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

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

Recruiting
21 years and older
All
Phase N/A

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Overview

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

Eligibility

Inclusion Criteria:

  • 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 Criteria:

  • 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.

Study details
    Smokeless Tobacco

NCT07107139

Roswell Park Cancer Institute

15 October 2025

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FAQs

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What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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