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Resistance based Group Intervention
Introduction
In the UK obesity is on its rise and there is an increased concern to whether there are any efficient
strategies to halt the problem. The U.S is estimated to be a decade ahead in terms of the evergrowing rise in obesity levels which is in-turn drastically increasing the rate of type 2 diabetes.
Results show obesity contributes to £3.5bn in economy costs, 30,000 deaths and 18 million days off
sick from work each year. It can also lead to major health problems such as diabetes, hypertension
and several more. Obesity is an overabundance of body fat and can be defined in relation to body
mass index (BMI), a BMI value >30 indicates an individual is obese and is reflected by an increased
waist circumference (Haslam, Sattar, & Lean, 2006).
Therefore, effective exercise prescription is essential to help with weight gain prevention and weight
loss maintenance, although it is evident that encouraging obese individuals to partake in physical
activity isn’t an easy task. Often people who are overweight or obese suffer from low self-esteem,
possible eating disorders, depression, and anxiety (Ehrman, Gordon, Visich, & Keteyian, 2018). Low
adherence to exercise is a common problem and can be due to high levels of displeasure, research
states individuals perform better with self-selected intensities which elicit a more pleasurable
response (Ekkekakis, 2009).
Multi-component behavioural weight management programs (BWMP) have been developed and
widely used most abundantly in primary care settings, they address physical activity, nutrition, and
behaviour therapy, although, these programs have seen to have varied outcomes. Loveman, et al.,
(2011) conducted a systematic review on the effectiveness of long=term weight management
schemes for adults and found the interventions had generally produced modest weight loss in
overweight or obese subjects, however weight regain was common, additionally these interventions
were likely to be cost-effective. An update review with a more calloborative approach used by NICE,
(2013) reported the effectiveness of 44 different BWMP’s compared to control coniditons,
participants in the control condition had produced acute weight loss over a 12+ month period,
whereas the intervention groups produced signifcantly greater results in most cases, 2-3kg more
weight reducution in a 12-18 month period. There had also been evidence that suggests
interventions involving face-to-face contact, set goals and supervised exercise yielded the most
benefit compared to other interventions, this indicates the the potential necessity for assistance and
contact to elciit greater results. Overall, BWMP’s may play a crucial role in the assistance of adopting
a healthier and active lifestyle.
Referral Criteria (ethnic groups include, week 2 lecture tier systems)
Participants will be eligible for the program if they match the referral criteria, this criterion is
evidence based using the guidelines associated with ACSM, (2013). Their body mass index (BMI)
should indicate that they’re overweight or obese, 25 – 29.9 kg/m2 (overweight), ≥30kg/m2 (obese).
In addition to BMI, waist girth measurements will also be taken, an obese individual will be
measured at a waist girth >102cm(40inch) for men and >88cm(35inch) for women (Executive
summary of the clinical guidelines, 1998).
Old age, physical inactivity and race are some of the factors that can contribute to hypertension,
participants may be referred if they have levels above normal, SBP – 120-139/ DBP – 80-89
(Prehypertension), Stage 1 & 2 hypertension are excluded from criteria.
An unhealthy diet with an abundant quantity of processed foods containing high saturated fat or
trans fats can increase cholesterol levels – leading to dyslipidaemia. Participants may be referred if
their LDL cholesterol is 130-159 mg∙dL-1, total cholesterol is 200-239 mg∙dL-1 , HDL cholesterol ≥60
mg∙dL-1 and triglycerides are 150-199 mg∙dL-1 .
Individuals at risk of Type 2 Diabetes with fasting plasma glucose levels exceeding optimal levels are
also considered, this is largely subject to an individual’s weight and waist circumference which can
lead to insulin resistance. Prediabetic plasma glucose ranges from 100 mg∙dL-1 to 125 mg∙dL-1 for
impaired fasting glucose and 140 mg∙dL-1 to 199 mg∙dL-1 for impaired glucose tolerance. Individuals
with higher values than prediabetic values will more than likely be diabetic and therefore excluded
from the criteria.
Cardiovascular disease (CVD) potential is exacerbated due to all above criteria; therefore, all are
leading causes of CVD. Additionally, cigarette smoking (or recent cessation/ in the last 6 months) and
sedentary lifestyle behaviours (failure to partake in at least 30 min of moderate intensity exercise 3
times per week) are considered lifestyle factors that may lead to increased risk of CVD – and are also
considered as referral criteria for this program.
Workshop entry process and progress monitoring
Pre-Participation Health Screening
Participants are required to complete a range of pre-participation processes that indicate the
physical readiness of the individual and to consider any metabolic complications one may have
before engaging in physical activity. Following a similar approach to ACSM, (2013), there will be a
multistage process, including AHA/ACSM Health/Fitness Facility Preparticipation Screening
Questionnaire ACSM, (2009), an informed consent, a CVD risk factor assessment and classification,
and medical evaluation (if required) that involves a physical examination and stress test by a
reputable health care professional. All individuals will be required to complete at minimum, the
health screening questionnaire and informed consent form.
