- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00000444
Timing of Smoking Intervention in Alcohol Treatment (Nicotine Patch)
February 10, 2011 updated by: Minneapolis Veterans Affairs Medical Center
Timing of Smoking Intervention in Alcohol Treatment
This study will attempt to determine the best time to begin a smoking cessation program in individuals who undergo intensive treatment for alcohol dependence.
The goal of this trial is to determine whether a smoking cessation program is more effective if it occurs at the same time as or after treatment for alcohol dependence.
The study also will attempt to determine the effect of smoking cessation programs on the outcome of treatment for alcohol dependence.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment
500
Phase
- Phase 4
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Minnesota
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Minneapolis, Minnesota, United States, 55417
- General Internal Medicine, VA Medical Center
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Meets criteria for alcohol use disorder and other drug dependence.
- Complete first week of alcohol treatment program.
- Current cigarette smoker (more than 5 cigarettes/day, smoking more than 1 year).
Exclusion Criteria:
- Lifetime diagnosis of an excluding psychiatric disorder: bipolar disorder, schizophrenia or other psychotic disorder, panic disorder with or without agoraphobia, obsessive-compulsive disorder, generalized anxiety disorder, eating disorder, post- traumatic stress disorder, antisocial personality disorder, or borderline personality disorder.
- Unable to participate in protocol due to functional deficits or severe depression.
- Suicidal or homicidal ideation.
- Current use of disulfiram (Antabuse) or naltrexone (Revia).
- Current use of pipes, cigars, or smokeless tobacco and unwillingness to stop.
- Lives more than 100 miles from alcohol treatment facility.
- No telephone.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Masking: None (Open Label)
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 1997
Primary Completion (Actual)
January 1, 2004
Study Completion (Actual)
January 1, 2004
Study Registration Dates
First Submitted
November 2, 1999
First Submitted That Met QC Criteria
November 2, 1999
First Posted (Estimate)
November 3, 1999
Study Record Updates
Last Update Posted (Estimate)
February 11, 2011
Last Update Submitted That Met QC Criteria
February 10, 2011
Last Verified
January 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Mental Disorders
- Chemically-Induced Disorders
- Alcohol-Related Disorders
- Substance-Related Disorders
- Alcoholism
- Physiological Effects of Drugs
- Neurotransmitter Agents
- Molecular Mechanisms of Pharmacological Action
- Autonomic Agents
- Peripheral Nervous System Agents
- Cholinergic Agents
- Ganglionic Stimulants
- Nicotinic Agonists
- Cholinergic Agonists
- Nicotine
Other Study ID Numbers
- NIAAAJOS11124
- R01AA011124 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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Virginia Polytechnic Institute and State UniversityCompletedCigarette Smoking Behavior | Smoking Behaviors | CigaretteUnited States
Clinical Trials on nicotine replacement patch
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Duke UniversityNational Institute on Drug Abuse (NIDA)Recruiting
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Ottawa Heart Institute Research CorporationSun Life Assurance Company of Canada; Vita Aid Professional Therapeutics; Pillway...Recruiting
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State University of New York at BuffaloMedical University of South Carolina; University of Pennsylvania; University... and other collaboratorsRecruitingRemote Visits | In-person Visits | Remote vs. In-PersonUnited States
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Wake Forest University Health SciencesNational Cancer Institute (NCI)CompletedBreast Cancer | Colorectal Cancer | Tobacco Use Disorder | Lung Cancer | Prostate CancerUnited States
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Chiao-Chiao LiaoRecruitingMental Disorders | Anxiety | Tobacco Use Disorder | Nicotine Dependence | Nicotine WithdrawalTaiwan
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University of Kansas Medical CenterPatient-Centered Outcomes Research InstituteCompletedSmoking | Pulmonary Disease, Chronic Obstructive | Tobacco Use DisorderUnited States
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Centre for Addiction and Mental HealthCanadian Cancer Society (CCS)RecruitingSmoking Cessation | Tobacco Smoking | Substance Use Disorders | Nicotine Dependence | Nicotine Use DisorderCanada
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The University of Texas Health Science Center,...RecruitingObesity | Overweight | Cigarette SmokingUnited States
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Ohio State University Comprehensive Cancer CenterNational Cancer Institute (NCI)RecruitingCigarette Smoking-Related CarcinomaUnited States