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Improving Smoking Abstinence Outcomes in the African American Community Through Extended Treatment — (KISV)  

Smoking Cessation Clinical Trial

Official title:
Improving Smoking Abstinence Outcomes in the African American Community Through Extended Treatment

Clinical Trial Summary

This study will evaluate the efficacy of extended bupropion(6 months) versus standard bupropion treatment (7 weeks) among African American daily smokers.

Clinical Trial Description

The primary objective of this study is to evaluate extended use of bupropion with the goal of enhancing abstinence in African American daily smokers, including the full spectrum of light, moderate, and heavy smokers. A two-arm, randomized design will be used to evaluate the efficacy of extended (6 months) bupropion treatment compared to standard (7 weeks) bupropion treatment. Baseline randomization stratified by gender and cpd (≤10, >10cpd) will assign participants (N=500) to receive extended treatment (EXT; 24 weeks of bupropion, n=250) or standard treatment (ST; 7 weeks of bupropion, n=250). All participants will receive culturally-relevant, individualized smoking cessation counseling, including support for medication adherence, and will be followed through Month 12. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05732272
Study type Interventional
Source University of Kansas Medical Center
Contact Tricia Snow, MPH
Phone 816-398-8960
Email psnow@kumc.edu
Status Recruiting
Phase Phase 3
Start date February 28, 2023
Completion date July 30, 2026
View Details
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