created by the Council of Social Service New South Wales. You can compare the steps in this guide with recruitment processes at your own agency. This guide to a good practice recruitment process contains the following steps: Plan for recruitment Prepare job descriptions and selection criteria Advertise Shortlist Select Do reference checks Make an offer of employment Note: Recruitment is a process which leads to a formal offer of employment. As such it is governed by legislation, particularly in relation to anti-discrimination law and equality of employment opportunities. Ensure that you are aware of the relevant legislation in your state/territory. Step one: plan for recruitment A good recruitment process takes time and is well planned. You need to prepare or revise the job description and selection criteria, convene a selection panel, advertise, conduct interviews and negotiate start dates. All these tasks should be scheduled in advance. It is also important to bear in mind that you may not successfully recruit during the first round of recruitment. The whole process can easily take months from the decision to recruit, to when the person actually starts in the position. The following is a checklist for managing the key steps in the recruitment process. Before you recruit: Confirm funding exists for the position Obtain necessary approvals to staff the position Develop a job description if the position is new or review the existing job description Establish the recruitment criteria Develop job-related and measurable selection criteria based on the job description, including the minimum (essential) experience and skills for the position Manage the recruitment process. Determine the best method for recruiting for the position including where to advertise and who should be included on the selection panel Develop the advertisement using the job description, minimum qualifications and selection criteria. The advertisement should also include: o Deadline for applications o Salary range and other key benefits o Contact person for further information o Anticipated date for interviews. Step two: prepare job description and selection criteria Job descriptions and section criteria are critically important to the recruitment process. The job description describes the role—what it does, how it does it, and reporting requirements (see job analysis below). 213 The related selection criteria describes the skills, knowledge, experience, qualifications and personal attributes that a candidate needs to meet the requirements of the job description. The selection criteria should also clarify whether these ‘competencies’ are essential or desirable. Clear and informed job descriptions and selection criteria are essential for both the employing agency and prospective candidates. For the agency, job descriptions provide the basis for not only recruitment but also performance appraisal and for ensuring that the work carried out by staff is aligned with the agency’s objectives. A well- developed job description assists candidates and job holders to understand their duties and responsibilities and also clarifies the boundaries of their role. If an existing job description is to be revised before recruitment, it’s a good idea to develop it with the person currently in the job. Alternatively, the job should be subject to a job analysis. A job analysis typically asks the following key questions: What is the overall purpose of the job? What are the main duties (e.g. the five main things the job holder does)? What are the typical working conditions (location, consumer interaction)? What are the supervision and reporting responsibilities? Selection criteria are based on the job description. They are the benchmarks that will be used to screen prospective candidates and select the most preferred person for the job. There are some key factors to consider when developing or revising the selection criteria including: What are the skills, experience or qualifications essential to the position? What are the skills, experience or qualifications that are desirable? It is also important to ensure that your criteria are specific, measurable and jobrelated. Also ensure that the selection criteria do not directly or indirectly discriminate against any potential candidates. This is often the stage at which potentially discriminatory values, explanations about how a job is done, or the ‘type’ of person required are inadvertently built into selection processes. It is useful to involve someone experienced in recruitment but outside the particular process, to check key documents and identify any potentially discriminatory practice Step three: advertise The most common way to advertise is through newspapers and more recently via job websites. With the increasing use of IT, many services may advertise in a high circulation newspaper but also promote the position via targeted e-bulletins or other email listings. Each method has a target audience or ‘demographic’ so it is important to consider who you are including (and therefore excluding) as potential job candidates. The information sent to prospective candidates should be accessible, including to those people with hearing and sight impairments and/or other disabilities. Effective strategies for responding to these needs include: Write in plain English 214 Use job websites compatible with software that can ‘read out’ web pages (e.g. Browse aloud) for people with literacy and visual impairments who might have difficulty reading online. If you are using an agent to recruit on your behalf remember they must be clear about your requirements and act in accordance with your agency’s employment practices and the relevant legislation. Step four: shortlist This part of the process should make full use of the selection criteria. It is also desirable that the same selection panel shortlists applications and conducts the interviews. All prospective candidates must be assessed against the essential and desirable criteria, in the same way, and by the same selection panel. The golden rule is to be consistent and document all decisions and the reasons for them. This documentation should be kept in a confidential file and referred to if there are any inquiries or complaints regarding the selection process. Step five: select There are a variety of ways to assess candidates against the required competencies for a position. It is important to consider the role and to employ a selection process or ‘setting’ that best suits the requirements of the position. The most common method is the interview, involving the candidate and a selection panel comprised of three to five people. Most job interviews take approximately 30–40 minutes, but are frequently longer for very senior positions such as CEOs or Directors. The selection panel often includes Board members and staff, as well as one independent or external member. Typically the candidate is asked a series of questions relevant to the position and designed to test their knowledge, experience and skills. It is essential that all candidates are asked the same questions and that the interview process gathers the information required to make a decision on the preferred candidate or candidates. Depending on the competencies being assessed, the interview may include a set exercise for the candidates. For example, asking them to analyse a budget or deliver a short presentation on a specific topic such as the Disability Advocacy Standards. Psychometric testing refers to personality and/or psychological assessments that are conducted with candidates, often prior to a formal interview. Psychometric tests are more often used for management positions or positions where high-level specific skills are required. Most of the tests available must be used under license to those who developed them, with associated costs. Step six: check references References checks often reveal useful information and are a key part of the selection process. They often provide information that a candidate may be unlikely to reveal about themselves and provide another perspective on their performance in previous roles. Always verify the nature of the relationship between the candidate and the referee and the length of time they have known each other. It is also essential that at least one of the referees is a previous supervisor. Notes from referee checks should also be documented and kept on file. 215 Step seven: make an offer Once the selection panel has received feedback regarding the referee checks, and is satisfied that the chosen candidate is the best person for the position, then the candidate is offered the position, usually verbally in the first instance. If the candidate accepts the position, then the start date needs to be agreed and the offer must be formalised in writing. It is important that the offer is accepted in writing before the other candidates interviewed are advised of the outcome. Once the formal offer has been accepted, then all other candidates should be advised in writing that they have been unsuccessful. It is also likely that some of the unsuccessful candidates may request feedback on their interview (strengths and weakness) and it is good practice and fair to ensure they receive useful feedback based on the notes from the selection panel. General principles Matters regarding sex, age, colour, race, religion, national origin, sexual orientation or disability are inappropriate to consider at any stage of the recruitment process (other than how people with specific needs might need to be supported to equitably access the process). It is also inappropriate to consider a person’s housing status, criminal record or credit history unless these factors are relate to a specific requirement for the position, and for which there should be separate formal processes (e.g. child protection procedures). Those involved in the recruitment process should be required to declare any conflict of interest relating to any candidate. For example, those involved in any stage of the recruitment process should make a declaration about any relationship with any candidates. Confidentiality must be maintained at all times. All documentation and communications with prospective candidates should re-iterate a commitment that applications will be treated in confidence. In addition, all recruitment files, from applications to interview assessments and the panel’s deliberations, should be held in secure locations with restricted access. 216 Standard 10: Protection of human rights and freedom from abuse 10.1 Sample policies and procedures Sample Policy: Human Rights65 Human rights, as outlined in the United Nations Declaration of Human Rights, include the rights to physical integrity, mental and moral integrity, civil rights and legal integrity, socio economic rights, and the right to a family. Our agency believes that people with disability have the same legal and civil rights as other people in the community and that advocacy has an important role in safeguarding people with disability against abuse. Abuse and/or harassment of a person/ people with disability will not be tolerated. Staff, volunteers or Committee Members who engage in such activity will be liable to dismissal from employment. Our agency will endeavour to ensure that all involved with our agency possess a full understanding of the legal and civil rights of people with disability. Our agency will seek potential staff, volunteers and Committee Members who are committed to defending the legal and human rights of people with disability. Our agency will provide adequate training for staff/ volunteers in reporting and supporting consumers in relation to abuse. Our agency will ensure that all staff recruited and potential advocates are screened as a safeguard to minimise the risk of exposing people with disability to abuse. Our agency will source and make available relevant information and resources which can assist in dealing with issues relating to abuse. Our agency has a commitment to upholding the legal and human rights of people with disability. Where people with disability are the consumers of the agency, our agency will: Provide information to consumers (and their families and carers, as appropriate) about their right to live free from abuse and their entitlement to independent advocacy and support if their human rights are infringed. Ensure that the legal and human rights of people with disability involved with our agency are upheld, both in the context of the advocacy undertaken and in the community in general. Outreach to people with disability Where people with disability are the consumers of the agency, consistent with our purpose and contractual obligation, our agency will: • • 65 Endeavour to seek people with disability who would not otherwise have come to the attention of our agency, or may have a limited ability to access our agency Seek out people with disability who may have been subject to abuse or neglect. National Disability Advocacy Program Quality Improvement Toolkit, FaHCSIA, 2009 217 Our agency may seek these consumers through outreach programs. 10.2 Tools Tool: Indicators of abuse assault and neglect66 Management, staff, volunteers, people with disability, their families, friends, carers, and advocates all play a significant role in preventing and detecting the occurrence of abuse, assault or neglect. The table below provides some examples of indicators of abuse and neglect of children and adults. It is important to remember that the indicators listed below are not the only indicators and that the presence of one or more indicators does not necessarily ‘prove’ that abuse, assault or neglect has occurred. This list of possible examples should not be considered a complete list of possible indicators. Type of abuse Physical indicators Behavioral signs Physical abuse - unexplained cuts, abrasions, bruising and/swelling: on face, lips, mouth, torso, back, buttocks thighs in various stages of healing - unexplained burns or scalds: cigarette burns especially on soles, palms, back or buttocks - rope burns on arms, legs neck or torso - unexplained fractures, strains or sprains - dislocation of limbs in various stages of healing - bite marks - dental injuries - ear or eye injuries - ligature marks - welts - avoidance of a particular staff member - fearfulness or fear of a particular person - sleep disturbance - obvious changes in behaviour - changes in appetite - changes in daily routine - unusual mood swings withdrawal - unusual passivity - out of character aggression - self-abuse - drowsiness - inappropriate or changing explanation of how an injury occurred - excessive compliance Psychological / emotional abuse - speech disorders - in the case of a child, there may be lags in physical development or a non-organic - self-abuse or selfdestructive behaviour - challenging or extreme 66 Disability Sector Quality System, Partners in Quality – Resources and Guide, Queensland. http://www.communities.qld.gov.au/disability/key-projects/disability-sector-quality-system/publications-toolsand-resources/resources/partners-in-quality-resources-and-guide 218 failure to thrive - injuries sustained from self-abuse or selfdestructive behaviours - suicide attempts - anxiety attacks behaviours - excessive compliance - extreme low self esteem - depression - feelings of worthlessness - lack of interpersonal skills necessary for adequate functioning - extreme attention seeking behaviour Sexual abuse - direct or indirect disclosure of abuse or assault - difficulty in walking or sitting - pain or itching in genital and/or anal area - vagina or penile bruising, bleeding or discharge - self-abusive or self-destructive behaviour - attempts at suicide - torn, stained or blood stained underwear or bedclothes - sexually transmitted diseases - trauma to the breasts, buttocks, lower abdomen or thighs - unexplained accumulation of money or gifts - pregnancy - sleep disturbances - changes to eating patterns - inappropriate or unusual sexual behaviour or knowledge - changes in social patterns - sudden or marked changes in behaviour or temperament - anxiety attacks - refusing to attend usual places egg work, school, respite - depression - going to bed fully clothed - excessive compliance of staff Financial abuse - no access or unwarranted restrictions to personal funds - no control over personal funds or bank accounts - no records or incomplete records kept of expenditure and purchases - no inventory kept of significant purchases - person controlling the finances does not have the proper legal authority - misappropriation of money, valuables or property - forced changes to wills or other legal documents - persistent failure to produce receipts - receipts indicating unusual or inappropriate purchases - person has insufficient money to meet normal budget expenses - person is persistently denied outings and activities due to a lack of funds 219 Tool: Human Rights Indicators Project – Queensland Advocacy Incorporated 67 Queensland Advocacy Incorporated (QAI) has been working on a Human Rights Indicators project – developing a set of human rights indicators for people with disability. “A human rights indicator is designed to be an objective measure of the degree to which persons with disability enjoy (or experience) a particular human right or freedom. Over time, QAI will use its Human Rights Indicators to build a database that records the lived experience of human rights of persons with disability in Queensland. The database will be compiled from a range of sources, including consultations with persons with disability and reports made by individuals and organisations. The database will provide evidence of the key issues that need to be addressed by governments and communities to improve recognition and respect for the human rights of persons with disability in Queensland.” There were a few drivers behind our project – we’d become aware of some unscrupulous operators of boarding houses for people with disability. For example, one boarding house had forty residents in its care although it no longer met the service conditions. We thought we needed to develop a set of indicators so that when someone went into a boarding house they could easily judge whether or not it was operating in a way that upheld the rights of people with disability. Although these services had to be accredited to operate, accreditation alone wasn’t enough to protect the rights of people with disability. In developing the indicators we consulted with agencies, the anti-discrimination board, service providers, the Office of the Public Advocate, advocacy groups and people with disability. At the first cut we developed a set of plain English standards. Now we have additional funding from a service provider for reviewing the first round of indicators and to produce a publication that will be a snapshot of how people with disability feel their human rights are being met in Queensland. It will also be a way of testing our indicators. We are running a set of hands-on workshops on human rights around scenarios for human rights for people with disability, their parents and service providers. We are taking an action learning approach and from that are hoping to develop a set of fact sheets for people with disability to understand when their rights are not being met. Queensland Advocacy Incorporated, http://www.qai.org.au/content/humanrights.cfm 67 220 Excerpt from Everyone has human rights Understand Yours!, 2006, Queensland Advocacy Incorporated, http://www.qai.org.au/content/humanrights.cfm 221 Excerpt from Everyone has human rights Understand Yours!, 2006, Queensland Advocacy Incorporated, http://www.qai.org.au/content/humanrights.cfm 222 Excerpt from Everyone has human rights Understand Yours!,2006, Queensland Advocacy Incorporated, http://www.qai.org.au/content/humanrights.cfm 223 5.2 Case studies Standard 1: Accessing advocacy Rights in Action Inc, Queensland Managing advocacy access is essential. We will never be able to provide advocacy for everyone – we have an agreed number of people based on our funding from FaHCSIA – so we want to make sure that we do help those who are most vulnerable. It’s about prioritising need. To do this we have developed a spectrum of vulnerability. The spectrum has three components – vulnerability, capacity and urgency of the issue. Previously, we used a numbered rating scale, but now we rank vulnerability and capacity as high, medium, or low. And the urgency of the issue is rated as urgent, non-urgent, or an issue that can be referred to another service. For example, a high rating for vulnerability would include those: at risk of suicide; homeless; with no income; living in a segregated setting (e.g. an institution); and from an Indigenous or Culturally and Linguistically Diverse (CALD) background. While a medium rating for vulnerability would include those with: communication difficulties; mobility impairment; and a health or justice order. Our view in ranking people from an Indigenous or non-English speaking background highly in terms of vulnerability, is that they have generally had less access to services and are more likely to have been left out of general community services. Referrals to other local services are made by telephone and if the person can be assisted at that time by providing information or linking them in with an existing service, this is done immediately. Whereas referrals identified as ones we might take up are reviewed and prioritised in regular staff meetings. At the moment we have reached capacity and can’t accept more referrals for about one month. That’s why it’s important we have strong networks in the community so we know what other services we can refer people to. Also, the agency can’t become a case manager, so it’s important to pressure existing services to assist people with disability as they would anyone else in the community, so they are integrated into the community. We don’t just say ‘no sorry we can’t help you’ when we can’t take up a referral. We try to find them the resources they need to resolve the issue themselves. It might take a few phone calls, helping people if they get stuck along the way. We don’t just give the person information, but try to put in place the steps they can follow through. Often we won’t just tell them about another organisation, we send them information or the organisation’s brochure; we might introduce them to someone from the organisation or offer to make an appointment for them – if we 224 don’t do this people might not take up the opportunity. Although it takes some time to do this, it is much better than the person calling back in three months in a crisis situation that might have been prevented. Where there aren’t other services to refer someone to in their local area, we might refer the issue to the local MP, or take up the issue on a systemic basis, lobbying for services in those areas. Accessing the most vulnerable people also involves proactive outreach, such as visiting people in group homes, nursing homes and the hospital psychiatric ward, because most people don’t self-refer – the bulk of our referrals come from social workers, disability service providers and legal services. We also visit our local Australian Business Enterprise Centres and talk to people with disability there on a monthly basis to raise awareness of the services they can access and develop some rapport so that if a situation does arise, they have the confidence to call us. We have had complaints from the people who have tried to access our service who were declined because they were outside of our geographic area. When this happens we refer people to the Complaints Resolution and Referral Service (CRRS) so they can make a complaint and also inform the Department through our quarterly reports so they know where there are areas of need. Gippsland Disability Advocacy Our agency is only funded for one EFT so it is important that we prioritise people at risk – it’s about urgency of need. In the last 12 months we’ve developed and introduced an intake document. We realised that we didn’t always have the information to hand that we needed, so we worked out the best way of getting that. We have a limited amount of time for administration so having the intake document as a tool is helpful because it provides a very quick snapshot. In the past, people phoning our agency to refer someone needing advocacy often provided little information about the person they were referring. But we find that the more information we have about a person, the easier it is to begin working with them on their issues. Also, from a safety perspective, it is important for us to have as much information about a person and their situation so that we can prepare our advocates for what to expect before they go to an initial meeting with a consumer. Having something down on paper is a safeguard for us and it also helps us comply with legislation. The intake document records demographic information, type of disability, the person’s issue, who they were referred by, and what supports they have. 225 Based on the information recorded in the intake document, we can prioritise cases for advocacy. When deciding which cases to prioritise, a range of issues come into play. We prioritise cases where people with disability are in a vulnerable situation and whose needs are urgent. Our promotional brochures outline the groups of vulnerable people for whom our agency will prioritise access, which include people who are experiencing discrimination, abuse or negligent treatment. It also includes those who are socially isolated; because our agency covers a large regional area and we find people who are isolated need support. Although some people referred may have multiple issues it is not as simple as prioritising those cases because consideration needs to be given to the urgency of those issues. It’s important to manage practice around advocacy access because it would be very easy to get caught up in a plethora of issues that could wait or issues that could be dealt with by another service. Because our resources are finite, we need to prioritise what we do and what advocacy we provide. If someone is referred to us and they have issues that aren’t as urgent, we will link them in with another support agency or specialist service where appropriate. It’s important that we don’t just let them fall through the cracks. That’s why it’s important that we have as much information as possible so that we have a sense of the issue, the person’s situation and then the urgency of need. Over time we will review the intake document and we may refine it, for example, we might refine the questions we ask when completing the intake form. A next step is also to develop a matrix for recording information about referrals for which we don’t end up providing advocacy but we do provide information and advice about the case. Sussex Street Community Law Service Inc Our agency introduced an exit survey for consumers collecting both feedback and demographic information. The survey is given to both consumers who come for a one-off visit and those with longer cases, and we usually receive about 20 responses per month. The demographic information in the survey collects includes: postcode, sex, year of birth, country of birth and Indigenous background. The data is collated and we can use this information for generating statistics regarding the populations accessing our agency in terms of sex, age and cultural background. We also monitor and compare these figures with local area demographics from time to time. That way we can see what percentage of various populations we are reaching. As an agency that covers a lot of the south of Western Australia, we have centres in several outreach areas. Consumers can access the agency via the central phone number and information service or they can contact the outreach centre in their 226 region directly. All consumers used to come through the central phone number, but as people in the community have become more aware of the local centres most calls are made directly to the local centre. Local communities are more aware of the outreach centres and able to access them directly because the centres have been active in getting out there talking to communities and business agencies to let them know about the services we provide and where we are and what we do. We’ve also advertised in local papers and on local radio stations about the services. In terms of intake, at this stage we haven’t needed a waiting list. We have been able to meet the demand for those in the areas we cover who have issues that we can handle. Some people who contact our agency just need us to send them information so they understand how they can deal with the issue. We also receive some referrals regarding issues we cannot handle, and when this happens, we’ll refer them to another appropriate agency. Although we don’t have the issue of a waiting list because we cover a large regional area, our agency encounters other issues in terms of providing advocacy for everyone referred. We know there is demand in some outlying areas where we don’t have centres. What we do in these cases is provide information and make referrals to local agencies that can help although they are not specific to disability. It is good to have policies and procedures around accessing advocacy not only when you have a waiting list but also in terms of prioritising how quickly a consumer is seen. Based on the urgency of the case, we can prioritise how soon people get an appointment. For example, an issue regarding accommodation, if a person is being evicted from their home, would be prioritised. If that is the case we try to set up an initial meeting as soon as possible, so that we can at least discuss with the consumer who they can speak to so that they can start the process. 