Primary dysmenorrhoea. Primary dysmenorrhoea
Conditions
Interventions
Intervention 1: 3 days before the onset of menstruation (as prophylaxis) until end of menstruation dry cupping for 3 menstrual periods at a time and rotations, use of the experimental group and the co
Treatment - Other
3 days before the onset of menstruation (as prophylaxis) until end of menstruation dry cupping for 3 menstrual periods at a time and rotations, use of the experimental group and the control group will
In the control group does not take place intervention
Sponsors
Vice chancellor for research, Qazvin University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
19 Years to 35 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: single women in the range of 35-19 years old; living in students dormitories of Qazvin University of Medical Sciences; with regular menstrual cycles; moderate to severe primary dysmenorrhea; lack of any known chronic diseases like diabetes; the absence of symptoms like burning, itching and abnormal vaginal discharge; no hormonal problems; no history of pelvic disease, fibroids and tumors; no usage of certain medications and no stressful factors (separation of parents, death of first-degree relatives and so on) in the last six months. Major excluding conditions: being under the age of 19 years and more than 35 years; irregular menstruation; menstrual without pain; mild primary dysmenorrhea; secondary dysmenorrhea; chronic disease; pelvic disease; being under the stressors in the past six months.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity and duration of primary dysmenorrhea. Timepoint: Before the intervention, one month, two months, three months after the intervention in case and control groups. Method of measurement: Verbal multidimensional scoring system. | — |
Secondary
| Measure | Time frame |
|---|---|
| Symptoms of dysmenorrhea. Timepoint: Before the intervention, one month, two months, three months after the intervention in case and control groups. Method of measurement: Verbal multidimensional scoring system. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Taherpour
Qazvin University of Medical Sciences, Qazvin, Iran
Outcome results
None listed