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Contingency Management for Chronic Recidivist Alcohol-Dependent Patients

This study is ongoing, but not recruiting participants.

Sponsors and Collaborators: University of Connecticut
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Information provided by: University of Connecticut
ClinicalTrials.gov Identifier: NCT00408161
  Purpose

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.


Condition Intervention Phase
Alcohol Dependence
Behavioral: Contingency Management
Behavioral: standard case management treatment
Phase I
Phase II

MedlinePlus related topics:   Alcoholism   

Drug Information available for:   Ethanol   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title:   Contingency Management for Chronic Recidivist Alcohol-Dependent Patients

Further study details as provided by University of Connecticut:

Primary Outcome Measures:
  • number of detoxifications [ Time Frame: 9, 12, and 18 months after intake ] [ Designated as safety issue: No ]
  • objective alcohol use [ Time Frame: 9, 12, and 18 months after intake ] [ Designated as safety issue: No ]
  • self-reported alcohol use [ Time Frame: 9, 12, and 18 months after intake ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • ASI composite scores [ Time Frame: 9, 12, and 18 months after intake ] [ Designated as safety issue: No ]
  • BSI scores [ Time Frame: 9, 12, and 18 months after intake ] [ Designated as safety issue: No ]
  • HRBS scores [ Time Frame: 9, 12, and 18 months after intake ] [ Designated as safety issue: No ]
  • objective drug use [ Time Frame: 9, 12, and 18 months after intake ] [ Designated as safety issue: No ]

Estimated Enrollment:   116
Study Start Date:   August 2003
Estimated Study Completion Date:   August 2009
Estimated Primary Completion Date:   August 2009 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
1: Active Comparator
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
Behavioral: Contingency Management
prize contingency management (CM) -- 6-month treatment plus standard case management treatment and follow-ups at 9, 12, and 18 months after intake
2: Active Comparator
standard case management treatment
Behavioral: standard case management treatment
6-month treatment standard case management treatment, and follow-ups scheduled at 9, 12, and 18 months after intake.

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.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

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:

-

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00408161

Locations
United States, Connecticut
University of Connecticut Health Center    
      Farmington, Connecticut, United States, 06030

Sponsors and Collaborators

Investigators
Principal Investigator:     Nancy M Petry, PhD     University of Connecticut Health Center    
  More Information


Research Studies at the University of Connecticut Health Center  This link exits the ClinicalTrials.gov site
 

Responsible Party:   UConn Health Center ( Nancy Petry, Ph.D. )
Study ID Numbers:   NIAAA-PET03510, NIH Grant P50-AA03510
First Received:   December 4, 2006
Last Updated:   July 31, 2008
ClinicalTrials.gov Identifier:   NCT00408161
Health Authority:   United States: Federal Government

Keywords provided by University of Connecticut:
Contingency Management  
Alcohol Dependence  

Study placed in the following topic categories:
Mental Disorders
Alcoholism
Substance-Related Disorders
Disorders of Environmental Origin
Alcohol-Related Disorders
Ethanol

ClinicalTrials.gov processed this record on October 22, 2008




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