227 Standard 2: Individual needs Regional Information and Advocacy Council, Victoria We approach advocacy based on the consumer’s best interests. An advocate has a discussion with the consumer about their wishes and needs. But in some cases a consumer’s expectations can be unrealistic. If an advocate is unclear about the actions to take on behalf of the consumer, they’ll talk to the consumer and let them know they are going get some advice from others in our agency. The advocate can then talk to their team leader or the manager of the agency about what actions will be in the best interests of the consumer, what actions are reasonable and what expectations are reasonable. It’s important to consider whether the consumer has given us the whole picture of their situation because if we go in and act without the whole picture our organisation’s credibility would take a hit. Other organisations wouldn’t want to relate or engage with us to solve problems for our consumers – it wouldn’t do us or our subsequent consumers any good. Consumers’ wishes and the organisation’s response are clearly documented in consumer files. It’s important to make file notes as things happen so that if a consumer makes a complaint or asks for a review, the file can be reviewed. In other cases, a family or carer contacts us on behalf of the person with disability. Before we act we have to consider whether the actions they’re asking for appear in the best interests of the person with disability. If they are, we usually go ahead. But if the parents/ carers interests don’t seem in the best interest of the person with disability, we usually take the case of the person with disability. For example, issues can occur when a person with disability reaches an age where they want some more independence and the family/ carer doesn’t agree with this. Our response would usually be to take up the consumer’s case. Where there are issues we can’t resolve, we can refer the case to the public advocate’s office, the Office of the Disability Services Commissioner, Health Services Commissioner etc. Rights in Action Inc, Queensland We meet with the person seeking advocacy (consumers) to get to know them, understand what the issue is, and who the people they want to be involved are, for example, a support person or friend. We make them aware of their rights, of possible actions they can take and what the consequences of those actions might be. It’s a very transparent process. It is part of QA that all actions are discussed with the person with disability. In most instances they also guide those actions, but in some cases what is in their best interest must be considered because we don’t want to put the person in a worse situation than they are in. 228 We have a process for obtaining informed consent which is guided by each individual case. Some people have reasonable literacy skills and can sign a consent form themselves. However, others might be confused about why they even have to sign – in our view having the documentation isn’t relevant if the consumer couldn’t understand it. Some people might nominate a person to sign forms on their behalf. Others, for example, a person with a severe acquired brain injury, may have legal decision makers, such as an adult guardian who can sign consent and authority forms on their behalf. Where the person has a formal guardian, we may not automatically agree with the guardian’s views, we remain loyal to the person we advocate for. If we don’t believe the action or decisions they want to take is in the best interests of the person with disability then we provide them with information about actions that we think would be more appropriate and might try and influence them to change their opinion. We develop strategy plans for each person containing information about the issue and the actions being taken. All plans are reviewed on a three-monthly basis to check the milestones that have been achieved and whether any barriers prevented achievement. Plans are never developed by one person – a number of us might come up with strategies that the advocate can then take back to their consumer to discuss the options and possible consequences. We want to make sure we’re implementing the best strategy. As well as the strategy plans, we record, number and file any contact we have with the person receiving advocacy. Keeping records and reviewing them keeps us accountable. It shows we don’t have a fixed agenda or a one-size fits all approach to advocacy. It’s a way of double checking that we’re doing what we say we’re doing and is a form of evidence to back that up. For us keeping records is just doing our jobs but it’s really about being accountable to the person with disability, that what we agreed with them is being done. Delivering a culturally appropriate service - Sussex Street Community Law Service Inc One of the important things we do, and I’d say this would be the case for other agencies with multiple sites, is to make provisions in the budget for bringing staff together at least once a year. There is quite a bit of money involved for travel and accommodation so we try to organise a two day session to get the most out of it. We allow time for general discussion of issues and also try to organise some formal training, for example on working with people from Indigenous or Culturally and Linguistically Diverse (CALD) backgrounds. We have received positive feedback about the value for the staff in meeting and having the opportunity to discuss mutual issues. The training for working with Indigenous people was delivered by members of the Indigenous community. It covered cultural values and beliefs; differences in how Indigenous people might expect things to be done; and issues of abuse and 229 discrimination related to race. It has impacted on how advocates feel. With the knowledge from the training, they can be more empathetic to the situation. We used another NDAP funded agency – the Ethnic Disability Advocacy Service – to provide the CALD training. Training briefly covered the migration patterns to Australia over time identifying the countries people have migrated from; how other agencies can help us with CALD consumers; and services and supports where we can refer CALD consumers. It’s become a valuable tool for advocates in knowing what consumers can access and what they can refer them to. 230 Standard 3: Decision making and choice Family Advocacy, South Australia Ensuring informed decision making and choice in advocacy is important because a quality life for people with disability is one in which they are given the opportunity to participate. Informed decision making and choice is key to what advocacy is about. The definition of advocacy states that you must not act contrary to the views of the person with disability and that you must keep their views in mind at all times in the advocacy process. As a family advocacy agency, we support the family member of the person with disability. However, whenever the person with disability is an adult, we make sure we meet with them so that we get to know them and what their preferences are. We might not meet them in the initial interview, but we meet them early in the case. In many cases, we get to know the whole family really well. Sometimes it is very difficult to find out what the person with disability’s preference is, but usually even people with profound disability are able to indicate ‘yes’ or ‘no’. In some difficult cases, we may arrange for an advocate to support the person with disability to ensure their voice is heard. So, depending on their capacity, we either speak to the person with disability directly to hear what they have to say; or we organise this with the support of an advocate for the person with disability. As it can be difficult to find out what the person with disability is really thinking, there are other clues we look for as to the true feelings of that person. In particular, there are some cases where the person with disability doesn’t describe the true situation because they are ‘seeking to please’. For example, a person who is uncomfortable in their work situation may not say this directly, but there might be physical factors indicating their discomfort. In this situation, we often find that family members know the person best and can help us find out what is really happening. On the other hand, acting according to the communicated wishes of the person with disability can raise concerns around duty of care. There are situations where parents approach agencies feeling distraught and disempowered because an advocate has supported the right of the person with disability to make their own decisions in taking drugs or other dangerous activities that have been impressed upon them by an outsider. A previous review of advocacy found evidence of cases where advocates were alienating the person with disability from their family. As an agency, we believe it is important to take a holistic approach, an inclusive approach, because family is so important. We are very careful not to alienate family members. It is one of the most delicate and sensitive aspects of our work. Where parents approach the agency suggesting an action that is not in the best interests of the person with disability, for example, placing them in a segregated 231 setting, we will try and work with the family. We work with them to consider the whole situation and what the consequences might be because it is an absolute priority that the outcomes are positive for the person with disability. In terms of duty of care, as an agency we are mandatory reporters – if we are aware of abuse of children under 18 we must report this to the Department. We have lobbied for this law to include adult children with intellectual disability, but this is not currently the case, which makes this situation more complex. Our approach is to involve the Office of the Public Advocate in situations where abuse is evident, whether that is physical abuse or issues around misuse of disability pensions. In some cases, families approach us in crisis situations, where there may be limited options available at the time, particularly in rural areas. For example, in one case, the strength of an adult child of an ageing rural couple was endangering himself and others around him. There were situations where he had grabbed the wheel of the car while his father was driving. The parents approached our agency for support. We agreed that on a short term basis he be admitted in Strathmont Centre to relieve his parents and for his own safety. However, instead of three months he ended up staying there for a year – it was distressing for his parents to see him in that situation, but they were unable to bring him home. We continued to advocate on their behalf, and he is now living in a regional centre that his parents can access, in a house with another male his age. They both receive a lot of support and he is involved with day activities. He is so much happier and some of his troubling behaviours have subsided. In terms of quality improvement, it is important to be flexible as an agency and work with the changing trends. We need to be adaptable to meet people’s evolving needs. This is also why staff training is absolutely essential as is providing staff with support in their work, which can be in very emotional situations. One such changing trend is the increased number of cases of mothers with an intellectual disability referred to us. Department Families South Australia approaches us to support mothers with intellectual disability who have had their children removed by the State. We discuss with the consumer their needs and wishes, and will advocate for them to have the most access to their children, for example, spending critical times like Christmas together, so that children are not alienated and get to know their mother. The use of consumer evaluation forms is also important in guiding our advocacy delivery, so that families can have an input into decision making on this level. When we have completed a case, the family completes an anonymous evaluation form. We provide a stamped self-addressed envelope so that they can fill out the forms at home rather than in front of an advocate. If you’re going to improve your agency, you really need feedback from the people you work with. You can think that you’re doing the right thing but, unless you check with those people you are funded to 232 support, you might be getting it wrong. We discuss the feedback at staff meetings and consider what is working well and where changes need to be made. Self advocacy groups - Gippsland Disability Advocacy Gippsland Disability Advocacy covers six local government areas – it’s a huge geographical area for our advocates to cover. We’ve recently been involved in a project to develop and support a network of self advocacy groups in the region. We are on the Steering Committee for the project. In our role, our advocates also rotate with advocates from other participating agencies to attend group meetings and support the members. In the project’s first year, there was philanthropic funding available for a project officer. So that the groups will not be dependent on funding, which can change, the aim for the future is that they will be self-sustainable. But to do that they will need a little help. This is why agencies have organised for their advocates to have a supporting role for the groups. The groups are a safe environment where people with disability can speak about their experiences and do the things they need to do. They provide a forum for people with disability to get together and talk about issues they are facing in their local community and how to manage them. In the start-up phase, meetings were held in day centres for people with disability. Members were mainly people living both in residential care and in the wider community, with minimal support, coping with issues including social isolation and economic disadvantage. People’s attendance at these groups increases our capacity to reach people with disability who may otherwise be hidden within a community. Sometimes families can be very supportive but often there is little or no family to offer support. Also, there are occasions when families are the issue. It is basically a community development project. The idea is to support community groups’ capacity to support people with disability and to support people with disability to be involved in their communities. People with disability have ownership of their group. They are empowered to speak out about what they think should happen in their community and the issues each group focus on are specific to their community. Supporting advocates help link the group to local organisations, as needed to work on solutions to issues. For example, one group is working on the lack of transport in their local area, and they have been able to link in with local council. An advocate attending either community advocacy or self advocacy groups improves access to services for these people, with an added benefit that people with disability will get to know the advocate and therefore feel more comfortable approaching them for support i.e. a familiar face. 233 Supporting these self advocacy groups’ work on advocacy issues in their local community means that our advocates are more available to work on individual advocacy cases. The people in the groups are also developing leadership skills and learning to network, which are key skills for their participation in the community. One of the self advocacy groups’ achievements to date is having organised a regional advocacy forum, which they were able to do with minimum help from advocacy agencies. They formed a Steering Committee to oversee the organisation, with one member from each group as a representative on the committee. They organised speakers, including relevant Members of Parliament. The forum was open to the general public and about 170 people attended. 234 Standard 4: Privacy, dignity and confidentiality Gippsland Disability Advocacy Gaining trust of people with disability is integral to advocacy so that we can work with them and build their confidence. We aim to provide an environment where consumers have the confidence to say what they want, are involved in directing advocacy actions and feel supported. One way of building consumers’ confidence and trust in us is having them sign a privacy document, which shows that we respect their rights and personal information. The consumer is given the privacy form in our initial meeting. The information on the form is brief, only a paragraph, and in plain English. It explains that their personal information will be collected and held by our agency and that it is our practice to disclose information to government departments for reporting and accountability, as well as other relevant parties. The advocate reads the form to the consumer and makes sure that they have understood the form before they are asked to sign. At the same time we explain that their information will be held securely – we have locked filing cabinets and our computers are password protected. As well as asking the consumer if they have understood the form, we might also ask them to feed the information back to us. We do this because often people will say they have understood when they haven’t. Where someone hasn’t understood we will break the information down for them into sections, always using appropriate language. The exact words we use depend on the capacity of the particular consumer. These practices are so important to building confidence and trusting relationships with consumers. It’s important that they understand a form before they sign it and understand their privacy rights. So we’re also explaining that with rights come responsibilities, which is important for them to be able to transfer this knowledge to another situation. It may take a bit of repetition and explaining, but taking the time to do this is really important. Now, we have also developed a specific agency privacy policy that documents how as an agency we adhere to the Privacy Act. We haven’t always had this but we had a new staff member who wasn’t used to dealing with privacy issues and she approached other staff about our practice in this area. Sometimes it’s something as simple as this that triggers a change in our practice. Something that makes us stop and think about how we can get better at what we do. We realised how important it is to remember that not everyone will be used to working in this context and aware of how to adhere to the Privacy Act – we decided we needed our own document. 235 We need to be good at what we do but we also need to be good at showing we’re doing what we say we’re doing. Privacy training, Nova Employment and Training, NSW We have a three tier approach to privacy. Firstly, staff are trained in what privacy means, using scenarios to emphasise important points. Secondly, the physical layout of our organisation has been altered to allow for private spaces. Thirdly, we have ongoing training participants/supported employees relating to their rights to privacy. Staff are trained to deliver information on all the Disability Service Standards, including privacy. Consider these questions: Do all staff members understand their obligations relating to privacy? How do we know? Do all participants/supported employees understand their rights relating to privacy? How do we know? Do we offer induction and refresher training in privacy issues? 236 Standard 5: Participation and integration Indigenous Disability Advocacy Service (IDAS) As a community service, we make sure that we keep our consumers informed of what is going on in their local communities. We keep them up to date with events and what is available. For example, we might let them know about men’s groups, carer’s meetings and workshops or training to help them work with their children. Then there are events like NAIDOC week to get involved in. We run information stalls to promote our service and invariably new consumers are enlisted on these days. There might be sessions in communities where a representative from the Ombudsman’s Office speaks to Indigenous people with disability about making complaints. IDAS has a complaints process which is explained to our consumers and which would end with the Ombudsman if no resolution could be found. We know the local communities and what is going on there. We’re always networking in the community and with other organisations – we’re made aware of lots of events through networking. We also find out about things through email and the web. The web is fantastic because we’re getting information all the time. We keep our eyes open for things that are coming up and, as soon as something does, we let consumers who would be interested know about it. If there is something in their area and relevant to them, we encourage them to get involved. We try to keep our consumers knowledgeable of what they can access and assist with support. IDAS is currently developing a consumer-friendly service directory which should be in circulation within the next few months. One of our consumers participated in “Shoulder to Shoulder” an initiative of the NSW Government, Stronger Together. We think of our agency as a family. Because we know our consumers on a personal level, we don’t have to search through our entire database to know who would be interested in a participating and who wouldn’t. Our personal relationship with our consumer, in keeping them informed, builds rapport and reassures them that they are important to us, which fosters the consumer’s confidence in IDAS doing our utmost for them. Knowing our consumers well also means they always lets us know what is happening and whether they are getting the right service. If our consumers are not happy with the agency, they feel confident in letting us know. This is something we encourage. We assure our consumers that complaints are welcome as they only serve to better our agency. IDAS has a good reputation and we intend to keep it. Our advocacy work is very relationship based. Our practice involves respectful listening – by being heartfelt in our communications, our consumers know that we care and they feel that they are being heard. Quality listening is an important aspect of our service as Aboriginal people’s needs are complex; it’s like throwing 237 a pebble in a pond, there is never just one issue, issues keep spiralling outwards. Respectful listening means that we can get to the bottom of our consumer’s issues. For example, issues around not having a voice, not being heard when accessing mainstream services. As Aboriginal advocates our role is to speak up for our consumers to ensure their voices are heard. Aboriginal people have different ways of communicating and thinking. When accessing mainstream services, some consumers feel misunderstood; not educated enough; that their voice is not being heard; and that the service does not understand our Aboriginal “way of being”. Feelings of intimidation and fear due to past history can stand in the way and keep our consumers from using mainstream services. That’s why individual advocacy is so important because we can act for our consumers and get the results that they cannot achieve on their own. People often ask me how they can better communicate with Aboriginal people. I can teach the way things are done but essentially one needs to be Aboriginal to understand. IDAS staff are Aboriginal people and, as such, we understand that providing time for consumer’s stories to come out is essential. Most times we sit with a consumer for several hours before the main issue surfaces. For example, one of our consumers didn’t want her child to undergo an intrusive assessment that was required by a disability service agency to continue to provide services. The agency didn’t want to take the support away, but they needed the assessment. Through sitting with, and listening to, the consumer, I eventually got to where the problem lay. The mother thought that her child was the only one who had undergo this procedure; she didn’t understand that it was standard practice. In this case, I was able to act as a go-between. In assuring the mother that all the other children had to have the assessment done she was then happy to cooperate and the services were able to continue. Basically we act on any issue that the disabled consumer is experiencing. In some cases, it might be as simple as liaising with an electricity or telephone company in regards to overdue accounts and making an alternative arrangement rather than having their electricity cut off. Individual advocacy is the most appropriate form of advocacy for people with disability from Indigenous communities. We have consumers who have tried to self advocate, but have not been able to get results. They feel as though they haven’t been listened to and they haven’t got a voice. There are a lot of issues around this and I couldn’t say for sure what the explanation is, but it could have to do with people’s perceived ideas of Indigenous people. Once we step in and act on our consumer’s behalf in most cases the consumer gets the desired results. We do make a big difference in improving their lives. Quality management in our agency is important to us. We care about our people and want to get the best outcomes possible. When our consumers turn around and tell us with heartfelt thanks that we have been a “blessing”, it truly makes all the hard work worth every moment. 238 Standard 6: Valued status Disability Advocacy Network, NSW There are so many things that make up valued status. It relates to integrity and treating people with disability the same way as other people – no more, no less. Promoting valued status just takes a common sense approach. As advocacy agencies, there are many ways that we can promote valued status. Over a decade ago, we started thinking about ways to celebrate the International Day of People with a Disability. What began as a small party within the deaf community in Wagga has grown to a large Dance Party for people with disability of all kinds from across the region that our agency covers. We have had approximately 300 people attending for the last three years. We applied for and now receive a community development grant from the local council. We work with a very small budget and we work hard to raise funds or to get businesses to donate products like food and drink for the party. In 2008, we also received a contribution from FaHCSIA. Funding helps pay for the venue, bus transport for people in the outreach areas, and carers for some of those attending. You don’t have to have a lot of money to do something like this, just commitment. We form a “Celebration of Ability” steering committee each year to organise the party. We include people with disability on the steering committee to help make the decisions. Our staff and staff from other disability services organise the party in their own time. We could get paid but we don’t want to, doing it voluntarily shows how we value people with disability. A high profile community member, like an MP (state or Federal) or the Mayor or whoever is available opens the night's proceedings and guests are able to talk to them. The party celebrates and includes people with disability and shows that they can do these things too. It celebrates their ability. Even the people in wheel chairs dance! If we as advocacy agencies don’t give people with disability opportunities to participate, how will they be appreciated and valued by the community? Another thing we do is talk to people with disability at disability employment agencies and group homes, so that they know their rights and have the confidence to complain when necessary, or to access other services if they need to. This helps ensure that they can be independent and have confidence to do the things that they need to. If consumers are not successful in achieving this, it leads to poor personal outcomes and self-worth, as well as enforcing the stigma associated with people with disability in the community. We also run community education presentations at schools and TAFE about disability awareness. People with different types of disability and disability agencies representatives (e.g. Vision Australia, Better Hearing, Mental Health, Carer Respite) talk to the students. 