Purpose of the project is to examine the effectiveness of Reinforcement-Based Treatment (RBT) on drug abuse and psychosocial outcomes of iner city opiate abusers who have recently completed a brief detoxification...
Date First Received: May 23, 2008
Last Updated: May 23, 2008
Verified by: National Institute on Drug Abuse (NIDA), May 2008
Clinical Trial Phase: Phase 4 | Start Date: August 2002
Overall Status: Completed
Estimated Enrollment: 463
Brief Summary
Official Title: “Reinforcement-Based Treatment and Abstinence-Contingent Housing for Drug Abusers”
Condition Keyword(s):
Intervention(s):
Purpose of the project is to examine the effectiveness of Reinforcement-Based Treatment (RBT) on drug abuse and psychosocial outcomes of iner city opiate abusers who have recently completed a brief detoxification.
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment
Study Primary Completion Date: February 2007
Detailed Clinical Trial Description
Participants are randomized into one of 3-groups: 1) those receiving intensive behavioral therapy plus abstinence-contingent housing, 2) those receiving recovery housing alone, and 3) those receiving standard care (referrals to community providers). For the two groups receiving recovery housing, rent payment is provided for a period of 3 months, as long as the participant remains drug-free.
Intervention(s) in this Clinical Trial
- Behavioral: Reinforcement-Based Treatment
- 3 group random assignment to receive, standard care, recovery housing alone, or recovery housing plus behavioral treatment
Arms, Groups and Cohorts in this Clinical Trial
- No Intervention: 1
- Standard care following detoxification
- Active Comparator: 2
- Recovery housing following detoxification
- Experimental: 3
- Recovery housing plus counseling
Outcome Measures for this Clinical Trial
Primary Measures
- Drug abstinence at follow-up
- Time Frame: 1, 3 and 6 months
Safety Issue?: No
- Time Frame: 1, 3 and 6 months
Secondary Measures
- Rates of employment
- Time Frame: 1, 3, and 6 months
Safety Issue?: No
- Time Frame: 1, 3, and 6 months
Criteria for Participation in this Clinical Trial
Inclusion Criteria:
- opiate dependent agree to live in recovery housing
Exclusion Criteria:
- acute psychiatric disorder pregnant over 65
Gender Eligibility for this Clinical Trial: Both
Minimum Age for this Clinical Trial: 18 Years
Maximum Age for this Clinical Trial: 65 Years
Are Healthy Volunteers Accepted for this Clinical Trial?: Accepts Healthy Volunteers
Clinical Trial Sponsor Information
Lead Sponsor: National Institute on Drug Abuse (NIDA)
Overall Clinical Trial Officials and Contacts
Maxine Stitzer, Ph.D. Principal Investigator Johns Hopkins
Additional Information
Information obtained from ClinicalTrials.gov on August 29, 2008
Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00685620
Study ID Number: BPR010213-01
ClinicalTrials.gov Identifier: NCT00685620
Health Authority: United States: Federal Government
Clinical Trials Authorship and Review
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.