Lifestyle Modifications for the Treatment of Sarcopenic Obesity
Sarcopenic Obesity, Sarcopenia, Obesity
About this trial
This is an interventional treatment trial for Sarcopenic Obesity
Eligibility Criteria
Inclusion Criteria:
- Independent living community-dwellers
- Sarcopenic
- Obese
- Montreal Cognitive Assessment test (MoCA) score > or = 26
Exclusion Criteria:
- Use of pacemaker
- Lactose intolerance
- Parkinson's disease
- Unmanaged pain
- Severe osteoporosis or arthritis
- Use of corticosteroids
- History of pulmonary embolus or myocardial infarction within the previous 2 years
- Heart disease
- Chronic obstructive pulmonary disease
- Chronic kidney disease
- Hypertension (resting systolic pressure >200mmHg, resting diastolic >100mmHg)
- Acute systemic illnesses
- Any other uncontrolled physical, psychological or mental condition that either prohibits adherence to the study protocol or increases significantly the health risks for the subject.
Sites / Locations
- Queen Margaret University
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Exercise & Protein Drink/Diet
Exercise
High-protein (1.2-1.5 g protein per kg bodyweight; a milk-based protein drink will provide 50 g protein/day) energy-restricted (500 kcal deficit) diet and a multimodal exercise program (balance, flexibility, aerobic, resistance) 3 times/week, each lasting 1 hour. 1 tablet of Vitamin D3 (25 micrograms) x three days/week. Total duration 16 weeks.
A multimodal exercise program (balance, flexibility, aerobic, resistance) will take place 3 times/week, each one lasting 1 hour. Participants in this group will follow their habitual diet. 1 tablet of Vitamin D3 (25 micrograms) x three days/week. Total duration 16 weeks.