239 We bring wheelchairs, walking aids, hearing aids, a hearing loop and glasses that simulate vision impairment so that the students experience what it would feel like to have a disability. We talk about myths and stereotypes and tips for communicating with people with disability. Valued status is more or less about communication and inclusion. If someone ignores you or speaks disrespectfully to you, that’s not valuing your status. We talk to the students about communication – not treating a person with disability as if they were a child, not yelling at them. If we impress this attitude on students then hopefully they will communicate well with people with disability. In terms of communication, it’s also important to think about the language you use – communicate clearly and don’t use a lot of jargon. Print your agency’s information and pamphlets in plain English and in other languages that are relevant to your local community. If people can’t understand the information that is supposed to be for them, they won’t feel valued. 240 Standard 7: Complaints and disputes Sussex Street Community Law Service Inc When consumers come to an initial interview, they are informed about our complaints procedure and where they can access more information. They also receive a hand-out outlining the complaints procedure. Where a consumer has made a complaint and is unhappy with the result they can also arrange to speak directly to the General Manager about the matter if they would like. About twelve months ago, we introduced exit surveys. If a consumer comes for a one-off visit they are given the form at the end of that visit, while consumers assisted over a period of time are given the form at the end of their case. Consumers get the survey and a stamped, addressed envelope to take home and return anonymously. As well as some basic demographic information, the survey asks consumers to comment on our agency. Questions include: how easy was it to contact the agency; how quickly did we respond to them; how did we treat them; did they understand the advice we gave; and did they find that advice useful? The responses allow consumers to choose between a range of answers and also allow room for them to provide further comments to support their answer. If consumers wish to make a complaint, there is also a feedback folder in reception where they can take a form and submit it. We weren’t getting much in there, which is one of the reasons we introduced the exit survey. People can take the survey home and reflect on whether they have something to complain about. It’s more confronting for people to submit a complaint in the reception area. Some consumers are disgruntled rather than extremely upset and they don’t want to make a fuss so they wouldn’t submit a form, but they might take the survey home to fill out. We can’t expect everyone to return the survey, but we generally receive about 20 per month. The surveys are collated monthly and staff are given general feedback. However, where there is a negative comment, we generally wouldn’t wait until the end of the month to deal with it. If an individual raises a particular issue, it is discussed with the relevant advocate. Addressing the issue straight away makes it easier to deal with because we can identify the context and discuss what we can do. For example, if a consumer comments that we were slow to respond, we consider whether we were particularly busy at that time and what could have been done. If a consumer was uncomfortable, we might consider whether there is something we can change in terms of our procedures. If a broader issue comes through in a few surveys, we’ll address it on an agency level. For example, there was a period where there was difficulty with phone calls getting through to the agency. People complained about having to wait too long before being transferred so we changed the phone system, making it quicker to divert from one phone to another. 241 The survey is a very useful tool to do something automatically. It might identify a problem we wouldn’t have been aware of otherwise. It is a really good tool for continuous improvement. Feedback is a real pointer to how your business is going. It’s easy to get lots of positive comments on a regular basis and not look deeper into your practice. If you’re continually patted on the back, you don’t necessarily stop to think about whether you’re pleasing all of your consumers. You might not stop to see that a minority of them are disaffected. With the exit survey, more often than not, we do get really positive comments and that’s important for the advocates to see where they’ve helped or been particularly understanding. Targeted feedback and investigating feedback trends68 We believe that having a strong mechanism for complaints and feedback is necessary for the organisation to be able to improve. Our feedback system used a survey sent out to all participants and employers asking them to rate the organisation on a 1–5 scale in different areas. We found that the positive responses were unreasonably high, which did not allow us to get the information we needed about where we could improve. Our strategy was to begin to target questions towards areas of potential weakness or negativity to try and bring issues more to light. We also began to investigate trends in the middle of the 1–5 scale, that is, areas that were described as “OK” by participants and employers. This allowed us to make better use of our feedback for the organisation. Job Support NSW, Disability Employment Services provider Consider these questions: Do we have an organisational culture that values complaints and feedback? Do we link complaints to continuous improvement? How useful is the feedback we receive? Could we target our feedback mechanisms to explore areas where we feel there are organisational weaknesses? *68 Quality Strategy Toolkit for Disability Employment and Rehabilitation Services, FaHCSIA: https://www.fahcsia.gov.au/sa/disability/pubs/employers/Documents/quality_strategy_toolkit 242 Standard 8: Agency management 8a Corporate governance Defining Board/CEO Roles Aware Industries, NSW Australian Disability Enterprise We were concerned that our Board should have its own separate sphere of operation from our management and CEO. We use a system called the “policy governance model”, which defines the specific and separate responsibilities of the Board and CEO, as well as how they engage with one another. The aim of this is to allow the Board to hold the CEO accountable regarding financial and quality measures, while giving the CEO and management sufficient creative freedom to perform his/her own job. We have found that this structured approach to Board–CEO relations works well to eliminate inefficient overlap, and allows both the CEO and Board to do better at fulfilling their own functions. We have also found it effective to set a work program for the Board at the start of each year. This way, Board members know when particular issues will be covered, allowing them to work through issues in a more systematic way. 8b Quality management systems Regional Information and Advocacy Council, Victoria It’s important to put the foundations in place before you build. Good agency management means clear management roles and responsibilities; sound administration practices; formal systems not dependent on individual staff members; and taking opportunities to improve. It’s important that it’s more than rhetoric; that there are solid practices to back us up. It takes time to do things properly. To continue providing better advocacy, we need to focus on good management systems, not only current advocacy provision. Four years ago, we started looking at our management systems, beginning with the Board; working from that overall organisational level down. There was a lack of clarity around management roles and responsibilities so we implemented an annual corporate governance program for the Board – a corporate governance trainer now spends one day a year with the Board. So the Board is clear about their role in providing strategic management, and about operational management issues that aren’t in their role to consider. Having the annual update tops up existing Board members’ knowledge and educates new Board members. Next, over a seven month period, we put resources into getting a comprehensive suite of policies and procedures together. So these remain up-to-date, the Board reviews them annually. Each of our three offices (Shepparton, Bendigo and Swan 243 Hill) can access policies and procedures electronically via a shared drive. Each office also has a hard copy, which is updated when changes are made. The distance between offices can be a challenge, but we focus on making sure the communication flows evenly between offices. We organise face-to-face team meetings monthly, which are important to cover issues, reinforce policy and practice, and provide debriefing for advocates. As we have grown and have more employees, we’ve also made sure there is a structure in place for management and clear lines of reporting to ensure clarity and accountability. It’s important to have the basics right, for example, having good administration practices in place. We’re disciplined about keeping an organised filing system, updating consumer files, and documenting important information in consumer files. All consumer files include an Intake form which includes details relating to the consumer, the issue they are seeking assistance with and details including their consent for their information to be shared and with whom. Good management also involves finding more efficient and effective use of time and resources – making good use of the resources we have. For example, thinking about the way we collect consumer data centrally so that we can adapt it to use for all of our different reporting requirements to funders. In terms of improvement, we’re just beginning a quality improvement partnership. We identified two other Victorian advocacy agencies that are on the same page as us and approached them about the partnership – they were very enthusiastic. We held our first meeting in February and will meet on a monthly basis to progress. We will work to develop performance standard measures for each year for an initial three year period. The plan is to develop a set of minimum standards and self and peer assessment tools we can each use to assess our agencies. Once it is developed, each agency will be able to use the self-assessment tool to assess their compliance with the performance standards. The Manager/CEO of one quality improvement partnership member agency will conduct a peer review of another member agency in March each year using the peer assessment tool. Following the review, a report will be forwarded to the Board Chair and CEO/Manager for rectification and each July, the three Board Chairs and CEOs/Managers will meet to verify the rectification is complete. The kinds of things we’ll assess are policies, procedures, practice and reporting. The idea behind the peer review is that although we think we’re doing pretty well, another agency might see a hole that we haven’t considered. By giving the results to the agency’s Board they will be able to see where things are working and where there are problems. 244 Citizen Advocacy South Australia We have developed and documented a vision of where we want to be in the next five years and how we want to get there. Working towards this vision keeps everyone focused on a united goal and on where we’re going. Planning and review are also key to management. We undertake strategic planning every three years; annual forward planning; annual Board program review; annual relationship review; bi-annual work flow review that preserves the focus on developing and sustaining citizen advocacy relationships and the organisational capacity to respond to the needs of vulnerable people with intellectual disability. Our practice evolves based on learning and environmental changes, for example, in relation to contemporary management practice. In reviewing our practice, where we find a weakness, we work to address that and identify the resources we need to help us do this. We think about the skills we need and seek out people with experience to advise us and to learn from. As a program we also focus on change management; identifying and seeking out people to advise us who may later become program associates who contribute to ensuring longevity. These associates may provide advice to the Board in areas including management, policy and government. As with anyone associated with CASA other than staff, they give their time freely because they believe in what the program is doing. We have found that having program associates around us helps to remain informed on some of the broader issues and to minimise staff time away from the core function. From time to time, we have engaged paid professionals for some issues. For example, we needed someone with experience to lead us through our strategic planning process so we hired a consultant. The OHS&W Audit was conducted by a registered auditor and a 12 month implementation plan was produced for Board consideration. In our view, Standards for Citizen Advocacy Program Evaluation (commonly referred to as CAPE) is also an important part of practice review. In our experience, CAPE assesses what a citizen advocacy program is doing, where the strengths and weaknesses are and makes recommendations that are designed to improve the program’s implementation of citizen advocacy over time. It encourages continuous improvement and contributes toward quality improvement. It all comes back to strengthening the probability that vulnerable people with disability will be matched with the most suitable citizen (the advocate), who will be supported by a program that is clear on its own role, independent and knows what it’s doing. It all impacts on the person with disability. The CAPE process we have undertaken has been a five day process, conducted by a team of six made up of a team leader (who is experienced in CAPE evaluation leadership) and other members who may be a mixture of coordinators and/or Board members from other citizen advocacy programs. We look at it as peer review – inviting people who do the same work as us in other places to come and listen to 245 what we are doing, talk to people being supported by the program and then give us some honest feedback. Sometimes when you’re heavily involved with what you’re doing, you can be missing something, and as humans we all tend to focus on what we’re doing well. As part of the process, staff are interviewed extensively, and all Protégés, Citizen Advocates, Advocate Associates, Program Associates and Board members are given the opportunity to participate and be interviewed by members of the CAPE team. The team rate the program against criteria in three categories: adherence to the principles of citizen advocacy, office effectiveness, program continuity and stability. After the evaluation is completed, the CAPE team leader compiles a written report of the team’s findings and recommendations for the Board’s consideration. 8c – Continuous improvement considerations Quality Improvement Partnership (QIP) In 2008 the Regional Information and Advocacy Council (RIAC) which operates in regional Victoria, was keen to assess the quality of its policies, procedures and practice by benchmarking with advocacy agencies with similar interests in quality improvement. It commenced the process by speaking with and identifying possible partners interested in participating in a network. After receiving a generally positive response the following steps were taken to design how the Quality Improvement Partnership (QIP) would work: Step one – design a Memorandum of Understanding to outline how the QIP would operate- this included each agency signing the MOU. The general principle established was for an equal sharing in the work of the QIP and for individual member agencies to be responsible for any costs associated with the QIP. The MOU also contained a Complaints Resolution procedure. Step two- It was agreed that each QIP member would participate in bi-monthly teleconferences, with the responsibility of organising the teleconference (and paying for it), developing an Agenda and taking Minutes. The teleconference was used to discuss policy, procedure and practice issues facing QIP members and would often result in the sharing of information (and policies and procedures) between member agencies. Step three – the development of a QIP Peer Assessment toolkit with which to undertake annual peer assessments of QIP members. The QIP toolkit was initially developed using the Draft Disability Advocacy Standards, and now uses the final Disability Advocacy Standards. Each year (in approximately April) a QIP member would visit another QIP member and undertake a peer assessment of the QIP member’s compliance with the standards. (This is not as rigorous as a NDAP QA audit as it does not involve interviewing consumers). The cost of the peer assessment is borne by the assessing agency. The assessor is to provide a report to 246 the agency to be assessed detailing its compliance in relation to the standards. All QIP members are assessed at a similar time. Step four – In approximately August of each year, the Managers and Chairpersons of the QIP members to meet together to confirm that any deficits identified during the Peer Assessment had been corrected, and to develop a work plan for the QIP for the following year. This meeting has proven valuable as it has developed a network among Board Chairs to share information relating to Board training, Managers Performance Evaluation, etc. Membership Currently the membership of the QIP consists of the following members: Regional Information and Advocacy Council (RIAC); Disability Advocacy and Information Service (DAIS); Disability Advocacy NSW; Advocacy Tasmania; The Speakout Association of Tasmania; and People With Disabilities Inc (PWD) Conclusion The QIP has proven to be a very effective means of ensuring a continuing focus for all members on the need for continuous improvement. It provides a means for the sharing of information and has made the development of policies and procedures an easier and more efficient process. It has also meant that through the annual QIP Peer Assessment evaluation member agencies have become very familiar with the Standards and audit processes. All members participated in a 1 day auditing training course in Victoria in 2011. The QIP encourages the development of similar networks of advocacy agencies to assist with the preparation of policies, procedures and practices and the NDAP QA. It has been the consistent view of the QIP that compliance with the Standards should be the major focus of all agencies in ensuring that consumers and staff are effectively and appropriately supported, and by so doing the NDAP QA audit becomes a far smaller issue. In 2012 some of the QIP members will be undertaking an exchange of Advocates between member agencies. For further information please contact Steve Doran, Chief Executive Officer, RIAC on 0358 221 944. 8d – Policies and procedures This section contains ideas and practices related to Standard 8 that have been put into place by different disability service providers. Although these are not disability advocacy agencies, the learnings from these disability employment services are useful. They are not intended to be prescriptive, but may help you think of ideas to develop your own policies and procedures 247 Disability Services Australia, NSW Australian Disability Enterprise and Disability Employment Services provider We have done substantial work to make the Disability Services Standards the centre of our corporate policies. Our policies detail the organisation's responsibilities against each Standard. That also means that whenever we create an operational procedure, it automatically rubs up against the Standards. We have centralised all of our policies, procedures and forms in a private intranet site. This site mirrors the organisation's shape, so that everyone can find what they need to do their jobs, as well as finding out what applies in different parts of the organisation. This ensures consistency in the organisation and also makes certain that no one is using out-of-date forms. Tulgeen Disability Services, NSW Australian Disability Enterprise When we were first going through QA Certification back in 2003 we decided to rewrite and replace our existing policies and procedures manual with 12 stand-alone manuals based around the 12 Disability Services Standards. The advantage of presenting policies and procedures manuals this way is, when our staff look at the policies and procedures, they are looking at the Standards at the same time, so it's all integrated. Each of the 12 manuals include information about additional supporting resources as well as a copy of all forms staff will need, and they are all cross referenced to the other relevant manuals, this way staff get to see the big picture. The handbooks are also displayed in a hanging file system, which means they are easy to handle and to pick up and read. Phoenix Society, SA Australian Disability Enterprise Because we comply with multiple quality systems, we have tried to find the most efficient system possible for dealing with the different requirements. What we have found works is to integrate all the different elements into our own internal policy and procedures manuals. Then, on the relevant pages of the manual, we have a reference to explain which quality system element this procedure relates to. That way, when it comes time to gather evidence for an audit process, we know where we need to go for the information. Where a particular quality system has something idiosyncratic, we explain that too, in a separate paragraph. Not all of our systems can be completely integrated this way, but we do manage to consolidate a large amount of material. For instance, our complaints manual contains both information relevant to Disability Services Standard 7, such how to contact advocates as well as the Complaints Referral and Resolution Service, and information about where to go for complaints about OH&S issues. 248 Standard 9: Staff, recruitment, employment and training Citizen Advocacy South Australia To attract and retain staff, Citizen Advocates and volunteers (i.e. Board members, Program Associates, Advocate Associates) we believe that it is important to be open and transparent; to have a clear vision and build on a shared sense of belief in the work, its importance and a commitment to seeing it done well. A lot of our work relies on networking and building relationships in our community – with Citizen Advocates, developing personal contacts of staff, Board contacts and people who have been identified as supporters and friends of the Program. In recent years, the same has been the case when recruiting staff i.e. ‘head hunting’ or going to people known in the broader network who are considered to have some of the skills and qualities believed to be important to be able to fulfil the role. Before hiring staff, we also consider what skills or knowledge we don’t currently have within the agency and seek to appoint someone who can bring a new set of skills and experiences thus broadening the skill base within the Program. With the current staff, all have worked in one capacity or another within the field of intellectual disability. We believe that such experience gives us an insight into the universal issues confronting people with intellectual disability and a greater awareness of the challenges and limitations service systems and providers face. When combined with taking the time to understand each individual in terms of their needs, identity, strengths, aspirations, such knowledge contributes significantly to determining the most suitable person to become the Citizen Advocate. In the main, Citizen Advocates are identified through our network which is constantly being built upon as Coordinators move throughout the community doing the work. The process of Citizen Advocate recruitment commences when we believe we have identified the most pressing need of the person with intellectual disability (Protégé). In this way, recruitment of prospective Citizen Advocates is highly personalised to the identity, needs and skills of the Protégé and the probability of a good ‘fit’ with the identity, skills and interests of a suitable citizen. Like Protégé recruitment, determining Citizen Advocate suitability is a very strategic and carefully considered process. Potential Citizen Advocates are offered the opportunity to learn more about a person in their community and what it would take to become that person’s Citizen Advocate. Called orientation, the process typically unfolds over a period of about 4–6 weeks (longer if necessary) and is conducted in people’s homes and the CASA office. CASA does not expect people to make a commitment straight away. Orientation is not only information sharing, it is the beginning of relationship building with the prospective Citizen Advocate. A relationship that will need to become 249 strong so that the Citizen Advocate will openly seek the support of the Program regardless of whether things are going well or not. The goal of orientation is to determine the suitability of this person or persons for the role identified for a specific Protégé. The process is done in such a manner as to give prospective Citizen Advocates all the information they need to make an informed decision about their capacity to undertake the role outlined by staff. Should a person be deemed unsuitable by staff, the person does not become a Citizen Advocate. Additional to this process is the 2008/09 funding agreement requirement that all people involved in the program, including Citizen Advocates undergo a national police clearance. CASA orientation typically involves four 1.5–2 hour sessions. We present material in a logical sequence using overheads. All people taking part in the process receive a copy of the material in a manual to refer to. In recognition of the importance of the prospective Citizen Advocate to be supported in their future role at home, spouses and/or partners are invited to take part. In so doing, they too come to understand how important the role of Citizen Advocate is and they can be supportive of it, thus further maximising the probability of Citizen Advocate longevity. This strategy has resulted in more husbands and wives both becoming involved with the Protégé and therefore broadening the Protégés support base. Advocate recruitment is so important because, at the end of the day, it’s about doing the very best we can on behalf of the person with intellectual disability. Citizen Advocacy staff should have the time needed to carefully think through the process and then determine the best possible person to invite to become a Citizen Advocate. However, no matter how much planning a Citizen Advocacy program may put into the ‘matching process’, things can still go wrong. When this happens, we have processes in place to try and determine the role we played in things not working out and why. It’s important to reflect on what role we had in the relationship not working i.e. what could be done differently next time; was there anything we missed etc. In so doing, we can work towards minimising the chances of something similar happening again; recognising, however, that all people are different and their situations unique. Performance management including appraisals of all staff as well as a commitment to ongoing training for Citizen Advocates and other Program volunteers is important to increase the likelihood of better outcomes for Protégés. Training and development includes visiting other Citizen Advocacy Programs, including peer training with other Coordinators; formal training sessions (e.g. governance and management training for the Board and staff); attending and presenting at conferences; and being a part of the national and international Citizen Advocacy network. Citizen Advocacy Program Evaluation (CAPE) is a great training ground for staff. Being involved in your own Program’s CAPE is an excellent learning and teaching 250 process. Our involvement in internal and external review mechanisms of other Citizen Advocacy Programs has positively influenced and even changed the way we think about your own practice. Ongoing training is important so to minimise the possibility of complacency creeping in to the practice. For example, staff attend Social Role Valorisation (SRV) training periodically which reminds us of the universal issues facing people from devalued groups in our society which in turn challenges our thinking; to become more aware and more in tune with the things in the community that devalue people with disability; and to think of ways we can counter this. Citizen Advocates and Program volunteers are also offered this training opportunity. Employment appraisal, Edge Employment Solutions, WA Disability Employment Service Every time a member of our staff has an employment appraisal, we contact either three participants they are assisting, three family members and three employers that they have worked with. That means that for every appraisal, nine people are surveyed about how the service is working for them. We orient the questions we ask towards the Disability Services Standards. We use this information not only in the staff appraisal, but also in a collated form to help us improve organisational performance overall. This gives us robust evidence about the needs of our stakeholders, and it also allows us to collect information gradually and continually for ongoing improvement. 