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)

Roswell Park

Buffalo, New York, United States

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NCT07107139