Actively Recruiting
Health Perceptions and Social Behaviors in Young Adults at Ohio State University to Develop Effective Oral Nicotine Pouch Risk Communication
Led by Ohio State University Comprehensive Cancer Center · Updated on 2026-03-05
2000
Participants Needed
1
Research Sites
N/A
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 research aims to understand the health perceptions and social behaviors related to oral nicotine pouch (ONP) use among graduate students at Ohio State University (OSU). The study focuses on young adults, exploring patterns of ONP use, social influences, and how social norms shape tobacco use. The goal is to develop effective, interactive messages that communicate the addictive risks of ONPs, which have become more popular due to factors like affordability, availability, and online advertising. Participants first complete an online survey that assesses their ONP use, perceptions of ONP use in their social circles, and their interaction with ONP content on social media. Those identified as at high risk for nicotine dependence are randomly assigned to receive one of two interventions: viewing either static or dynamic visual ONP risk messages designed to influence knowledge, risk perceptions, and sharing intentions. Participants in one intervention group view four randomized messages and complete brief questionnaires about message effectiveness and attitudes toward ONPs. Throughout the study, participants' susceptibility to ONP use, perceived harm, social norms, exposure to ONP information, self-efficacy to avoid use, and intentions to share messages on social media are measured using various scales. Sociodemographic data and tobacco use history are also collected. The study spans up to two years, with all participation conducted online, requiring approximately 5-10 minutes for the initial survey and additional time for intervention message exposures and questionnaires.
CONDITIONS
Brief Title
Studying the Health Perceptions and Social Behaviors of Graduate Students at the Ohio State University for the Development of Effective Oral Nicotine Pouch Addictive Risk Communication
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be a graduate student at Ohio State University
- Be aged 21 years or older
- For Aim 2 and Aim 3, be identified as susceptible to, have experimented with, or currently use oral nicotine pouches
- Consent to participate in follow-up studies if identified as high risk for nicotine dependence
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 online screening and enrollment visit
Duration - 5 to 10 minutes
Participants complete an online survey assessing oral nicotine pouch use patterns, perceptions of use within their social circles, and interactions with oral nicotine pouch content on social media.
1 online visit
Duration - Single session on study day
Participants identified as high risk view preventive oral nicotine pouch messages which may be static or dynamic visual risk messages depending on random assignment.
1 online visit
Duration - Up to 2 years
Participants complete follow-up assessments of knowledge, perceptions, attitudes, self-efficacy, and intentions related to oral nicotine pouch use for up to 2 years.
Follow-up assessments as scheduled online
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
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
4
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