Evaluating Narrative Vaping Prevention Video Ads for Adolescents and Young Adults
NCT07767929 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1910
Last updated 2026-09-02
Summary
The purpose of this study is to evaluate the persuasive effectiveness of narrative advertisements: with acted-out plots (where characters enact a vaping-related experience) versus narrative advertisements without acted-out plots and control. Using a 3-arm between-subjects randomized design, approximately 1,910 adolescents and young adults (aged 13-20) in the U.S. who vape or are susceptible to vaping will be recruited online. Participants will be randomly assigned to view video ads from one of three conditions (narrative with acted-out plots, narrative without acted-out plots, or control videos) and complete a post-exposure survey evaluating message engagement, emotional response, perceived effectiveness, and psychological reactance.
Conditions
- Vaping
Interventions
- BEHAVIORAL
-
Acted-Out Narrative Ads
Participants view 3 randomly ordered vaping prevention video ads featuring characters enacting a vaping-related experience or consequence (e.g., experiencing addiction/withdrawal symptoms).
- BEHAVIORAL
-
Non-Acted-Out Narrative Testimonial Ads
Participants view 3 randomly ordered narrative testimonial video ads featuring testimonial narration with static visual presentations, without character enactment.
- BEHAVIORAL
-
Neutral Control Videos
Participants view 3 neutral/informational text-and-voice-only control ads about vaping without any testimonial element.
Sponsors & Collaborators
-
Food and Drug Administration (FDA)
collaborator FED -
National Institute on Drug Abuse (NIDA)
collaborator NIH -
UNC Lineberger Comprehensive Cancer Center
lead OTHER
Principal Investigators
-
Seth M Noar, PhD · UNC Lineberger Comprehensive Cancer Center
-
Sarah Kowitt, PhD · UNC Lineberger Comprehensive Cancer Center
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 13 Years
- Max Age
- 20 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2026-09-30
- Primary Completion
- 2028-08-31
- Completion
- 2028-08-31
Countries
- United States
Study Locations
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