Having both premenstrual syndrome and dysmenorrhea.
Conditions
Interventions
Intervention 1: Intervention group: (n=74) reception of curcuminoids (500 mg/day), for seven days before the start of bleeding until three days after that for three menstrual cycles. Intervention 2: C
Sponsors
Birjand University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 25 Years
Inclusion criteria
Inclusion criteria: Simultaneous diagnosis of premenstrual syndrome and primary dysmenorrhea Being single BMI between 19 and 25 Ages 18-25 years Informed consent to participate in the project
Exclusion criteria
Exclusion criteria: Acute or chronic illness during study The occurrence of a traumatic event such as the death of a relative during the studyMarriage Marriage during study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| People with premenstrual syndrome and dysmenorrhea. Timepoint: Before intervention, 3 months later. Method of measurement: Premenstrual Syndrome severity questionnaire, digital barometer, digital scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAfsane Bahrami
Birjand University of Medical Sciences
Outcome results
None listed