Tobacco Education and Lung Health Study (TEAL)

Recruiting Phase 3 Interventional Study
Smoking Cessation
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
50 – 80
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
1,188 (estimated)
Sponsor
Georgetown University · Other
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About This Trial
Primary Objective To compare two smoking cessation interventions among individuals undergoing lung cancer screening. Primary outcomes are: 3-month self-reported abstinence from cigarettes and 6-month self-reported and bioverified abstinence from cigarettes. Secondary Objectives 1) To evaluate reach and engagement overall and by subgroup (e.g., race and ethnicity, underinsured, readiness to quit).…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * eligible for a screening or diagnostic scan, * USPSTF eligibility criteria (50-80 years old and \>20-pack years); * currently smoking cigarettes (\>1 in the past 30 days); * English speaking; * able to provide meaningful consent. Exclusion Criteria: * prior lung cancer, * he…
Contacts

Kathryn L Taylor, PhD

2022159402

taylorkl@georgetown.edu

CONTACT

Randi M. Williams, PhD

rmw27@georgetown.edu

CONTACT