About this trial
People with HIV experience earlier impairments in physical function compared to people in the general population. They also exhibit an earlier presentation and more rapid development of frailty, a multisystemic syndrome of aging characterized by reduced activity, fatigue, slowness, weakness, and weight loss. While exercise can improve physical function in people with HIV, it is less effective in doing so than in the general population and is difficult to sustain in the long-term.
The goal of this clinical trial is to learn whether the medication tesamorelin will improve physical function and muscle health in adults with HIV when combined with exercise. Tesamorelin is a growth hormone-releasing hormone analogue that is FDA-approved to treat abdominal fat accumulation in people with HIV. While tesamorelin has also been shown to increase muscle mass and improve measures of muscle health, its effects on physical performance and muscle strength have not yet been evaluated.
During a 24-week intervention phase, half of participants will be randomly assigned to receive tesamorelin and half of participants will be randomly assigned to receive placebo (a look-alike substance that contains no drug). All participants also will engage in a home-based exercise intervention supervised by an exercise coach. During a subsequent 24-week extension phase, individuals will be monitored off study drug and supervised exercise, and be encouraged to continue to exercise independently.
The investigators will investigate effects of tesamorelin on physical function, muscle mass and quality, quality of life, and exercise adherence and self-efficacy. They also will evaluate whether effects of tesamorelin are maintained following treatment cessation. This study may identify an important strategy to improve how individuals aging with HIV function and feel with potential applications to other patient populations.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Men and women, 50-80 years old
Documented HIV infection on suppressive antiretroviral therapy for at least 1 year with HIV-1 RNA <200 copies/mL and CD4+ T cell count >200/µL 3
Sedentary lifestyle, defined as self-reported physical activity that breaks a sweat <3 days/week with no regular resistance exercise in the past 3 months
≥1 Fried frailty criterion (weakness, slow gait speed, exhaustion, decreased physical activity, or unintentional weight loss as defined by specific thresholds)
Disqualifiers
Use of tesamorelin or other growth hormone (GH)-based therapy within 6 months
Insulin-like growth factor 1 (IGF-1) z-score >2.0
HbA1c >8%
Active or suspected malignancy (with the exception of non-melanoma skin cancer) within 24 months
Trial design
Parallel
Treatments tested in this trial
Tesamorelin
DrugTesamorelin WR 1.28 mg given subcutaneously daily
Placebo
DrugIdentical placebo injection given subcutaneously daily
Exercise
BehavioralHome-based semi-supervised exercise program
Treatment groups
Trial outcomes
Primary outcomes
Change in Repeated Chair Stand Time
Time to complete 10 repeated chair stands
Secondary outcomes
Change in Standard and Modified Short Physical Performance Battery (SPPB)
Objective assessment of physical function that includes measures of balance, gait, and strength
Change in 1-Repetition Maximum Leg Press
Maximal weight that can be lifted by lower extremities once using correct form through full range of motion
Change in 400-Meter Walk Time
Time to walk 400 meters at the fastest pace possible
Change in Appendicular Lean Tissue Mass
Dual-energy x-ray absorptiometry (DXA) lean tissue mass in all four extremities
Sponsors and contacts
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Massachusetts General Hospital
Lead sponsor
University of Colorado, Denver
Collaborator