Influence of Authorized Smokeless Tobacco Product Modified Risk Claims II: Laboratory Assessment of Sensory and Subjective Effects
Part of paid clinical trials in Buffalo, New York.
- Sponsor
- Roswell Park Cancer Institute
- Study ID
- NCT07107139
- Status
- Recruiting
Conditions
- Smokeless Tobacco
Eligibility Criteria
- Sex
- ALL
- Age
- 21 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Copenhagen group — OTHERParticipants use product for up to 30 minutes
- Snus group — OTHERParticipants use product for up to 30 minutes
Study Details
This study seeks to measure the effects of smokeless tobacco product risk messages on sensory experiences and future intentions to use.
Key Dates
- Start date
- May 11, 2026
- Status verified
- May 2026
- Primary completion
- May 1, 2027
- Completion
- May 1, 2027
Study Design
- Enrollment
- 50 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- FACTORIAL
- Primary purpose
- BASIC_SCIENCE
Arms
- Active Comparator: Copenhagen groupParticipants will place .66 grams of Copenhagen between cheek and gums for up to 30 minutes.
- Active Comparator: Snus GroupParticipants will place one pouch of snus beween cheek and gums for up to 30 minutes.
Primary Outcome Measure
Change in sensory response [ Time Frame: Before viewing study ads and immediatley after viewing ]
Central Contacts
- ASK RPCI1-877-275-7724
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Roswell Park | Buffalo | New York | 14263 | Richard O'Connor, PHD (PRINCIPAL_INVESTIGATOR) |
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