- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00408161
Contingency Management for Chronic Recidivist Alcohol-Dependent Patients
April 5, 2019 updated by: UConn Health
The purpose of this study is to evaluate the efficacy of prize contingency management (CM) in reducing in-patient detoxification services for chronic recidivist alcohol-dependent patients.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study evaluates the efficacy of prize contingency management (CM) in reducing in-patient detoxification services for chronic recidivist alcohol-dependent patients.
116 alcohol-dependent patients who have received 4 or more alcohol detoxifications in a calendar year will be randomly assigned to one of two 6-month treatment conditions: standard case management treatment, or standard case management treatment plus CM.
In the CM condition, patients earn the chance to win prizes by submitting negative breath samples and by complying with steps toward treatment goals, such as attending outpatient substance abuse treatment services, attending appointments with low income housing programs, or complying with outpatient psychiatric treatment.
Treatment services received, alcohol and drug use, psychosocial functioning, and HIV risk behaviors will be measured pre-treatment and at months 1, 3, and 6 (post-treatment), and at follow-ups scheduled for 9, 12, and 18 months after intake.
Study Type
Interventional
Enrollment (Actual)
104
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Connecticut
-
Farmington, Connecticut, United States, 06030
- University of Connecticut Health Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- age 18 years or older
- Four or more inpatient alcohol detoxifications in the previous 12 months
- current diagnosis of DSM-IV alcohol dependence
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: 1
prize contingency management (CM) plus standard case management treatment -- patients earn the chance to win prizes by submitting negative breath samples and by complying with steps toward treatment goals
|
prize contingency management (CM) -- 6-month treatment plus standard case management treatment and follow-ups at 9, 12, and 18 months after intake
Other Names:
|
Active Comparator: 2
standard case management treatment
|
6-month treatment standard case management treatment, and follow-ups scheduled at 9, 12, and 18 months after intake.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
number of detoxifications
Time Frame: 9, 12, and 18 months after intake
|
9, 12, and 18 months after intake
|
objective alcohol use
Time Frame: 9, 12, and 18 months after intake
|
9, 12, and 18 months after intake
|
self-reported alcohol use
Time Frame: 9, 12, and 18 months after intake
|
9, 12, and 18 months after intake
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
ASI composite scores
Time Frame: 9, 12, and 18 months after intake
|
9, 12, and 18 months after intake
|
BSI scores
Time Frame: 9, 12, and 18 months after intake
|
9, 12, and 18 months after intake
|
HRBS scores
Time Frame: 9, 12, and 18 months after intake
|
9, 12, and 18 months after intake
|
objective drug use
Time Frame: 9, 12, and 18 months after intake
|
9, 12, and 18 months after intake
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2003
Primary Completion (Actual)
September 1, 2008
Study Completion (Actual)
September 1, 2008
Study Registration Dates
First Submitted
December 4, 2006
First Submitted That Met QC Criteria
December 4, 2006
First Posted (Estimate)
December 6, 2006
Study Record Updates
Last Update Posted (Actual)
April 9, 2019
Last Update Submitted That Met QC Criteria
April 5, 2019
Last Verified
April 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NIAAA-PET03510
- NIH Grant P50-AA03510
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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