AzTrials
AzTrials

VapingNCT07540780

Social Media Support Groups for Adolescent Vaping Cessation

A study testing Social Media Intervention in people with Vaping and Vaping Cessation, run by University of California, San Francisco at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The purpose of this study is to pilot test feasibility and acceptability of the Quit the Hit Toolkit, a social media-based nicotine vaping cessation program for adolescents and young adults, adapted for use in community settings. Read more about this study

Who is it for?
Ages 13 years and olderHealthy volunteers can take part
Conditions the study is for
Vaping, Vaping Cessation, Nicotine Dependence
What is being tested?
Social Media Intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteUnited States
Study dates
15 Apr 2026to 31 Oct 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 13 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • English literacy
  • Age between 13-21 years (group participants) or 18+ (coaches, peer mentors)
  • Indicate they use social media "most" (>= 4) days per week (group participants)
  • Have vaped at least once per week in the past 30 days (90 percent of participants) (group participants)
  • Access to a computer or mobile phone with photo capability to verify abstinence from vaping (group participants)
  • Indicate they are considering quitting or are interested in quitting with the next 6 months or within the next 30 days (group participants)
  • Currently reside in California, Minnesota, Oklahoma, or South Carolina

Who cannot join

  • No English literacy
  • Age under 13 or over 21 (group participants) or under 18 (coaches, peer mentors)
  • Insufficient social media use (3 or fewer days per week) (group participants)
  • Have not vaped at least once per week in past 30 days (group participants)
  • No access to computer or mobile phone with photo capability to verify abstinence from vaping (group participants)
  • Not considering or interested in quitting vaping in the next 30 days or 6 months (group participants)
  • Not a resident of California, Minnesota, Oklahoma, or South Carolina

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Sarah Rosen, BA contact

415-502-0758

quitthehit@ucsf.edu

United States1 site, 1 recruiting
  • University of California, San Francisco

    San Francisco, California, 94143

    Sarah Rosen, BA, 415-502-0758, quitthehit@ucsf.edu

    Pamela M Ling, MD, MPH

    Recruiting

Other trials in United States

About this study

The purpose of this study is to pilot test feasibility and acceptability of the Quit the Hit Toolkit, a social media-based nicotine vaping cessation program for adolescents and young adults, adapted for use in community settings.

Read the detailed description

This is a single-arm pilot study testing training materials for the Quit the Hit Toolkit. Community-based coaches will be recruited then receive training on the intervention, then they will recruit and lead 5-week vaping cessation groups online.

Being tested
Social Media Intervention
Keywords
single arm, pilot, intervention, vaping, adolescent, young adult
Medical subject headings
Vaping, Tobacco Use Disorder

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Social Media InterventionBehavioural

    Social media based intervention using Instagram with up to 3 posts per day for 30 days

Study groups in NCT07540780
Study groupRoleWhat they receive
Vaping InterventionExperimentalIndividuals will receive training on how to implement the vaping intervention (Quit the Hit Toolkit) in their own community settings. These individuals will serve as coaches and will recruit and facilitate vaping support groups on Instagram, where group participants will receive up to 3 Instagram posts per day for 30 days. Group coaches will work with a Cessation Counselor, Principal Investigator, Co-Investigators and a Pediatrician on demand if additional expertise or clinical advice is needed. Group participants will be educated about signs of nicotine dependence and if they express interest in pharmacotherapy will be encouraged to access this through their personal healthcare providers. The Instagram groups will provide educational and social support, troubleshooting and advice about nicotine replacement therapy (NRT) or other forms of treatment. Groups will also include trained peer mentors to provide additional support.
Receives: Behavioral: Social Media Intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of coaches who complete training and coach a vaping cessation group for 5 weeks

    Participants will be trained to serve as group coaches, implementing the intervention ("Quit the Hit Toolkit") to help teens and young adults stop vaping. Coaches will complete training and each will recruit approximately 10 participants for a vaping cessation group for 5 weeks. Investigators will track the number of coaches who successfully complete both training, recruit participants, and coach the groups for 5 weeks.

    Measured: 5 weeks

Secondary outcomes (3)
  1. Number of participants recruited and enrolled in the pilot study

    Coaches will work through their networks to recruit approximately 10 participants age 13-21 to participate in vaping cessation groups. The number of participants who qualify for the study on the study website, and the number who enroll in the study will be tracked.

    Measured: From time that coaches complete training to pilot group kickoff not greater than 4 weeks

  2. Number of participants who complete vaping cessation group over 5 weeks

    The number of participants who remain in the vaping cessation groups and like, post, or otherwise respond to the intervention posts or texts over 5 weeks, and who complete the survey at the end of the intervention will be tracked.

    Measured: From start of cessation groups to end of the intervention over 5 weeks.

  3. Acceptability of training protocol and intervention procedures to coaches and participants measured by qualitative interviews

    All coaches, peer mentors, and participants in the pilot intervention will be invited to participate in interviews or focus groups. Study investigators will solicit feedback on acceptability of the study procedures, training, recruitment, intervention experience, payment systems, and other engagement procedures.

    Measured: Following the end of pilot groups over about 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Apr 2026
  2. Study start15 Apr 2026
  3. Primary completion30 Sep 2026 (estimated)
  4. Study completion31 Oct 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07540780
Sponsor's protocol ID
20204627
Other IDs
R01CA292971
Status last verified
Jul 2026
First submitted
14 Apr 2026
Last updated
17 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: This is limited qualitative pilot data that may not be able to be sufficiently deidentified to be ethically shared. Investigators' ability to successfully deidentify the data to protect participant privacy will dictate whether or not a de-identified dataset could be made available to other researchers.

Publications

  • Lyu JC, Olson SS, Ramo DE, Ling PM. Delivering vaping cessation interventions to adolescents and young adults on Instagram: protocol for a randomized controlled trial. BMC Public Health. 2022 Dec 10;22(1):2311. doi: 10.1186/s12889-022-14606-7.

    PubMed 36496358
  • Ling PM, Lyu JC, Lisha NE, Nguyen N, Gribben V, Ramo DE. Social Media Support Groups for Youth Nicotine Vaping Cessation: An RCT. Am J Prev Med. 2026 Aug;71(2):108314. doi: 10.1016/j.amepre.2026.108314. Epub 2026 Feb 20.

    PubMed 41724253

Questions about this trial

What is this clinical trial studying?

A study testing Social Media Intervention in people with Vaping and Vaping Cessation, run by University of California, San Francisco at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 17 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Sarah Rosen, BA (415-502-0758, quitthehit@ucsf.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of coaches who complete training and coach a vaping cessation group for 5 weeks (time frame: 5 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07540780, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Jul 2026.

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