251 Standard 10: Protection of human rights and freedom from abuse Villamanta Disability Rights Legal Service Inc. The necessity to protect human rights is one of Villamanta Disability Rights Legal Service Inc’s foundation beliefs. It underlies everything that Villamanta does. Our whole service is built on the belief that people’s human rights are paramount. The reason our service exists is to help people with disability, in particular people who have an intellectual disability, to get to know their rights and the relevant law and to learn how to use the law to protect those rights. The protection of human rights informs all of our policies and procedures. We believe that having clear, well thought out policies and procedures about how we manage our service is vital to ensuring we consistently recognise and protect our consumers’ human rights. The Management Committee would not sign off on a policy, procedure or document without consideration of human rights. We recently reviewed all of our policies and procedures as a whole, drawing on a range of resources for guidance. When we are writing policies and procedures we do not just make them up, we go to respected sources. We have drawn on resources from the Eastern Community Legal Centre (Victoria), which received a grant for a consultant to develop a policies and procedures manual; the Federation of Community Legal Centres; VCOSS whose website has some example policies and procedures; and the Law Institute of Victoria. In Victoria, we also have a Disability Advocacy Resource Unit (DARU), which is in the process of developing, and setting up, a library of resources which advocacy agencies can draw on. We also believe that it is extremely important that we ensure our staff members and volunteers always treat consumers (and others) with the utmost respect and dignity. One of the questions we ask people who want to work or volunteer for Villamanta is “what, if any, are your views on human rights?” We also ask whether they have experience working with people with disability. That is not to say that people who do not have that experience cannot work for Villamanta, but they may need training in that regard before they are able to do a good job for our consumers. Workers and volunteers need to understand where our agency is coming from. We are not providing a charitable service for the “down and out”. Our consumers have human and legal rights and dignity. Our job is to stand up for the rights of people with disability – and support them to stand up for their own rights - and to redress the imbalance in society, so that people with disability have the same rights and opportunities as other people in the general community. A number of our service’s activities promote the human rights of people with disability. We provide community legal education (CLE) for people with disability and their carers. We also provide training on disability related issues for service agencies as well as the general community. At the CLE sessions we hold for people 252 who have an intellectual disability, we provide participants with a free copy of our booklet ‘Your Rights Your Choices’, produced in plain English, so that they are aware of, and understand, their rights. The sessions we run for others in the community aim to teach them about the rights of people with disability and what they need to do to avoid infringing those rights. We also work on systemic advocacy issues. For example, in response to the overrepresentation of people who have an intellectual disability in the criminal justice system, we recently got funding to research and produce a publication to be read by people working in the criminal justice system (police, courts, judiciary, lawyers and corrections) to ensure better understanding and treatment of those people who have an intellectual disability. Much of our work is done on individual legal cases where the human rights of a person with disability are not being upheld. It is Villamanta’s view (and that of many other people) that the rights of a person with disability cannot be met if that person is placed in an institution. There is an extensive history of abuse of people living in institutions which clearly illustrates that people’s human rights cannot be protected in such a setting. For those rights to be fully met the person should be living in the community with appropriate levels of support. Today there are many community residential units (CRUs) dotted throughout the community which have gradually been replacing the large institutions. We are frequently involved in cases where a CRU placement of a consumer who has a disability is failing, often including physical abuse. In these cases it is sometimes suggested that the best option is to place either our consumer, or another resident of the CRU, in an institution. In such cases we strongly oppose this suggestion. We have found that when a residential placement is not working it is often because there has been an inappropriate placement. For example, one person in the residence may be abusing others who are more vulnerable and unable to defend themselves. In some cases the abuse comes from a direct care worker. In some cases, increased and better trained staffing can solve the problem. In other cases, where this is not so, we lobby the Department of Human Services, or other relevant service provider organisations, to arrange an alternative and more appropriately supported CRU placement for the person whose behaviours are causing the problem. We would always oppose the placement of any of the residents of the CRU in an institution. We also consider issues of negligence and victims of crime in these matters. As a legal advocacy agency, we are different from many other advocacy agencies that advocate in the ‘best interests’ of people with disability. We are consumer directed and act on the consumer’s instructions and wishes. Our service considers that there will always be someone there, such as a parent/ relative or a public advocate, to indicate what would be in the consumer’s ‘best interests’; we are there at a tribunal or talking to a service agency to indicate the wishes of the person with disability. It is about ensuring their voice is heard and they have their human and legal rights recognised and acted upon. We always aim to communicate with our 253 consumer in person using whatever means of communication works best for them. In cases where it is impossible for us to communicate with the person with disability, or they have limited capacity, we find families often know how best to communicate with the person and what their wishes would be. In some cases a guardian is appointed to make decisions on the person’s behalf and we may receive instructions from them. We are always careful to check out whether families might have an ulterior motive for trying to ensure a certain outcome. If we did not protect the human rights of people with disability, we would be failing in our work both morally and ethically and we would be doing our consumers a grave disservice. Queensland Advocacy Incorporated The definition of advocacy is to protect, promote and defend people’s human rights. This comes through in the key elements of advocacy (functioning by speaking out, acting or writing; minimal conflict of interest; sincerely perceived interests; promotion of person’s welfare, wellbeing and justice; vigour of action; and costs). Considering quality practice in this area involves unpacking what things mean. For example, acting in ‘best interests’ is not about taking away a person’s rights; and there are differences between expressed need, perceived need and fundamental need. Where an action is not considered in someone’s ‘best interests’, a paternalistic approach would be to block or deny that action; but, as advocates, we work with the person, discuss the issues and the possible consequences of the actions. It is the person’s right to be involved in decision making. Also, it’s important to recognise that the way we perceive a need does not necessarily make it right. As advocates we must stop and ask ourselves if we’re really pursuing an action in a person’s ‘best interests’? There are a range of tools we can use in considering our practice in relation to human rights – the Convention on the rights of persons with disability (CRPD) social justice principles; community development principles; and social role valorisation theory. Personally I find the vulnerability schema, developed by David Massy, a useful tool in planning advocacy strategies that recognise, from a systems point of view, how society is affecting the life situation of the person with disability (e.g. how they are portrayed by people in power). Other people might not relate to this or certain tools I’ve mentioned – what is important is finding a tool that best articulates things for you to help you consider your practice. The issue here is to understand that the common response to vulnerable people in social policy, political motivated responses is always to locate the problem in the individual 'blame the victim' as opposed to understanding the problem genesis arising from exclusion, prejudice, rejection, fear and hatred of people with disability. 254 With increasing workloads, it’s not as easy as it once was, but it’s important to find the time to reflect on your practice. We try and make time for this in staff meetings. Or, where there is a particular issue, we may organise a meeting and involve the staff available. We also try to organise an external peer review every five years. Where the budget is not available for this, we’re considering engaging an external consultant to run some workshops to get feedback from our stakeholders and people with disability because you have to engage people face-to-face to really get feedback. Over the last few years, our agency has also developed a set of human rights indicators for people with disability in consultation with a range of stakeholders, including people with disability. Now we also have the UN Charter of Rights for People with Disabilities (CRPD). When we started the project, there wasn’t a set of human rights indicators for people with disability anywhere, which is surprising considering there are indicators for women, children and other groups. The human rights indicators are now another tool we can use in considering our practice as agencies as well as informing how you shape your advocacy strategies. Advocacy often is the last resort; the last stop for vulnerable people. Advocacy is ultimate safeguard for people with disability’s fundamental need and human rights being upheld in the community and by government. As we will never be able to provide enough advocacy, it’s important that the advocacy we provide is strong, clear and coherent. 255 5.3 Links to other resources Standard 1: Accessing advocacy Policy Templates and Procedures on Community Door Policy Templates and Procedures relevant to Standard 1 have been developed by the Department of Communities, Queensland specifically to assist organisations as they implement the Standards for Community Services. They are a good place to start for developing policies for this Disability Advocacy Standard (Accessing Advocacy) and to tailor them to your agency’s needs. The templates and guidelines are available on the Community Door website. Culturally Inclusive Service Delivery This Culturally Inclusive Service Delivery resource is part of the QUT Centre of Philanthropy and Non-Profit Studies, Developing Your Organisation website. Access and Equity Policy Template Here is a link to an Access and Equity Policy which has a strong cultural diversity consideration component. MDAA developed resources – Working with multicultural consumers with disability MDAA has produced a range of resources to assist you in working with people from a NESB with disability. The “building Cultural Competence” publication is a brief standard-by-standard guide including cultural competence across all of the standards for disability services in NSW. Standard 2: Individual needs Multicultural Disability Advocacy Association of NSW, among the resources available on this website, including information in 10 community languages on their different communities understanding of disability related issues, there are several resources prepared specifically to help agencies work with people from Culturally and Linguistically Diverse (CALD) backgrounds, including a manual on cultural competency. National Ethnic Disability Alliance, the national peak organisation representing the rights and interests of people from CALD backgrounds with disability, their families and carers nationally. Resources include publications and fact sheets. Standard 3: Decision making and choice Policy Templates and Procedures on Community Door 256 Policy Templates and Procedures relevant to Standard 3 have been developed by the Department of Communities, Queensland specifically to assist organisations as they implement the Standards for Community Services. They are a good place to start for developing policies for this Disability Advocacy Standard (Decision making and choice) and to tailor them to your agency’s needs How To: A Practical Guide to CALD Consumer Participation The link provides a work sheet that has different strategies to encourage effective participation from CALD consumers. An Introduction to consumer participation by the National Resource centre for Consumer Participation in Health, 2002. This fact sheet covers definitions, benefits, models and methods, barriers to participation, and evidence of effectiveness. Effective Engagement The Victorian Government has produced three downloadable books to “assist service users to take part in making decisions that affect them”: Standard 4: Privacy, dignity and confidentiality Information Privacy Principles, Australian Government, Office of the Privacy Commissioner, Public Sector Information Sheet - Information Privacy Privacy Act 1988 (latest version), including Information Privacy Principles, ComLaw, National Privacy Legislation for Not-For-Profits This link provides useful information for not-for-profit organizations including a ‘privacy checklist’. Privacy Templates and Information Our Community is a world-leading social enterprise that provides advice and tools for Australia's 600,000 not-for-profit community groups and state, private and independent schools, as well as practical linkages between the community sector and the general public, business and government. A range of information around privacy considerations, including sample templates are provided. Policy Templates and Procedures on Community Door Policy Templates and Procedures relevant to Standard 4 have been developed by the Department of Communities, Queensland specifically to assist organisations as they implement the Standards for Community Services. They are a good place to start for developing policies for this Disability Advocacy Standard (Privacy, dignity and confidentiality) and to tailor them to your agency’s needs. 257 Worksheets for the National Privacy Principles (NPP’s) The Quality Strategy Toolkit for Disability Employment Services provides worksheets designed to develop a working knowledge of the NPP’s. The worksheets also compare the National Privacy Principles with the Information Privacy Principles (IPP). Standard 5: Participation and integration Inclusion Works – a community organisation that aims to build better communities through the inclusion of people with disability. The publications/ articles page has a range of information resources on community inclusion that you may find useful. Nican – provides information on its website about recreation, tourism, sport and the arts for people with disability nationally, with the aim of creating links that improve access to recreation experiences for people with disability and their communities. Community Development and Community Education guidance is available on the Community Door website. Community Inclusion is discussed on the Our Community website with reference to a wide variety of resources. Standard 6: Valued status Disability WA, Disability Services Commission has a range of training resources around their Disability Services Standards, including Valued Status. Standard 7: Complaints and disputes Policy Templates and Procedures on Community Door Policy Templates and Procedures relevant to Standard 7 have been developed by the Department of Communities, Queensland specifically to assist organisations as they implement the Standards for Community Services. They are a good place to start for developing policies for this Disability Advocacy Standard (Complaints and disputes) and to tailor them to your agency’s needs. The templates and guidelines are available on the Community Door website. The Complaints Resolution and Referral Service VOICE – Valuing Organisational Improvement and Community Excellence This resource has a special emphasis on Indigenous managed organisations, and has an excellent template for a complaints policy and consumer feedback sheet. 258 Complaints Handling System – Developing Your Organisation Collecting Feedback – Community Toolbox - this American website has some simple and creative ideas to collect consumer feedback. Standard 8: Agency management Corporate Governance Handbook for the Board, FaHCSIA, 2nd edition, 2010, for more information on corporate governance: The Council on Quality and Leadership - has resources on leadership and Board development available on their website. Disability Services Queensland, for tools and resources The Disability Advocacy Resource Unit (DARU), Victoria The National Association of Community Legal Centres’ National Management Committee Guide for Community Legal Centres Volunteering Queensland, a range of resources for organisations recruiting and involving volunteers Community Door has an extensive range of generic templates and guidelines addressing corporate governance. Victorian Employers’ Chamber of Commerce and Industry (VECCI) produce training on Corporate Governance which has been highly recommended by disability advocacy agencies. Our Community website provides further information on corporate governance: Standard 9: Staff, recruitment, employment and training Best Practice guidelines for creating a productive workplace environment were created by the Human Rights and Equal Opportunities Commission (HREOC – now known as the Australian Human Rights Commission - AHRC). You can use them to assess the systems and practices at your agency and consider how you could improve. Employing People – DYO managed by the QUT Centre of Philanthropy and NonProfit Studies, the DYO site deals with Employing People and has subsections under Recruitment of Staff, and Employment Issues. Recruitment Policy Template – Our Community The Our Community Policy Bank website has a nine page recruitment policy. 259 Volunteers (Help Sheet) The Australian Institute of Community Practice and Governance website provides a help sheet on why screening of volunteers is important. Standard 10: Protection of human rights and freedom from abuse Queensland Advocacy Incorporated, Human Rights Indicators Project, Easy English booklet on Human Rights ‘Everyone has human rights Understand Yours!’ Public guardianship bodies in all states/territories In each state and territory there is a body which facilitates the appointment of a public guardian in situations where an individual may lack decision making capacity. Where necessary, you should refer to the relevant Office in your state/territory. ACT: Office of the Community Advocate Queensland: The Adult Guardian Northern Territory: Office of Adult Guardianship NSW: Office of the Public Guardian South Australia: Office of the Public Advocate Tasmania: The Office of the Public Guardian Victoria: Office of the Public Advocate Western Australia: The Public Advocate Information on the Convention on the Rights of Persons with Disabilities Australian Human Rights Commission National Anti-Discrimination Information Gateway 260 Section 6: Complaints handling mechanisms 6.1 Complaints associated with the NDAP Quality Strategy Strong and impartial complaints and appeals processes are vital components of the Quality Strategy. The following contacts may be important where disability advocacy agencies wish to make a complaint about certification or issues relating to their relationship with their funding body. The Easy Read Guide to Quality Assurance and auditing of the National Disability Advocacy Program (available on the FaHCSIA website) provides advice to people with disability about how they can complain about aspects of the audit process Australian Government Department of FaHCSIA What it investigates: The Department of Families, Housing, Community Services and Indigenous Affairs (FaHCSIA) has complaints handling mechanisms which disability advocacy agencies can access. The types of issues disability advocacy agencies may complain to FaHCSIA about include: 1. funding issues 2. complaints about the Complaints Resolution and Referral Service 3. complaints relating to departmental contract management How to contact them: FaHCSIA National Office Complaints Team Phone: 1800 634 035 Fax: (02) 6133 8442 fahcsiafeedback@fahcsia.gov.au Further information about the types of complaints that can be made by the public about FaHCSIA’s service(s), or the services of a FaHCSIA funded service provider can be found on the FaHCSIA website. Certification Bodies Types of complaints: Certification Bodies are required to have an internal complaints handling system. The types of complaints that disability advocacy agencies might make to a Certification Body could include (in the first instance): • • complaints about audit results complaints about certification revocation or suspension 261 complaints about the conduct of an audit team. How to contact them: Refer to the JAS-ANZ website for details of accredited Certification Bodies. Joint Accreditation System of Australia and New Zealand (JASANZ) Types of complaints: You can contact JAS-ANZ with a complaint about a Certification Body if you are not satisfied with the outcome of the Certification Body's complaints process. The types of complaints might include: complaints about audit results complaints about certification revocation or suspension complaints about the conduct of an audit team. JAS-ANZ does not have authority to overturn a certification decision, although it can question the judgement of the Certification Body and reassess its accreditation status if accreditation requirements have not been met. How to contact them: Tel: 02 6232 2000 Fax: 02 6262 7980 Mail: GPO Box 170 Canberra ACT 2601 Administrative Appeals Tribunal (AAT) What it investigates: If you are not happy about a decision FaHCSIA has made under the Disability Services Act 1986 (Cth) you may be able to lodge an appeal with the AAT. The AAT provides independent review of a wide range of administrative decisions made by the Australian Government and some non-government bodies. How to contact them: Tel: 1300 366 700 Email: aatweb@aat.gov.au. Postal contact details for Offices in each state are available from the AAT website. Commonwealth Ombudsman What the Ombudsman investigates: The Commonwealth Ombudsman can investigate complaints about the actions and decisions of Commonwealth departments and authorities to see if they are wrong, unjust, unlawful or discriminatory or unfair. The Ombudsman also seeks remedies for those affected by defective administration, and acts to improve public administration generally. This means that the Ombudsman can look at complaints raised by service providers 262 about the way FaHCSIA has dealt with them. The Ombudsman cannot override the decisions of agencies, or compel them to comply with his or her recommendations. However, agencies generally do accept the Ombudsman's recommendations. How to contact the Ombudsman: Tel: 1300 362 072 Postal contact details for Offices in each state, and an online complaints form are available from the Commonwealth Ombudsman's website. 6.2 External referrals Although most complaints from people with disability should be handled by disability advocacy agencies in the first instance, particular complaints may require an external referral. In the case of complaints that have not reached a resolution through the agency's internal systems, the Complaints Resolution and Referral Service (CRRS) will often be an appropriate external referral. This section provides information about the CRRS and some other complaints handling bodies that may be useful to you when seeking to make an external referral. The Complaints Resolution and Referral Service (CRRS) What it investigates: CRRS is an independent organisation funded by the Australian Government to resolve and investigate complaints about service providers relating to the Disability Advocacy Standards, Disability Services Standards (FaCSIA) 2007 and Disability Services Standards (DEWR) 2007. The CRRS encourages and supports the local resolution of complaints, but can facilitate conciliation between parties or investigate complaints when local resolution is not appropriate. How to contact the CRRS: Phone: free call 1800 880 052 Fax: 02 8412 7199 TTY: free call 1800 301 130 Mail: PO Box 126 St Leonards NSW 2065 Email: crrs@workfocus.com National Relay Service: Call 1800 555 677 and ask them to call the CRRS for you. Translating and Interpreting Service: Call 13 14 50 and ask them to call the CRRS for you. The CRRS website has further information 263 The National Disability Abuse and Neglect Hotline What it investigates: The Hotline is a single contact point for anyone to report claims of abuse and neglect in government funded services. The Hotline refers complainants to other relevant agencies, such as FaHCSIA or the police. Its role is to provide support and a link between the complainant and the service. How to contact the Hotline: Phone: Free call 1800 880 052 Fax: 02 8412 7199 TTY: Free call 1800 301 130 Mail: PO Box 126 St Leonards NSW 2065 Email: hotline@workfocus.com National Relay Service: Call 1800 555 677 and ask them to call the Hotline for you. Translating and Interpreting Service: Call 13 14 50 and ask them to call the Hotline for you. The Hotline website has further information. Police When to contact them: Any issue that arises at a service where there may have been a criminal act should be referred to the police. This might include: any action that in the normal community sense would involve reference to the police sexual assault/harassment alleged physical abuse fraud. Where criminal activity may have taken place the case should also be referred to the relevant department. The Department of Families, Housing, Community Services and Indigenous Affairs (FaHCSIA) will not investigate the criminal element of the allegation but will make sure that an agency is still meeting its contractual obligations (including meeting the Disability Advocacy Standards). How to contact the police: Refer to the police service in your local area through the Government Services section of your phonebook (by looking under 'Police'); or refer to: NSW Police Force Australian Federal Police Queensland Police Service Northern Territory Police Western Australia Police South Australia Police Tasmania Police Victoria Police 264 The Australian Human Rights Commission (AHRC - formerly HREOC) What it investigates: The AHRC can deal with complaints about discrimination under any of the four Acts administered by the Commission: Human Rights and Equal Opportunity Commission Act 1986 (Cth), Sex Discrimination Act 1984 (Cth), Racial Discrimination Act 1975 (Cth) and Disability Discrimination Act 1992 (Cth). Each of these Acts has Specific grounds for complaint including race, sex, pregnancy, marital status, disability, sexual reference, age and trade union activity. How to contact them: Phone: 1300 656 419 (local call) or 02 9284 9888 +Fax: 02 9284 9611 TTY: 1800 620 241 (toll free) Email: complaintsinfo@humanrights.gov.au Free interpretation and translation services are available by contacting 13 14 50 and asking for the Australian Human Rights Commission. WorkCover/SafeWork authorities What they investigate: If you cannot resolve complaints about occupational health and safety within your agency, complainants can contact state-based authorities. These authorities provide information and complaints-handling relating to occupational health and safety (OH&S) issues. How to contact them: WorkCover/WorkSafe ACT Phone: (02) 6205 0200 Fax: (02) 6205 0336 Email: workcover@act.gov.au WorkCover NSW Phone:13 10 50 NT WorkSafe Phone: 1800 019 115 (free call) Email: ntworksafe.deet@nt.gov.au Qld Workplace Health and Safety Phone: 1300 369 915 SA SafeWork Phone: 1300 365 255 265 Tas WorkCover Phone: 03 6233 7657 Fax: 03 6233 8338 Email: wstinfo@justice.tas.gov.au WorkSafe Victoria Phone: 03 9641 1444 Email: info@worksafe.vic.gov.au WA WorkSafe Phone: 1300 307 877 Switchboard: (08) 9327 8777 Email: safety@docep.wa.gov.au Mail: PO Box 294 WEST PERTH WA 6872 State/Territory Government authorities Health, Disability, Legal Services: Depending upon the issue, complainants may need to contact State/Territory-based authorities in the areas of health, disability and legal services. Please check the internet for up-to-date and relevant contact details for these authorities. 