Condition 1: primary dysmenorrhea. Condition 2: Premenstrual syndrome. Primary Dysmenorrhea Pain localized to other parts of lower abdomen
Conditions
Interventions
Intervention 1: Intervention group: In the intervention group, mint oral capsule will be used once a day from 7 days before the start of menstruation until the first 3 days of menstruation. Interventi
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Be Iranian and single. Be a resident of the dormitories of Mashhad University of Medical Sciences. Have regular menstruation Have premenstrual syndrome and primary dysmenorrhea at the same time. Be 18-35 years old. No medication No allergies to mint No alcohol or drugs or tobacco No diet No disease
Exclusion criteria
Exclusion criteria: Discontinuation of medication or irregular use of medication (not taking medication twice or more) Have a BMI of more than 30. Be a professional athlete. Suffer from depression, stress and anxiety . Experience an unfortunate or stressful event while studying. Has used traditional medicine methods to reduce symptoms and improve pain. Married while studying.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean score of total premenstrual syndrome symptoms, severity and duration of dysmenorrhea. Timepoint: Mean score of total symptoms of premenstrual syndrome, severity and duration of dysmenorrhea at the beginning of the study (before the intervention) and 1 and 2 months after the intervention. Method of measurement: The mean total score of premenstrual syndrome symptoms will be assessed by COPE premenstrual events calendar form and the severity and duration of dysmenorrhea in the first and second months of the treatment cycle, by visual pain scale and COX scale and by patients' self-report. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSamira Ebrahimzadehzagami
Mashhad University of Medical Sciences
Outcome results
None listed