Actively Recruiting
An Online Intervention to Reduce E-cigarette Use and Susceptibility to Smoking in Young Adults
Led by University of Southern California · Updated on 2026-01-16
100
Participants Needed
1
Research Sites
29 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
An Online Intervention to Reduce E-cigarette Use and Susceptibility to Smoking in Young Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be between the ages of 18 to 24
- Be able to read English
- Vape at least one day per week in the past month
- Have no history of cigarette use at screening and baseline
You will not qualify if you...
- Have severe mental health, illicit drug use, or alcohol use disorder
- Currently receiving nicotine cessation services
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Southern California
Los Angeles, California, United States, 90089
Actively Recruiting
Research Team
I
I-Wen Contracts and Grants Coordinator
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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