Influence of Authorized Smokeless Tobacco Product Modified Risk Claims I: Consumer Product Demand

NCT ID: NCT07102082

Last Updated: 2025-12-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

160 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-09-25

Study Completion Date

2026-11-30

Brief Summary

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To explore consumer responses to the announcement and implementation of new modified risk claims for Copenhagen and General Snus (brands of smokeless tobacco (ST) products) using a series of complementary and innovative research activities and methods.

Detailed Description

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Primary Objectives:

To assess the influence of smokeless tobacco products' modified risk claims on:

1. Product demand (measured as willingness to pay in USD) using an experimental auction approach; and
2. Perceived risk of tobacco-associated diseases as assessed using questionnaire-based measures.

Conditions

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Smoking Behaviors

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Group A - no claim

Participants view smokeless tobacco ads with no claims

Group Type SHAM_COMPARATOR

Modified Risk - None

Intervention Type BEHAVIORAL

Participants view ads with no modified risk claim

Group B - Modified Risk Tobacco Product Claim

Participants view ads with a modified risk claim

Group Type ACTIVE_COMPARATOR

Modified Risk Claim

Intervention Type BEHAVIORAL

Participants view ads with a modified risk claim

Interventions

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Modified Risk - None

Participants view ads with no modified risk claim

Intervention Type BEHAVIORAL

Modified Risk Claim

Participants view ads with a modified risk claim

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Residing in one of the 8 counties of Western New York (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 access to a device (ie: computer/tablet/smartphone) with internet capabilities to participate in an online survey study.
* Have the ability to read, write, and communicate in English.
* Participant must understand the investigational nature of this study and an Independent Ethics Committee/Institutional Review Board approved information sheet prior to receiving any study related procedure

Exclusion Criteria

* Plan to quit smoking in the next 30 days.
* Use of smokeless tobacco at least weekly in the last 6 months.
* Lifetime use (that is, ever used at any time prior to the study) of Copenhagen or General Snus.
* Unwilling or unable to follow protocol requirements.
* Pregnant or planning to become pregnant (by self report)
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

Roswell Park Cancer Institute

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Richard O'Connor

Role: PRINCIPAL_INVESTIGATOR

Roswell Park

Locations

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Roswell Park

Buffalo, New York, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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ASK RPCI

Role: CONTACT

1-800-767-9355

Other Identifiers

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R21CA289541

Identifier Type: NIH

Identifier Source: secondary_id

View Link

I-4008824

Identifier Type: -

Identifier Source: org_study_id

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