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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00732342
Other study ID # 08-053-2
Secondary ID P60AA003510
Status Completed
Phase N/A
First received
Last updated
Start date February 2008
Est. completion date May 2015

Study information

Verified date April 2019
Source UConn Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

310 alcohol abusing or dependent patients beginning intensive outpatient day treatment at community-based clinics will be randomly assigned to one of four conditions: (a) standard treatment as usual (ST) at the clinic without contingency management (CM); (b) standard treatment with contingency management for 12 weeks with a 0.5 probability of winning prizes for each negative sample submitted; (c) standard treatment with contingency management for 24 weeks with a 0.34 probability of winning prizes for each negative sample submitted; or (d) standard treatment with contingency management for 24 weeks with a 0.5 probability of winning prizes for each negative sample submitted. We expect that contingency management will decrease alcohol use to a greater extent than non-contingency management treatment, and that availability of contingency management for 24 weeks may result in longer term benefits than 12 week exposure to contingency management. This study will be the first to evaluate the effects of probability of winning prizes on response to contingency management.


Recruitment information / eligibility

Status Completed
Enrollment 310
Est. completion date May 2015
Est. primary completion date May 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age > 18 years

- current DSM-IV diagnosis of alcohol abuse or dependence

- willing to sign informed consent and able to pass an informed consent quiz

Exclusion Criteria:

- serious, uncontrolled psychiatric illness (e.g., acute schizophrenia, bipolar disorder, severe or psychotic major depression, or suicide risk) on the basis of history or medical examination

- current DSM-IV diagnosis of opioid dependence

- in recovery from pathological gambling

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Contingency Management
Prizes given for targeted behavior of abstinence

Locations

Country Name City State
United States 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 Carlson Recovery Center Springfield Massachusetts
United States Morris Foundation Waterbury Connecticut

Sponsors (2)

Lead Sponsor Collaborator
UConn Health National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary longest duration of negative breath samples submitted active phase and throughout follow-up phase
Secondary subjective reports of alcohol use baseline and each follow-up
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