The AHA/ACSM Health/Fitness Facility Preparticipation Screening Questionnaire (see figure 1),
allows individuals with multiple CVD risk factors to be properly assessed by a professional prior to
engaging in physical activity, this is mandatory as part of regular effective medical practice and
should progress incrementally alongside their prescribed exercise program (ACSM, 2009).
A CVD risk factor assessment allows the health care professional to acquire relevant information
regarding the patient’s development and on-going progression/regression. Determining the
presence of metabolic and cardiovascular disease is essential for when making decisions regarding
the level of medical clearance, the need for exercise testing and the level of exercise supervision and
exercise frequency (ACSM, 2013).
The informed consent is required before exercise in any health/fitness or clinical setting, this
documentation is an important part of ethical and legal consideration. The form allows the
participant to understand what is required of them and the purpose and risks associated with the
exercise test/program (ACSM, 2013).
Figure 1
AHA/ACSM Health/Fitness Facility Preparticipation Screening Questionnaire
Note: Adopted from American College of Sports Medicine. (2013). ACSM's guidelines for exercise
testing and prescription. Lippincott Williams & Wilkins. p25, fig 2.2.
Figure 2 and 3 adopted from ACSM, (2013) are representative of the CVD assessments that the
health practioner will require from each patient. This is necessary to identify the level of risk which
will therefore determine the exercise regime. For example, if the patient has numerous CVD risk
factors (≥2) they will likely be classified as moderate or high risk, or a combination of both, in this
case, with the given referral criteria, the individuals will more than likely be classified as moderate
risk. This can then be progressed to identify which level of intensity is or isn’t advised when working
with patients, In Figure 3, this model allows the practioner to address whether a medical
examination, exercise test and physician supervision are necessary for pre-participation health
screening, however, if not required, the patient may still be eligible to request the examination if
they believe they’re at risk.
Figure 2
Logic model for classification of risk
Note: Adopted from American College of Sports Medicine. (2013). ACSM's guidelines for exercise
testing and prescription. Lippincott Williams & Wilkins. p26, fig 2.3.
Figure 3
Medical examination based on risk classification
Note: Adopted from American College of Sports Medicine. (2013). ACSM's guidelines for exercise
testing and prescription. Lippincott Williams & Wilkins. p28, fig 2.4.
If the patient has answered the CV assessment (see figure 2) and shows signs of metabolic
complications, they will be required to consult a physician prior to starting an exercise program,
there is evidence that if an individual of whom is unaccustomed to physical activity and performs
bouts of vigorous intensity exercise, the likelihood of an exercise-related event such as sudden
cardiac death or acute MI is increased (Giri, et al., 1999; Siscovick, et al., 1984). Therefore, the most
appropriate approach would be to start with light-to-moderate intensity levels of exercise and
progress incrementally as their physical fitness increases.
Pre-participation – Assessments (Physiological, Psychological & Nutrition)
Once the patient has completed their initial step within the pre-participation process, they will then
be taken through various assessments that will be repeated throughout the 12-week intervention,
patients will be required to take part in the tests at the start, after six weeks and the twelfth week –
totalling three compulsory testing events. The patients will be asked to participate in a 6-month
follow up post-intervention to highlight the long-term effects and thus asked to repeat all the range
of assessments below to evaluate the long-term health effects of this program.
Blood Pressure (BP)
Patients will have their blood pressure measurement taken before exercise participation. This is an
important factor to consider when addressing an individual’s health and well-being. Prehypertensive
individuals included in the referral criteria require health-promoting lifestyle alterations to prevent
the progressive rise in blood pressure, as this indefinitely increases the likelihood of developing CVD
(Chobanian, et al., 2003). As this intervention involves overweight and obese patients, they will most
likely need modifications when undergoing a blood pressure test, one main modification is that the
individual will likely require a larger cuff size. Measurement of blood pressure will follow the same
methodology from Prineas, (1991).
It is expected that, by the halfway point of the program, patients will see a decrease in their BP, with
further reductions by the end point of 12 weeks, with the future expectation to return to normal
levels (<120 mm Hg SBP, <80 mm Hg DBP) (ACSM, 2013). Numerous substantial epidemiological
studies have shown that a reduction in weight leads to a BP lowering effect, likely due to improving
insulin sensitivity (Mertens and Van Gaal, 2000).
Cholesterol Levels
Next, the patients will be required to have their blood taken to examine cholesterol levels NHS
(2019), with the aim to reduce low-density lipoproteins (LDL), as this is a major risk factor for CVD,
thus lowering LDL results in a significant reduction in the incidence of CVD (12), further, to increase
the levels of high-density lipoproteins (HDL) to combat the chances of developing CVD (ACSM, 2013).
Smoking, overweight/obese status, sedentary lifestyle, and poor nutrition habits all contribute to the
raise in cholesterol levels (NHS, 2019). The program hopes to reduce cholesterol levels, seeing a
decline by week 6 and further reductions by week 12 – with the expectation to reach normal levels
by the end of the intervention. Normal levels = LDL – 100-129 mg∙dL-1, Total cholesterol <200 mg∙dL1
, HDL – 40-60 mg∙dL-1, Triglycerides <150 mg∙dL-1 (NCEP, 2004).
