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Collaborative Injection Drug Users Study III/Drug Users Intervention Trial (CIDUS III/DUIT)
The purpose of this study is to test whether a six-session behavioral intervention for HIV and HCV seronegative injection drug users is effective in reducing sexual and injection risk behaviors that could lead to primary HIV and HCV infection.
CIDUS III/DUIT is a five-city (Baltimore, Chicago, Los Angeles, New York, and Seattle) randomized controlled trial to develop and evaluate the efficacy of a six-session behavioral intervention for HIV and HCV uninfected injection drug users between the ages of 15 and 30 years. The primary goals of the intervention are to: 1. decrease the shared use of syringes and other injection paraphernalia, 2. decrease sexual risk behaviors associated with HIV and HCV infection, and 3. decrease the incidence of hepatitis C virus (HCV) infection. The intervention arm consists of six small-group training and skills-building sessions to teach and reinforce peer education activities around decreasing sex and injection risk behaviors for HIV and HCV infection. In the fifth session, participants practice peer education around sex or injection risk behaviors within their community. The control arm consists of six video and discussion sessions to control for attention. Prior to study enrollment, all participants in both arms receive HIV and HCV testing with client-centered pre- and post-test counseling to also control for the demand for risk reduction information. Behavioral assessments (by audio computer assisted self interviewing) and blood draws (for serologic testing) occur at baseline, 3 and 6 month follow-up. 3285 participants completed the baseline visit, of whom 1564 tested HIV and HCV seronegative and returned for test results making them eligible to enroll in the intervention trial. Of the eligible participants, 854 were randomized into the trial. 606 and 591 returned for 3 and 6 month follow-up assessments, respectively, and 712 participants completed at least one follow-up visit.
Age
15 - 30 years
Sex
ALL
Healthy Volunteers
Yes
Health Research Association
Los Angeles, California, United States
University of Illinois at Chicago
Chicago, Illinois, United States
Johns Hopkins University
Baltimore, Maryland, United States
New York Academy of Medicine
New York, New York, United States
Public Health Seattle and King County
Seattle, Washington, United States
Start Date
May 1, 2002
Primary Completion Date
December 1, 2006
Completion Date
December 1, 2006
Last Updated
September 27, 2012
1,400
Estimated participants
Peer Education Intervention
BEHAVIORAL
Lead Sponsor
Centers for Disease Control and Prevention
NCT04142047
NCT06694805
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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