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NCT06586619Recruiting

A Remotely Delivered Tai Chi/Qigong Intervention for Older People Living With HIV

A Remotely Delivered Tai Chi/Qigong Intervention for Older People Living With HIV: A Randomized Clinical Trial

Source: ClinicalTrials.gov · Last updated 16 Sept 2026

Brief summary (registry, in English)

The goal of this randomized clinical trial is to learn if tai chi/qigong decreases depressive symptoms among older people living with HIV compared to a health education class. The main questions it aims to answer are: Does tai chi/qigong reduce depressive symptoms among older people living with HIV more than a health education class? What are the behavioral, psychological, and biological mechanisms in which tai chi/qigong affects depressive symptoms? Does tai chi/qigong affect depressive symptoms among older people living with HIV differently for men compared to women? Researchers will compare a 12-week, twice a week remotely delivered tai chi/qigong intervention to a health education class of the same duration to determine if it improves depressive symptoms among older people living with HIV. Participants will: Attend either a tai chi/qigong class twice a week for 12 weeks or a health education class of the same duration delivered via Zoom. Each class will be 45-60 minutes in length. Participate in 3 separate interviewer-administered interviews: at the time of enrollment, 3 months after the last class, and 9 months after the last class. Keep a tracking log of their home practice of tai chi/qigong (only participants in the intervention group). Use a biosensor (an earlobe sensor or chest strap) to measure their heart variability. Go to their local lab (e.g., Quest or Labcorp) for blood draw at the time of enrollment and at 9 month post intervention (this will only be a subset of participants).

Status (registry)
Recruiting
Study type
Interventional
Enrollment
326 (estimated)
First submitted
4 Sept 2024
Start date
4 Aug 2025
Primary completion date
Jul 2029
Lead sponsor
Florida International University
Diseases
HIV
NCT number
NCT06586619

What you commit to

  • Study type: Interventional
  • Planned participants: 326
  • From 4 Aug 2025 to the primary completion date, Jul 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • An individual who meets any of the following criteria will be excluded from participation in this study:
  • Reports high risk for suicide based on the CCSR screening tool.
  • Has participated in a study on mental health in the last 12 months.
  • Currently exercising at least 150 minutes a week

Who the study is looking for

  • In order to be eligible to participate in this study, an individual must meet all of the following criteria:
  • The ability to provide consent assessed by the GAIN Cognitive Impairment Scale
  • Provision of signed and dated informed consent form
  • Must be 50 - 75 years old.
  • Must have been diagnosed with HIV by a healthcare professional (status confirmed at baseline by an uploaded picture of a recent lab report or medication bottle with name),
  • Must have reliable internet access,
  • Must have a smart phone
  • No substantial experience (regular weekly practice for more than 3 months in the past 12 months) with mind-body interventions,
  • Willing to participate for the length of the 12-week intervention and follow up assessments (a total of 12 months).
  • Must report stable housing for the past 60 days and the next 60 days;
  • Must have mild to moderate depressive symptoms (a score more than 5 but less than 19 on the PHQ-9 scale)
  • Must speak and understand English

Age in the registry: 50 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Florida International University
Coordinator of this site? Confirm its status
MiamiUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.