About this trial
This study will be conducted to study the effect of virtual reality therapy on prostaglandin levels in adolescent females with primary dysmenorrhea.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age 17- 21 years old.
The body mass index (BMI) < 30 kg/m2.
Unmarried females.
Females with dysmenorrhea pain.
Disqualifiers
Have a pathological disease related to reproduction.
Students who use analgesic drugs for 3 months/3 menstrual cycles.
Students with menstrual pain secondary to diagnosed organic or inflammatory causes.
Trial design
Parallel
Treatments tested in this trial
Pharmacological treatment
DrugAll participants in the two groups will receive pharmacological treatment in the form of ibuprofen 400 mg, three times per day, during the first 2 days of menstruation, for 3 menstrual cycles.
Virtual reality
Other interventionThe experimental group will receive virtual reality during the first 2 days of menstruation, for 3 menstrual cycles.
Treatment groups
Trial outcomes
Primary outcomes
Visual Analogue Scale (VAS)
Participants in both groups will complete the visual analogue scale (VAS) before the start of treatment and after 3 menstrual cycles of treatment. The VAS is a 10 cm horizontal line on which the participants' pain intensity is represented by a point between the extremes of "no pain at all "and "worst pain imaginable". Each girl will be asked to mark a point on the line between the extreme that was related to her pain intensity. Then, the distance will be measured each time from the left end of the line to the marked point to obtain the VAS score for pain intensity of dysmenorrhea.
Assessment of Prostaglandin Levels
Blood samples will be collected from each girl in both groups to measure the levels of plasma PGF2α before the start of treatment and after 3 menstrual cycles of treatment.
Sponsors and contacts
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