RecruitingNot ApplicableNCT07107139
Influence of Authorized Smokeless Tobacco Product Modified Risk Claims II: Laboratory Assessment of Sensory and Subjective Effects
Sponsor
Roswell Park Cancer Institute
Enrollment
50 participants
Start Date
May 11, 2026
Study Type
INTERVENTIONAL
Conditions
Summary
This study seeks to measure the effects of smokeless tobacco product risk messages on sensory experiences and future intentions to use.
Eligibility
Min Age: 21 Years
Inclusion Criteria9
- Age ≥ 21 years of age
- Residing in 8 counties of Western NY (Erie, Niagara, Cattaraugus, Chautauqua, Allegheny, Livingston, Genesee, Orleans, Wyoming)
- Smoke cigarettes every day, at least 5 cigarettes per day, for at least 1 year
- Open to trying a non-combusted oral tobacco product
- Have the ability to read, write, and communicate in English
- Have successfully completed our preliminary Auction study I-4008824 with a bid for Copenhagen and/or General Snus > $0
- Willing to abstain smoking 8-10 hours prior to each laboratory session and complete breath CO test for verification (<8ppm)
- Female participants must be amenable to taking a pregnancy test (urine) prior to beginning study procedures.
- Participant must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure.
Exclusion Criteria9
- Age ≥ 21 years of age
- Residing in 8 counties of Western NY (Erie, Niagara, Cattaraugus, Chautauqua, Allegheny, Livingston, Genesee, Orleans, Wyoming)
- Smoke cigarettes every day, at least 5 cigarettes per day, for at least 1 year
- Open to trying a non-combusted oral tobacco product
- Have the ability to read, write, and communicate in English
- Have successfully completed our preliminary Auction study I-4008824 with a bid for Copenhagen and/or General Snus > $0
- Willing to abstain smoking 8-10 hours prior to each laboratory session and complete breath CO test for verification (<8ppm) .
- Female participants must be amenable to taking a pregnancy test (urine) prior to beginning study procedures.
- Participant must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure.
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Interventions
OTHERCopenhagen group
Participants use product for up to 30 minutes
OTHERSnus group
Participants use product for up to 30 minutes
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07107139