Actively Recruiting
HIV Prevention Intervention for Latino Male Couples
Led by University of Central Florida · Updated on 2024-12-06
400
Participants Needed
1
Research Sites
258 weeks
Total Duration
On this page
Sponsors
U
University of Central Florida
Lead Sponsor
N
National Institute on Minority Health and Health Disparities (NIMHD)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
HIV Prevention Intervention for Latino Male Couples
Who Can Participate
Eligibility Criteria
You may qualify if you...
- At least 18 years old
- Reside in one of the 50 Ending the HIV Epidemic (EHE) jurisdictions or 17 areas with high HIV rates among Latinxs
- Identify as Latinx, Hispanic, Afro-Latinx or have a main partner who identifies as Latinx, Hispanic, or Afro-Latinx
- Have a main male partner with an ongoing sexual relationship for at least 3 months
- At least one member of the couple reports three or more acts of unprotected anal sex with main or other partners
- Able to speak English and/or Spanish
You will not qualify if you...
- Either partner reports severe intimate partner violence in the past year
- Either partner has language or cognitive impairments preventing informed consent
- Adults unable to consent
- Pregnant women
- Prisoners
- Individuals who are not yet adults
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Central Florida
Orlando, Florida, United States, 32816
Actively Recruiting
Research Team
O
Omar Martinez, JD, MPH, MS
CONTACT
A
Amoy Fraser, PhD, CCRP, PMP
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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