266 Section 7: Key contacts QA Administration Contacts Organisation/function Contact details Australian Government Refer to FaHCSIA website. Department of Families, Housing, Community Services and Indigenous Affairs (FaHCSIA) State and Territory offices – funding body for NDAP Joint Accreditation System of Australia and New Zealand (JAS-ANZ) – accreditation body Certification Bodies – accredited to conduct QA audits and grant certification Level 1,Members Equity Building, 11 London Circuit, Canberra, ACT 2600 GPO Box 170, Canberra, ACT 2601 Phone: 02 2 6232 2000 (Switchboard) Fax: 02 6262 7980 Email: contact@jas-anz.com.au Refer to JAS-ANZ website for details of accredited Certification Bodies. 267 Complaints and Appeals Contacts Organisation Contact details Administrative Appeals Tribunal Phone: 1300 653 227 (local call cost) Australian Human Rights Commission Level 3, 175 Pitt Street SYDNEY NSW 2000 Complaints Infoline: 1300 656 419 Commonwealth Ombudsman Phone: 1300 362 072 Complaints Resolution and Referral Service (CRRS) PO Box 126 St Leonards NSW 2065 Phone: Free call 1800 880 052 TTY: 1800 301 130 Fax : 02 8412 7199 Email: crrs@workfocus.com Legal Services Commission Refer Internet for details within each State/Territory National Disability Abuse and Neglect Hotline PO Box 126 St Leonards NSW 2065 Phone: Free call 1800 880 052 TTY: 1800 301 130 Fax: 02 8412 7199 Email: hotline@workfocus.com 268 Disability peak bodies Peak Body DANA (Disability Advocacy Network of Australia) Contact details PO Box 96 DICKSON ACT 2602 Phone: 02 61541983 AFDO (Australian Federation of Disability Organisations) NCID (National Council on Intellectual Disability) NDS (National Disability Services) NEDA (National Ethnic Disability Alliance) 247 Flinders Lane Melbourne Victoria 3000 Phone: 03 9662 3324 Fax: (03) 9662 3325 TTY: (03) 9662 3724 Email: office@afdo.org.au PO Box 771 Mawson ACT 2607 Phone: (02) 6296 4400 Fax: (02) 6296 4488 Email:ncid@ncid.org.au Locked Bag 3002 Deakin West ACT 2600 Ph/TTY: (02) 6283 3200 Fax: (02) 6281 3488 PO Box 9381 Harris Park NSW 2150 Phone: (02) 9687 8933 Fax: (02) 9635 5355 Email: office@neda.org.au 269 Disability agency contacts – multicultural Agency National Ethnic Disability Alliance (NEDA). NEDA is the national consumer peak for people from a NESB with disability, their families and carers. ACT Contact details PO Box 9381 Harris Park NSW 2150 Phone: (02) 9687 8933 Fax: (02) 9635 5355 Email: office@neda.org.au Post: PO Box 394 Civic Square ACT 2608 ACT Multicultural Council (ACTMC). ACTMC is the ACT state member of the NEDA network. The ACTMC provides a source of advocacy and representation for migrants of non- English speaking cultures, including those with disabilities. NSW Multicultural Disability Advocacy Association of NSW (MDAA). Phone: (02) 6249 8994 Fax: (02) 6248 6767 Email: actmc@bigpond.com.au Post: PO Box 884 Granville NSW 2142 Phone: (02) 9891 6400 MDAA is the NSW state member of the NEDA Fax: (02) 9635 5355 network. MDAA provides individual and TTY: (02) 9687 6325 systemic advocacy supports to people from a Toll Free: 1800 629 072 NESB with disability, their families and carers. Email: mdaa@mdaa.org.au NT Post: PO Box 1160 Multicultural Community Services of Central Alice Springs NT 0871 Australia (MSCSA). Phone: (08) 8952 8776 MCSCA is the NT member of the NEDA Fax: (08) 8952 5176 network. Email: mcsca@alicesprings.net.au Qld Post: 9 Chippendall Street Milton QLD 4064 AMPARO Advocacy Inc. Tel: (07) 3369 2500 AMPARO Advocacy Inc is the QLD state Fax: (07) 3399 2511 member of the NEDA network. Email: amparoadvoc@optusnet. com.au SA Post: PO Box 23 Multicultural Advocacy & Liaison Services of Findon SA 5023 SA (MALSSA). Phone: (08) 8351 9500 MALSSA is the SA state member of the NEDA Fax: (08) 8152 0396 network. Email: malssaadmin@malssa.org.au 270 Tas Post: GPO Box 798H Hobart TAS 7001 Multicultural Council of Tasmania Phone: (03) 6231 5067 Fax: (03) 6231 5069 Email: mcot@tassie.net.au Vic Action on Disability in Ethnic Communities (ADEC). ADEC: 175 Plenty Road Preston, Vic 3072 ADEC is not a member of the NEDA network. ADEC is the peak body in Victoria for people from a NESB with disability, their families and carers. ADEC provides individual and systemic advocacy supports to people from a NESB with disability, their families and carers. Phone: (03) 9480 1666 Fax: (03) 9480 3444 Email: info@adec.org.au MRCNW: 45 Main Road St Migrant Resource Centre North West Region Albans VIC 3021 (MRCNW). Phone: (03) 9367 6044 MRCNW is the Victorian member of the NEDA Fax: (03) 9367 4344 network. MRCNW provides information and Email: mrcnw@mrnorthwest.org.au support to migrants and refugees. WA 320 Rokeby Road Subiaco WA 6008 Ethnic Disability Advocacy Centre (EDAC) Phone: (08) 9388 7455 EDAC is the WA state member of the NEDA Freecall: 1800 659 921 network. EDAC aims to promote and Fax: (08) 9338 7433 safeguard the rights of ethnic people with Email: admin@edac.org.au disabilities and their carers. Privacy Organisation Privacy Commissioner Contact details GPO Box 5218 Sydney NSW 2001 Phone: 1300 363 992 TTY: 1800 620 241 Fax: (02) 9284 9666 Email: privacy@privacy.gov.au 271 Section 8: Glossary Accreditation Process by which an authoritative body, JAS-ANZ, gives formal recognition that a Certification Body is competent to carry out Certification. This assessment is carried out by JAS-ANZ against criteria set out in Requirements for Bodies Providing Audit and Certification of Advocacy Agencies under the National Disability Advocacy Program (Procedure 29) Advocacy Supporting people to exercise their rights and freedoms recognised or declared by the United Nations Convention on the Rights of People with Disabilities, or seeking to achieve societal change to ensure that people with disabilities attain the rights and freedoms recognised or declared by the Convention. ATSI Stands for 'Aboriginal or Torres Strait Islander'. Audit All activities related to the Certification of an agency to determine whether the agency meets all the requirements of the Disability Advocacy Standards necessary for granting Certification, and whether they are effectively implemented. This includes documentation review, audit, preparation and consideration of the audit report and other relevant activities necessary to provide sufficient information to allow a decision to be made as to whether Certification shall be granted. Audit cycle A three-year cycle of annual surveillance audits, ending with a full reassessment against all the Disability Advocacy Standards. Audit team A team of competent personnel identified by a Certification Body as meeting the required team competencies set down in JAS-ANZ Procedure 29. A person with disability will be included in the team either as a lead auditor, or a technical expert. Auditor A member of an audit team who has knowledge in the area of disability and quality management practices and skills in collecting and analysing data. Auditors gather evidence, consumer feedback, and have input into audit ratings. CALD Stands for 'culturally and linguistically diverse'. 272 Certification Process by which a third party gives written assurance that an agency conforms to the requirements of the Disability Advocacy Standards. Certification Body A third party which assesses and certifies with respect to the Disability Advocacy Standards. Certification document Document indicating that an agency conforms to specified Disability Advocacy Standards. Citizen Advocacy A type of Individual Advocacy, which seeks to support people with disability (also called protégés) by matching them with volunteers. Some of the matches made may last for life. Through citizen advocacy: people with disability who are vulnerable, isolated and may have no family or community supports or networks are sought out; Citizen advocates(who are volunteers) are encouraged to represent the interests of a person with disability as if they were their own and be free from conflict of interest; and • Citizen advocates are recruited, trained and supported by a coordinator who manages the work of the citizen advocacy agency. Complaints The independent and impartial service funded by the Australian Resolution and Government to assist in the resolution of complaints about Referral Service Australian Disability Enterprises, Disability Employment Services, (CRRS) and FaHCSIA funded advocacy agencies. Conformity When the requirements of a performance indicator associated with a Disability Advocacy Standard are met. Consumer A person with disability who is a member of the audit team, technical expert engaged for his/her specialist knowledge and abilities (e.g. (CTE) empathy with the life experience of people with disability, and ability to plan and facilitate the effective input of people with disability in an audit process). A CTE shall provide evidence to the Certification Body of the CTE having been a service recipient of a State or Commonwealth funded disability organisation in Australia. Note: every audit team must include a CTE. If appropriately qualified, the CTE may also perform the functions of an auditor/lead auditor other technical experts (with or without disability) may also be attached to the audit team to supplement the background knowledge of the team (e.g. where there are 273 Continuous improvement critical requirements and special procedures). An agency's striving for excellence in establishing and maintaining quality services that continually improve performance to achieve better outcomes for consumers. CRRS See Complaints Resolution and Referral Service. Cultural competence Cultural competence is the idea that that individuals, agencies and systems have the capacity, skills and knowledge to respond to the needs of a culturally diverse population. Disability Advocacy Standards The Standards under the Disability Services Act 1986 (Cth), plus the relevant key performance indicators (KPIs), as determined by the Minister(s). These 10 standards and 25 KPIs define the government's requirements for quality and directly link to outcomes required of each disability advocacy agency funded under the National Disability Advocacy Program. DAS See Disability Advocacy Standards. FaHCSIA Department of Families, Housing, Community Services and Indigenous Affairs Family Advocacy A type of individual advocacy, which works with parents and family members to enable them to act as advocates with and on behalf of a family member with disability. Family advocates work with parents and family members on either a short-term or an issue-specific basis. Family advocates work within the fundamental principle that the rights and interests of the person with disability are upheld at all times. Individual Advocacy Through family advocacy: • family members are provided with advice and support; • the person with disability is assisted via the family member being directly supported by the agency to advocate on their behalf. Supports people with disability to exercise their rights, through either one-to-one support, or by supporting people to advocate for themselves individually, through a third party, or on a group basis. Individual advocates work with people with disability on either a short-term or issue-specific basis. Individual advocates: work with people with disability requiring one-to-one advocacy support; develop a plan of action (sometimes called an individual advocacy plan) in partnership with the person with a disability that maps out clearly defined goals; educate people with disability about their rights; and work through the individual advocacy plan in partnership 274 Internal Audit JAS-ANZ with the person with disability. Internal audits are a means of checking that a disability advocacy agency’s systems, processes and procedures are working as intended, reviewed regularly and amended as necessary. Selfassessments check the extent to which documents in the management system meet the requirements of the Disability Advocacy Standards. Internal audits do this, as well as a check to see if those processes and procedures are implemented and followed. The Joint Accreditation System of Australia and New Zealand. JAS-ANZ is a not-for-profit, self-funding international organisation established under a Treaty between the governments of Australia and New Zealand on 30 October 1991. JAS-ANZ is the government-appointed peak accreditation body for Australia and New Zealand for Certification of management systems, products, personnel, training course providers and sector-specific schemes. JAS-ANZ accreditation of a Certification Body provides the necessary confidence that the Certification Body has undergone and passed a JAS-ANZ assessment to test its independence, impartiality, integrity and competence. Key Measures of performance against the Disability Advocacy Performance Standards. Indicators (KPIs) Lead auditor Same as 'auditor', but with additional leadership experience. Responsible for organising and directing the activities of the audit team, as well as participating in general audit activities. Legal advocacy A type of individual advocacy, which seeks to uphold the rights and interests of people with all types of disabilities on a one-toone basis by addressing legal aspects of instances of discrimination, abuse and neglect. Legal advocates may: provide legal representation for people with disability as they come into contact with the justice system; pursue positive changes to legislation for people with disability; and people with disability to understand their legal rights. 275 Major nonconformity When the requirements of a KPI associated with a Disability Advocacy Standard are not met, or the outcome is ineffective. A number of related nonconformities may also constitute a major nonconformity. The Certification Body's procedures shall ensure that: verification of effective corrective action shall require a follow-up visit by the Certification Body before Certification. If the agency is already certified, evidence of a corrective action plan shall be presented to the Certification Body within five working days, and verification of effective corrective action shall require a follow-up visit by the Certification Body within three months failure to action the major nonconformity within three months, or take action sufficient to downgrade the major nonconformity to a nonconformity, shall result in automatic suspension of Certification if the major nonconformity is downgraded to nonconformity, that nonconformity is actioned within a further three months (total of six months to fully action a major nonconformity). FaHCSIA may subsequently issue such instructions as it sees fit to the disability advocacy agency to deal with the major nonconformity. National The NDAP provides people with disability access to effective Disability disability advocacy that promotes, protects and ensures their full Advocacy and equal enjoyment of all human rights enabling community Program (NDAP) participation. The NDAP is funded and administered by the FaHCSIA. Nonconformity When the requirements of a key performance indicator associated with a Disability Advocacy Standard are not fully met, or the outcome is only partly effective. The Certification Body's procedures shall ensure that: corrective action taken is verified as effective before Certification, or within six months if the disability advocacy agency is already certified failure to action a nonconformity within six months may lead to the nonconformity being upgraded to a major nonconformity; and in addition, a major nonconformity may be raised with the disability advocacy agency's corrective action process Notifiable issue Evidence or allegations of a serious health, safety or abuse risk, financial impropriety and/or professional misconduct. If such 276 evidence is found or specific allegations are made, the Certification Body's procedures shall require it to record the details of the disclosure, allegation or witnessed event, and also to immediately notify the disability advocacy agency's manager (unless there is justifiable reason for not doing so, such as risk of compromising collection of evidence in subsequent investigations), and FaHCSIA. The Certification Body is not responsible for resolving the issue, but has a duty of care to report the allegation. Certification cannot proceed until FaHCSIA advises the Certification Body that the notifiable issue is resolved. If the disability advocacy agency is already certified, the Certification Body shall seek advice from FaHCSIA. Observations Opportunity for improvement or positive feedback, provided by a Certification Body during the audit process. Observations which are opportunities for improvement do not prevent Certification, but they should be carefully considered by management and addressed wherever possible, to ensure that conformity is not compromised in the future. Ongoing support Advocacy support that is or has been of an ongoing nature and shall not include phone calls or requests for information that are one off in nature only. Person with disability Person with disability include those who have long-term physical, mental, intellectual or sensory impairments which in interaction with various barriers may hinder their full and effective participation in society on an equal basis with others. Privacy Act Privacy Act 1988 (Cth) as amended 2000. Principles and Objectives The Principles and Objectives of the Disability Services Act 1986 (Cth) set out the basic human rights which all services supporting people with disability should meet. The Principles recognise that people with disability have the same fundamental rights as do other members of society. The Objectives relate more directly to service delivery, that is, the way in which a service operates. Procedure 29 The document Requirements for Bodies Providing Audit and Certification of Advocacy Agencies under the National Disability Advocacy Program which sets down the requirements (accreditation criteria) for bodies seeking accreditation by the Board of JAS-ANZ, to assess disability advocacy agencies and certify that they meet the Disability Advocacy Standards. Quality A systematic way of checking that a disability advocacy agency 277 assurance (QA) meets set standards. Quality management systems and practices Systems to establish quality policy and quality objectives and to achieve those objectives. Rating scale The system used to rate conformity of a disability advocacy agency. Each KPI associated with a Disability Advocacy Standard is to be rated according to the scale below. A Disability Advocacy Standard is to be rated the same as the lowest rating of any of its associated KPIs: Self advocacy major nonconformity is 0 nonconformity is 1 conformity is 2. A type of Individual advocacy, which supports people with disability to advocate on their own behalf, to the extent possible, or on a one-to-one or group basis. Through self advocacy: advocates work with people with disability to develop their personal skills and self-confidence to enable them to advocate on their own behalf. people with disability are educated about their rights. Self-assessment A critical review, conducted internally, that documents the extent to which the advocacy agency’s existing management system (policies, procedures and practices) ensures that they meet the DAS. Self-Assessments may be conducted by peer agencies. Surveillance audit An audit conducted at least annually by a Certification Body to verify that a certified agency continues to comply with the Disability Advocacy Standards. Systemic advocacy Seeks to introduce and influence long-term changes to ensure that the rights and freedoms of people with disability, being rights and freedoms recognised or declared by the Disabilities Convention, are attained and upheld so as to positively affect the quality of their lives. The systemic advocacy agency: pursues positive changes to legislation, policy and service practices in partnership with groups of people with disability, advocacy agencies and other relevant organisations; seeks to address barriers and discriminatory practices to produce long-term positive changes. Target group for The target group for advocacy support provided by NDAP 278 NDAP agencies, as required under section 8 of the Disability Services Act 1986 (Commonwealth), consists of people with disability that: a. ‘is attributable to an intellectual, psychiatric, sensory or physical impairment or a combination of such impairments; b. is permanent or likely to be permanent; and c. results in: i. a substantially reduced capacity of the person for communication, learning or mobility; and ii .the need for ongoing support services. Technical expert A member of the assessment or audit team engaged to supplement the background knowledge of the team; (e.g. where there are critical requirements and special procedures). A technical expert need not meet all the requirements of ISO 100112, and in this case, they should always work under the direct supervision of an auditor, except where the particular circumstances of interviews with people with disability preclude this. All technical experts shall at least meet the requirements of Clause 7 of ISO 10011-2. 279 Attachment 1 Joint Accreditation System of Australia and New Zealand JAS-ANZ Procedure 29 Issue 2 Requirements for bodies providing audit and certification of advocacy agencies under the national disability advocacy program 12 July 2012 Authority to Issue Dr James Galloway Chief Executive with Authority of the Governing Board 280 Contents 0 1 2 3 4 4.1 4.2 4.3 4.4 4.5 4.6 Introduction 282 Scope 284 References 284 Definitions 284 Certification body 288 General provisions 288 Organization 288 Operations 288 Subcontracting 288 Quality system 288 Conditions and procedures for granting, maintaining, extending, suspending and withdrawing certification 289 4.7 Internal audits and management reviews 289 4.8 Documentation 289 4.9 Records 289 4.10 Confidentiality 289 5 Certification body personnel 290 5.1 General 290 5.2 Qualification criteria 290 6 Changes in certification requirements 291 7 Appeals, complaints and disputes 291 8 Application for certification 291 8.1 Information on the procedure 291 8.2 The application 292 9 Preparation for evaluation 292 10 Evaluation 293 11 Evaluation report 294 12 Decision on certification 295 13 Surveillance 296 14 Use of licences, certificates and marks of conformity 297 15 Complaints to suppliers 297 Annex A - Audit Duration 298 Annex B - Certification of advocacy agencies with multiple sites 299 Annex C - Audit planning and consumer sampling 301 Annex D - Code of Ethics 304 281 0 Introduction 0.1 Object and field of application 0.1.1 This procedure, including the attached Annexes, sets down the requirements (accreditation criteria) for bodies seeking accreditation by the Governing Board of the Joint Accreditation System of Australia and New Zealand (JAS-ANZ), to audit advocacy agencies and certify that they meet the Disability Advocacy Standards (DAS) set down by the Australian government. The advocacy agencies referred to in this procedure are those funded under the Commonwealth Disability Services Act 1986, for the National Disability Advocacy Program (NDAP) administered by the Department of Families, Housing, Community Services and Indigenous Affairs (FaHCSIA). 0.1.2 The focus of the NDAP certification scheme is to ensure that advocacy agencies have appropriate management systems in place which are used to achieve the outcomes identified through the DAS and associated Key Performance Indicators (KPIs). The outcomes identified through the DAS and KPIs define the elements of quality support which should be achieved for people with disability receiving advocacy support. Advocacy agencies will need to comply with, and demonstrate continuous improvement against the DAS and KPIs. 0.1.3 Accreditation in conformity with ISO/IEC Guide 65 and the criteria in this procedure acknowledges that bodies possess the necessary competence and reliability to operate a conformity assessment system for advocacy agencies, and will thereby facilitate their acceptance or recognition on a national basis. 0.1.4 Only those certification bodies that have been accredited by JAS-ANZ to ISO/IEC Guide 65, IAF Guidance on the Application of ISO/IEC Guide 65 (IAF GD 5:2006) and this procedure shall carry out audits and issue certificates against the DAS. It is the responsibility of an advocacy agency seeking certification to the DAS to verify the accreditation status of the chosen certification body, by either requesting a copy of their accreditation certificate (or acknowledgement of application) and scope; by contacting JAS-ANZ; or by searching the JAS-ANZ Register, which is available on-line at www.jasanz.org. 0.1.5 FaHCSIA may review criteria or set additional criteria, in consultation with all stakeholders. In any case, these criteria will be reviewed within two years after implementation; or as the need arises. Revised or additional criteria will be the subject of an agreement between JAS-ANZ and FaHCSIA and will be regarded as part of these accreditation criteria. Where there is inconsistency between the revised or additional procedure and this procedure, the requirements of the revised or additional procedure will prevail. 0.1.6 The criteria against which an advocacy agency is audited shall be those outlined in the DAS relevant to the function performed. 0.2 Background 0.2.1 ISO/IEC Guide 65 is an International Standard that sets out the requirements for certification bodies providing audit and certification of product certification systems. The term ‘product’ includes ‘service’ and ‘process’. 0.2.2 To facilitate the uniform interpretation and application of ISO/IEC Guide 65 for audit and certification of advocacy agencies in Australia, this procedure incorporates the work of the JAS-ANZ National Disability Advocacy Program Technical Committee (NDAP TC), aligned with the requirements of ISO/IEC Guide 65, to produce normative criteria, comprising all of this document including the Annexes. 0.2.3 The JAS-ANZ NDAP TC, whose members represent the significantly interested parties, developed these criteria in line with ISO/IEC Guide 65 clause 4.1.3. This procedure shall be read in conjunction with ISO/IEC Guide 65 and IAF GD 5. 