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HIV Prevention Counseling for Men Who Have Sex With Men

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Behavioral intervention
Risk-reduction counseling
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections focused on measuring Homosexuality, Male, Risk-Taking, Behavior Therapy, HIV Seronegativity

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria Participants may be eligible for this study if they: Are an HIV-negative man who has had anal sex with another man in the 12 months prior to study entry. Are able to attend all scheduled study visits. Are able to provide information for locator purposes (address, phone number, etc.). Are at least 18 years old. Exclusion Criteria Participants will not be eligible for this study if they: Have been in a monogamous relationship for 2 years or more with an HIV-negative man. (Monogamous is defined as a relationship in which the members of the couple engage in sexual activities with only each other.) Have an obvious mental disorder or any another condition that would prevent them from completing the study. Are currently enrolled in any Phase III HIV vaccine trial, including the AIDSVAX Phase III trial sponsored by VaxGen, Inc. Are currently enrolled in HIVNET Protocol 014. Were enrolled in the HIVNET 015 Pilot Study.

Sites / Locations

  • San Francisco Dept of Hlth / AIDS Office
  • Denver Dept of Public Health / HIVNET
  • Howard Brown Health Ctr
  • Fenway Community Health Ctr
  • New York Blood Ctr
  • Univ of Washington

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
September 8, 2008
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT00000931
Brief Title
HIV Prevention Counseling for Men Who Have Sex With Men
Official Title
A Randomized Clinical Trial of the Efficacy of a Behavioral Intervention to Prevent Acquisition of HIV Among Men Who Have Sex With Men
Study Type
Interventional

2. Study Status

Record Verification Date
November 2006
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to see if a behavioral intervention, a special kind of counseling, can reduce the risk of HIV infection in men who have sex with men. The behavioral intervention will be compared to the standard risk reduction counseling that is given before and after getting an HIV test. In standard pre- and post-test counseling, everyone is told the same things about how to prevent HIV. The behavioral intervention used in this study is designed to help each individual prevent HIV according to his specific problems and needs.
Detailed Description
The intervention being evaluated in this trial is based on the extensive literature on behavioral approaches to risk reduction in MSM. These reviews recommend an intervention that, unlike the current standard HIV pre-test and post-test risk-reduction counseling, is tailored to an individual's unique problems and needs, lifestyle, and situations that contribute to high-risk behavior. Furthermore, there is a need for HIV-prevention intervention trials using biological endpoints (e.g., HIV seroconversion) in addition to behavioral change indices. Participants are randomly assigned to receive either the behavioral intervention or the control risk-reduction counseling. The same counseling staff provides the two types of treatment. The behavioral intervention consists of 10 counseling sessions within a 4-month period followed by quarterly maintenance sessions for the remainder of the 3-year follow-up. The intervention is conducted on a one-to-one basis and targets condom use, change in sexual practices associated with HIV risk, and change in sexual practices in the context of alcohol and drug use. Participants in the control group receive pre- and post-test counseling at enrollment, then semiannually through Month 36. Beginning at Month 6, all participants complete routine semiannual visits. At each visit, Risk Assessment and phlebotomy for specimen collection for HIV antibody tests are administered. As is routine in most public counseling and testing venues, participants in the control condition do not see the same counselor consistently.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Homosexuality, Male, Risk-Taking, Behavior Therapy, HIV Seronegativity

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Enrollment
4350 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Behavioral intervention
Intervention Type
Behavioral
Intervention Name(s)
Risk-reduction counseling

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria Participants may be eligible for this study if they: Are an HIV-negative man who has had anal sex with another man in the 12 months prior to study entry. Are able to attend all scheduled study visits. Are able to provide information for locator purposes (address, phone number, etc.). Are at least 18 years old. Exclusion Criteria Participants will not be eligible for this study if they: Have been in a monogamous relationship for 2 years or more with an HIV-negative man. (Monogamous is defined as a relationship in which the members of the couple engage in sexual activities with only each other.) Have an obvious mental disorder or any another condition that would prevent them from completing the study. Are currently enrolled in any Phase III HIV vaccine trial, including the AIDSVAX Phase III trial sponsored by VaxGen, Inc. Are currently enrolled in HIVNET Protocol 014. Were enrolled in the HIVNET 015 Pilot Study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chesney M, Coates T
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Koblin B
Official's Role
Study Chair
Facility Information:
Facility Name
San Francisco Dept of Hlth / AIDS Office
City
San Francisco
State/Province
California
ZIP/Postal Code
94102
Country
United States
Facility Name
Denver Dept of Public Health / HIVNET
City
Denver
State/Province
Colorado
ZIP/Postal Code
80204
Country
United States
Facility Name
Howard Brown Health Ctr
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60613
Country
United States
Facility Name
Fenway Community Health Ctr
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
New York Blood Ctr
City
Bronx
State/Province
New York
ZIP/Postal Code
10456
Country
United States
Facility Name
Univ of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
15234855
Citation
Koblin B, Chesney M, Coates T; EXPLORE Study Team. Effects of a behavioural intervention to reduce acquisition of HIV infection among men who have sex with men: the EXPLORE randomised controlled study. Lancet. 2004 Jul 3-9;364(9428):41-50. doi: 10.1016/S0140-6736(04)16588-4.
Results Reference
result

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HIV Prevention Counseling for Men Who Have Sex With Men

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