Tobacco Education and Lung Health Study (TEAL)

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.

Trial Details

NCT ID
NCT06290869
Phase
PHASE3
Sponsor
Georgetown University
Status
RECRUITING
Cancer Type
Lung Cancer
Interventions
  • Phone-based Tobacco Treatment, Nicotine Replacement, and Stepped Care Intervention
  • E-Referral to the Tobacco Quitline
Locations (sample)
  • Washington D.C., District of Columbia, United States|38.89511,-77.03637

Key Eligibility 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;

For full eligibility, visit ClinicalTrials.gov.

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