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Completed

NCT Number: NCT04221750

Diet and Exercise Plus Metformin to Treat Frailty in Obese Seniors

The continuing increase in prevalence of obesity in older adults including many older Veterans has become a major health concern. The clinical trial will test the central hypothesis that a multicomponent intervention consisting of lifestyle therapy (diet-induced weight loss and exercise training) plus metformin will be the most effective strategy for reversing sarcopenic obesity and frailty in older Veterans with obesity.

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Key information

Age range

65 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Michael E. DeBakey VA Medical Center, Houston, TX

Houston, Texas, 77030-4211, United States

About this study

The growing prevalence of obesity in older adults including many older Veterans, has become a major concern in the US already strained health care system in general and in the VA in particular. In older adults, obesity exacerbates the age-related decline in physical function resulting in frailty, decrease in quality of life, loss of independence, and increase in nursing home admissions. The investigators' group demonstrated that weight loss from lifestyle therapy improves physical function and ameliorates frailty but the improvement was modest at best and most obese older adults remained frail. More importantly, there are concerns that the weight-loss induced loss of muscle and bone mass could worsen underlying age-related sarcopenia and osteopenia in the subset of frail obese elderly. Metformin, a biguanide, is a widely available drug used as first line treatment of type 2 diabetes. Animal studies suggest that metformin improves health span and increases lifespan, hence may represent a novel intervention for frailty. Because metformin reduces cellular senescence and senescence-associated phenotype (SASP), it is believed to retard accelerated aging most especially in older adults with obesity. The objective is to conduct a head-head comparative efficacy, placebo controlled, randomized controlled trial to test the hypothesis that lifestyle therapy + metformin for six months will be more effective than lifestyle therapy alone or metformin alone in improving physical function and preventing the weight loss-induced reduction in muscle and bone mass in obese (BMI > 30 kg/m2) older (age 65 - 85 years) Veterans with physical frailty.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 65 - 85 years
  • BMI = or > 30 kg/m2
  • Mild to moderate frailty (score of 18 to 31 in the modified Physical Performance Test)
  • Stable body weight (plus/minus 2 kg) during the past 6 months
  • Sedentary (regular exercise <1 h/wk or <2 x/wk for the last 6 months)
  • Willing to provide informed consent

Exclusion criteria

  • Any major chronic diseases, or any condition that would interfere with exercise or dietary restriction, or use of metformin, in which exercise, dietary restrictions, or metformin are contraindicated, or that would interfere with interpretation of results
  • Cardiopulmonary disease (e.g. recent MI, unstable angina, stroke) or unstable disease (e.g., NYHA Class III or IV congestive heart failure, severe pulmonary disease requiring steroid pills or the use of supplemental oxygen) that would contraindicate exercise or dietary restriction
  • Severe orthopedic (e.g. awaiting joint replacement) and/or neuromuscular (e.g. multiple sclerosis, active rheumatoid arthritis) disease or impairments that would contraindicate participation in exercise
  • Renal impairment as defined by an estimated glomerular filtration rate (eGFR of less than 30 mL/min/1.73 m2) in which metformin is contraindicated
  • Other significant co-morbid disease that would impair ability to participate in the exercise intervention (e.g. severe psychiatric disorder [e.g. bipolar, schizophrenia], excess alcohol use [>14 drinks per week])
  • Severe visual or hearing impairments that would interfere with following directions
  • Significant cognitive impairment, defined as a known diagnosis of dementia or positive screening test for dementia using the Mini-Mental State Exam (i.e. MMSE score <24)69
  • Uncontrolled hypertension (BP>160/90 mm Hg)
  • History of malignancy during the past 5 years (except non-melanoma skin cancers)
  • Current use of bone acting drugs (e.g. use of estrogen, or androgen containing compound,raloxifene, calcitonin, parathyroid hormone during the past year or bisphosphonates during the last two years)
  • Osteoporosis (T-score -2.5 and below on hip or spine scan) or history of fragility fractures
  • Known history of diabetes mellitus or any of the following:
  • Fasting blood glucose of 126 mg/dl, or HbA1c of 6.5% or >
  • Terminal illness with life expectancy less than 12 months, as determined by a physician
  • Use of any drugs or natural products designed to induce weight loss within past three months
  • History of excessive alcohol consumption (e.g. 8 or more drinks a week for women and 15 or more drinks a week for men)
  • Positive exercise stress test for ischemia or any indication for early termination of exercise stress testing
  • Taking metformin or any other glucose lowering drug
  • Lives outside of the study site or is planning to move out of the area in the next 2 years

Treatment and study plan

Lifestyle Therapy

Behavioral

Weight management program, in which participants are prescribed a balanced diet that provides and energy deficit of 500 to 750 kcal per day to induced ~10% weight loss plus Supervised combined aerobic and resistance exercise training three times weekly

Other names: Diet-induced weight loss and exercise training

Metformin Hydrochloride

Drug

Given orally starting at 500 mg (one tablet) taken orally once a day with meals. After a week, the dose of metformin will be increased to 1000 mg (two tablets) daily. After another week, the dose of metformin will be increased to 1500 mg (three tablets) daily.

