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Contingency Management for Smoking Cessation in Adolescent Smokers - Phase IV, Enhancing a High School Based Smoking Cessation Program

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City:   New Haven
State:   Connecticut
Zip Code:   06519
Conditions:   Nicotine Dependence
Purpose:   The purpose of this study is to examine the the efficacy of adjunctive nicotine replacement therapy when used in combination with the contingency management (CM) + cognitive behavioral therapy intervention. Subjects will be randomly assigned to receive either a nicotine transdermal patch or a placebo patch as well as being randomly assigned to receive either CM or no CM; all subjects will receive cognitive behavioral therapy. We hypothesize that that subjects receiving both active nicotine patch and CM will have higher rates of abstinence from tobacco than subjects in the other groups.
Study Summary:  
Criteria:   Inclusion Criteria: - High School aged - Desire to quit smoking - Smoking >5 cigarettes per day - Able to read and write in English Exclusion Criteria: - Current dependence on other substances - Medical conditions that would contraindicate the use of a nicotine patch
NCT ID:   NCT01145001
Primary Contact:   Principal Investigator
Suchitra Krishnan-Sarin, Ph.D.
Yale University

Dana Cavallo, Ph.D.
Phone: 203-974-7607
Email: dana.cavallo@yale.edu
Backup Contact:   Email: thomas.liss@yale.edu
Thomas Liss, BS
Phone: 203-974-7555
Location Contact:   New Haven, Connecticut 06519
United States

Tom Liss, BS
Phone: 203-974-7555
Email: thomas.liss@yale.edu

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 20, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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