Impact of Virtual Reality on Painful Menstruation
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Relaxation Technique, Pain treatment.
- Who it may be relevant to
- Registry conditions: Painful Menstruation, Relaxation; Back Ligaments. Basic parameters: 13 years — 20 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt, Jordan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Impact of Virtual Reality Combined With Manual Diaphragmatic Release on Adolescent Female With Painful Menstruation
Overview
To investigate the effect of virtual reality on painful menstruation in adolescent female
Detailed description
The focus of relatively recent work has been on non-pharmacological pain management techniques. The usage of virtual reality (VR) devices that can replicate three-dimensional (3D) immersive worlds is one particularly exciting advancement. This technology is becoming more widely available in healthcare settings and has shown promise in lowering pain and anxiety levels for people receiving minor gynecological disorders, dental work, burn wound care, and labor. So, the research purpose is targeted to look into the impact of virtual reality combined with diaphragmatic release as an active relaxation technique on painful menstruation in adolescent female
Interventions
- Device Relaxation Technique
utilizing virtual reality and a relaxation technique called diaphragmatic release to treat menstrual pain sufferers - Device Pain treatment
utilizing cold laser and a relaxation technique called diaphragmatic release to treat menstrual pain sufferers
Primary outcome measures
- pain intensity [Time frame: 1o days for successive three months]
Secondary outcome measures (1)
- Menstrual Distress Questionnaire [Time frame: 1o days for successive three months]
Eligibility 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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- Mohamed Abdel Moenem Abo El Ros — Ismailia
Jordan · 1 center
- Zaytona University in Jordon — Amman
Identifiers
NCT: NCT06961396 · IRB # 21/3/20242025 · IRB # 21/3/20242025