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Clinical Trial Summary

This project will address research gaps and advance the science of smoking cessation by conducting a randomized controlled trial of an evidence-based, population-level quit smoking text messaging program with or without a smartband.


Clinical Trial Description

Aim 1 of this study is to test within-treatment effects for smoking cessation. The primary outcome will be biochemically (cotinine)-confirmed 7-day point-prevalence abstinence (PPA) at end of treatment (8 weeks). Secondary outcomes will be percent days smoke-free, time to relapse, and rated treatment satisfaction. Aim 2 of this study is to explore sex/gender differences in treatment effects for smoking cessation. Given established sex/gender differences in smoking behavior and cessation,randomization will be stratified by sex/gender and we will measure effects of sex/gender on outcomes. Effect sizes will be estimated for smoking outcomes by sex. Outcomes will be evaluated for those who complete enrollment, defined as those who complete study onboarding. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06111755
Study type Interventional
Source Yale University
Contact Kathleen A Garrison, PhD
Phone 203-737-6232
Email kathleen.garrison@yale.edu
Status Recruiting
Phase N/A
Start date March 26, 2024
Completion date February 2025

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