Plasma Glucose Levels
Testing for glucose levels can be done via blood samples NHS (2020), like testing for cholesterol
levels, therefore both can be checked simultaneously. Prediabetic patients within this program will
have both impaired glucose tolerance (IGT) and impaired fasting glucose (IFG) and are at a
significantly high risk for developing diabetes (10).
Reduction in weight can make it easier to achieve a lower blood sugar level, leading to improved
insulin response and sensitivity, this program aims to reduce body weight and improve blood sugar
levels week by week with appropriate diet and exercise. By the end of the 12 weeks, the patient will
have lowered both (IGT & IFG) levels appropriately, aiming for close to 100 mg∙dL-1.
Anthropometric Measures
Patients would have already identified their BMI and waist circumference (WC) prior to joining the
program, their BMI and (WC) will be recorded at the point of starting the program, in the middle and
at the end (1,6,12 weeks). Along with BMI, circumference measures will be taken by the practioners
using a measuring tape, measures of the waist, upper arm, hips, calf, mid-thigh, neck, and calf will all
be required for recording at the same intervals throughout the program (1,6,12 weeks). Using the
same methodology seen in the manual of Callaway and colleagues, (1988). It is essential that all
patients achieve reduction in girth measurements, with the addition of a lower BMI score
throughout the program, with the emphasis of reducing WC to prevent the probability of CVD,
hypertension, diabetes, and early death (Pi-Sunyer, 2004). According to the guidelines addressed by
ACSM (2013), normative values of WC for men and female are as follows: 28.5–35inch / 31.5–
39.0inch, therefore these values will be the target for individuals of this program, achieving a
reduction in both BMI and WC respectfully.
Resting Heart Rate (RHR)
In addition to the measures above, practioners will need to take a resting heart rate from all
participants, this is not included in the referral criteria, so a varied range of RHR are expected.
However, it is known that a RHR ≥90 beats per min(bpm) compared to <60bpm yields at least a twofold increase in CVD mortality, the method associated with taken RHR is adopted from Cooney, et
al., (2010).
6 Minute Walk Test (6MWT)
To test exercise capacity, this program will involve a 6-minute walk test, the distance the individual
covers is the prime outcome measure of the test, secondary measurements will include fatigue and
dyspnoea that will be rated via a borg scale Williams (2017), and will be administered at the start,
middle and end of the intervention. The method for this specific test is adopted from Enright (2003)
and inherits a non-intrusive approach to gaining knowledge as to where the patient is in terms of
their fitness level. Furthermore, this test requires no equipment and can be performed anywhere if
the patient has a means of recording distance travelled via electronic device plus a stopwatch.
The table below contains an equation that is an acceptable method to predict VO2 peak from the
6MWT:
Table 1:
VO2 peak equation
Note: Adopted from Cahalin, et al., (1996)
Strength Testing
To test muscular strength, a gym facility will be used, all participants will partake in a six-repetition
max test (6RM) using both a leg press and chest press machine. They will be supervised by a
practioner to ensure adequate technique and methodology behind the test will be adopted from
Logan and colleagues (2000). A 6RM can be deemed more appropriate than singular maximal rep
due to the population used for this study; as they’re at risk to developing CVD and other health
conditions.
This test will commence at the start, middle and end of the exercise program, practioners will record
the weights lifted for each patient and the goal will be to increase the weight used for each future
test.
Psychological Testing/Questionnaire
Each patient will fill and complete a quality-of-life questionnaire (QOLQ) created by Moorehead and
colleagues (2003). It will be assigned to patients at the start and end of the intervention, this
questionnaire covers multiple areas of an individual’s life and can be used to assess whether some if
not all elements have improved. Further, the QOLQ can be completed in less than one minute, and
can be administer to patients via email,
Nutritional Analysis
Participants will be asked to provide a 3-day food diary at the start of the intervention for the health
practioner to assess, it is very likely that there should be amendments to the participants eating
habits to allow for progressive weight loss. The diary should provide all food and beverages with as
close to exact measures of each.
12-Week Program Content and Delivery
Week 1:
Day 1
•Screening
& Testing
Day 2
Day 3
Day 4
Day 5
Day 6
You should clearly outline content of the 12-week mutli-component BWMP and how it will be
delivered. Make reference to equipment / facilities that are required. Also ensure that you choose
an underpinning psychological model for your programme to follow. (Transtheoretical Model)
Programme content must include elements of diet, physical activity and behavioural therapy. You
should be making individuals aware of the consequences and prevalence of obesity,
acknowledging and quantifying lifestyle and risk factors associated with overweight / obesity.
Promote healthy lifestyle options. This can be delivered in a commercial or non-commercial
setting such as those delivered in primary care setting.
Delivery of the programme needs to be made clear and may include group workshops or
individual consultations on a range of topics that would be beneficial for the patients. You may
also provide them with supplementary materials that you feel is important. There may also be online aspects of the programme.
Where possible use peer-reviewed scientific research to compliment your choice of methods and
content.
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