Using virtual reality to improve outcomes for patients undergoing gallbladder surgery
The Effect of Patient Education and in the Operating Room Family Interview Practices on Patient Outcomes Using Virtual Reality in Cholecystectomy Patients: A Randomized Controlled Trial
This study is testing if using virtual reality for patient education can help people getting gallbladder surgery feel less stressed and more satisfied with their preparation process.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Marmara University Academic / other |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06634615 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the impact of virtual reality (VR) patient education and family interview practices on various outcomes for patients undergoing laparoscopic cholecystectomy. It is a randomized controlled trial that will assess stress intensity, anxiety levels, information needs, sleep quality, and overall satisfaction with the surgical preparation process. A total of 60 patients will be enrolled, with participants assigned to either a control group or groups receiving VR interventions. The study will also include a preliminary pilot application to ensure the usability of data collection forms.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are scheduled for elective laparoscopic cholecystectomy and have a stress intensity score above 3.
Not a fit: Patients with psychiatric disorders, persistent sleep problems, or those who experience discomfort during VR application may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce anxiety and improve overall satisfaction for patients undergoing gallbladder surgery.
How similar studies have performed: Other studies have shown promising results using virtual reality in healthcare settings, indicating potential for success in this novel application.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients who volunteered to participate in the study, * who were 18 years of age or older, * who would undergo elective laparoscopic cholecystectomy surgery, * who had no vision, hearing and communication problems, * whose relatives had a smartphone and internet connection, * whose stress intensity was higher than 3 points (between 1-10 points) met the inclusion criteria. Exclusion Criteria: * Patients with complaints of dizziness, * psychiatric disorders, * persistent sleep problems were excluded from the study. * Patients who voluntarily left the study, * interrupted the family video call with VR, * felt discomfort during VR application, * developed any allergy to the goggle material, * filled out the data collection forms incompletely and/or incorrectly will be excluded from the study.
Where this trial is running
Istanbul
- Marmara University Pendik Training and Research Hospital Prof. Dr. Asaf Ataseven Additional Service Building — Istanbul, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Çağla Islattı Mutlu
- Email: caglaislatti@gmail.com
- Phone: 905434568906
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.