NCT04707911

Brief Summary

Social media based intervention to support teens in their efforts to quit vaping.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2021

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 11, 2021

Completed
2 days until next milestone

First Posted

Study publicly available on registry

January 13, 2021

Completed
10 months until next milestone

Study Start

First participant enrolled

November 18, 2021

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 18, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 18, 2024

Completed
Last Updated

June 21, 2024

Status Verified

June 1, 2024

Enrollment Period

2.6 years

First QC Date

January 11, 2021

Last Update Submit

June 18, 2024

Conditions

Keywords

Nicotine DependenceSocial Media

Outcome Measures

Primary Outcomes (3)

  • Point Prevalent Abstinence (PPA) from vaping

    7-day point prevalence abstinence (PPA) from all tobacco products will be assessed over the course of the study. Participants reporting no vaping in the past 7 days will be coded as abstinent. Those reporting 7-day abstinence and not using nicotine replacement therapy will be mailed saliva cotinine test kit and saliva tetrahydrocannabinol (THC) test kit for biochemical verification of abstinence.

    1 month

  • Point Prevalent Abstinence (PPA) from vaping

    7-day point prevalence abstinence (PPA) from all tobacco products will be assessed over the course of the study. Participants reporting no vaping in the past 7 days will be coded as abstinent. Those reporting 7-day abstinence and not using nicotine replacement therapy will be mailed saliva cotinine test kit and saliva tetrahydrocannabinol (THC) test kit for biochemical verification of abstinence.

    3 months

  • Point Prevalent Abstinence (PPA) from vaping

    7-day point prevalence abstinence (PPA) from all tobacco products will be assessed over the course of the study. Participants reporting no vaping in the past 7 days will be coded as abstinent. Those reporting 7-day abstinence and not using nicotine replacement therapy will be mailed saliva cotinine test kit and saliva tetrahydrocannabinol (THC) test kit for biochemical verification of abstinence.

    6 months

Secondary Outcomes (6)

  • Change in the number of participants with reduction in vaping

    Up to 6 months

  • Change in the number of vape quit attempts

    Up to 6 months

  • Number of participants with at least 1 quit attempt

    Up to 6 months

  • Change in response on Stages of Change Questionnaire

    Up to 6 months

  • Change in the score on the Thoughts About Abstinence (TAA) Questionnaire

    Up to 6 months

  • +1 more secondary outcomes

Study Arms (2)

Vaping Intervention

EXPERIMENTAL

The vaping intervention will be implemented on Instagram. Participants in the treatment condition will be assigned to groups on Instagram, where they will receive up to 3 posts per day for 30 days. Groups are facilitated by a trained Guide, working with the Principal Investigator, Co-Investigators and a Pediatrician on demand if additional expertise or clinical advice is needed. 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.

Behavioral: Social Media Intervention

Control Condition

NO INTERVENTION

Participants in the control condition will be directed to the Truth Initiative e-cigarette texting quit program. This innovative and free text message program was created with input from teens, college students and young adults who have attempted to, or successfully, quit e-cigarettes using text coaching methods

Interventions

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

Vaping Intervention

Eligibility Criteria

Age13 Years - 21 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of California, San Francisco

San Francisco, California, 94143, United States

Location

Related Publications (1)

  • 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.

MeSH Terms

Conditions

VapingTobacco Use Disorder

Condition Hierarchy (Ancestors)

SmokingBehaviorSubstance-Related DisordersChemically-Induced DisordersMental Disorders

Study Officials

  • Pamela Ling, MD

    University of California, San Francisco

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 11, 2021

First Posted

January 13, 2021

Study Start

November 18, 2021

Primary Completion

June 18, 2024

Study Completion

June 18, 2024

Last Updated

June 21, 2024

Record last verified: 2024-06

Data Sharing

IPD Sharing
Will not share

Locations