Placebo

Drug

Given orally starting at 500 mg (one tablet) taken orally once a day with meals. After a week, the dose of placebo will be increased to 1000 mg (two tablets) daily. After another week, the dose of placebo will be increased to 1500 mg (three tablets) daily.

Healthy lifestyle

Behavioral

Group educational sessions that focus on healthy diet, exercise, and social support once a month

Primary outcomes

  1. Change in the modified Physical Performance Test (PPT)

    Time frame: 6 months

    The Physical Performance Test includes seven standardized tasks (walking 15.2 m [50 ft], putting on and removing a coat, picking up a penny, standing up from a chair, lifting a book, climbing one flight of stairs, and performing a progressive Romberg test) plus two additional tasks (going up and down four flights of stairs and making a 360-degree turn). The score for each task ranges from 0 to 4, with higher scores indicating better physical performance; a perfect score would be 36.

Secondary outcomes

  1. Change in muscle strength

    Time frame: 6 months

    Assessed by biodex dynamometer and1-repetition maximum

  2. Change in gait speed

    Time frame: 6 months

    Assessed by time need to walk a certain distance

  3. Change in peak aerobic power

    Time frame: 6 months

    Assessed by indirect calorimetry during a graded exercise test

  4. Change in lean body mass

    Time frame: 6 months

    Assessed by dual-energy x-ray absorptiometry (DXA)

  5. Chang in body fat

    Time frame: 6 months

    Assessed by DXA

  6. Change in thigh muscle

    Time frame: 6 months

    Assessed by magnetic resonance imaging (MRI)

  7. Change in bone microarchitecture

    Time frame: 6 months

    Assessed by high-resolution peripheral quantitative computed tomograph (HR-pQCT)

  8. Change in bone strength

    Time frame: 6 months

    Assessed by finite-element analyses

  9. Change in hip, lumbar spine, and wrist bone mineral density (BMD)

    Time frame: 6 months

    Assessed by DXA

  10. Change in serum C-telopeptide

    Time frame: 6 months

    Assessed by immunoassay

  11. Change in telomere length

    Time frame: 6 months

    Assessed by Q-PCR

  12. Change in mood

    Time frame: 6 months

    Assessed by geriatric depression scale (score range: 0 to 30, where lower scores indicating better mood)

  13. Change in serum procollagen type 1 N propeptide

    Time frame: 6 months

    Assessed by radioimmunoassay

  14. Change in serum 25-OH vitamin D

    Time frame: 6 months

    Assessed by immunoassay

  15. Change in serum parathyroid hormone

    Time frame: 6 months

    Assessed by immunoassay

  16. Change in high-sensitivity c-reactive protein

    Time frame: 6 months

    Assessed by immunoassay

  17. Change in p16 and other markers of cell arrest

    Time frame: 6 months

    Assessed by immunohistochemistry

  18. Change in protein expression of senescence associated secretory phenotype

    Time frame: 6 months

    Assessed by elisa or western blotting

  19. Change in Medical Outcomes 36-Item short form Health survey (SF-36)

    Time frame: 6 months

    Assessed by Physical component summary and mental component summary score (score range 0 to 100, with higher scores indicating better health status)

  20. Change in Impact of Weight on Quality of Life_Lite (IWQOL-lite) score

    Time frame: 6 months

    Assessed by IWQO-liteL questionnaire

  21. Change in serum adiponectin

    Time frame: 6 months

    Assessed by ELISA

  22. Change in serum leptin

    Time frame: 6 months

    Assessed by ELISA

  23. Change in fasting serum insulin

    Time frame: 6 months

    Assessed by immunoassay

  24. Change in fasting serum glucose

    Time frame: 6 months

    Assessed by glucose oxidase method

  25. Change in blood pressure

    Time frame: 6 months

    Assessed by sphygmomanometry

  26. Change in serum lipids

    Time frame: 6 months

    Assessed by automated enzymatic/colorimetric assays

  27. Change in insulin growth factor 1

    Time frame: 6 months

    Assessed by immunoassay

  28. Change in Cognitive composite scores

    Time frame: 6 months

    Using cognitive toolbox which yields the following summary scores: Cognitive Function

    Composite Score, Fluid Cognition Composite Score, and Crystallized Cognition Composite Score (score range: -3 to +3 for each with higher scores indicating better cognitive status

Sponsors and collaborators

Lead sponsor

VA Office of Research and Development

Fed

Collaborators

  • Baylor College of Medicine
  • Michael E. DeBakey VA Medical Center

Registry information

Official study title

Lifestyle Intervention Plus Metformin to Treat Frailty in Older Veterans With Obesity

Acronym: DEMFOS

Important dates

Study start
2021
Primary completion
2025
Study completion
2025
First posted
Jan 9, 2020
Registry last updated
Jan 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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