- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07437196
Social Media Vaping Cessation Pilot With Peer Mentors
February 25, 2026 updated by: University of California, San Francisco
Single-Arm Social Media Vaping Cessation Trial With Peer Mentors
The purpose of this study is to understand the feasibility and acceptability of integrating peer mentoring into a social media-based intervention to help adolescents and young adults quit e-cigarette use.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study is a one-arm pilot trial with adolescent and young adult e-cigarette users.
This study tested a peer-mentored program to help teens and young adults quit vaping using social media.
Participants joined one of two inter groups and received messages from a trained counselor over 5 weeks.
Each group also included two peer mentors who had successfully quit vaping and offered support.
Participants completed surveys before and after the program.
Study Type
Interventional
Enrollment (Actual)
27
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
San Francisco, California, United States, 94143
- University of California, San Francisco
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion criteria for intervention participants:
- English literacy;
- aged 13 to 21;
- use social media at least four days per week;
- vape at least once per week in the past 30 days;
- are considering or interested in quitting within the next six months or 30 days; and
- resided in California.
Inclusion criteria for peer mentors:
- English literacy;
- aged 18-29;
- have quit e-cigarettes for more than 3 months;
- are willing to participate in an approximately 2-hour online training and pass the test after training; and
- will commit to provide support to help peers quit vaping in Instagram groups for 5 weeks (approximately 20 mins/day).
Exclusion criteria for intervention participants:
Individuals who do not meet the inclusion criteria.
Exclusion criteria for peer mentors:
Those who report using other tobacco products or substances and those with active mental health conditions will be excluded
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Peer-Mentored Vaping Cessation Intervention
Adolescents and young adults received the Quit the Hit (QTH) vaping cessation program delivered via Instagram over 5 weeks.
A trained counselor posted 1-3 evidence-based vaping cessation messages per weekday.
Each group included two peer mentors, aged similarly to participants, who had successfully quit vaping and provided social support and guidance.
Participants completed baseline and follow-up surveys.
|
The QTH program delivered 1-3 evidence-based vaping cessation messages per weekday via Instagram over 5 weeks.
Peer mentors, aged similarly to participants and who had successfully quit vaping, provided social support, encouragement, and one-on-one direct messaging.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility: Engagement and retention
Time Frame: 5 Weeks
|
Engagement measured by number of posts and likes in the Instagram group.
Retention defined as proportion completing the 5-week follow-up survey.
|
5 Weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Usefulness of Peer Mentoring
Time Frame: 5 Weeks
|
Perceived usefulness was assessed in the follow-up survey with 9 statements, measuring agreement using a 5-point Likert scale (1 disagree a lot to 5 agree a lot).
Example items included "the peer mentors helped me quit vaping," "the peer mentors shared useful information on quitting," and "the peer mentors increased my confidence that I can quit."
|
5 Weeks
|
|
Satisfaction with Peer Mentoring
Time Frame: 5 Weeks
|
Satisfaction with peer mentoring was assessed with six statements on the follow-up survey, measuring agreement using a 5-point Likert scale (1 = disagree a lot to 5 = agree a lot).
Items included "I liked the peer mentoring in the program," "I felt comfortable with the messages I got from peer mentors," "the peer mentors sent messages at convenient times of day," etc.
Additionally, participants rated their satisfaction with the quantity of peer mentor posts on a 5-point scale by responding to the item
|
5 Weeks
|
|
Evaluation of the program
Time Frame: 5 Weeks
|
The overall evaluation of the peer mentored vaping cessation program was measured using four statements, measuring agreement on a 5-point Likert scale (1 = disagree a lot to 5 = agree a lot).
The four items were "I would recommend this program to others", "The program gave me something new to think about", "I thought about what I read in the program", and "The program was easy to understand."
|
5 Weeks
|
|
Self-Reported 7-Day Point Prevalent Abstinence (PPA) from vaping
Time Frame: 5 Weeks
|
7-day point prevalence abstinence (PPA) will be assessed via the question about the number of days they used e-cigarettes in the past 7 days at the end of the intervention.
Participants reporting no vaping in the past 7 days will be coded as abstinent.
|
5 Weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Pamela M Ling, MD, University of California, San Francisco
- Principal Investigator: Chen Joanne Lyu, PhD, University of California, San Francisco
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 19, 2024
Primary Completion (Actual)
July 30, 2024
Study Completion (Actual)
August 3, 2024
Study Registration Dates
First Submitted
February 20, 2026
First Submitted That Met QC Criteria
February 20, 2026
First Posted (Actual)
February 27, 2026
Study Record Updates
Last Update Posted (Actual)
February 27, 2026
Last Update Submitted That Met QC Criteria
February 25, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- F32CA265059 (U.S. NIH Grant/Contract)
- T31IR1910 (Other Grant/Funding Number: Tobacco Related Diseases Research Program)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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