Mindfulness and Behavior Change for Cardiovascular Health in Older People with HIV
This study is looking at how a program called "One-Mind One-Heart" can help older people living with HIV improve their heart health. This program combines mindfulness (a type of meditation) and behavior change skills to help with stress, physical activity, diet, and substance use. Another group will receive education on reducing heart disease risks, like increasing activity and improving diet. The study aims to see if it's possible to recruit participants, if the eligibility rules work, and if people can be easily assigned to a group. You may be able to join if you are 50 or older, have HIV, and your viral load is suppressed (meaning the virus is at very low levels). The study plans to enroll 50 people, but its current status is unclear.
- Study design
- This is an interventional study planning to enroll 50 participants. It will compare two approaches: the "One-Mind One-Heart" program and an education program.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Not specified.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Mindfulness and Behavior Change to Improve Cardiovascular Health of Older People With HIV
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Feasibility of recruitmentBaseline (pre-intervention)
70% or more of participants consent to screening, meet screening criteria, are eligible, and agree to participate in the study
- Feasibility of eligibility criteriaBaseline (pre-intervention)
Less than 20% of participants are ineligible due to each criterion
- Feasibility of randomizationPre-intervention
70% or more of participants are randomized and complete the first intervention session
- Feasibility of the OM-OM interventionDuration of intervention
70% or more of participants attend all sessions and complete all homework
- Feasibility of research assessmentsDuration of intervention; 0 and 12-week follow-up
70% or more of weekly and follow-up research assessments are completed
- Feasibility of blood drawsBaseline; 12-week follow-up
70% of more are collected
- Acceptability of OM-OH intervention0-weeks post-intervention
Rating of 7.5 or greater/10 on: session satisfaction, helpfulness, and utility; overall program satisfaction; plan to use the skills; and would recommend the intervention program to a friend
- Acceptability of text-enhanced delivery0-weeks post-intervention
Rating of 7.5 or greater/10 on: ease, and confidence of use; and rating of 2 or less/10 on interference of technical problems
- Acceptability of blood draws0- and 12-weeks post-intervention
Rating of 7.5 or greater/10 on ease of collection; and rating of 2 or less/10 on pain