Actively Recruiting

Phase Not Applicable
Age: 21Years +
All Genders
Healthy Volunteers
ID07346092

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

Age: 21Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 online screening and enrollment visit

Survey Completion

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

Preventive Intervention

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

Follow-up Monitoring

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

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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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