Yale University
New Haven, Connecticut, 06511, United States
NCT Number: NCT04172623
This study will use wearable technology to test the feasibility and efficacy of delivering a novel real-time smoking intervention to improve standard tobacco treatment.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
New Haven, Connecticut, 06511, United States
The goals of this project include evaluating the feasibility, acceptability, and helpfulness of the real-time smoking intervention and to assess the preliminary efficacy of the real-time intervention as an adjunct to standard tobacco treatment. Rates of adherence, participant satisfaction, and perceived usefulness will be evaluated through post-treatment interviews and ratings. Biochemically confirmed 7-day point prevalence abstinence will be compared between the experimental and control groups at the end of treatment (week 8).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Adult smokers will use wearable technology in order to receive real-time feedback as a smoking intervention in addition to standard treatment.
Adult smokers will receive standard outpatient tobacco treatment.
Time frame: Baseline and Week 8
Self-reported cigarette use (Timeline follow-back data) during the 8-week study to estimate effect sizes between groups.
Time frame: Week 8
Timeline follow-back data will be collected to determine the % of days abstinent from cigarettes.
Yale University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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