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Clinical Trial Summary

The main goal of this study is to pilot test the community-based buprenorphine treatment (CBBT) intervention, examining buprenorphine treatment initiation, opioid use, and HIV risk behaviors. Two groups of participants will be followed for 60 days, with 3 research visits. One group will be enrolled prior to the CBBT intervention (pre-intervention), and one group after the CBBT intervention (post-intervention). Data sources will include questionnaires, urine toxicology tests, and medical record data. Investigators hypothesize that compared to the participants in the pre-intervention group, participants in the post-intervention group will be more likely to initiate buprenorphine treatment, reduce opioid use, and reduce high-risk HIV risk behaviors.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01761110
Study type Interventional
Source Albert Einstein College of Medicine, Inc.
Contact
Status Completed
Phase N/A
Start date December 2012
Completion date February 2014

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