About this trial
This study seeks to measure the effects of smokeless tobacco product risk messages on sensory experiences and future intentions to use.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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
Disqualifiers
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
Trial design
Factorial
Treatments tested in this trial
Copenhagen group
Other interventionParticipants use product for up to 30 minutes
Snus group
Other interventionParticipants use product for up to 30 minutes
Treatment groups
Trial outcomes
Primary outcomes
Change in sensory response
assessed with a 0-100 visual analog scale - anchored by word descriptors at each end.
Secondary outcomes
Change in nicotine boost
Will be measured after use of products with gas chromatography-mass spectrometry
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Roswell Park Cancer Institute
Lead sponsor
National Cancer Institute (NCI)
Collaborator