Virtual reality for reducing pain and anxiety in women with menstrual cramps
Official title: Effect of Virtual Reality on Pain and Anxiety in Women With Dysmenorrhea: A Randomized Controlled Trial
Run by Tokat Gaziosmanpasa University · NCT07853508 · Data updated 2026-11-12
In women with primary dysmenorrhea, this study tests whether a relaxing virtual reality experience can lower pain and anxiety during a 3-day period.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 68 (estimated) |
| Sponsor | Tokat Gaziosmanpasa University Academic / other |
| Locations | 2 sites (Erbaa, Tokat Province and 1 other locations) |
| Status | Recruiting |
| Started | September 30, 2026 |
| Main results expected | October 30, 2026 |
| Study ends | November 30, 2026 |
| Registry record updated | November 9, 2026 |
| Trial ID | NCT07853508 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are university students with a diagnosis of primary dysmenorrhea, regular menstrual cycles, and no vision/hearing impairments.
✕Probably not a fit
Individuals with secondary dysmenorrhea, pelvic pain from other causes, psychiatric disorders, hormonal therapy use, or sensory impairments may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized trial compares a 3-day VR session to a 3-day 2D video session in university students with primary dysmenorrhea. Participants will use a VR headset or a 2D screen for 20 minutes daily and report pain and anxiety before and after each session. The goal is to see if the immersive VR experience provides greater relief than standard video viewing. The study focuses on non-pharmacological management of menstrual pain and anxiety. Findings could inform patient-facing options for symptom relief during menstruation.
Why it matters
Potential benefit: If effective, VR could offer a non-drug method to reduce pain and anxiety during menses.
How similar studies have gone: Other non-pharmacological pain-relief approaches have shown promise, but VR for primary dysmenorrhea is comparatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * University students, * Diagnosed with primary dysmenorrhea, * Having a regular menstrual cycle, * Willing to participate in the study, * Having no vision or hearing problems. Exclusion Criteria: * Individuals diagnosed with secondary dysmenorrhea, * Individuals experiencing chronic pelvic pain, * Individuals with a psychiatric disorder, * Individuals using hormonal therapy, * Individuals using analgesics during menstruation, * Individuals with visual or hearing impairments, * Individuals wishing to withdraw at any stage of the study, * Individuals who fill out the forms incompletely or fail to fill them out.
Where it's running
-
Tokat Gaziosmanpasa University
Erbaa, Tokat Province, Turkey (Türkiye) Recruiting -
Tokat Gaziosmanpasa University
Erbaa, Tokat Province, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Abdurrahim Uyanık, MSc
- Email: abdurrahim.uyanik@gop.edu.tr
- Phone: 05419634590
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.