The Impact of Brief Behavioral Treatment for Insomnia Versus Brief Mindfulness Treatment on Cognition and Sleep Health in Adults (Age 50+) With HIV (NCT07272863)
The Impact of BBTI on Cognition and Sleep Health in Older Adults With HIV
๐ฉบ Plain-English Summary (8th-Grade Level)
The goal of this clinical trial is to examine the effects of a telephone-delivered Brief Behavioral Treatment Insomnia (BBTI) versus a Brief Mindfulness Treatment (BMT) on cognitive and sleep outcomes in older adults with HIV. The main questions it aims to answer are: What are the effects of BBTI vs BMT on self-reported and observed sleep outcomes in older adults with HIV and insomnia up to 1-year post-intervention? What are the effects of BBTI vs BMT on self-reported and observed cognitive comes in older adults with HIV and insomnia up to 1-year post-intervention? What is the association between Alzheimer's Disease biomarkers and sleep and cognitive outcomes in older adults with HIV receiving BBTI vs BMT? Participants will: * Complete 4 weeks of telephone-delivered BBTI or BMT * Attend baseline, post-intervention, and 1-year post in-person visits for sleep and cognitive assessments * Have blood collected at all three time points
Who can join: Review the eligibility criteria below.
Location: The University of Alabama at Birmingham โ Birmingham, Alabama
Age range: 50 Years to 99 Years
๐งช Interventions in This Study
- BBTI (BEHAVIORAL)
- BMT (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (2 Sites)
- The University of Alabama at Birmingham โ Birmingham, Alabama
- The University of Alabama โ Tuscaloosa, Alabama
๐ Contact the Study Coordinator
Phone: (205) 348-3374
Email: slcody@ua.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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- Perinatal Research on Improving Sleep and Mental Health โ San Francisco, California
- Improving Sleep With a Digital Cognitive Behavioral Therapy for Insomnia Application โ Boston, Massachusetts
- Wearable Transcranial Electrical Stimulation (tES) for Insomnia โ Bethesda, Maryland
- Evaluation of a Neurostimulation Device for Insomnia: A Randomized Trial โ New York, New York
- Remote STATE Training for Insomnia in Older Adults โ San Francisco, California
Explore by condition: All Insomnia clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.