Clinical trial Recruiting at 2 sites Interventional Ages 18 and up Women only

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.

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Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment68 (estimated)
SponsorTokat Gaziosmanpasa University
Academic / other
Locations2 sites (Erbaa, Tokat Province and 1 other locations)
StatusRecruiting
StartedSeptember 30, 2026
Main results expectedOctober 30, 2026
Study endsNovember 30, 2026
Registry record updatedNovember 9, 2026
Trial IDNCT07853508 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

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.