Actively Recruiting
Human Laboratory Study of the Effects of Nicotine Product Claims on Appeal, Perceptions, and Use Behavior
Led by Ohio State University Comprehensive Cancer Center · Updated on 2026-02-05
450
Participants Needed
1
Research Sites
236 weeks
Total Duration
On this page
Sponsors
O
Ohio State University Comprehensive Cancer Center
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study evaluates knowledge, feelings and thoughts regarding nicotine products among young adults who are susceptible to but do not use tobacco/nicotine and adults who use tobacco/nicotine.
CONDITIONS
Official Title
Human Laboratory Study of the Effects of Nicotine Product Claims on Appeal, Perceptions, and Use Behavior
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Young adult susceptible non-users aged 18 to 24 who have never used oral nicotine pouches (ONPs) and are susceptible to combustible tobacco only, non-combustible tobacco only, or both
- Adult tobacco users aged 18 to 65 who have never used ONPs or used ONPs more than 3 months ago and 10 times or less in their lifetime
- Adult tobacco users may be exclusive combustible tobacco users, exclusive non-combustible tobacco users, or dual users
- Current adult tobacco users must have used combustible and/or non-combustible tobacco every day or some days for 6 months or longer
- Willing and able to complete an in-person laboratory visit
You will not qualify if you...
- Younger than 18 years or older than 65 years
- Not susceptible non-users or current tobacco users
- Unwilling or unable to complete an in-person laboratory visit
- Used ONPs within the past 3 months
- Used ONPs more than 10 times in their lifetime
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ohio State University Comprehensive Cancer Center
Columbus, Ohio, United States, 43210
Actively Recruiting
Research Team
T
The Ohio State University Comprehensive Cancer Center
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
9
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