Opioid Dependence Clinical Trial
Official title:
Development of a Community-based Buprenorphine Treatment Intervention
Verified date | April 2018 |
Source | Albert Einstein College of Medicine, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 77 |
Est. completion date | February 2014 |
Est. primary completion date | February 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - at least 18 years old - English or Spanish fluency - ever injected drugs - not receiving buprenorphine treatment (no prescribed buprenorphine in the previous 6 months) - clients of our collaborating community-based organization - interested in buprenorphine treatment Exclusion Criteria: - pregnant - taking more than 60mg of methadone daily in the previous 30 days |
Country | Name | City | State |
---|---|---|---|
United States | Washington Heights Corner Project | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Albert Einstein College of Medicine, Inc. | National Institute on Drug Abuse (NIDA), The City University of New York, Washington Heights Corner Project |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | HIV risk behaviors | Drug- and sex-related HIV risk behaviors will be assessed using a standardized risk assessment tool used in NIDA's Clinical Trials Network. | 60 days | |
Primary | initiation of buprenorphine treatment | Medical record information will be extracted to determine initiation of buprenorphine treatment, which will be defined as a visit with a medical provider in which buprenorphine is prescribed. | 60 days | |
Secondary | opioid use | Opioid use will be determined via self-report using the Addiction Severity Index and via urine specimens (e.g., urine toxicology testing). | 60 days |
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