Effect of Virtual Reality on Pain and Anxiety in Women With Dysmenorrhea: A Randomized Controlled Trial

NCT ID
NCT07853508
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Tokat Gaziosmanpasa University
Conditions
Anxiety, Menstrual Pain, Primary Dysmenorrhea

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Enrollment: 68 participants (Estimated).

What is being studied

  • Behavioral: Virtual Reality

Who may be eligible

Ages
18 Years to no maximum
Sex
Female
Healthy volunteers accepted
Yes

ClinicalTrials.gov lists the following eligibility 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.

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: Turkey (Türkiye)

  • Tokat Province, Turkey (Türkiye): 1

Sample of listed locations

  • Tokat Gaziosmanpasa University — Erbaa, Tokat Province, 60500, Turkey (Türkiye) — Site recruitment status not specified in the registry data

Study details

Start date
September 30, 2026
Primary completion date
October 30, 2026
Completion date
November 30, 2026
First posted
October 1, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07853508
Registry last updated
October 1, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07853508 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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