Using virtual reality to relieve painful menstruation in young women
Impact of Virtual Reality Combined With Manual Diaphragmatic Release on Adolescent Female With Painful Menstruation
This study is testing if using virtual reality along with relaxation techniques can help young women aged 16 to 22 feel less pain during their periods.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 13 Years to 20 Years |
| Sex | Female |
| Sponsor | New Ismailia National University Academic / other |
| Locations | 2 sites (Ismailia and 1 other locations) |
| Trial ID | NCT06961396 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of virtual reality (VR) combined with a diaphragmatic releasing technique on painful menstruation in adolescent females aged 16 to 22. The research focuses on non-pharmacological pain management methods, utilizing immersive VR technology to potentially reduce pain and anxiety associated with primary dysmenorrhea. Participants will engage in relaxation techniques while experiencing VR environments designed to promote comfort and relaxation during menstruation. The study aims to provide insights into innovative pain management strategies for young women.
Who should consider this trial
Good fit: Ideal candidates for this study are adolescent females aged 16 to 22 who experience primary dysmenorrhea and have a normal body mass index.
Not a fit: Patients with conditions such as polycystic ovarian syndrome, obesity, severe menstrual bleeding, or low back pain due to orthopedic issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could offer a non-invasive and effective method for managing menstrual pain in adolescent females.
How similar studies have performed: While the use of virtual reality in pain management is gaining traction, this specific application for painful menstruation in adolescents is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Ismailia and 1 other locations
- Mohamed Abdel Moenem Abo El Ros — Ismailia, Egypt (Recruiting)
- Zaytona University in Jordon — Amman, Jordan (Recruiting)
Study contacts
- Study coordinator: Mohamed AM Abo El Ros, Ph.D
- Email: mohamed.aboelros@pt.ninu.edu.eg
- Phone: 01206530584
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.