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N/A Completed N=33 Randomized Single-blind Other

Strength Training and Endurance Exercise for LIFE

Source: ClinicalTrials.gov NCT02101060 ↗
Enrolled (actual)
33
Serious AEs
0.0%
Results posted
May 2021
Primary outcomePrimary: Aerobic Capacity — 0.15; 0.02 Liters/minute

Summary

Research is needed to determine safe and effective exercise rehabilitation programs to prevent and improve physical disability in older adults living with HIV. This problem is of great importance to the VA. The majority of the 25 thousand HIV-infected veterans are over 50 years of age (64%). The combined effect of aging and inflammation increase the risk for physical disability in older HIV-infected veterans. This translational exercise training trial will examine the cardiac and skeletal muscle effects of combined aerobic exercise and resistance training to attenuate the functional declines of aging with HIV by reducing the deleterious consequences of chronic inflammation. Findings will guide future rehabilitation research on cardiac remodeling and inflammation of skeletal muscle. The proposed research will advance the goal to develop effective rehabilitation strategies that improve the health of older HIV-infected veterans.

Outcome Measures

OutcomeResultp-value
PRIMARY
Aerobic Capacity
0.15; 0.02
PRIMARY
Diastolic Function
1.8; 0.5
SECONDARY
Biomarkers of Systemic Inflammation
-0.04; -0.03

Eligibility Criteria

Inclusion Criteria

  • HIV-infected veterans adult 50 years of age and older under medical care for HIV
  • Antiretroviral Therapy

Exclusion Criteria

  • Patients with comorbid conditions that could have a potential impact on their ability to perform exercise testing and training will be excluded according to the American College of Sports Medicine
  • Only sedentary adults will be eligible. Individuals that participate in regular structured aerobic exercise or resistance training in the prior 6-months will be excluded
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02101060). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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