My Path to Quit Tobacco
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- University of Wisconsin, Madison
- Study ID
- NCT07419425
- Phase
- PHASE4
- Status
- Recruiting
Conditions
- Smoking Cessation
Eligibility Criteria
- Sex
- ALL
- Age
- 21 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Nicotine patch — DRUGPatch dosing will be consistent with the package insert
- Quitline Counseling Phone Calls — OTHER4, 10 to 15-minute counseling sessions (the duration of a typical quitline call) will occur via phone one week prior to the TQD, 1 day after the TQD, and 1 and 2 weeks after the TQD.
- Counseling Sessions — OTHERParticipants will have the option of choosing 8, 30-minute counseling phone calls or 8, 60-minute video group counseling sessions
- Pathways to Freedom — OTHERPathways to Freedom video content, a 60-minute video that addresses key issues such as emotional dependence, nicotine replacement, identifying smoking triggers, developing coping skills, and other behavioral strategies people can use to support a quit attempt.
- Monetary Incentive — OTHERup to $50 for completing counseling sessions ($5 for completing sessions 1-6 and $10 for completing sessions 7 and 8)
Study Details
The overarching goal of this program of research is to reduce smoking-related health disparities by increasing smoking cessation among Black adults. The goal of this research proposal is to determine whether more intensive, culturally specific, evidence-based interventions are more effective at promoting long-term cessation and other key patient-centered outcomes compared to the usual evidence-based standard of care: services provided by a state-run quitline. This study compares the relative effectiveness of three different treatments (Standard, Intensive, and Intensive Incentivized) on long-term smoking cessation (biochemically confirmed abstinence from combusted tobacco at 26-weeks post-target quit day) among Black adults who smoke and want to quit.
Key Dates
- First listed
- Feb 19, 2026
- Start date
- Jul 6, 2026
- Status verified
- May 2026
- Primary completion
- Jan 31, 2030
- Completion
- Jan 31, 2030
Study Design
- Enrollment
- 1,550 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: Standard InterventionThe Standard Intervention will include 2 weeks of nicotine patches + 4 quitline-style counseling phone calls.
- Experimental: Intensive InterventionThe Intensive Intervention will include 8 weeks of nicotine patches (if eligible) + 8 counseling sessions (choice of individual phone or virtual group) + the Pathways to Freedom video content on the study website with additional smoking cessation content.
- Experimental: Intensive Incentivized InterventionThe Intensive Incentivized Intervention will include all components provided in the Intensive intervention (8 weeks of nicotine patches (if eligible) + 8 counseling sessions (choice of individual phone or virtual group) + the Pathways to Freedom video content on the study website with additional smoking cessation content) and up to $50 for completing counseling sessions ($5 for completing sessions 1-6 and $10 for completing sessions 7 and 8)
Primary Outcome Measure
Biochemically confirmed abstinence from combusted tobacco at 26-weeks post-target quit day [ Time Frame: 26 weeks post-TQD ]
Central Contacts
- Megan Piper, PhD608-265-5472
Locations (5)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Arizona State University | Phoenix | Arizona | 85004 | - |
| Indiana University | Indianapolis | Indiana | 46202 | - |
| University of Kansas Medical Center Research Institute, Inc | Kansas City | Kansas | 66160 | - |
| Virginia Commonwealth University | Richmond | Virginia | 23298 | - |
| UW School of Medicine and Public Health | Milwaukee | Wisconsin | 53233 | - |
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