- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00164320
Project TEAM: Teaching HIV Prevention in the HIV Clinic
September 9, 2005 updated by: Centers for Disease Control and Prevention
The purpose of this study is to determine if the TEAM prevention intervention delivered by a physician and an HIV-positive counselor is effective.
It is hypothesized that those who receive the intervention will report a higher reduction in risky sex than those who were in the standard-care condition.
Study Overview
Study Type
Interventional
Enrollment
600
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Florida
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Miami, Florida, United States, 33136
- University of Miami School of Medicine
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 1) 18 years or older, 2) HIV-infected, 3) Sexually active, 3)Receiving HIV primary care at participating clinic, 4) Can communicate in English or Spanish, 5) No previous enrollment in the TEAM study or intervention.
Exclusion Criteria:
- 1) Participation in a similar study run by the TEAM PI.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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Self-reported unprotected (without condoms)anal or vaginal sex with HIV-negative or unknown-status persons.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Dogan Eroglu, PhD., Centers for Disease Control and Prevention
- Principal Investigator: Lisa Metsch, PhD., University of Miami
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2004
Study Completion
May 1, 2006
Study Registration Dates
First Submitted
September 9, 2005
First Submitted That Met QC Criteria
September 9, 2005
First Posted (Estimate)
September 14, 2005
Study Record Updates
Last Update Posted (Estimate)
September 14, 2005
Last Update Submitted That Met QC Criteria
September 9, 2005
Last Verified
September 1, 2005
More Information
Terms related to this study
Other Study ID Numbers
- CDC-NCHSTP-3699
- R18/CCR420971-01
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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