Actively Recruiting
Tobacco Education and Lung Health Study (TEAL)
Led by Georgetown University · Updated on 2026-02-17
1188
Participants Needed
1
Research Sites
209 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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). 2) To conduct an economic analysis to evaluate intervention costs from the health system perspective.
CONDITIONS
Official Title
Tobacco Education and Lung Health Study (TEAL)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Eligible for a screening or diagnostic lung cancer scan
- Between 50 and 80 years old and meet USPSTF criteria of over 20 pack-years smoking history
- Currently smoking cigarettes (at least one cigarette in the past 30 days)
- Able to speak English
- Able to provide meaningful consent
You will not qualify if you...
- Prior diagnosis of lung cancer
- Hearing impairment
- Cognitive impairment
- Living in the same household as another enrolled participant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Georgetown University Medical Center
Washington D.C., District of Columbia, United States, 20007
Actively Recruiting
Research Team
K
Kathryn L Taylor, PhD
CONTACT
R
Randi M. Williams, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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