NCT06131931 HIV Prevention Intervention for Latino Male Couples
| NCT ID | NCT06131931 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Central Florida |
| Condition | HIV |
| Study Type | INTERVENTIONAL |
| Enrollment | 400 participants |
| Start Date | 2023-06-21 |
| Primary Completion | 2028-06 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 400 participants in total. It began in 2023-06-21 with a primary completion date of 2028-06.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The primary objective of this proposal is to test the efficacy of Connecting Latinxs en Pareja (CLP). CLP is a four-session intervention grounded in social cognitive theory and a relationship oriented ecological framework. The investigators will examine whether participants assigned to CLP report an increase in the proportion of HIV protected anal sex acts to those assigned to a Wellness Promotion (WP) time and attention matched control condition. The primary outcome, relates to use of HIV protection.
Eligibility Criteria
Inclusion Criteria: * at least 18 years * reside in the 50 local jurisdictions identified by the EHE initiative or 17 jurisdictions with most HIV diagnoses among Latinxs * identify as Latinx/Hispanic/Afro-Latinx or reports having a main partner who identifies as Latinx/Hispanic/Afro-Latin * report having a main/primary male partner operationalized as a man with whom he has a primary ongoing sexual relationship, for at least 3 months * at least one member of the dyad report three acts of unprotected of anal sex (with main or other partners) * able to speak English and/or Spanish Exclusion Criteria: Either partner: * reports severe intimate partner violence (IPV) within the dyad during the past year on the Revised Conflict Tactic Scale\[1-4\] * has a language or cognitive impairment that would prevent informed consent. Inclusion of dyads reporting severe IPV could pose dangers and ethical concerns and will be referred to domestic abuse organizations for screening and services. * adults unable to consent * pregnant women * prisoners * individuals who are not yet adults
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06131931 clinical trial?
This trial is open to male participants only, aged 18 Years or older, up to 100 Years, studying HIV. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06131931 currently recruiting?
Yes, NCT06131931 is actively recruiting participants. Contact the research team at omar.martinez@ucf.edu for enrollment information.
Where is the NCT06131931 trial being conducted?
This trial is being conducted at Orlando, United States.
Who is sponsoring the NCT06131931 clinical trial?
NCT06131931 is sponsored by University of Central Florida. The trial plans to enroll 400 participants.
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