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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06129123
Other study ID # UP-23-00005-AM001
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 1, 2026
Est. completion date March 1, 2027

Study information

Verified date November 2023
Source University of Southern California
Contact Shirin Contracts and Grants Coordinator
Phone 310-918-0538
Email shirin.mistry@med.usc.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this intervention development and pilot clinical trial is to determine whether receiving the brief online intervention results in greater reductions in past 7-day e-cigarette use frequency and smoking susceptibility over an 8-week period compared to receiving the control condition in young adults who currently use e-cigarettes. Participants in the experimental condition will be asked to complete the 30-minute mobile-based program. Participants in the assessment-only control will be given the option to access the intervention after they complete their final survey at 8 weeks. All participants will complete our online surveys at baseline as well as 2-weeks, 4-weeks, and 8-weeks post-randomization. Researchers will compare outcomes among the intervention and control groups to determine the efficacy of the intervention.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date March 1, 2027
Est. primary completion date March 1, 2027
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 24 Years
Eligibility Inclusion Criteria: - be between the ages of 18 to 24 - be able to read English - report vaping at least one day per week in the past month - report no history of cigarette use at screening and baseline. Exclusion Criteria: - reporting mental health, other drug, or alcohol use problems - currently receiving nicotine cessation services

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Live Free From E-cigarettes
This is a 30-minute online educational program that focuses on providing information about e-cigarette and smoking social norms, harms of e-cigarettes and cigarettes, and ways to quit or reduce using e-cigarettes.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Southern California

Outcome

Type Measure Description Time frame Safety issue
Primary E-cigarette Use Participants will report the number of (1) days they vaped, (2) times they picked up their device to vape per day, and (3) puffs they took before putting their vaping device away per day in the past 7 days and 30 days 8 weeks
Primary Smoking Susceptibility 4-item Expanded Susceptibility to Smoking Index (ESSI) 8 weeks
Secondary Perceived harms and benefits of vaping Using the 21-item Short Form Vaping Consequences Questionnaire (S-VSQ), participants will rate the likelihood that each consequence will occur when they vape. 8 weeks
Secondary Perceived harms and benefits of smoking Using the 21-item Short Form Smoking Consequences Questionnaire (S-SCQ), participants will rate the likelihood that each consequence will occur when they smoke. 8 weeks
Secondary Motivation to vape Participants will select which option best describes their interest in e-cigarette use: plan to stop (coded as 1), decrease (2), continue (3) or increase (4) vaping. 8 weeks
Secondary Motivation to smoke Participants will report if they plan to start smoking (yes/no). 8 weeks
Secondary Quitting vaping self-efficacy Participants rate their confidence about quitting vaping "someday" and "in the next 6 months" on a 5-point scale. 8 weeks
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