0.2.4 The term ‘should’ is used in this document to indicate recognised means of meeting the requirements of the standard. A certification body can meet these in an equivalent way provided this can be demonstrated to JAS-ANZ. 282 0.2.5 The term ‘shall’ is used in this document to indicate those provisions which, reflecting the requirements of the relevant standard, are mandatory. 0.2.6 All the major headings (numbers 1-15) of this procedure have been reproduced from ISO/IEC Guide 65. 0.2.7 This procedure does not diminish any of the requirements of ISO/IEC Guide 65. The clause numbers in this procedure are prefixed with the letter ‘J’ to indicate mandatory criteria developed by the JAS-ANZ NDAP TC for auditing and certifying advocacy agencies. 0.2.8 The text of ISO/IEC Guide 65 and IAF GD5:2006 is not included in this document and shall be referred to separately. 0.2.9 References in this procedure to specific clauses of ISO/IEC Guide 65 shall be read to mean references to ISO/IEC Guide 65 in conjunction with the IAF GD 5:2006 and the corresponding criteria in this procedure. 283 Conformity assessment – requirements for bodies providing audit and certification of agencies under the National Disability Advocacy Program 1 Scope No additional requirements 2 References 1993 National Disability Services Standards. Disability Services Standards (Advocacy Standards) (FaHCSIA) Determination 2012 – the Disability Advocacy Standards. National Disability Agreement (NDA). Disability Discrimination Act (Cwlth) 1992. Disability Services Act (Cwlth) 1986. IAF GD 5:2006 - Guidance on the Application of ISO/IEC Guide 65:1996; available at www.iaf.nu. IAF MD 1:2007 (issue 1) – IAF Mandatory Document for the Certification of Multiple Sites Based on Sampling; available at www.iaf.nu. IAF MD 2:2007 (Issue 1) – IAF Mandatory Document for the Transfer of Accredited Certification of Management Systems; available at www.iaf.nu. IAF MD 5:2009 (Issue 1) – IAF Mandatory Document for the Duration of QMS and EMS Audits; available at www.iaf.nu. ISO/IEC Guide 65:1996 - General requirements for bodies operating product certification systems. ISO 19011:2011 - Guidelines for quality and/or environmental management system auditing. Privacy Act (Cwlth) 1988 as amended 2000. JAS-ANZ Procedure 03 – Rules of procedure governing the use of the accreditation symbol. United Nations Convention on the Rights of People with Disabilities; available at http://www.un.org/disabilities/. 3 Definitions J.3.1 The following definitions also apply to this procedure: Advocacy supporting people to exercise the rights and freedoms recognised or declared by the United Nations Convention on the Rights of People with Disabilities, or seeking to achieve societal change to ensure that people with disabilities attain the rights and freedoms recognised or declared by the Convention. Advocacy agency advocacy agencies funded by the Australian Government. Advocacy agency with an advocacy agency with one central office and multiple full-time and/or 284 multiple sites part-time sites at which activities are fully or partially carried out. Advocacy models any of six advocacy models currently funded under the NDAP program: Individual Advocacy Individual advocacy supports people with disability to exercise their rights, through either one-to-one support, or by supporting people to advocate for themselves individually, through a third party or on a group basis. The types of NDAP-funded advocacy that are provided under individual advocacy include but are not limited to: self, family, citizen, and legal: Self-Advocacy Supports people with disability to advocate on their own behalf, to the extent possible, or on a one-to-one or group basis. Family Advocacy Works with parents and family members to enable them to act as advocates with and on behalf of a family member with disability. Family advocates work with parents and family members on either a short-term or an issue-specific basis. Family advocates work within the fundamental principle that the rights and interests of the person with disability are upheld at all times. Citizen Advocacy Seeks to support people with disability (also called protégés) by matching them with volunteers. Legal Advocacy Seeks to uphold the rights and interests of people with all types of disabilities by addressing legal aspects of instances of discrimination, abuse and neglect. Systemic advocacy Seeks to introduce and influence longer term changes to ensure the rights of people with disability are attained and upheld to positively affect the quality of their lives. In all these models, the target group of advocacy support is the person with disability. Audit team a team of at least two persons appointed to conduct an audit. An audit team normally comprises a lead auditor and a CTE. However, while a CTE may also perform the role of lead auditor (or auditor) if appropriately qualified, in that case the audit team shall still comprise at least two persons. CB certification body. Central office the office of an advocacy agency that has the responsibility to administer its Australian Government’s advocacy funding and the right to implement corrective actions at any site. The central office is the central point for the administration of the common management system. Certification audit all activities related to the initial certification of an advocacy agency to determine whether the advocacy agency meets the requirements of the DAS. Certification body a body accredited as conforming to the criteria specified in this procedure which audits and certifies to the DAS. 285 Close out verification by a CB that corrective action has been implemented by an advocacy agency to address a major nonconformity or nonconformity. Conflict of interest a relationship between the CB, or a person working for the CB (paid or unpaid, staff or contractor), and an advocacy agency, disability service or person, that threatens the impartiality of the CB. Such relationships apply to past, present or future involvement and include: a) having worked with, or been a consumer of, or consulted to the advocacy agency in the last two years, or reasonable prospects of such work in the next two years b) any financial interest in the advocacy agency or relatives or friends with a financial interest in the advocacy agency c) being in competition with the advocacy agency d) any other commercial or voluntary arrangement or directorship with the advocacy agency e) having immediate family members employed by an advocacy agency, or in any of the above situations f) any personal bias or inclination which would affect decisions in relation to the advocacy agency g) having worked with or audited a disability service that has been subject to advocacy from the advocacy agency. Conformity the requirements of a KPI associated with a DAS are met. See Rating scale. Consent the voluntary agreement of a person or a person's authorised representative about a proposed action – e.g. participate in an interview; review personal records. Consulting participating in designing, implementing or maintaining an NDAP management system. Note: Identifying opportunities for improvement is not consulting. Consumer primarily, a person with disability who is receiving / has received within the last 3 months support from the advocacy agency being audited. Consumer may also mean family member/s or an unpaid primary carer or advocate of that person with disability. Some advocacy agencies may use the terms “client”, “participant”, “service user” etc. in lieu of “consumer”. Consumer technical expert a person with disability, engaged for his/her specialist knowledge and abilities; e.g. empathy with the life experience of people with disability, and ability to plan and facilitate the effective input of people with disability in an audit process. A CTE shall provide evidence to the CB of having been a service recipient of a State or Commonwealth funded disability organisation in Australia. CRRS Complaints Resolution and Referral Service. The independent and impartial service funded by the Australian Government to assist in the resolution of complaints about advocacy agencies, disability employment service providers funded under the Disability Services Act. CTE consumer technical expert. DAS the Disability Advocacy Standards, plus the relevant Key Performance Indicators (KPIs) define the elements of quality support which should be achieved for people with disability receiving advocacy support from advocacy agencies. 286 External stakeholder in the context of Annex C, clauses C.2.10 and C.4.4, a person or other agency that is connected with the work of the advocacy agency. FaHCSIA Australian Government Department of Families, Housing, Community Services and Indigenous Affairs (FaHCSIA), including where acting as administrator of the National Disability Advocacy Program on behalf of the Australian Government. Full-time site a service location for an advocacy agency that operates on a full-time basis – normally five days per week during normal working hours (e.g. 8:30 AM to 4:30 PM, Monday to Friday) or more. IAF International Accreditation Forum. IAF GD5: 2006 IAF GD5:2006 - Guidance on the Application of ISO/IEC Guide 65:1996. Independent advocate an independent person who can support someone. With respect to consumers and the audit process, an independent person who can support a consumer to participate in the audit process. If an advocate is required during an audit process, in this instance the independent advocate shall not be a paid employee or volunteer of the organization being audited. JAS-ANZ NDAP TC JAS-ANZ National Disability Advocacy Program Technical Committee. KPI the Key Performance Indicators identify the requirements which need to be demonstrated or measured in order to achieve compliance with each Standard within the DAS. Major nonconformity the requirements of a KPI associated with a Disability Advocacy Standard are not met, or the outcome is ineffective. A number of related nonconformities may also constitute a major nonconformity. See Rating scale. NDAP National Disability Advocacy Program. Nonconformity the requirements of a KPI associated with a Disability Advocacy Standard are not fully met, or the outcome is only partly effective. Notifiable issue evidence or allegations of a serious health, safety or abuse risk, financial impropriety and/or professional misconduct. Ongoing support advocacy support that is or has been of an ongoing nature and shall not include phone calls or requests for information that are one off in nature only. Other technical expert a person other than a CTE who provides specific knowledge or expertise to an audit team, and is engaged by the CB to participate in the audit or relevant part of the audit. Outcomes outcomes for the purposes of this Procedure are those identified through the DAS and KPIs which define the elements of quality support which should be achieved for people with disability receiving advocacy support. Outreach site a service location for an advocacy agency set up in the premises of another organisation. An outreach site is not permanently open but may operate for a period on a regular basis such as weekly or monthly, or on demand. Outreach sites do not include consumers’ private homes. Part-time site a permanent service location for an advocacy agency that regularly operates on only some days of the working week or for part of normal 287 working hours on some days. Person with disability persons with disabilities include those who have long-term physical, mental, intellectual or sensory impairments which in interaction with various barriers may hinder their full and effective participation in society on an equal basis with others. Rating scale the system used to rate conformity of an advocacy agency. Each KPI associated with a Disability Advocacy Standard is to be rated as follows: a) major nonconformity rating = 0 b) nonconformity rating = 1 c) conformity rating = 2 A standard is to be rated the same as the lowest rating of any of its associated KPIs. Self assessment 4 a critical review, conducted internally, that documents the extent to which the advocacy agency’s existing management system (policies, procedures and practices) ensures that they meet the DAS. Self assessments may be conducted by peer organisations. Certification body 4.1 General provisions J.4.1.1 If an explanation is required for the consistent application of this procedure or reference standards, it shall only be acceptable if approved and published by the JAS-ANZ NDAP TC. 4.2 Organization J.4.2.1 The CB shall ensure that the structure that safeguards impartiality shall be an impartial committee which includes a CTE and another person with disability. J.4.2.2 The CB shall have a documented, publicly available policy on handling gifts or hospitality offered by an advocacy agency to which it is contracted to provide certification services. 4.3 Operations No additional requirements 4.4 Subcontracting No additional requirements 4.5 Quality system J.4.5.1 The CB's procedures for internal audits, required by ISO/IEC Guide 65 Clause 4.5.3 n), shall be based on the provisions of ISO 19011. J.4.5.2 The CB shall document monitoring procedures for all audit team members, including CTEs and other technical experts. Procedures shall include on-site observation. The CB should establish the frequency of observation to take account of the criticality and volume of the work being undertaken, the experience and performance history of the audit team members and any data obtained from other types of monitoring activity such as review of audit reports and client feedback. 288 4.6 Conditions and procedures for granting, maintaining, extending, suspending and withdrawing certification J.4.6.1 For the initial certification, the CB shall confirm that the agency has: implemented its policies and procedures implemented a program for conducting self assessments covering its compliance with all the DAS standards and KPIs during the certification cycle completed at least one self assessment. J.4.6.2 The CB shall have documented procedures that shall be made available on request for: a) the certification, surveillance and recertification audits of an advocacy agency (including reporting), in accordance with the provisions of ISO 19011 identifying and recording nonconformities and the need for appropriate corrective action by advocacy agencies. 4.7 Internal audits and management reviews No additional requirements 4.8 Documentation J.4.8.1 CBs shall include the following in public information: a) consumers will be offered information about the audit process and independent advocacy support to engage in the process prior to any consent being obtained b) participation by consumers in audits is at all times voluntary and shall be based on the principle of consent. Where possible, a consumer’s consent for interview shall also grant permission for the audit team to review that consumer’s file. It is desirable to obtain consents in writing. Where the capacity of a consumer to provide consent is uncertain, an independent advocate should be involved to determine that capacity and to support an appropriate level of involvement by the consumer. Where written consent is not obtained, the reason for this, and evidence supporting the assumption that consent was sought and has been obtained, should be recorded in file notes c) consumers shall be invited by their advocacy agency to both the opening and closing meetings of all audits d) the process for transferring certification shall be in accordance with IAF MD 2:2007 4.9 Records J.4.9.1 The CB’s records shall include the following information: a) clear, up to date documentation of the supporting information and rationale for all decisions to sample advocacy agencies with multiple sites b) sufficient information to trace all on-site audit durations, and the basis for the calculations c) justification for, and documentation of any departure from the requirements in the Annexes d) the number of consumers consulted during each audit and the methods of consultation e) how it ensured that consumers provided their consent to participate in the audit and for the CB to access their files 4.10 Confidentiality J.4.10.1 The CB shall treat all information about an advocacy agency, comprising documentation, records, data either in hard copy or electronic format, or verbal information that comes into 289 the possession of a CB or any of its representatives in accordance with the Privacy Act and any relevant state or territory legislation. J.4.10.2 The CB shall not disclose information about a consumer of an advocacy agency that is identifiable directly or indirectly to that consumer without the written consent of that person, unless required by law. Where written consent is unobtainable or impracticable, the consumer shall be supported by a family member, carer, guardian or advocate empowered to make an informed decision about consent. J.4.10.3 The CB shall not use information about a consumer for any purpose other than the assessment of conformity with the DAS. J.4.10.4 Where the CB wishes to disclose information about an agency (other than a notifiable issue – see clause J.10.6) to FaHCSIA it must first seek the agency’s permission. If permission is denied it may still disclose this information to FaHCSIA if it takes the view that to do so would be in the best interests of the agency consumers. 5 Certification body personnel 5.1 General J.5.1.1 Auditors shall meet the guidance for competence of auditors in ISO 19011. J.5.1.2 The CB shall have processes to ensure that personnel have appropriate knowledge. It shall determine and define the competence required for each function in the certification activity, including functions undertaken by management and administrative personnel, as well as audit and certification activities. 5.2 Qualification criteria J.5.2.1 All audit personnel shall comply with the code of ethics. See Annex D. J.5.2.2 All audit team members shall have experience and/or training in disability services auditing or evaluation. J.5.2.3 All audit team members shall demonstrate that they have the following knowledge and skills: a) understanding of the legislative and regulatory requirements applicable to advocacy agencies, including the DAS b) understanding of the nature of advocacy, the NDAP quality assurance system and the role of people with disability and other stakeholders in quality processes c) understanding of the diversity of advocacy agency models and organisational structures and how this impacts on management practices d) understanding of the diversity of people using advocacy agencies and their needs in relation to the audit process e) ability to communicate effectively in writing or orally or using alternative communication systems with all parties involved in the audit process f) ability to gather, review and report on evidence against the DAS. J.5.2.4 CTEs shall have the personal attributes listed in ISO 19011. J.5.2.5 All auditors and CTEs shall successfully complete the training required by FaHCSIA, which includes the nature of advocacy and advocacy models, and an understanding of the DAS, KPIs and Evidence Guidelines, before auditing in the system. J.5.2.6 All audit team members shall have a current national police check, along with all necessary checks required by state or territory legislation before working with children or vulnerable people. J.5.2.7 Where an advocacy agency already holds a JAS-ANZ-accredited certification to another set of standards, the CB shall consider the extent of the demonstrated conformance for any common or significantly similar criteria and rely on this to avoid audit duplication. 290 Every audit report shall record any eligible audit report and the criteria partially or fully relied upon. J.5.2.8 When selecting the audit team for any on-site audit, the CB shall ensure that the skills brought to each assignment are appropriate. The team shall: a) as a minimum comprise two people, i.e. a two person team is required even if the lead auditor is also a CTE. In deciding the size and composition of the audit team and the need (if any) for other technical experts (in addition to the CTE), consideration shall always be given to the range of disabilities and consumer communication styles likely to be encountered during the audit b) understand the geographic or cultural context in which the advocacy agency operates c) inform the CB, prior to the audit, of any potential, current or perceived conflict of interest they have in conducting the audit J.5.2.9 6 The CB shall provide appropriate training and support to assist the CTE to function effectively in the audit team. Such training may include auditor training or lead auditor training where appropriate. A supervising auditor or lead auditor shall always provide ongoing supervision to maintain the necessary level of communication and support to the CTE and other technical expert(s). The CB shall evaluate the competence of the CTE and other technical expert(s) to interview consumers face-to-face or by telephone without other members of the audit team present before authorising them to do so. The CB shall keep records of this evaluation. Changes in certification requirements No additional requirements 7 Appeals, complaints and disputes J.7.1.1 The CB shall include a CTE in each appeal hearing. J.7.1.2 The CB shall have a documented process to receive, evaluate and make decisions on complaints. J.7.1.3 The complaints-handling process shall include at least the following elements and methods: a) an outline of the process for receiving and investigating a complaint, and for deciding what actions are to be taken in response to it b) a system for tracking and recording complaints, including actions undertaken in response to them c) a system to ensure that any appropriate corrective action is taken. J.7.1.4 The decision to be communicated to the complainant shall be made by, or reviewed and approved by, individual(s) not previously involved in the subject of the complaint. J.7.1.5 The CB shall copy matters referred to it by FaHCSIA into its complaints system and action them according to its procedures for handling complaints. 8 8.1 Application for certification Information on the procedure No additional requirements 291 8.2 The application J.8.2.1 The CB shall require the advocacy agency to supply the following information: a) the scope of the management system, services delivered and location(s) of the advocacy agency b) a copy of its documented policies and procedures relating to its management system c) a copy of the latest self assessment d) a copy of its current funding agreement with FaHCSIA J.8.2.2 The CB shall have a legally enforceable agreement for providing certification services to the advocacy agency. The agreement shall: a) extend to all the sites covered by the scope of a multiple site certification b) where possible, extend to any sites and/or outlets of relevant subcontractors to the client. Note: this depends on whether the client can obtain its subcontractors’ agreement to do this. c) require the advocacy agency to inform it of the opening or closing of a site. A CB may seek confirmation from FaHCSIA of the number of sites an advocacy agency delivers services from d) require the advocacy agency to make available to the CB the records of all communications and action taken in relation to the requirements of the DAS. This includes correspondence, recommendations and actions documented by the CRRS or FaHCSIA; or correspondence with any other advocacy agency or disability service provider relating to complaints about the advocacy agency seeking certification. 9 Preparation for evaluation J.9.2.1 The audit program shall include an initial audit and periodic surveillance and recertification audits. See Clause 13. J.9.2.2 The CB shall plan audits to allow sufficient time and resources for the activities listed at Clause J.10.8; e.g. to report compliance against each KPI, and to fully comply with the reporting requirements in this procedure. J.9.2.3 The CB should commence planning with the advocacy agency as early as possible to ensure adequate consumer participation. J.9.2.4 The CB shall send the advocacy agency the list of suggested consumer participants as early as possible, to ensure that the advocacy agency has adequate time to arrange interviews. J.9.2.5 The CB shall ensure that the CTE has discussions with the advocacy agency about the support needs and sensitivities of the selected consumers as early as possible, to ensure the advocacy agency has adequate time to prepare for the Stage 2 audit. J.9.2.6 The CB shall follow up at audit any matters referred to it by FaHCSIA that relate to conformity with the DAS or to a potential notifiable issue, and provide any further information on them to FaHCSIA if requested. J.9.2.7 The CB shall inform the advocacy agency of the names of the members of the audit team who will carry out the audit, with sufficient notice to appeal against the appointment of any particular auditor, CTE or technical expert. The CB shall seek the advocacy agency’s agreement to the audit plans prior to conducting the audit. J.9.2.8 The CB shall provide the advocacy agency with a list of all the disability organisations that it audits. If the agency subsequently perceives a potential conflict of interest and wishes to choose another CB to provide certification services, the CB shall respect the agency’s decision. J.9.2.9 The CB shall check that the advocacy agency has invited consumers to the opening and closing meetings of all audits. 