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N/A N=455 Prevention

Evaluating a Structural and Behavioral HIV Risk Reduction Program for Black Men

HIV

Enrolled (actual)
455
Serious AEs
0.0%
Results posted
Dec 2018
Primary outcome: Primary: Condom Use/Unprotected Sex - Redefined as Sexual Risk - 12 Month Follow-up — 28; 18; 26; 40 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
MEN Count (Behavioral); Comparison (Behavioral)
Age
Adult · 18+ yrs
Sex
Male
Sponsor
University of California, San Diego
Primary completion
Apr 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Condom Use/Unprotected Sex - Redefined as Sexual Risk - 12 Month Follow-up
28; 18; 26; 40; 30; 34
PRIMARY
Condom Use/Unprotected Sex - Redefined as Sexual Risk - 6 Month Follow-up
15; 18; 32; 29; 25; 28
SECONDARY
Non-viral STI - 12 Month Follow-up
17; 15; 87; 98; 16; 10
SECONDARY
Non-viral STI - 6 Month Follow-up
7; 13; 83; 85; 5; 7

Summary

The purpose of this study is to evaluate the effectiveness of the Making Employment Needs (MEN) Count intervention, an HIV intervention and prevention program for heterosexual Black men. The MEN Count model integrates HIV risk reduction and gender-equity counseling with housing and employment case management via multiple one-on-one sessions delivered by a peer case manager over 60-90 day period. MEN Count was developed and pilot tested using a Community-based participatory research (CBPR) approach via funding from a National Institutes of Health (NIH) R21, in Boston, Massachusetts. A more larger scale, two-armed quasi-experimental controlled trial design will be used to test MEN Count among Black men recruited/enrolled from an STD clinic and other community-recruitment methods in Washington, DC. Study participants (N=504) will be Black men reporting heterosexual risk for HIV [unprotected sex with a woman and 2+ female sex partners in the past 6 months] and either current unemployment or homeless in the past 6 months. To evaluate the effectiveness of MEN Count, a two-armed quasi-experimental design will be conducted in which participants will receive either MEN Count or an attention comparison program similar to MEN Count in structure. We will assess program impact on reduction in number of unprotected sex episodes and incident cases of STI (Chlamydia, gonorrhea, syphilis) via survey and STI testing, respectively, at baseline and 6 and 12 month follow-ups. Additionally, quality assurance and process evaluation efforts will be conducted to ensure high quality program adherence and delivery, as well as to support program replication should the model prove effective.

Eligibility Criteria

Inclusion Criteria: Black men aged 18 and older, reporting heterosexual risk for HIV [unprotected sex with a woman and 2+ female sex partners in the past 6 months] and either current unemployment or homeless in the past 6 months. Exclusion Criteria: planned to leave Washington D.C., Maryland, or Virginia in the next 6 months, were cognitively impaired (based on Folstein Mini-Mental Exam at recruitment or baseline testing), and/or had self-reported health status that prohibited them from participating in the program
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01694121). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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