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Effects of E-cigs vs Pouches on Cigarette Smoking and Addiction

Recruiting

Evaluating The Effects Of E-cigarettes Versus Oral Nicotine Pouches and Product Constituents (Menthol Flavor, Nicotine Concentration) On Adult Cigarette Smoking and Addiction

Who can join

Ages 21 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* 21+ years old
* English literate
* Currently smoking cigarettes, biochemically confirmed

Exclusion Criteria:

* Currently using smoking cessation pharmacotherapies (NRT, bupropion, varenicline)
* Currently pregnant or breastfeeding
* Significant current medical or psychiatric condition
* Known hypersensitivity to propylene glycol

About the study

The study will recruit an anticipated 256 adults who currently smoke cigarettes and report a willingness to try switching to alternative, non-combustible products. Participants will be randomized to receive either e-cigarettes or nicotine pouches for a duration of 4 weeks and to 1 of 4 possible regulatory scenarios within products where flavor availability is either menthol and tobacco/unflavored available or tobacco/unflavored only available, and nicotine concentration is either higher (5% e-cig, 6mg pouch) or lower (2.4% e-cig, 3mg pouch). Participants will return for bi-weekly research visits (in person or remote videocall) to complete measures for study aims. Participants will complete a final follow-up at Week 6 to assess maintenance of cigarette reduction and willingness to continue using products once they are no longer provided. The investigators expect to observe which products and constituents lead to greater smoking reduction.

What is being tested

Sponsor: Yale University · Participants: 256 · Started: Aug 20, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06077240

Locations in the U.S.

ConnecticutYale University, New Haven

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.