RECRUITING

Influence of Authorized Smokeless Tobacco Product Modified Risk Claims II: Laboratory Assessment of Sensory and Subjective Effects

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study seeks to measure the effects of smokeless tobacco product risk messages on sensory experiences and future intentions to use.

Official Title

Influence of Authorized Smokeless Tobacco Product Modified Risk Claims II: Laboratory Assessment of Sensory and Subjective Effects

Quick Facts

Study Start:2025-09-01
Study Completion:2027-03-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07107139

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age ≥ 21 years of age
  2. * Residing in 8 counties of Western NY (Erie, Niagara, Cattaraugus, Chautauqua, Allegheny, Livingston, Genesee, Orleans, Wyoming)
  3. * Smoke cigarettes every day, at least 5 cigarettes per day, for at least 1 year
  4. * Open to trying a non-combusted oral tobacco product
  5. * Have the ability to read, write, and communicate in English
  6. * Have successfully completed our preliminary Auction study I-4008824 with a bid for Copenhagen and/or General Snus \> $0
  7. * Willing to abstain smoking 8-10 hours prior to each laboratory session and complete breath CO test for verification (\<8ppm)
  8. * Female participants must be amenable to taking a pregnancy test (urine) prior to beginning study procedures.
  9. * 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.
  1. * Age ≥ 21 years of age
  2. * Residing in 8 counties of Western NY (Erie, Niagara, Cattaraugus, Chautauqua, Allegheny, Livingston, Genesee, Orleans, Wyoming)
  3. * Smoke cigarettes every day, at least 5 cigarettes per day, for at least 1 year
  4. * Open to trying a non-combusted oral tobacco product
  5. * Have the ability to read, write, and communicate in English
  6. * Have successfully completed our preliminary Auction study I-4008824 with a bid for Copenhagen and/or General Snus \> $0
  7. * Willing to abstain smoking 8-10 hours prior to each laboratory session and complete breath CO test for verification (\<8ppm) .
  8. * Female participants must be amenable to taking a pregnancy test (urine) prior to beginning study procedures.
  9. * 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.

Contacts and Locations

Study Contact

ASK RPCI
CONTACT
1-877-275-7724
askrpci@roswellpark.org

Study Locations (Sites)

Roswell Park
Buffalo, New York, 14263
United States

Collaborators and Investigators

Sponsor: Roswell Park Cancer Institute

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-09-01
Study Completion Date2027-03-01

Study Record Updates

Study Start Date2025-09-01
Study Completion Date2027-03-01

Terms related to this study

Additional Relevant MeSH Terms

  • Smokeless Tobacco