292 J.9.2.10 J.9.2.11 10 J.10.1 The CB shall have documented procedures for reviewing applications. In particular, and as part of the review process applied to each application for certification, the CB shall: a) review the outcomes of observations and discussions during any pre-audit site visits b) review any legal requirements that may impact on the advocacy agency’s management system c) confirm the availability of the required audit team competencies d) calculate the audit duration in accordance with Annex A (single site) or Annex B (multi-site) as applicable e) plan its sampling of an advocacy agency with multiple sites in accordance with Annex B f) make appropriate arrangements for seeking consumer feedback in accordance with Annex C. Where a single site advocacy agency (or any site of a multi-site advocacy agency) provides multiple advocacy models, the CB shall always sample consumers from every advocacy model. The time spent auditing the different advocacy models (and hence the number of consumers / stakeholders sampled per model) should be proportional to the level of funding provided for each model. Evaluation The CB shall perform the initial audit in a 2 stage process. The CB may conduct the stage 1 audit remotely. During the stage 1 audit, the CB shall: a) review the advocacy agency’s policies and procedures for complying with the DAS including its self assessment b) evaluate the advocacy agency’s logistical needs and preparedness for the stage 2 audit J.10.2 The CB shall document stage 1 audit findings and communicate them to the advocacy agency before the stage 2 audit, identifying any areas of concern that could be classified as nonconformities during the stage 2 audit. J.10.3 The Stage 2 audit shall not proceed until the advocacy agency advises the CB that they are ready to proceed and the CB agrees. In determining the interval between stage 1 and stage 2 audits, the CB shall consider whether the advocacy agency wishes to resolve areas of concern identified during the stage 1 audit before the stage 2 audit can proceed. J.10.4 The purpose of the stage 2 audit is to evaluate the implementation and effectiveness of the advocacy agency’s management system. The stage 2 audit shall take place at the site(s) of the advocacy agency. During the stage 2 audit, the CB shall at least evaluate the evidence to demonstrate the advocacy agency’s effective implementation of their policies, procedures and practices to comply with the DAS. J.10.5 The CTE shall actively participate in the following audit activities with other team members and this involvement shall be traceable via reports or other documents on the CB's files: a) developing and agreeing the final audit plan and reviewing the stage 1 audit findings b) planning and preparing the methods of consumer participation in the audit and evaluating the need for independent support for consumers c) participating for the full duration of the stage 2 audit, including the opening meeting, audit team review meeting(s) and closing meeting. If the stage 1 audit is done on site, the CTE shall be present for the duration of the visit d) engaging consumers during the audit to collect, examine and analyse evidence with respect to the DAS e) reviewing consumer files or following up issues with consumers 293 f) reviewing audit findings, determining audit ratings and preparing the written audit report J.10.6 If an audit team finds evidence of a notifiable issue, the CB's procedures shall require it to record the details, and to immediately notify the advocacy agency’s manager (unless there is justifiable reason for not doing so, such as a risk of compromising collection of evidence in subsequent investigations), and FaHCSIA. J.10.7 The CB is not responsible for resolving a notifiable issue, but shall report the evidence. Certification cannot proceed until FaHCSIA advises the CB that the notifiable issue is resolved. If the advocacy agency is already certified, the CB shall seek advice from FaHCSIA. J.10.8 At all on-site audits the audit team shall hold a closing meeting with the advocacy agency’s management and any consumers who wish to be involved, prior to concluding the on-site audit. At the closing meeting, the audit team shall: a) explain its initial audit findings regarding the conformity of the advocacy agency with each standard and KPI b) if applicable, provide the advocacy agency with documented major nonconformities and nonconformities, including the DAS KPIs they relate to, explanatory comments, and the close out dates c) summarise any notifiable issue raised during the audit, unless there is justifiable reason for not doing so - see Clause J.10.6 d) summarise any audit follow-up activities briefly summarise all the available avenues for resolving complaints and appeals including via the CB, CRRS or JAS-ANZ summarise the timing of, and requirements for, preparing for and conducting surveillance and recertification audits 11 J.11.1 Evaluation report Written reports of DAS on-site audits require more than generic summary statements. The content of all reports shall include: a) a brief description of the advocacy agency, including the advocacy model(s) offered b) the number and roles of stakeholders consulted with during each audit, including the model of advocacy accessed by them (eg. individual, systemic, citizen etc.) and methods of consultation c) an executive summary of the overall findings (conclusions) of the audit, including comments on the effectiveness of the advocacy agency's system to ensure conformity with the DAS and a summary of major nonconformities and nonconformities at on-site audit completion, even if the agency has addressed nonconformities before the report is finalised d) ratings of conformity against each KPI and each standard, in accordance with the rating scale e) an adequate description of the main evidence and audit trails to support the ratings of KPIs f) positive and negative observations; noting that while negative observations (eg. opportunities for improvement) do not prevent certification, CBs should advise advocacy agencies to carefully consider them and address them wherever possible, to ensure that conformity is not compromised in the future times allocated for stage 1 and stage 2 audits, the number and type of interviews with consumers. J.11.2 Where applicable, reports of surveillance or recertification audits shall document: a) close out of each major nonconformity and nonconformity revealed previously 294 b) any useful comparison with the results of previous audits J.11.3 The CB shall prepare stand-alone reports of any follow-up audits outlining any major nonconformity or nonconformity and clearly documenting the evidence provided to support decisions to close them out or downgrade them. It is not acceptable to report follow up activity as an amendment to the original audit report. J.11.4 In an audit that covers more than one type of certification standard (e.g. ISO 9001 in addition to the DAS), the report shall clearly identify all requirements of the DAS. J.11.5 The CB shall provide the draft written report to the advocacy agency within 10 working days of completing the on-site component of the audit (single site agency) or 20 working days (multiple site agency), even if the draft decision is not to certify. J.11.6 The advocacy agency shall have 10 working days from receiving the draft written report in which to provide a response to the CB. J.11.7 The CB shall consider any response provided by the advocacy agency, make the final certification decision and provide the final report to FaHCSIA and the advocacy agency within a further seven working days, even if the decision is not to certify. J.11.8 The CB’s procedures shall ensure that in the instance of a major nonconformity: a) the major nonconformity is closed out before certification or expiry of certification b) close out shall normally require a follow-up visit by the CB. For a certified advocacy agency, evidence of a corrective action plan shall be presented to the CB within 5 working days of the date of issue of the major nonconformity, and close out shall normally require a follow-up visit by the CB within three months c) the CB shall be able to justify circumstances where close out of a major nonconformity, or downgrading the major nonconformity to a nonconformity did not require a follow-up visit d) for a certified advocacy agency, failure to close out the major nonconformity within three months of the date of issue, or take action sufficient to downgrade the major nonconformity to a nonconformity, shall result in automatic suspension of certification e) for a certified advocacy agency, if the major nonconformity is downgraded to a nonconformity, that nonconformity shall be closed out within a further three months (maximum of six months from the date of issue to fully action a major nonconformity) J.11.9 The CB’s procedures shall ensure that in the instance of a nonconformity: a) the nonconformity is closed out before certification or expiry of certification b) for a certified advocacy agency, the nonconformity shall be closed out within six months of the date of issue c) for a certified advocacy agency, failure to close out a nonconformity within six months of the date of issue will result in a major nonconformity being raised with the advocacy agency’s corrective action process 12 Decision on certification J.12.1 The CB shall make decisions on renewing certification based on the results of the recertification audit, as well as the results of its review of the system over the period of certification, and complaints received. J.12.2 If an audit team submits advice of a notifiable issue to FaHCSIA, the CB shall withhold the advocacy agency’s certification until FaHCSIA advises it in writing that certification can proceed. J.12.3 The CB shall advise FaHCSIA of all certification decisions within 5 working days of the date of the decision. The CB shall provide FaHCSIA with reasons for any decisions to vary, suspend or withdraw certification, together with a copy of the certification document(s). 295 J.12.4 The CB shall include a CTE in the certification decision-making process. J.12.5 Certification documents shall include: a) the effective date of certification which shall be on or after the date of the formal decision by the CB b) the expiry date or recertification due date consistent with the recertification cycle c) the JAS-ANZ symbol. Refer to JAS-ANZ Procedure 3 J.12.6 13 If an advocacy agency ceases to provide advocacy support or FaHCSIA revokes its funding for any reason, FaHCSIA will notify JAS-ANZ and the CB that issued certification within 10 working days of revocation becoming effective. Surveillance J.13.1 In the context of this procedure, ‘surveillance’ includes surveillance audits in the first and second years of a three-year certification cycle, and a recertification audit in the third year prior to expiration of certification. The cycle begins with the certification or recertification decision. J.13.2 Surveillance and recertification audits are on‐site audits and shall be planned together with any other surveillance activities so that the CB can maintain confidence that the certified services continue to fulfil requirements. J.13.3 Once certification is achieved, the date of the first surveillance audit shall not be more than 12 months from the date of the last day of the on‐site component of the certification or recertification audit. The second surveillance audit shall be conducted not more than 13 months after the last day of the first surveillance audit. J.13.4 Surveillance audits shall include: a) reviewing the effectiveness of actions taken on nonconformities identified during the previous audit b) progress of planned activities aimed at continual improvement of performance against the DAS c) continuing operational control d) review of any changes to systems or personnel e) standards 2, 7, 8, and 10 and other selected standards f) use of marks and/or any other reference to certification g) interviewing the responsible managers and a sample of consumers in accordance with Annex C J.13.5 Following a surveillance audit, the CB shall maintain certification based on demonstration that the advocacy agency continues to satisfy the requirements of the DAS. It may rely on a positive conclusion by the audit team leader without further independent review, provided that: a) for any major nonconformity or other situation that may lead to suspension or withdrawal of certification, the CB has a system that requires the audit team leader to report to the CB the need to initiate a review by appropriately competent personnel, different from those who carried out the audit, to determine whether certification can be maintained b) competent personnel of the CB monitor its surveillance activities, including monitoring the reporting by its auditors, to confirm that the certification activity is operating effectively J.13.6 The purpose of the recertification audit is to confirm the continued conformity and effectiveness of the advocacy agency’s system against the DAS as a whole. The recertification audit shall consider the performance of the system over the period of certification, and include a review of previous surveillance audit reports. 296 J.13.7 Recertification audit activities may need to have a stage 1 audit in situations where there have been significant changes to the management system, the client, or the context in which the management system is operating (e.g. changes to legislation). J.13.8 The recertification audit shall include an on-site audit that addresses the following: a) the scope of the management system in its entirety in the light of internal and external changes and its continued relevance to the requirements of the DAS b) evidence to demonstrate the advocacy agency’s effective implementation of their policies, procedures and practices to comply with the DAS including positive outcomes for consumers J.13.9 14 When, during a recertification audit, instances of nonconformity or lack of evidence of conformity are identified, the CB shall define time limits for correction and corrective actions to be implemented prior to the expiry of certification. Use of licences, certificates and marks of conformity No additional requirements 15 J.15.1 Complaints to suppliers In the context of this procedure, a ‘supplier’ is an advocacy agency. Complaints to advocacy agencies include records of all communications and action taken in relation to the requirements of the DAS. See clause J.8.2.2. 297 Annex A - Audit Duration A.1 Planning for an audit of an advocacy agency will typically take longer than planning for other types of audits (such as ISO 9001) and large individual variations are likely to occur. This is partly due to the complexities of sourcing information and obtaining the necessary consents to arrange effective and representative consumer sampling. A.2 The on-site audit duration for the stage 2 audit of a single site advocacy agency shall be not less than one auditor day, and is expected to fall in the range of one to five auditor days. The duration will depend on a number of factors. The CB shall have a procedure for determining the amount of audit time necessary, based on the relevant requirements of IAF MD5:2009 and the following factors: a) an advocacy agency’s existing accredited certification to another standard b) results of self assessments conducted by the advocacy agency in the last 12 months c) the number and type(s) of advocacy models delivered d) number of consumers attached to the agency, if any (see C.2.10) e) types of disability of the consumers f) geographic location of consumers g) consumers’ preferred method of engagement (e.g. interview at home, by telephone, group setting) h) level and type of support needed by consumers to enable them to participate in the audit including access to appropriate methods of communication i) ratio of staff to consumers. A.3 The CB shall demonstrate that in planning the audit with the advocacy agency it has undertaken a thorough analysis of the above factors and developed an appropriate process for engaging consumers. This process shall be based on the strategy provided to the CB by the advocacy agency. See Annex C. A.4 Audit duration calculations (i.e. auditor days) shall be based on an 8 hour working day including 1 hour for lunch, and exclude all activities other than auditing. The times are to be regarded as true minimums: planning, preparation, travel time and reporting shall not be included. Time spent conducting the document review or other stage 1 audit activities shall not be included, even if done on-site. The same applies to on-site report writing. The CB may arrive at the required audit duration by working part-time hours to suit the advocacy agency. A.5 Where two or more team members work together (e.g. auditor plus CTE or other technical expert or another auditor), that time shall be counted as if a single auditor was involved. When, in exceptional circumstances, CTEs work alone (see Clause J.5.2.10), that time shall not be counted as contributing to the audit duration, unless the CTE is also qualified as an auditor or lead auditor. A.6 Where two or more auditors are used along with one CTE, the CB shall demonstrate that the CTE has adequate time to conduct the required amount of consumer interviews and meet the requirements of Clause J.10.5. 298 Annex B - Certification of advocacy agencies with multiple sites B.1 Introduction B.1.1 Auditing an advocacy agency with multiple service outlets differs from a single-site audit. The aim of this Annex is to establish criteria for the audit and, if appropriate, the certification of advocacy agencies with a network of full-time and/or part-time sites, thus ensuring that the audit provides adequate confidence in the conformity of the advocacy agency, while being practical and economically feasible. B.1.2 The requirements of IAF MD 1:2007 apply except as otherwise indicated in this Annex. B.1.3 Auditing sites and/or outlets of sub-contractors relies on the sub-contractor providing the relevant information or the CB obtaining agreement from the sub-contractor to conduct the audit. B.2 Structure of advocacy agencies with multiple sites B.2.1 Advocacy agencies with multiple sites include: a) multiple sites delivering a single advocacy approach b) multiple sites delivering one or more advocacy approaches from each site. B.2.2 Some advocacy agencies may make use of outreach sites. These sites shall be sampled in accordance with the requirements of this Annex, but do not need to be visited if the advocacy agency can provide evidence that services provided at the outreach sites meet the DAS, and if information, including policies, procedures, and consumer files and individual plans associated with an outreach site can be provided to the CB for physical sampling remotely. If this evidence cannot be provided, the CB shall sample and visit outreach sites as if they were full-time or part-time sites. B.3 Eligibility criteria for the advocacy agency B.3.1 The advocacy agency’s management system shall be centrally administered under a centrally controlled plan and be subject to self assessment. All the sites (including the central office) shall be assessed under the advocacy agency’s self assessment program before the CB starts its audit. B.3.2 The advocacy agency shall demonstrate that it has established a system that complies with the DAS and that the entire network of sites i meets the requirements of the DAS. B.3.3 The advocacy agency shall demonstrate its ability to collect and analyse data (including but not limited to the items listed below) from all sites including the central office, and its authority and ability to initiate organisational change if required: a) system documentation and system changes b) handling of complaints c) evaluation of corrective actions d) self assessment planning and evaluation of the results e) consumer engagement. B.4 Sampling methodology for advocacy agencies with multiple sites B.4.1 The site selection criteria should include: a) results of self assessments by the advocacy agency or previous audits by the CB b) records of complaints and communications (see clause J.8.2.2) and other relevant aspects of corrective and preventive action c) significant variations in the size of the sites and number of consumers d) the advocacy models delivered e) modifications since the last CB audit f) geographical location and dispersion 299 g) whether sites are operated by subcontractors h) outreach sites B.5 Size of sample B.5.1 The minimum number of non-central office sites to be visited per audit is: initial audit and recertification audit: the size of the sample shall not be less than the square root of the number of full-time and part-time sites (y= x ), rounded to the upper whole number. surveillance audit: the size of the annual sample shall not be less than the square root of the number of full-time and part-time sites with 0.6 as a coefficient (y=0.6 x ), rounded to the upper whole number. B.5.2 In all audits, the central office shall be visited at least once, in addition to the sites sampled. B.5.3 Where consumers are collocated with the central office, the consumer population shall be treated as a separate site. B.5.4 The size of the sample shall be increased where the CB’s analysis of the advocacy agency indicates special circumstances such as might apply to any of the site selection criteria at clause B.4.1. B.5.5 Where one or more sites of a multi-site advocacy agency delivers more than one advocacy model, the CB shall sample the models in accordance with Clause J.9.2.11. B.5.6 Where the advocacy agency also has a hierarchical structure and would otherwise be sampled at each level, the sampling model which results in the largest sample shall be applied. B.6 Audit duration B.6.1 The stage 2 audit duration for an advocacy agency with multiple sites shall be not less than two auditor days, and is expected to fall in the range of two to six auditor days. See Annex A for requirements applying to auditor days. B.7 Additional sites B.7.1 Where a certified multi-site advocacy agency wishes to include new sites in the scope of its certification, the CB shall require it to provide sufficient information to demonstrate that its management system has been fully implemented in the new sites so as to meet the requirements of the DAS. Each new group of sites should be considered as an independent set to determine the sample size, with those chosen for audit to be included during the next scheduled audit activity. The CB need not conduct additional audits, or move forward the next scheduled audit, solely due to the operation of additional sites by an advocacy agency. 300 Annex C - Audit planning and consumer sampling C.1 Introduction C.1.1 Seeking direct feedback from consumers is a critical element of the audit process. CBs shall ensure that wherever possible, consumers have been offered the opportunity to participate in the audit process. However it is not usually practicable for all consumers to provide direct feedback, and for this reason a sampling approach is normally required to ensure appropriate levels and types of feedback during the audit. C.1.2 The CB should select the sample of consumers to be interviewed. This ensures that the sample is not influenced by other stakeholders which might inhibit the collection of accurate data. C.2 Sampling principles C.2.1 Consumer sampling shall be determined at the site level on a case-by-case basis. C.2.2 CBs may sample from all consumers who have received ongoing support, where the agency has contact details. C.2.3 A proposed strategy for sampling consumers should be developed by the advocacy agency in consultation with relevant stakeholders, and negotiated with the CB, so that the CB may quote for certification services. This strategy shall be made available to other CBs, on request. C.2.4 Ideally, emphasis should be placed on the agency inviting consumers to participate in the audit and in turn, the CB should select from a list of willing participants. C.2.5 The CB shall negotiate the proposed sample numbers and sampling approach, including methods of communication and sampling methods (face-to-face interview, focus groups, telephone survey, mail survey) with the advocacy agency when planning the audit. C.2.6 CBs should maintain a flexible approach to consumer involvement methods, ensuring that priority is given to methods encompassing direct communication. C.2.7 In sampling consumers, the CB shall have regard to the vulnerability of some consumers which may lead them to be unable to participate. C.2.8 The CB shall ensure that the sampling approach is appropriate to the service delivery context of the advocacy agency. An advocacy agency with a small number of consumers would not need an extensive consultation mechanism around sampling. C.2.9 The CB shall attempt to represent the demographics of the consumers assisted by the advocacy agency, when sampling consumers. Some of the demographics to consider are: a) disability type b) gender c) age d) cultural or language differences e) complexity of support needs, including communication f) length of tenure with organisation (includes those exited). C.2.10 Although the key focus of this Annex is on sampling consumers, in the case of systemic advocacy, CBs will need to sample consumers who are associated with the systemic advocacy work of the agency through stakeholder committees and groups. Where such consumers are not available, the CB should sample other external stakeholders connected with the advocacy work. C.2.11 Where an advocacy agency delivers more than one advocacy model, the CB shall sample consumers receiving each model of advocacy in accordance with Clause J.9.2.11. C.2.12 The sampling approach does not preclude consumers talking to an audit team member if the opportunity arises and they choose to during an audit. 301 C.2.13 The CB shall verify that the advocacy agency has: a) developed the sampling approach in consultation with relevant stakeholders b) made all reasonable attempts to inform all its consumers in accessible and varying formats of all scheduled audits and provide them with an opportunity to participate in the process and in the consumer sample c) made it clear to all consumers that they are entitled to involve an independent advocate or support person of their choice in the audit process if they wish. C.3 Process for determining consumer sample size C.3.1 Noting that consumers have the right not to be involved, the minimum number of consumers to be sampled for an audit of an advocacy agency (or per site, for a multi-site advocacy agency) is: a) initial and recertification audits: the square root of the number of consumers receiving advocacy support over the last three months (y= x ), rounded to the upper whole number b) surveillance audit: 0.6 times the square root of the number of consumers receiving advocacy support over the last three months (y=0.6 x ), rounded to the upper whole number. C.3.2 The CB should aim for a minimum of 5, and a maximum of 10 consumers per advocacy model and per site. C.3.3 The CB should aim to have one to one direct contact with 50% of the proposed sample of consumers. It is understood that in the advocacy context, many of these interviews will be conducted via telephone or other technologies, as consumers are not normally present on site at advocacy agencies. In using some technologies, CBs shall be mindful of the possibility of others accessing the conversations, and shall take steps to ensure confidentiality is maintained in remote interview situations. However, one to one face to face interviews are preferable to remote interviews, where practicable. If the 50% ratio cannot be achieved (e.g. refusals or clear preference by consumers for another consultation method), the CB shall clearly document its justification for the sampling approaches used. The remaining 50% may be sampled using other methods including: a) focus group b) written survey c) other innovative ways to involve consumers. C.4 Consumer file sampling C.4.1 Consumer file sampling aims to cross check verbal information gathered from consumers and to confirm outcomes for consumers. However, there will be times when consumers agree to be interviewed, but not to allow access to their files; and vice versa. While the principles applying to consumer sampling also initially apply to file sampling, the CB may also need to follow up on file specific issues identified during interviews with consumers or others. This requires wider access to files, and the CB shall try to obtain appropriate additional consents, to maximise the number of files available for review. C.4.2 To ensure validity of the audit, files reviewed at each site should normally cover all of the consumers sampled and should not be less than the number of consumers interviewed. C.4.3 All file access shall be by consent by the consumer and shall comply with the provisions of the Privacy Act and any relevant state or territory legislation. C.4.4 Where advocacy agencies deliver advocacy models where no consumers are attached to the agency, sampling consumer files is not applicable for those models. See clause C.2.10. In this case CBs shall sample whatever documents or records are available to cross-check information gathered in interviews of external stakeholders. C.5 Traceability of audit planning and consumer sampling processes C.5.1 A CB shall be able to justify how it samples consumers for any audit. Any reduction in the sample size shall be justified and documented in each case (e.g. where an insufficient number of consumer consents are received). The CB shall pay particular attention to the 302 validity of the results of the audit where the sample size is likely to be 30% or more below the numbers which would apply using the above sampling approaches. If in doubt about the validity, advice should be sought from FaHCSIA before the audit begins. C.5.2 Sampling strategies shall be sufficiently documented for each audit so as to be able to trace compliance with all the requirements of this Annex. This information may be included in, or attached to the audit plan, or may be separately recorded. 