Study on the Effect of Digital Smoking Cessation Education Intervention on Outpatients
- Conditions
- Smoking Cessation
- Registration Number
- NCT07013084
- Lead Sponsor
- National Taiwan Normal University
- Brief Summary
This study aimed to assess the novel approach of an immersive three-dimensional (3D) virtual reality (VR) smoking cessation program and its effectiveness on smoking outpatients
- Detailed Description
A randomized controlled trial (RCT) was conducted with 100 outpatients from a smoking cessation clinic in Taiwan. Participants were randomly assigned to either the experimental group (n=50) or the comparison group (n=50) through a coin toss. The experimental group received standard outpatient smoking cessation services in combination with an immersive 3D VR smoking cessation program, while the comparison group received only standard outpatient services. The VR program included five interactive modules that used immersive scenarios to simulate smoking-related cues and provide educational content, employing cognitive-behavioral techniques and practicing coping strategies to promote behavior change.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
- currently receiving outpatient care at the smoking cessation clinic
- self-reported current tobacco use
- aged between 20 and 64 years
- no participation in any smoking cessation intervention within the past 12 months
- Patients with medical contraindications that could prevent them from engaging with the VR equipment
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method smoking status indicator1 From enrollment to the end of intervention at 12 weeks Participants reported the number of days they smoked in the past 30 days
smoking status indicator2 From enrollment to the end of intervention at 12 weeks Participants reported the average number of cigarettes consumed per day in the past 30 days
smoking status indicator3 From enrollment to the end of intervention at 12 weeks Nicotine dependence was measured using the FTND.
smoking status indicator4 From enrollment to the end of intervention at 12 weeks exhaled CO levels were measured using a handheld CO monitor
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
Trial Locations
- Locations (1)
Tri-Service General Hospital SongShan Branch ,Taipei,Taiwan
🇨🇳Taipei, Taiwan