- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03278496
Recovery Housing and Drug Abuse Treatment Outcome
Study Overview
Status
Intervention / Treatment
Detailed Description
Aims To conduct a randomized, controlled trial of abstinence-contingent recovery housing delivered with or without intensive day treatment among individuals exiting residential opioid detoxification.
Design Random assignment to one of three conditions: recovery housing alone (RH), abstinence-contingent recovery housing with reinforcement-based treatment RBT (RH + RBT) or usual care (UC). RH and RH + RBT participants received 12 weeks of paid recovery housing contingent upon drug abstinence. RH + RBT participants also received 26 weeks of RBT, initiated concurrently with recovery housing. Assessments were conducted at 1, 3 and 6 months after treatment enrollment.
Setting Out-patient drug-free substance abuse treatment program in Baltimore, Maryland.
Participants Patients (n = 243) who completed medication-assisted opioid detoxification.
Measurements Primary outcome was drug abstinence (opioid- and cocaine-negative urine and no self-reported opioid or cocaine use in the previous 30 days). Secondary outcomes included abstinence at all time-points (1, 3 and 6 months), days in recovery housing and employment.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Maryland
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Baltimore, Maryland, United States, 21224
- Behavioral Pharmacology Research Unit
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- completes residential detoxification for use of opiates and/or cocaine
- willing to go to outpatient aftercare
- agrees to random assignment; signs informed consent
Exclusion Criteria:
- moving out of town
- primary substance use does not include opiates or cocaine
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Recovery housing plus counseling
Intensive counseling in a 5-day per week program plus abstinence-contingent rent payment in a community recovery house.
Intervention lasts 12 weeks with follow-up at 12 and 24 weeks post treatment entry.
|
Participants receive 3 months of abstinence-contingent program-supported rent payment in community recovery housing.
They also receive intensive outpatient counseling (both individual and group) focused on relapse prevention skills training, goal setting, employment seeking and recreational activities.
|
|
Experimental: Recovery Housing only
Abstinence-contingent payment for recovery housing rent in absence of any formal counseling.
Intervention lasts 12 weeks with follow-up at 12 and 24 weeks post treatment entry.
|
Participant may receive up to 3 months of abstinence-contingent rent payment in community recovery housing but is not invited to participate in intensive counseling.
|
|
Active Comparator: Usual Care Referral
Participants receive referral resources for community substance abuse counseling and recovery housing but no formal treatment or help with rent payments.
All participate in follow-up data collection.
|
Participants are referred to an outpatient program of their choosing with an appointment made for them.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
abstinence from opiates and cocaine
Time Frame: 6 months post randomization
|
Free in the community plus self report of no drug use in past 30 days verified with negative urine screen.
|
6 months post randomization
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Maxine Stitzer, Ph.D., Johns Hopkins University
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DA13003
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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