ClinicalTrials.Veeva

Menu

Stanford Tobacco Treatment Services - Virtual Reality Treatment for Smoking Cessation

Stanford University logo

Stanford University

Status

Completed

Conditions

Smoking Cessation
MindCotine Virtual Reality Mindful Exposure Therapy

Treatments

Behavioral: MindCotine's VR app

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05220254
P30CA124435 (U.S. NIH Grant/Contract)
IRB-60253

Details and patient eligibility

About

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

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Daily cigarette smoker or some day smoker (>9 cigarettes per week)
  • Age 18+
  • 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

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

MindCotine mobile app program
Experimental group
Treatment:
Behavioral: MindCotine's VR app

Trial documents
2

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems