Evaluating Narrative Vaping Prevention Video Ads for Adolescents and Young Adults
2 other identifiers
interventional
1,910
1 country
2
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2026
Typical duration for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 11, 2026
CompletedFirst Posted
Study publicly available on registry
August 17, 2026
CompletedStudy Start
First participant enrolled
September 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2028
September 2, 2026
September 1, 2026
1.9 years
August 11, 2026
September 1, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Message engagement
Assessed using a standard 3-item self-report scale (e.g., " I could picture myself in the scene of the events described in the ad", "I was mentally involved while watching the ad"). Responses are scored on a 1-5 Likert scale, with higher averaged scores indicating deeper engagement.
Baseline (after each video exposure)
Secondary Outcomes (5)
Perceived Message Effectiveness
Baseline (after each video exposure)
Negative Affect
Baseline (after each video exposure)
Psychological Reactance
Baseline (after each video exposure)
Vaping Susceptibility
Baseline (after each video exposure)
Vaping beliefs
Baseline (after each video exposure)
Study Arms (3)
Condition 1
EXPERIMENTALActed-Out Narrative Video Ads
Condition 2
EXPERIMENTALNon-Acted-Out Narrative Video Ads
Condition 3
ACTIVE COMPARATORControl Videos
Interventions
Participants view 3 randomly ordered vaping prevention video ads featuring characters enacting a vaping-related experience or consequence (e.g., experiencing addiction/withdrawal symptoms).
Participants view 3 randomly ordered narrative testimonial video ads featuring testimonial narration with static visual presentations, without character enactment.
Participants view 3 neutral/informational text-and-voice-only control ads about vaping without any testimonial element.
Eligibility Criteria
You may qualify if:
- Age 13-20 years old.
- Current vaper or at risk of vaping. Participants will be considered as a current vaper if they report using e-cigarettes in the past 30 days. Participants will be considered as "at-risk of vaping" if they answer anything other than "definitely not' to 3 screening items assessing their susceptibility to vaping (e.g., "If one of your best friends were to offer you a vape, would you use it?" Response options: definitely not, probably not, probably yes, definitely yes).
- Live in the United States
You may not qualify if:
- Younger than 13 years or older than 21 years.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Fairfield University
Fairfield, Connecticut, 06824, United States
University of North Carolina, Chapel Hill
Chapel Hill, North Carolina, 27599, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Seth M Noar, PhD
UNC Lineberger Comprehensive Cancer Center
- PRINCIPAL INVESTIGATOR
Sarah Kowitt, PhD
UNC Lineberger Comprehensive Cancer Center
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 11, 2026
First Posted
August 17, 2026
Study Start
September 1, 2026
Primary Completion (Estimated)
August 1, 2028
Study Completion (Estimated)
August 1, 2028
Last Updated
September 2, 2026
Record last verified: 2026-09