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| Sponsor: | Yale University |
|---|---|
| Collaborator: |
National Institute on Alcohol Abuse and Alcoholism (NIAAA) |
| Information provided by (Responsible Party): | Ned Cooney, Yale University |
| ClinicalTrials.gov Identifier: | NCT00861146 |
Purpose
The majority of individuals with alcohol problems remain current smokers, and the negative health consequences of smoking among these individuals are substantial. This study will investigate the impact of smoking cessation interventions initiated during intensive alcohol treatment on processes reflecting risk of alcohol relapse.
| Condition | Intervention | Phase |
|---|---|---|
|
Tobacco Use Cessation Alcohol-related Disorders |
Behavioral: behavioral counseling plus contingency management |
Phase II |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Concurrent Alcohol and Smoking Treatment: Effects on Alcohol Relapse Risk |
| Estimated Enrollment: | 144 |
| Study Start Date: | April 2009 |
| Estimated Study Completion Date: | July 2012 |
| Estimated Primary Completion Date: | July 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1 concurrent smoking cessation
smoking cessation delivered concurrent with intensive alcohol treatment
|
Behavioral: behavioral counseling plus contingency management
Individual counseling sessions with voucher rewards for smoking abstinence, transdermal nicotine patch and nicotine gum
|
|
Active Comparator: 2 deferred smoking cessation
smoking cessation delivered 12 weeks after intensive alcohol treatment
|
Behavioral: behavioral counseling plus contingency management
Individual counseling sessions with voucher rewards for smoking abstinence, transdermal nicotine patch and nicotine gum
|
Objectives:
Most alcohol and drug treatment programs do not systematically address cigarette smoking during treatment. One obstacle is a concern that smoking cessation early in recovery might increase risk of alcohol relapse. This study will follow patients enrolled in intensive outpatient alcohol treatment to compare the effects of a Concurrent Smoking Cessation (CSC) intervention to a Deferred Smoking Cessation (DSC) control group on process measures reflecting risk of alcohol relapse.
Research Design:
Participants will be enrolled in intensive outpatient alcohol treatment and then randomized to CSC or DSC groups in a 2:1 ratio. The CSC group will receive smoking treatment concurrent with intensive alcohol treatment and the DSC group will receive smoking treatment three months after alcohol treatment. The smoking treatment protocol will include behavioral counseling, contingency management with voucher rewards for verified smoking abstinence, and prescribed nicotine patch and gum. During a three-month period after the CSC target smoking quit date, both groups of subjects will be asked to participate in a prospective daily monitoring procedure, calling into an Interactive Voice Response system once a day to complete self-report assessments of relapse risk factors. By comparing participants in the CSC group composed of many participants who have stopped smoking with the DSC group who are expected to continue smoking during this daily monitoring period, we will determine the impact of smoking cessation on alcohol relapse risk factors.
This study will be conducted in the substance abuse day treatment programs located at Newington and West Haven campuses of VA Connecticut Healthcare System. These are three-week treatment programs meeting Monday-Friday for 4-5 hrs/day. Participants may be recruited either before or soon after day program admission. Participants will be 144 individuals that are 18 years of age or older, meet DSM-IV diagnostic criteria for current alcohol abuse or dependence, report currently smoking 10 or more cigarettes per day, and are screened for medical contraindications for nicotine patch and gum use. Dependent variables are process assessments reflecting alcohol relapse risk obtained using daily Interactive Voice Response (IVR) technology. These relapse risk processes include alcohol craving, negative affect, alcohol abstinence self efficacy, alcohol outcome expectancies, motivation for alcohol abstinence, and self-control demands. Given the mixed results from previous clinical trials, we will conduct bidirectional tests of the hypothesis that smoking cessation has an impact on alcohol relapse risk factors, examining whether smoking cessation leads to increased or decreased alcohol relapse risk.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Lucienne Levy | 860-667-6748 | lucienne.levy@va.gov |
| Contact: Ned Cooney, PhD | 860-667-6842 | ned.cooney@va.gov |
| United States, Connecticut | |
| VA Connecticut Healthcare System | Recruiting |
| Newington, Connecticut, United States, 06111 | |
| Contact: Lucienne Levy 860-667-6748 | |
| Principal Investigator: Ned Cooney, PhD | |
| VA Connecticut Healthcare System | Recruiting |
| West Haven, Connecticut, United States, 06516 | |
| Contact: Helen Sackler, PhD 203-479-8054 | |
| Sub-Investigator: Helen Sackler, PhD | |
| Principal Investigator: | Ned L Cooney, PhD | Yale University |
More Information
| Responsible Party: | Ned Cooney, Associate Professor, Yale University |
| ClinicalTrials.gov Identifier: | NCT00861146 History of Changes |
| Other Study ID Numbers: | NIAAA-Cooney-AA011197, R01AA011197, NIH Grant R01AA011197 |
| Study First Received: | March 11, 2009 |
| Last Updated: | January 25, 2012 |
| Health Authority: | United States: Federal Government |
|
nicotine dependence tobacco dependence smoking cessation |
alcoholism self-efficacy relapse |
|
Smoking Alcohol-Related Disorders Habits Substance-Related Disorders Mental Disorders Ethanol Anti-Infective Agents, Local |
Anti-Infective Agents Therapeutic Uses Pharmacologic Actions Central Nervous System Depressants Physiological Effects of Drugs Central Nervous System Agents |