NCT06142877

Brief Summary

The goal of this clinical trial is to test the effects of social media use on e-cigarette use in young adults who use e-cigarettes. The main questions it aims to answer are:

  • Does reducing social media use change young adults' e-cigarette use?
  • Does reducing social media use change things such as young adults' mental health and what they see on social media? Participants will complete surveys and submit screenshots showing how much time they spend on social media. Researchers will compare young adults who reduce their social media use to young adults who use social media as usual, to see if their e-cigarette use differs.

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Dec 2023

Geographic Reach
1 country

1 active site

Status
recruiting

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

November 15, 2023

Completed
7 days until next milestone

First Posted

Study publicly available on registry

November 22, 2023

Completed
12 days until next milestone

Study Start

First participant enrolled

December 4, 2023

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2025

Completed
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2025

Completed
Last Updated

May 7, 2024

Status Verified

May 1, 2024

Enrollment Period

1.2 years

First QC Date

November 15, 2023

Last Update Submit

May 6, 2024

Conditions

Keywords

social mediayoung adulte-cigarettenicotine vaping

Outcome Measures

Primary Outcomes (1)

  • Past-month vaping days

    Number of days the participant vaped nicotine in the past 30 days

    Collected at baseline, 1mo, 3mo, 6mo

Secondary Outcomes (2)

  • Episodes per vaping day

    Collected at baseline, 1mo, 3mo, 6mo

  • Puffs per vaping episode

    Collected at baseline, 1mo, 3mo, 6mo

Study Arms (2)

Social Media Use Reduction

EXPERIMENTAL
Behavioral: Social Media Use Reduction

Social Media Use as Usual

NO INTERVENTION

Interventions

Participants will be incentivized to reduce their social media use by a pre-specified percentage from baseline.

Social Media Use Reduction

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Age 18-25
  • Daily social media use
  • Ownership of a smartphone
  • Vaping (i.e., use of a nicotine e-cigarette) on 1-19 days of the past 30 days
  • Residing in the United States

You may not qualify if:

  • Lack of capacity to provide informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Oklahoma Health Sciences Center

Oklahoma City, Oklahoma, 73104, United States

RECRUITING

MeSH Terms

Conditions

Vaping

Condition Hierarchy (Ancestors)

SmokingBehavior

Study Officials

  • Erin A Vogel, PhD

    University of Oklahoma

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Erin A Vogel, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants will be randomized to one of two groups: 1) social media use reduction (intervention), or 2) social media use as usual (control).
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 15, 2023

First Posted

November 22, 2023

Study Start

December 4, 2023

Primary Completion

February 1, 2025

Study Completion

March 1, 2025

Last Updated

May 7, 2024

Record last verified: 2024-05

Data Sharing

IPD Sharing
Will not share

Deidentified data will be available from the Principal Investigator upon reasonable request.

Locations