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). 2) To conduct an economic analysis to evaluate intervention costs from the health system perspective.
Eligibility criteria
Qualifiers
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;
Disqualifiers
prior lung cancer,
hearing impairment,
cognitive impairment,
household member already enrolled.
Trial design
Treatments tested in this trial
- Phone-based Tobacco Treatment, Nicotine Replacement, and Stepped Care Intervention
- E-Referral to the Tobacco Quitline