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Clinical Trials in Egypt / NCT06961396
Recruiting Not applicable

Impact of Virtual Reality on Painful Menstruation

NCT06961396 · tracked via the Priya Life Science Egypt tracker
Sponsor
New Ismailia National University
Phase
Not applicable
Started
2025-04-01
Last updated
2025-05-07

Condition(s) studied

Painful MenstruationRelaxation; Back Ligaments

Investigational drug(s) / intervention(s)

Relaxation TechniquePain treatment

Relaxation Technique: utilizing virtual reality and a relaxation technique called diaphragmatic release to treat menstrual pain sufferers

Pain treatment: utilizing cold laser and a relaxation technique called diaphragmatic release to treat menstrual pain sufferers

Study summary

To investigate the effect of virtual reality on painful menstruation in adolescent female

Eligibility

Sex
FEMALE
Min age
13 Years
Max age
20 Years
Healthy volunteers
Accepted
Inclusion Criteria: * age from 16 to 22 year * cases of primary dysmenorrhea * Normal body mass index (20-25) Exclusion Criteria: * cases with polycystic ovarian syndrome * Obese female or body mass index more than 25 * severe bleeding with menstruation * cases with low back pain due to orthopedic origin like disc herniation or spinal malalignment

Primary outcome measure(s)

  • pain intensity — 1o days for successive three months
    Measurement of pain intensity using a visual analogue scale via the application of a virtual reality device combined with diaphragmatic release exercises

Trial sites (2)

FacilityCityRegionStatus
Mohamed Abdel Moenem Abo El Ros Ismailia Egypt Recruiting
Zaytona University in Jordon Amman Jordan Recruiting

More New Ismailia National University trials in Egypt

Evaluation of Exercise Capacity in Teenage Females Using Virtual Reality and Plyometric Workout Recruiting
Combined Effect of Sensory-motor Integration in Individuals With Postmenopausal Polyneuropathy Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06961396 on ClinicalTrials.gov ↗ ← All trials in Egypt