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
NA
310 participants
INTERVENTIONAL
2008-02-29
2015-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
FACTORIAL
TREATMENT
NONE
Study Groups
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1
Standard Treatment
No interventions assigned to this group
2
Standard Treatment with Contingency Management for 12 weeks with a 0.5 probability of winning prizes for each negative sample submitted
Contingency Management
Prizes given for targeted behavior of abstinence
3
Standard Treatment with Contingency Management for 24 weeks with a 0.34 probability of winning prizes for each negative sample submitted
Contingency Management
Prizes given for targeted behavior of abstinence
4
Standard Treatment with Contingency Management for 24 weeks with a 0.5 probability of winning prizes for each negative sample submitted
Contingency Management
Prizes given for targeted behavior of abstinence
Interventions
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Contingency Management
Prizes given for targeted behavior of abstinence
Eligibility Criteria
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Inclusion Criteria
* current DSM-IV diagnosis of alcohol abuse or dependence
* willing to sign informed consent and able to pass an informed consent quiz
Exclusion Criteria
* current DSM-IV diagnosis of opioid dependence
* in recovery from pathological gambling
18 Years
ALL
No
Sponsors
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National Institute on Alcohol Abuse and Alcoholism (NIAAA)
NIH
UConn Health
OTHER
Responsible Party
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Principal Investigators
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Nancy M Petry, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
UConn Health
Locations
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Prospect House
Bridgeport, Connecticut, United States
Alcohol and Drug Recovery Centers, Inc.
Hartford, Connecticut, United States
The Hospital of Central Connecticut at New Britain General
New Britain, Connecticut, United States
Morris Foundation
Waterbury, Connecticut, United States
Carlson Recovery Center
Springfield, Massachusetts, United States
Countries
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Other Identifiers
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08-053-2
Identifier Type: -
Identifier Source: org_study_id
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