Stanford Tobacco Treatment Services - Virtual Reality Treatment for Smoking Cessation
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Stanford University
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- Number of Patients With Interest in the MindCotine Application
Study Overview
Brief Summary
This study aims to see how feasible a mobile app based virtual reality program for smoking cessation (MindCotine) would be among Stanford cancer center patients
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Health Services Research
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Daily cigarette smoker or some day smoker (>9 cigarettes per week)
- •English or Spanish fluent
- •Smartphone compatibility
- •Available to interact with a smartphone app for 6-weeks
- •Available to complete the EOT assessment at end of 6-weeks
- •Ability to understand and the willingness to personally sign the written IRB-approved informed consent document.
- •Confirm phone, email, address during consent
Exclusion Criteria
- •Ever had epilepsy
- •Less than 10 cigarettes per week
- •Not English or Spanish fluent
- •No smartphone compatibility
- •Unavailable to interact with the VR program,
- •Unavailable to answer questions about the intervention post-treatment
Arms & Interventions
MindCotine mobile app program
Intervention: MindCotine's VR app (Behavioral)
Outcomes
Primary Outcomes
Number of Patients With Interest in the MindCotine Application
Time Frame: 6 weeks
Total number of patients who expressed interest in the app, out of total number of participants who were screened for enrollment. This measure is to assess whether MindCotine is a feasible smoking cessation option among patients who smoke cigarettes.
Number of Patients Who Registered With the MindCotine Application
Time Frame: 6 weeks
Total number of patients who registered with the app, out of total number of participants who were enrolled (eligible and willing to accept help with quitting). This measure is to assess whether MindCotine is a feasible smoking cessation option among patients who smoke cigarettes.
Number of Patients Who Would Recommend the MindCotine Application as a Measure of Feasibility Among Patients Who Smoke.
Time Frame: 6 weeks
Learning whether MindCotine is a feasible smoking cessation option among patients who smoke cigarettes. Interest in using the app will be calculated as total number of patients who recommend the app to others.
Secondary Outcomes
- Number of Patients Using Cessation Medication by End of Treatment(6 weeks)
- Average Change in Cigarette Use(baseline to end of treatment, up to 6 weeks)
- Number of Patients Who Attempt to Quit Smoking by Using the Application(6 weeks prior to end of treatment survey)
- Number of MindCotine App Coaching Engagements Completed(6 weeks)
- Number of MindCotine App Program Activities Completed(6 weeks)
- MindCotine Dropout(6 weeks)
- Number of MindCotine App Journal Entries Completed(6 weeks)
Investigators
Judith Prochaska
Professor of Medicine
Stanford University