Using virtual reality to reduce preoperative anxiety before abdominal surgery
The Effect of Virtual Reality on Preoperative Anxiety Before Abdominal Surgery
This study is testing if using virtual reality can help people feel less anxious before having abdominal surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 96 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | Trakya University Academic / other |
| Locations | 1 site (Edirne) |
| Trial ID | NCT05718661 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of virtual reality in managing preoperative anxiety in patients scheduled for abdominal surgery. Participants will watch videos using virtual glasses to determine if this intervention can lower their anxiety levels compared to those who do not use the glasses. Data will be collected through a patient information form, a Visual Anxiety Scale (VAS-A), and a smart wristband that measures stress levels. The study will analyze the frequency of anxiety and the impact of virtual reality on anxiety management during the pre-surgical period.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are scheduled for abdominal surgery and can communicate in Turkish.
Not a fit: Patients who are not undergoing abdominal surgery or have health issues preventing the use of virtual glasses may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce anxiety levels in patients before surgery, leading to improved surgical outcomes.
How similar studies have performed: Other studies have shown promising results in using virtual reality for anxiety management, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Being 18 years or older, * To be able to communicate in Turkish, * Volunteering to participate in the research * To have abdominal surgery * Not applying isolation to the patient * It was determined that there is no obstacle to communication. Exclusion Criteria: * Not volunteering to participate in the research * To have a surgical intervention other than abdominal surgery * Failure to communicate * The patient is in isolation * Having a vision problem * Having a health problem that prevents using virtual glasses * Premedication has been applied
Where this trial is running
Edirne
- Trakya University Hospital — Edirne, Turkey (Recruiting)
Study contacts
- Principal investigator: Dogan Albayrak, Dr — Trakya University
- Study coordinator: Sevim Sen, PhD
- Email: sen.sevim13@gmail.com
- Phone: 00905319906926
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.