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Behavioral Economic Intervention to Improve HIV Behaviors in Sexual Minority Individuals

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoint reworded 2 of 8 changed
See other at-risk trials from The University of Texas Health Science Center at San Antonio

Record History

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  1. Notable Primary endpoint(s) modified
    • Eligibility criteria expanded, about 16 words
    • Secondary endpoints: details revised at 5 of 5 entries
  2. Minor Eligibility criteria shortened, about 1 wordv3
  3. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Feb 1, 2025 to Mar 3, 2025
    • Site details revised
    v2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This research study is testing a new behavioral therapy called Episodic Future Thinking or EFT can help people reduce drug use and risky sexual behaviors while helping them adhere to their HIV prevention medication (PrEP). Participants will be randomly assigned to one of two groups. One group will receive standard care, which includes counseling on HIV prevention, drug use reduction, and sexual health. The other group will receive standard care plus a new program called Episodic Future Thinking (EFT), where participants will think about and plan for their future goals using a mobile app and counseling sessions. Study procedures that are not part of regular care include filling out surveys, providing blood, urine, and swab samples for testing, and using the EFT app.
Trial Details
NCT Number NCT06745947
Lead Sponsor The University of Texas Health Science Center at San Antonio
Collaborators: National Institute on Drug Abuse (NIDA)
Conditions
(from sponsor)
HIV Prevention
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov