Skip to main content
Clinical Trials/NCT00968188
NCT00968188
Completed
N/A

A Randomized Control Trial of an Internet-based HIV/STI Prevention for Young MSM Receiving HIV Testing.

University of Illinois at Chicago1 site in 1 country102 target enrollmentAugust 2009

Overview

Phase
N/A
Intervention
Not specified
Conditions
HIV
Sponsor
University of Illinois at Chicago
Enrollment
102
Locations
1
Primary Endpoint
Sexual Risk Behavior
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study is to develop an empirically validated, scientifically-based HIV and STI prevention program that can be delivered online to young men who have sex with men (YMSM) who were recently tested for HIV.

Detailed Description

Presently, there are a limited number of proven HIV interventions culturally tailored to young men who have sex with men (YMSM). This is alarming because Men who have sex with men comprise 68% of HIV/AIDS diagnoses in men, despite representing a much smaller proportion of the population. In addition, MSM are reporting more sexual risk behavior than in previous years and there is significant concern that HIV infection rates may once again be on the rise after more than a decade of remaining relatively stable. The Internet is a viable intervention avenue because of it's high percentage of accessibility and usage, especially among young adults. Moreover, it might hold a strong appeal for YMSM, since its anonymity confers a sense of perceived safety against stigma surrounding HIV prevention information. The purpose of this study is to compare two different versions of an online HIV/STI intervention for YMSM. This study is part of an overall program of research designed to understand and prevent HIV infection among high-risk youth. Participation in this study will help us to determine the usefulness of an tailored and interactive HIV Internet-assisted intervention.

Registry
clinicaltrials.gov
Start Date
August 2009
End Date
September 2010
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Brian Mustanski

PhD / Assistant Professor and Director, IMPACT Program, University of Illinois at Chicago

University of Illinois at Chicago

Eligibility Criteria

Inclusion Criteria

  • Between 18 and 24 years of age
  • Self-identify as a biological male
  • Understand and read English
  • Have tested HIV negative at an approved clinic within 6 weeks
  • Report at least one (male) sex partners in the past three months, and unprotected anal sex with at least one male sex partner in the past three months.

Exclusion Criteria

  • Have been diagnosed with HIV within the past three months
  • Participation in another HIV prevention program
  • No access to the Internet or an email address

Outcomes

Primary Outcomes

Sexual Risk Behavior

Time Frame: 3 months

Secondary Outcomes

  • HIV knowledge, Decisional Balance, condom errors, safer sex self-efficacy, intentions(3 months)

Study Sites (1)

Loading locations...

Similar Trials