Actively Recruiting
Development of a Behavioral Economic Intervention to Improve HIV-related Behaviors Among Sexual Minority Individuals
Led by The University of Texas Health Science Center at San Antonio · Updated on 2025-06-22
60
Participants Needed
1
Research Sites
25 weeks
Total Duration
On this page
Sponsors
T
The University of Texas Health Science Center at San Antonio
Lead Sponsor
N
National Institute on Drug Abuse (NIDA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating a new behavioral therapy called Episodic Future Thinking (EFT) to help sexual minority individuals reduce drug use and risky sexual behaviors while improving adherence to HIV prevention medication (PrEP). The study is a two-phase research project, with the second phase involving a randomized controlled trial comparing standard care alone to standard care plus the EFT program. The study focuses on HIV prevention behaviors, including methamphetamine use and sexual risk, among adults aged 18 to 34 who are HIV negative and currently taking PrEP. Participants will be randomly assigned to one of two groups. One group receives standard care, which includes counseling on HIV prevention, reducing drug use, and sexual health. The other group receives the same standard care plus the EFT intervention, which involves thinking about and planning future goals using a mobile app and in-person counseling sessions delivered by a trained counselor. The EFT intervention aims to improve decision-making through cognitive training exercises supported by mobile health technology. During the study, participants will complete surveys and provide blood, urine, and rectal swab samples for testing PrEP adherence, drug use, and sexually transmitted infections from Day 1 to Day 180. HIV rapid tests and psychological assessments will also be conducted throughout the study period. Researchers will monitor PrEP-related intentions, attitudes, stigma, and self-efficacy, along with mental health measures. Participants are expected to attend all study visits and use the EFT app as part of the intervention group. The study duration is approximately six months for each participant.
CONDITIONS
Brief Title
Behavioral Economic Intervention to Improve HIV Behaviors in Sexual Minority Individuals
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 to 34 years of age
- HIV negative as confirmed by Rapid HIV Antibody Test
- Identify as gay or bisexual
- Recent methamphetamine use within the past 3 months
- Currently prescribed and taking HIV PrEP medication
- Self-reported nonadherence to HIV PrEP in the past 3 months
- Urine screen test indicating PrEP nonadherence
- Self-reported condomless anal sex or diagnosis of a sexually transmitted infection in the past 3 months
- Able to attend all study visits
- Fluent in English
You will not qualify if you...
- Currently receiving treatment for any substance use disorder
- HIV positive
- Medical or psychiatric illness that may interfere with participation
- Unable to provide informed consent
- Unable to attend study visits as required
- Plans that would prevent study completion such as surgery, major medical treatments, incarceration, or moving away from the study area
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 6 months
Participants receive the Episodic Future Thinking behavioral economic intervention through a combination of in-person counseling sessions and mobile health technology via an app to improve HIV-related behaviors. The control group receives standard supportive counseling and information.
Multiple visits during the 6-month period including counseling sessions and assessments
Duration - Up to 6 months
Participants are monitored for HIV-related behaviors and health outcomes after the intervention period.
Periodic assessments during the follow-up period
Trial Site Locations
Total: 1 location
1
University of Texas Health Science Center at San Antonio
San Antonio, Texas, United States, 78229
Actively Recruiting
Research Team
E
Emeka Okafor, PhD, MPH
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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