A Naturalistic Study of Adolescents and Young Adults in Treatment for Opioid Dependence
NCT ID: NCT02718352
Last Updated: 2018-06-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
8 participants
OBSERVATIONAL
2016-03-31
2018-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Interventions
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Naturalistic Prospective Cohort
Follow subjects through 1 year of naturalistic buprenorphine treatment
Eligibility Criteria
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Inclusion Criteria
* Meet criteria for enrollment in the APT Adolescent and Young Adult Suboxone Program (Opioid Dependence per DSM-V criteria; no contraindications to buprenorphine (concomitant benzodiazepine, alcohol use, sedative use),
* Stable enough to participate in outpatient care/intensive outpatient care for at least 12 weeks;
* Can commit to at least 12 weeks of treatment through the APT Adolescent and Young Adult Suboxone Program
* Are willing to provide locator information for follow-up.
* Are fluent in English and have a 6th grader or higher reading level
Exclusion Criteria
* Are physically dependent on alcohol, benzodiazepines, or other sedatives.
* Are in custody of the Department of Children and Families
16 Years
25 Years
ALL
No
Sponsors
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Yale University
OTHER
Responsible Party
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Principal Investigators
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Deepa Camenga, MD
Role: PRINCIPAL_INVESTIGATOR
Yale University
Locations
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APT Foundation
New Haven, Connecticut, United States
Countries
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Other Identifiers
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16010 17074
Identifier Type: -
Identifier Source: org_study_id
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