NCT07328061Completed
Virtual Reality for Anxiety and Pain Management in Transvaginal Ultrasound for Endometriosis
Effect of Virtual Reality on Anxiety and Pain During Trans-vaginal Ultrasound for Endometriosis: A Prospective Randomized Controlled Study.
Source: ClinicalTrials.gov · Last updated 8 Jan 2026
Brief summary (registry, in English)
The goal of this study to evaluate whether virtual reality (VR)-based technology, designed to promote relaxation and support pain self-management, can reduce anxiety and pain during trans-vaginal ultrasound (TVUS) for endometriosis. Participants, women undergoing TVUS for endometriosis will be randomly assigned to either VR distraction group (VR-TVUS) or a standard examination group (control). Anxiety and pain levels will be assessed immediately before and after the TVUS.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 155 (actual)
- First submitted
- 28 Dec 2025
- Start date
- 10 Dec 2023
- Primary completion date
- 20 Aug 2024
- Lead sponsor
- Sheba Medical Center
- Diseases
- Endometriosis
- NCT number
- NCT07328061
What you commit to
- Study type: Interventional
- Participants enrolled: 155
- From 10 Dec 2023 to the primary completion date, 20 Aug 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- History of epilepsy or seizure disorders.
- History of migraines.
- Visual or hearing impairment.
- Diagnosed anxiety disorders.
- Active respiratory tract infection.
Other
- Claustrophobia.
- Current symptoms of dizziness or nausea.
- Any contraindication to transvaginal ultrasound examination.
Who the study is looking for
- Women aged 18 to 50 years.
- Confirmed or suspected diagnosis of endometriosis.
- Scheduled to undergo transvaginal ultrasound examination.
- Ability to understand the study procedures and independently complete study questionnaires.
- Provided written informed consent.
Age in the registry: 18 years to 50 years · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Endometriosis Center, Sheba Medical Center Coordinator of this site? Confirm its status | Ramat Gan | Israel | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.