Using virtual reality to manage acute pain during outpatient hysteroscopy
Effect of Virtual Reality Technology for Managment of Acute Pain in Outpatient Hysteroscopy: A Randomised Controlled Trial
This study is testing whether using virtual reality can help reduce pain and anxiety for patients during outpatient hysteroscopy procedures.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 50 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | Female |
| Sponsor | Egymedicalpedia Industry-sponsored |
| Locations | 1 site (Cairo) |
| Trial ID | NCT06424093 on ClinicalTrials.gov |
What this trial studies
This study investigates the use of virtual reality (VR) technology as a non-pharmacological method to alleviate acute pain and anxiety during outpatient hysteroscopy procedures. By immersing patients in a computer-generated environment through a headset, the study aims to provide distraction and improve the overall patient experience. The research addresses the growing trend of outpatient gynecological procedures, which, while beneficial, can still be associated with discomfort. The study seeks to fill a gap in existing literature regarding the effectiveness of VR in this specific medical context.
Who should consider this trial
Good fit: Ideal candidates for this study are patients scheduled for diagnostic hysteroscopy due to conditions like infertility or abnormal uterine bleeding.
Not a fit: Patients with absolute contraindications to office hysteroscopy or those with psychological, hearing, or visual disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce pain and anxiety for patients undergoing outpatient hysteroscopy, enhancing their overall experience.
How similar studies have performed: Previous studies have shown promise for VR in managing pain in various medical fields, but its application in outpatient hysteroscopy remains relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: \- Patients scheduled for diagnostic hysteroscopy e.g. Infertility, AUB Exclusion Criteria: * Absolute contraindication to office hysteroscopy such as acute pelvic infection , active genital herpes , heavy bleeding or pregnancy. * Psychological ,hearing or visual disorders. * known anatomical condition that make performing office hysteroscopy is difficult such as cervical stenosis ,fibrosis or cervical amputation . * Previous history of failed office hysteroscopy * Patients scheduled for operative hysteroscopy.
Where this trial is running
Cairo
- Ain Shams University Hospitals — Cairo, Egypt (Recruiting)
Study contacts
- Principal investigator: Radwa Rsaheedy Ali, M.D — Department of obstetrics & gynecology, Faculty Of Medicine, Ain Shams University
- Study coordinator: Waleed Mohamed shawky, MSC
- Email: Waleed.shawky.94@gmail.com
- Phone: +201093699004
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.