Behavioral Counseling for Alcohol Dependent Smokers (Nicotine Patch)
Mood Management Training for Alcohol Dependent Smokers
2 other identifiers
interventional
144
1 country
1
Brief Summary
This study is to evaluate the effectiveness of a mood management intervention on abstinent alcoholic smokers with a history of major depression. The second aim is to determine the effect of smoking treatments on alcohol abstinence and to identify factors associated with smoking and alcohol outcomes (e.g., more days of abstinence). A randomized, two-group design will be used to evaluate the added benefit of mood management compared to a state-of-the-art smoking cessation treatment. Treatment will consist of 8 weekly group sessions and 1, 3, 6, and 12-month follow-up.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_4
Started Feb 1999
Longer than P75 for phase_4
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 1999
CompletedFirst Submitted
Initial submission to the registry
February 3, 2000
CompletedFirst Posted
Study publicly available on registry
February 4, 2000
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2003
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2003
CompletedSeptember 29, 2010
September 1, 2010
3.9 years
February 3, 2000
September 28, 2010
Conditions
Interventions
Eligibility Criteria
You may qualify if:
- Meets criteria for alcohol dependence.
- Currently abstinent from alcohol and other drugs for at least 3 months.
- Meets criteria for history of major depression independent of alcohol use.
- Smoked an average of 10 or more cigarettes per day during the past month.
- Able to fully participate in all aspects of the study.
- Willing to participate in eight 2-hour treatment sessions and 12 months of followup.
- Willing to stop smoking and wear a nicotine patch for six consecutive weeks and refrain from participating in additional smoking interventions for the duration of treatment.
You may not qualify if:
- Current episode of major depression (within the last 3 months) or current or lifetime history of bipolar disorder, schizophrenia or other major psychiatric disorders.
- Current use of antidepressant, other psychotropic medications, smokeless tobacco, nicotine replacement or other smoking cessation therapy.
- Any medical condition that would preclude use of the nicotine patch including current unstable angina, recent history (within 1 month) of myocardial infarction or stroke, history of severe skin allergies or evidence of severe chronic dermatoses.
- Currently pregnant, breast feeding or likely to become pregnant during the nicotine patch phase of the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Internal Medicine, Mayo Foundation
Rochester, Minnesota, 55905, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Christ A. Patten, PhD
Mayo Clinic
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
February 3, 2000
First Posted
February 4, 2000
Study Start
February 1, 1999
Primary Completion
January 1, 2003
Study Completion
January 1, 2003
Last Updated
September 29, 2010
Record last verified: 2010-09