Clinical Trials Directory

Trials / Completed

CompletedNCT00296647

Smoking Cessation Intervention: Effectiveness in Primary Care

Tobacco Dependence: Treatment and Outcomes; Pharmacotherapies: Effectiveness in Primary Care

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
1,346 (actual)
Sponsor
University of Wisconsin, Madison · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The information gathered in this study may help to develop more effective ways to help people quit smoking and stay quit in the future.

Detailed description

Randomized clinical trials may not accurately reflect the public health benefit of tobacco dependence pharmacotherapies when used in real-world clinical settings due to differences in patient selection, motivation, and adherence. To have a positive public health impact, a treatment must be accessible and acceptable to a broad range of smokers and effective under normal use conditions. The proposed project will assess primary care patients willingness to use cessation treatment and will determine the relative effectiveness of five cessation pharmacotherapies. This research builds on a primary care clinic-based recruitment strategy that was highly successful in a previous study. In the proposed research, 1320 primary care patients presenting for a regular outpatient visit will be recruited by medical assistants to participate in a free smoking cessation program and will be randomly assigned to one of five active pharmacotherapies: patch, lozenge, bupropion, patch+lozenge, and bupropion+lozenge (n = 264/condition). Interested participants who pass medical screening will pick up their medications at clinic pharmacies and will receive proactive telephone counseling from the Wisconsin Tobacco Quit Line. Assessment will be limited to preserve the generalizability of the findings, but select individual differences will be assessed pre-quit to validate algorithms (from Project 1: Efficacy) designed to optimize pharmacotherapy selection for smokers based on gender, level of dependence, and other factors. Smoking behavior will be assessed at six months and one year post-quit so that abstinence rates across pharmacotherapy conditions can be compared. The cost of incorporating tobacco dependence treatment into primary care will also be estimated.

Conditions

Interventions

TypeNameDescription
DRUGnicotine patchDecreasing dosages from 21 to 7 mg over 12 week period
DRUGnicotine patchDecreasing dosage from 21 to 7 mg over 12 weeks
DRUGnicotine lozenge4 mg nicotine lozenge: dosage according to package directions for 16 weeks
DRUGbupropiondosage according to prescription directions: 12 weeks
DRUGpatch + lozengedosage of each according to package insert directions (12 weeks patch, 16 weeks lozenge)
DRUGbupropion + lozengedosage of each according to prescription or package insert (12 weeks bupropion, 16 weeks lozenge)

Timeline

Start date
2004-09-01
Primary completion
2009-07-01
Completion
2010-12-01
First posted
2006-02-27
Last updated
2015-10-14
Results posted
2011-11-30

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00296647. Inclusion in this directory is not an endorsement.