Investigating the Prevalence and Risk Factors for Sarcopenia Amongst Adults Seeking Treatment for Obesity

ConditionObesity
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age21-100
SponsorSingapore General Hospital

About this trial

Sarcopenia, a condition where individuals lose muscle mass and strength, is associated with poorer health and function. While aging is a well-known cause of sarcopenia, obesity is increasingly recognised as a significant factor. When sarcopenia and obesity occur together, it can result in more severe health problems. This is especially concerning because weight loss, the treatment for obesity, can further reduce muscle mass and potentially worsen the situation. Despite this, it is unknown how common sarcopenia is among people with obesity, as only a few studies have looked into this using the most accurate diagnostic criteria, showing a prevalence of 4-13%.

In this study, the investigators will examine the prevalence of sarcopenia in 300 adults with obesity at a specialized Obesity Center. The investigators expect to find a higher prevalence among Asian participants due to differences in body composition compared to other ethnic groups.

The investigators will also explore various factors that might be linked to sarcopenia in these individuals, such as age, gender, race, body mass index, smoking and alcohol use, medical conditions, medications, physical activity, aerobic capacity, and dietary protein intake. Some of these factors could help in identifying those at risk of sarcopenia and could be targeted for future treatments.

Currently, screening for sarcopenia is not a standard part of routine obesity care as it requires specialized equipment and trained staff. By determining how common sarcopenia is in people with obesity, this study will help healthcare providers better understand the problem and allocate resources effectively. Identifying factors associated with sarcopenia will also help streamline diagnosis and monitoring for those at risk.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

body mass index ≥ 27.5kg/m2

able to provide informed consent.

Disqualifiers

unable to undergo the physical function tests (handgrip strength testing and chair-stand tests)

pregnant women

history of bariatric procedures or surgeries

on medications for treatment of obesity (glucagon-like peptide 1 receptor agonists, phentermine, naltrexone-bupropion, orlistat)

Trial population

Adults with obesity seeking treatment at Singapore General Hospital Obesity Centre

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Sarcopenia

Skeletal muscle mass Skeletal muscle mass measurement will be obtained via bioimpedance analysis using the TANITA MC 780 MA Multi-frequency Segmental Body Composition Analyser. Low skeletal muscle mass will be defined by percentage of skeletal muscle mass divided by body weight of ≤ 37% in males and ≤ 27.6% in females.

Time frame
Outcome measures will be recorded at baseline only.
2

Handgrip strength

Handgrip strength will be measured using the Jamar handgrip dynamometer. Two trials will be performed for each hand, and the maximum strength will be used for diagnosis.

Time frame
Outcome measures will be recorded at baseline only.
3

5-time chair stand test

Time taken (seconds) to perform 5 sit-to-stand repetitions

Time frame
Outcome measures will be recorded at baseline only.
4

30-second sit-to-stand test

Number of sit-to-stand repetitions performed in 30 seconds

Time frame
Outcome measures will be recorded at baseline only.

Secondary outcomes

1

Aerobic capacity

The study will use a validated non-exercise prediction model comprising a physical activity questionnaire to estimate peak oxygen uptake, VO2 milliliter/kg/minute (ml/kg/min). This simple physical activity questionnaire consists of age, gender, height, weight, estimated maximum heart rate, frequency of exercise, length of time for each workout, intensity of each workout, waistline diameter, and resting heart rate. It will be self-administered or administered with the assistance of the clinical research coordinator if required.

Time frame
At baseline
2

Physical activity questionnaire

Number of minutes per week spent on moderate to vigorous physical activity will be recorded

Time frame
At baseline
3

Dietary questionnaire

72 hour dietary recall questionnaire will be administered and dietary macronutrient composition will be calculated

Time frame
At baseline

Other outcomes

Sponsors and contacts

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