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

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07767929 on ClinicalTrials.gov