Risk Reduction Behavior Clinical Trial
Official title:
HIV Prevention Among Latino MSM: Evaluation of a Locally Developed Intervention
Wake Forest University is partnering with Chatham Social Health Council (a community-based
organization) to conduct a randomized controlled trial to evaluate the efficacy of Hombres
Ofreciendo Liderazgo y Apoyo (HOLA) en Grupos (Men Giving Leadership and Support in Groups),
a Spanish-language HIV risk behavior intervention for Latino men who have sex with men (MSM)
in rural North Carolina.
Participants in the HOLA intervention, when compared to those in the comparison
intervention, will report: increased consistent use of condoms during sexual intercourse;
increased use of HIV and sexually transmitted disease (STD) counseling, testing, and
treatment services; greater knowledge concerning the impact of HIV on communities (including
Latino and MSM)and HIV risk behaviors and prevention strategies; more positive attitudes
towards abstinence and condom use; increased self-efficacy to use and assert the use of
condoms with sex partners; increased condom-use mastery scores; decreased barriers to risk
reduction (e.g. health-compromising aspects of machismo); and enhanced partner and provider
communication and sexual negotiation skills.
Status | Completed |
Enrollment | 304 |
Est. completion date | August 2015 |
Est. primary completion date | August 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Male gender - Self-identify as Latino or Hispanic - 18 years of age or older - Speak Spanish - Have had sex with another man since attaining age 18 - Have not participated in HOLA, HOLA en Grupos, HoMBReS or other Latino Partnership interventions developed and delivered by the Chatham Social Health Council or Wake Forest University during the past 12 months Exclusion Criteria: - Have had sex with at least one woman since attaining age 18 but who have not had sex with at least one man since attaining age 18 |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | Wake Forest University Health Sciences | Winston-Salem | North Carolina |
Lead Sponsor | Collaborator |
---|---|
Centers for Disease Control and Prevention |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Increased self-reported consistent use of condoms during sexual intercourse | 6 months post-intervention | No | |
Secondary | Increased self-reported use of HIV and sexually transmitted disease (STD) counseling, testing, and treatment services | 6 months post-intervention | No |
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