Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 11:53 AM
Ignite Modification Date:
2025-12-24 @ 11:53 AM
NCT ID:
NCT01860261
Eligibility Criteria:
Inclusion Criteria:
* HIV-positive
* Age \>=50 years on date of enrollment visit
* Less than 60min/week of vigorous exercise on average in the 90d prior to enrollment
* Able to complete study documents and activities in English (in this pilot we are only prepared to use English language questionnaires and instructional materials)
* Interested in and willing to do an exercise program
* Receiving continuous antiretroviral therapy (ART) for at least six months with an undetectable viral load at most recent clinic visit, or if not on ART then must have been off continuously for six months with no plan to start ART and have CD4 count \> 400 cells/µl (to avoid enrolling patients at risk of developing opportunistic infections or other HIV-associated illnesses).
Exclusion Criteria:
* Medical conditions likely to limit the ability to participate in the planned exercise, including renal failure (creatinine \> 2 mg/dl, congestive heart failure, significant lung disease, or severe osteoarthritis, Any health condition(s) that the study physician determines would preclude safe participation in the intervention or may require special modification of the exercise protocol (e.g. angina or myocardial infarction in the past 6 months)
* Substantial deconditioning or current impairment of physical function; this will be tested for by assessing whether patients can climb up and back down one flight of stairs (approximately 3 meters of elevation gain) without stopping 8.
* Unable or unwilling to actively participate in the intervention for the duration of the pilot study
* Unable to provide informed consent.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
50 Years
Study:
NCT01860261
Study Brief:
Protocol Section:
NCT01860261