303 Annex D - Code of Ethics D.1 Auditors, CTEs, other technical experts and staff of CBs must abide by this code of ethics when auditing within the Disability Advocacy sector. D.2 Audit team selection, ongoing work and training should be inclusive and supportive of the unique needs and talents of people with disability, as per the Disability Discrimination Act. Depending on the circumstances, this may include, but is not limited to: a) providing accessible information through Braille, Auslan interpreters, Easy English or a support person b) providing an accessible workplace, noting that some modifications to the office environment and equipment can be purchased under the government-run Workplace Modifications Scheme c) ensuring that all CB staff are given some information on disability awareness as part of their induction, and those who require it, such as human resources personnel, are given more in-depth training as required d) working collaboratively with people with disability to ensure that they are given meaningful roles within the organisation in which their input and feedback can be valued and used in a positive and constructive manner. For example, this could be achieved through offering structured peer support and mentoring, or engaging with an independent advocate to resolve any work-related issues. An independent advocate of a staff member's choice should always be allowed to assist them to resolve work-related matters when requested, and all staff members should be aware of this option e) developing a Disability Action Plan and submitting it to the Australian Human Rights Commission. D.3 CBs should document all requests for modifications and adaptations by people with disability in an interview or as part of their job or training (e.g. asking for an interpreter or large print documents), along with the outcomes of the requests. D.4 CBs should be mindful of the human rights of people with disability as outlined in the United Nations Convention on the Rights of Persons with Disabilities, in particular the Principles and Objectives, and Articles (http://www.un.org/disabilities/). D.5 CBs should be considerate of the working hours of advocacy agency staff when planning the audit. D.6 The CB should promote available complaint mechanisms to advocacy agencies and participating consumers. D.7 During the audit: a) all consumers have the right and opportunity to be involved and consulted at no substantive cost to themselves b) consumers have the right not to be involved c) consumers' confidentiality and privacy shall be respected in all aspects of the audit including communications in person and remote communication via technology such as video conferencing d) the CB should encourage sampling methods that maximise the confidentiality of participants e) the CB shall ensure that the advocacy agency has invited consumer representation at the opening and closing meetings of all audits f) the CB shall ensure that the advocacy agency has advised consumers about opportunities to participate in the audit, including opportunities for family, other support or guardians to participate g) the CB shall ensure that people with disability receive timely and accessible information about the audit process to allow for full and informed contribution 304 h) consumers have the right to independent advocacy and support to assist with having their say i) consumers should have appropriate support to facilitate genuine participation. D.8 The CB shall facilitate transfer of certification if requested by an advocacy agency it has certified. It shall not revoke certification simply because an advocacy agency advises of its intent to change its CB. D.9 CBs and their staff (external or internal) should promote the benefits of the National Disability Advocacy Program to all interested parties, and not openly criticise the Government’s initiatives in this sector. CBs should actively participate in the continuous improvement of the Program by identifying and raising issues with the relevant infrastructure element, i.e. FaHCSIA or JAS-ANZ. D.10 Auditors, CTEs, other technical experts and staff of CBs involved in audits within the disability sector must be free of conflicts of interest. 305 Attachment 2 - Consent for the Release of Information The person giving consent needs to read this page, or have its contents explained to him / her before signing on the next page. Why is the information collected? The Australian Government gives disability advocacy agencies money to help people with disability. In return, the Government expects every disability advocacy agency in Australia to follow the Disability Advocacy Standards. These are rules that tell them what they need to do to make sure that they give people with disability good quality support. An audit team from a Certification Body will visit your disability advocacy agency to check if it is following the Standards. The more the audit team can learn about your disability advocacy agency, and what it is you need, the better chance there is that you will get the right type of support. To help during these audits, the Audit team may need to have a look at personal files. What information is collected? The information listed below may be collected from you by your disability advocacy agency. By signing this form you are saying it is OK for them to give information about you to the Audit team for the purpose of checking to see how they provide good quality advocacy support. The information that may be collected may include such information as: - Your full name; - Your date of birth, sex, address, and if you are an Australian citizen or permanent resident; - The type of disability you have; - Who referred you to the agency; - Why you have been referred to the agency; - Your individual plan with the agency; and - The reason why you leave the agency. Protection of information Your disability advocacy agency is obliged to observe strict privacy rules called Information Privacy Principles which are contained in the Privacy Act 1988. This means that they must: - Tell you why they need to collect your information; - Tell you what they do with your information and who they will give it to; - Store the information securely; - Only use the information for the purposes they obtained it; and - Only pass your information on when you have been advised of the other parties to whom your information may be given and you have consented, or when the law allows. The information that is forwarded to the audit team will be stored in a secure manner and your personal information will only be used or disclosed by the certification body, as described on this form. The person giving consent may keep this page for information. 306 Consent Form for the Release of Information __________________________________________________ Consent I Of (address) give consent for: the agency providing me with advocacy support, to provide some or all of my personal information to an audit team from: the Certification Body, or to another organisation as directed by the Commonwealth. I acknowledge that the disclosure of some or all of my personal information to the certification body, or to another organisation as directed by the Commonwealth, will occur for the purpose of checking to see how the agency provides good quality advocacy support. Client’s (or legal guardian’s) Signature Date: Compliance with Information Privacy Principle 2 I (name of Authorised officer) Of (agency name) have explained to the person giving consent, and I believe they understand that personal information is collected for the purpose of determining access to and delivery of advocacy support under the Disability Services Act 1986 through a disability advocacy agency; and this disability advocacy agency may be required, from time to time, to pass some or all of their personal information to the certification body, or to another organisation as directed by the Commonwealth. Signature (Authorised officer) Date 307 Attachment 3 - Disability Advocacy Standards, key performance indicators and examples of evidence Standard Key Performance Indicator Examples of Evidence Standard 1: Accessing advocacy 1.1 The advocacy agency adopts, applies and promotes non-discriminatory policies in respect of age, gender, race, culture, religion, disability or living arrangements, consistent with the contractual obligations and purpose of the advocacy agency and the relative need and available resources. All agencies Purpose statement that makes it clear who the agency works with to promote, protect and defend the welfare of and justice for people with disability. Evidence of staff participation in anti-discrimination and cultural awareness training and/or evidence of links with relevant specialist agencies as appropriate, such as MOUs or participation in joint projects with multicultural or indigenous advocacy agencies. Evidence that the organisation is aware of demographic information/ABS statistics and match of this to the profile of people with disability who receive advocacy support. Documented and implemented non-discriminatory practices and policies for identifying and/or responding to requests for information, referral and/or advocacy support. Each person with disability has opportunities to access advocacy on the basis of relative need and available resources. 1.2 The advocacy agency has processes to determine how the individuals or issues supported are chosen and prioritised based on relative need and available resources. 1.3 Each person with disability is informed about how decisions are made in relation to access and advocacy issues. Agencies undertaking individual advocacy/ legal advocacy Documented and implemented entry and exit policies and procedures highlighting non-discriminatory practice, which may include ongoing access for people with disability who receive advocacy support after their issue/case is closed. Agencies undertaking systemic advocacy Documented and implemented practices and/or policies for deciding and communicating which systemic issues the agency will work on. Documented and implemented practices and policies showing how people with disabilities influence/contribute to the prioritising processes that determine which issues receive attention. Agencies undertaking citizen advocacy Annual protégé recruitment plan that reflects diversity and level of vulnerability of people with disability. Consistent practice of “seek-out” recruitment of people with a disability who need advocacy, but who would not ordinarily come to the attention of the agency if it relied solely on (self- or other-initiated) referrals. Established Advisory Support Group (e.g. Sub-Committee), which can assist in the implementation of the appropriate Protégé entry and exit policies and procedures. 308 Standard 2: Individual needs Each person with disability receives advocacy that is designed to meet their individual needs and interests. 2.1 The advocacy agency has a process for determining and documenting the advocacy objectives that reflect the wishes, needs or interests of each person with disability. 2.2 Advocacy activities are directed to meeting the advocacy objectives of each person with disability. 2.3 Each person with disability engaged in determining advocacy objectives is provided with opportunities to involve a support person of their choice. 2.4 In meeting the needs of a person with disability, the advocacy agency avoids, where possible, any conflict of interest or the perception of any conflict of interest in relation to the conduct of its advocacy work, and deals with any conflict or perceived conflict transparently. 2.5 The advocacy agency helps to empower people to advocate for themselves or their family or others with appropriate strategies (e.g. information, training, mentoring, support). All agencies Evidence of practice of supporting/educating people with disabilities to advocate for themselves and/or of supporting/educating families to advocate on their behalf. Examples of how the agency has taken into account the specific needs of people from Indigenous and CALD backgrounds, people with specific disabilities such as hearing impairment, people with literacy difficulties. Interpreters are provided where requested or where a need is identified. Agency promotional material that makes it clear the extent, if at all, the agency provides training and support. Documented and implemented policies and practice of responding to the information needs of people with disabilities/families and providing referrals as appropriate. Agency policy on conflict of interest. Documented and implemented practices and policies for identifying and transparently dealing with conflicts of interest that arise for the organisation, Board and staff, for example, a Conflict of Interest register maintained for staff and Boards of Management, or evidence in minutes of a standing agenda item that flags the need to declare any conflict of interest. Management, staff and volunteer training in recognising and dealing with conflicts of interest. Agencies undertaking individual advocacy/ legal advocacy Documented and implemented policies and practices for developing and implementing individual advocacy plans in partnership with people with disability and/or their families/guardians (as appropriate). Evidence of collecting and reviewing feedback about the extent to which the needs of the person with a disability are met. Agencies undertaking self advocacy Observations of people with disabilities receiving support to develop advocacy action plans to address their wishes, needs or goals. Agencies undertaking systemic advocacy Documented and implemented practices and policies showing how people with disabilities influence the choice of advocacy objective. Evidence of reporting of outcomes / review of advocacy process. Evidence of advocacy plan, actions taken and people/agencies involved, or file notes detailing progress or justification for not having a plan in place. Policies and procedures to address how the agency selects and prioritises the systemic issues it addresses. 309 Agencies undertaking citizen advocacy Standard 3: Decision making and choice Each person with disability has the opportunity to participate as fully as possible in making decisions about the advocacy activities undertaken. 3.1 3.2 The advocacy agency’s policies support each person with disability to direct, within the limits of their capacity or interest, the advocacy activities undertaken to meet their advocacy objectives. In all circumstances the advocacy activity is informed by ethical guidelines. Documented and implemented practices and policies for developing confidential individual written profiles detailing ‘need’ and seeking advocates based on their skills in relation to these needs. Observations of individual being given opportunity to discuss their advocacy needs and advocate role. Details of completed relationships, and/or those being rematched or awaiting rematching. Documented and implemented practices and policies for reviewing the extent to which the needs of the person with a disability are being met. Practice of one-to-one (or near one-to-one) matching of people with a disability with advocates to ensure that the individual needs of the person with the disability remains the focus of the advocacy relationship. Practice of recruiting advocates whose role is strictly voluntary, thereby avoiding any conflicts of interest arising from receipt of monetary and/or in-kind payments. All agencies Observations of the way advocates interact with people with disability in making decisions about advocacy activities. Evidence of the involvement of people with disability in agency decision-making (e.g. representation on the Board, participation in consultations that feed into agency’s strategic plan or lead to improve practices, involvement in surveys that inform agency policies and procedures). Evidence of the involvement of people with disability in the agency’s quality assurance activities. Observation of information, strategies and ideas presented to people with disabilities and families in ways that they can understand. Agencies undertaking individual advocacy/legal advocacy Ethics guidelines for supporting people with disability in making decisions about advocacy activities. Procedures are established and implemented for the regular review of advocacy actions and these require review of the extent to which the agency promotes the person’s choices and decisions. 310 Feedback is sought from people with disability on the extent to which the agency promotes choice and decision making. Documented and implemented practices and policies for determining a decision on behalf of a person who has impaired decision making capacity e.g. consultation with them, documenting factors taken into account including knowledge gathered over time. Agencies undertaking citizen advocacy Evidence of induction and or training that orientates advocates to the need to support people with a disability, where appropriate, to make decisions and choices. Practice of supporting advocates tofacilitate the process, where appropriate, of decisions and choices made by people with a disability. Evidence of feedback gained from people with disability about how they are supported to make their choices. Agencies undertaking systemic advocacy Documented and implemented practices and policies that demonstrates that people with disabilities influence decision making about advocacy activities. Observations of individual people with disability and/or their families becoming involved in systemic advocacy activities of their choice. Ethical guidelines inform systemic advocacy policy and practice. Agencies undertaking family advocacy Standard 4: Privacy, dignity and confidentiality The right of each person with disability to privacy, dignity and confidentiality is recognised and respected. 4.1 The advocacy agency complies with the Information Privacy Principles of the Privacy Act 1988 in order to protect and respect the rights of each person with disability. 4.2 The advocacy agency promotes privacy, dignity and respect for each person with disability. Documented and implemented practices and policies for encouraging families to include the views of the person with disability in advocacy efforts where appropriate. All agencies Observations of the way advocates and agency staff talk and write about people with a disability. Clear privacy policy ensuring compliance with relevant State/Territory and Federal legislation. Documented and implemented practices and policies for obtaining consent where relevant and possible, examples could include consent to use photographs for publicity or to share information. Confidential information safely stored e.g. locked filing cabinets. Staff [and volunteers and contractors] sign confidentiality agreements. 311 Evidence that information about right to privacy is provided to people with disabilities and their families when they receive advocacy support. Evidence that the feedback from people with disability who receive advocacy support is used to influence the development of policies, procedures and practice of the agency. Feedback from people with disability who receive advocacy support about the attitude of agency staff to people with a disability. Feedback from external observers on the attitudes of the advocacy agency to people with disability. Agencies undertaking citizen advocacy Feedback from people with disability who receive advocacy support about the attitude of agency staff to people with disability. Feedback from people with disability who receive advocacy support on the attitudes of the advocacy agency to people with disability. Feedback from people with disability who receive advocacy support. Content and practice of orienting advocates to the importance of recognising and respecting the right of people with disability to privacy, dignity and confidentiality. Agencies undertaking family advocacy Documented and implemented practices and policies for encouraging families to obtain the approval of the person with disability before sharing information about the person with disability in the pursuit of advocacy efforts, where appropriate. 312 Standard 5: Participation and integration Each person with disability is supported and encouraged to participate and be involved in the community. 5.1 Through advocacy, opportunities for participation and involvement in the community are promoted. 5.2 Where appropriate, the advocacy agency takes action to introduce, influence or produce positive systemic change in the community. All agencies Purpose statement that makes it clear that the agency seeks to promote participation and inclusion. Examples of barriers to community participation being raised with other agencies and authorities for the purpose of promoting change. People with disability connected to the organisation report that they feel valued and accepted by agency staff. Agencies undertaking individual advocacy/legal advocacy Evidence of advocacy taken on behalf of individual people with disabilities aimed at increasing their participation and inclusion in the community. Agencies undertaking citizen advocacy Examples of activities people with disability who receive advocacy support and advocates are involved in – while recognising that the citizen advocates and the person with a disability make their own decisions outside of the control of the funded agency. Observation that community participation is covered in citizen advocate orientation. Practice of recruiting advocates who—by virtue of being non-service, “ordinary” members of the community—can facilitate the participation and integration of people with a disability. Content and practice of orienting advocates to their potential role in facilitating the participation and integration of people with a disability. Agencies undertaking family advocacy /systemic advocacy/ self advocacy Examples of events /activities hosted or engaged in which promote the inclusion of people with disabilities as valued and contributing members of community. Examples of evaluation forms from events or activities hosted by the organisation. 313 Standard 6: Valued status The intrinsic value of each person with a disability is recognised and each person is supported and encouraged to enhance their valued status in the community. 6.1 Through advocacy, the aspirations and strengths of each person with disability is promoted. 6.2 The advocacy agency promotes the intrinsic value and the valued status of each person with disability in all its activities. All agencies The valued status of people with disability is promoted in reports and promotional material. Details of public speaking at conferences, lectures and professional gatherings to promote a positive image of people with disabilities. Examples of issues raised or referrals made to systemic advocacy agencies and/or other agencies and authorities. Examples of activities and issues that the agency engages in that supports the valued status of people with a disability. Agencies undertaking citizen advocacy Standard 7: Complaints and disputes Each person with disability, who has a complaint or dispute with the advocacy agency, is encouraged to raise it, and have it resolved, without threat of retribution. 7.1 7.2 The advocacy agency informs each person with disability about how to raise a complaint or initiate a dispute about any areas of dissatisfaction with the advocacy agency, without threat of retribution. The advocacy agency seeks to resolve complaints or disputes raised or initiated by each person with disability, with access to both internal complaints resolution mechanisms and external complaints resolution mechanisms. Examples of activities people with disability who receive advocacy support and advocates are involved in that promote the intrinsic value and the valued status of people with disability– while recognising that the citizen advocates and the person with a disability make their own decisions outside of the control of the funded agency. Citizen advocacy orientation documentation includes information about valued status and what this means in practice. All agencies Documented complaints policy and procedures. Documented and implemented practices and policies for investigating and resolving complaints – cover both internal and external complaints resolution mechanisms, including the Complaints Resolution and Referral Service (CRRS). File review demonstrates that the agency completes complaints investigations in accordance with its complaints procedures. People with disability who access the advocacy agency are provided with information about the agency’s complaints policy and procedures. The agency reviews its complaints policy, procedures, processes and practices to ensure implementation is appropriate to complainants. Service user feedback about the complaints mechanism. Complaints register. 314 Standard 8: Agency management 8.1 The advocacy agency has clearly stated aims and objectives that communicate to each person with disability and other relevant stakeholders the scope and limitations of the advocacy agency. 8.2 The advocacy agency has governance and management systems in place that facilitate quality management practices and continuous improvement. 8.3 The advocacy agency operates independently and is structured in such a way that it is as free as possible from conflicts with other service provision and the interests of each person with disability. Standard 9: Staff, recruitment, employment and training 9.1 The advocacy agency ensures that its staff have relevant skills and competencies. Each person who has an employment or volunteer relationship with the advocacy agency has appropriate skills and competencies. 9.2 The advocacy agency provides opportunities for the appropriate and continuing training and skills development for each staff member. Each advocacy agency adopts quality management systems and practices that optimise the effectiveness of advocacy for each person with disability and facilitates continuous improvement. All agencies Documented agency aims and objectives. Documented and implemented practices and policies for promotion and communication of agency aims and objectives with people with disability who receive advocacy support and stakeholders. Reviews of agency management systems involving service users (eg. people with disability who receive advocacy support, family members, citizen advocates) – including documented annual self assessments and continuous improvement plans. Clear governance arrangements. Documented and implemented policies and practices for performance and risk management are undertaken. Documented policy on agency independence. Agency management and staff can provide practical examples of how they operate to ensure they are as free as possible from things that conflict with the best interests of people with disability. Policies and procedures include referral to another agency if required to prevent a conflict of interest. Evidence of the involvement of people with disability in the agency’s quality assurance activities. Minutes of management committee meetings. Documented roles and responsibilities of management committee office bearers. All agencies Current list of all people who have an employment relationship with the advocacy agency. Position descriptions of all paid and unpaid staff that describe skills and competencies needed for their role. Documented and implemented practices and policies for recruitment & induction that ensure paid and unpaid staff have the necessary skills and competencies for their position, including relevant qualification (where appropriate). Staff appraisals conducted at least annually. Training and development plans for all staff. Agencies undertaking citizen advocacy Independent evaluations of practices for developing the capacity of citizen advocates to assist people with disability meet their advocacy objectives. 315 Standard 10: Protection of human rights and freedom from abuse The advocacy agency acts to prevent abuse and neglect and to uphold the legal and human rights of each person with disability. 10.1 The advocacy agency takes all practical and appropriate steps to prevent abuse, neglect and discrimination of each person with disability. 10.2 The advocacy agency upholds and promotes the legal and human rights of each person with disability. Regular opportunities for the staff and board of management to avail themselves of Citizen Advocacy-related training, including participation in the independent evaluation of other Citizen Advocacy agencies, as a means to enhance conceptual and practical knowledge. All agencies Staff knowledge and skills in recognising and reporting criminal activities, abuse and neglect. Evidence of staff knowledge/learning about human and legal rights. Agency management and staff can provide practical examples of how they act to prevent abuse and neglect – (eg an outreach program which seeks out people with disability who are abused or neglected and who would not normally come to the attention of other agencies; community education to raise awareness about abuse of people with disabilities and strategies to prevent and respond to it, etc). Documented and implemented policies and procedures around responding to/reporting in situations of abuse and neglect. Examples could include a flow chart on who to notify and/or stages of reporting sequence/steps. Documented and implemented policies and procedures reflect prevention of abuse that could occur internal to the agency and external to the agency. Evidence of advocacy agency activities to promote and uphold the legal and human rights of people with disabilities on either an individual or systemic basis. Agencies undertaking citizen advocacy Practice of recruiting advocates for people with a disability who are isolated and otherwise vulnerable, in order to ensure their protection of human rights and freedom from abuse, consistent with the mission of Citizen Advocacy. Content and practice of orientating advocates to their role in ensuring the protection of the human rights, and prevention from abuse, of peoples with a disability. Practice of supporting advocates in their role of ensuring the protection of the human rights, and prevention from abuse, of people with a disability. 316