Prevention of HIV Infection in High-Risk Social Networks of African American Men Who Have Sex With Men (MSM)

Not Applicable

Completed

• Conditions: HIV
• Interventions: Behavioral: Counsel, Test, and Treat; Behavioral: Social Network Intervention

• Registration Number: NCT01825252
• Lead Sponsor: Medical College of Wisconsin

Brief Summary

During the formative research phase, investigators will undertake formative studies to locate, understand, and characterize high-risk social networks of African American MSM in the community; gain community participation, involvement, and input; and undertake interviews with key informants and community members to gain information needed to pilot test study recruitment procedures, measures, and intervention content.

During a 4-year main outcome trial phase, the investigators will enroll 24 separate sociocentric ("bounded") social networks composed predominantly of Black MSM. Each sociocentric network will consist of the ring of friends surrounding an initial high-risk index as well as all friends surrounding persons in this second ring and then friends surrounding a successive third snowball ring of enrollees. Each 3-ring sociocentric network is expected to consist of approximately 40 unique members (n=24 networks, each with 40 members = approximately 960 individual participants).

All participants will be assessed at baseline to measure sexual practices, substance use, and other risk characteristics over the past 3 months; asked to provide biological specimens to be tested for HIV and other sexually transmitted diseases (STDs); and counseled in HIV/STD risk reduction. STDs will be treated and those with HIV will be referred for treatment.

The investigators will identify the individuals in intervention condition networks with the greatest number of reciprocal interconnections and the most favorable sociometric standing in the network. These individuals--expected to constitute approximately 20% of the sociocentric network and designated as network leaders--will be recruited to attend a 9-session program that provides training and guidance in how to deliver on-going, theoretically-based, and culturally tailored risk reduction advice and counseling to other members within the same network.

Six and 18 months following the intervention, all participants will be reassessed on risk behavior and STD/HIV laboratory measures as well as measures of intervention exposure, with positive STD and HIV cases respectively treated or referred to care at each assessment point. Outcome analyses will test whether there is greater reduction in high-risk sexual practices, substance use associated with risky sex, and HIV/STD incidence within social networks in the intervention condition. The primary trial endpoints are reductions in prevalence and frequency of unprotected anal intercourse with nonexclusive partners, increased condom use, and lower incidence on a composite biological measure of new HIV/STD disease during the followup period.

Detailed Description

Not available

Study Timeline

• Study Start: 2011-08
• Study First Submitted: 2013-04-02
• Study First Submitted QC: 2013-04-04
• Study First Posted: 2013-04-05
• Primary Completion: 2016-07
• Study Completion: 2017-12
• Status Verified: 2018-02
• Last Update Submitted: 2018-02-13
• Last Update Posted: 2018-02-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 856

Inclusion Criteria

• are age 18 or older;
• except for the initial index, were named as part of a friendship circle of an already-enrolled participant;
• provide written informed consent and do not exhibit intoxication, drug use,or psychiatric impairment that leads the research staff member to question capacity to provide informed consent;
• can complete study measures and participate in study activities in English;
• reside in or near the study city and do not have definite plans to leave the area in the next 12 months.

Exclusion Criteria

• are age 17 or younger;
• exhibit intoxication, drug use, or psychiatric impairment such that they are unable to provide written informed consent;
• cannot complete study measures or adequately comprehend study activities conducted in English; or
• live in a location distant from the study city.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Counsel, Test, and Treat	Counsel, Test, and Treat	People in this arm will only receive standard-of-care counseling, testing, and treatment for HIV and STDs.
Social Network Intervention	Social Network Intervention	Approximately 20% of people in this condition will be trained to have discussions endorsing less risky behaviors with their social network members.

Primary Outcome Measures

Name	Time	Method
Reduction of unprotected anal intercourse with nonexclusive partners	24 months	We will compare the prevalence and frequency of unprotected anal intercourse with nonexclusive partners pre- and post-intervention.
Condom use	24 months	We will measure rates of condom pre- and post-intervention
HIV/STD incidence rates	24 months	We will compare HIV/STD incidence rates pre- and post-intervention

Trial Locations

Locations (2)

Medical College of Wisconsin; 🇺🇸 Milwaukee, Wisconsin, United States

AIDS TaskForce of Greater Cleveland; 🇺🇸 Cleveland, Ohio, United States