Effects of FDA Authorized Smokeless Tobacco Claims Among US Adults Who Smoke Cigarettes
NCT06927700 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1257
Last updated 2026-03-04
Summary
This study will be an online survey experiment conducted with adults who smoke cigarettes (ages 21+) to examine their reactions to modified risk advertising claims authorized by the Food \& Drug Administration (FDA) for two smokeless tobacco brands (General Snus and Copenhagen), which describe the lower risks of these products compared to cigarette smoking. The study will compare effects of ads with different two different claim types (i.e. claims about reduced lung cancer risk and claims about reduced risks for multiple disease) versus ads with no reduced-risk claims, and examine effects on message and product perceptions, and interest in using the smokeless tobacco products. This study will also examine how smokers' reactions/interest may vary based on the product brand, and asses prior awareness/exposure to the authorized claims.
Conditions
- Tobacco Product Beliefs and Use
Interventions
- BEHAVIORAL
-
Modified Risk Claim Type - None
Participants will view smokeless tobacco ads with no modified risk claim (control)
- BEHAVIORAL
-
Product Brand - General Snus
Participants will views ads for the smokeless tobacco brand General Snus
- BEHAVIORAL
-
Product Brand - Copenhagen
Participants will views ads for the smokeless tobacco brand Copenhagen
- BEHAVIORAL
-
Modified Risk Claim Type - Multiple Diseases
Participants will view smokeless tobacco ads with a claim about lower risks for multiple diseases
- BEHAVIORAL
-
Modified Risk Claim Type - Lung Cancer
Participants will either view smokeless tobacco ads with a modified risk claim about lower risks for lung cancer only
Sponsors & Collaborators
-
National Cancer Institute (NCI)
collaborator NIH -
Rutgers, The State University of New Jersey
lead OTHER
Principal Investigators
-
Olivia A Wackowski, PhD, MPH · Rutgers University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2025-04-24
- Primary Completion
- 2025-05-04
- Completion
- 2025-05-04
Countries
- United States
Study Locations
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