drugset / Trial / NCT06822049

Summary

The study will employ a randomized, parallel-group design with two-stage randomization. After an initial brief screen for basic eligibility, participants will be randomized (within site) to either Remote (R) or In-Person (IP) Intake Groups. During the Intake, detailed consent and eligibility assessment will be completed. Participants who are eligible at the Intake will be randomized (within site and Intake Group) to R or IP Treatment and Assessment Groups. Participants will be followed for 3 months.

Timeline

Start
2025-03-10
Primary completion
2026-07-31
Completion
2027-02-28

Drugs

EvaluationDrugModalityDoseRoute
Background Nicotine Unknown Oral

Indications

No indication recorded.