primary dysmenorrhea. Primary dysmenorrhoea
Conditions
Interventions
Intervention 1: After providing the necessary information, taking written consent, and allowing female students in accepting or rejecting participation in the research, the students are randomly alloc
Treatment - Other
After providing the necessary information, taking written consent, and allowing female students in accepting or rejecting participation in the research, the students are randomly allocated to four int
The second group: Initially, demographic and VAS questionnaires are completed by a researcher for each student. Then, chopped and packed candy is given to the participants. At the beginning the menstr
The third group: Initially, demographic and VAS questionnaires are completed by a researcher for each student. Then, chopped and packed candy is given to the participants. At the beginning the menstru
The fourth group: Initially, demographic and VAS questionnaires are completed by a researcher for each student. Then, chopped and packed candy is given to the participants. At the beginning the menstr
Sponsors
North Khorasan University of Medical Science
Eligibility
Sex/Gender
Female
Age
18 Years to 25 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: At reproductive age (18-25 years), unmarried, without reproductive system diseases, no cyst, not taking medications prescribed for cysts, not taking contraceptive drugs such as LD, HD, and levonorgestrol, menstrual period of 30 ± 3in the past three months, primary dysmenorrhea in all menstrual cycles, lack of sensitivity to hot candy, and lack of an underlying disease such as diabetes. Exclusion criteria: Married students, taking antidepressants, anti-serotonin, barbiturates, and psychotropic drugs, taking NSAID pills and herbal medicines, lack dysmenorrhea during their menstrual period, and participants with reproductive system problems, infections, and cysts.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary dysmenorrhea. Timepoint: Before intervention and 1,2,3,4,5,6 hours after intervention. Method of measurement: Validated Scale (VAS)AnologVisual,SF-MPQ. | — |
Secondary
| Measure | Time frame |
|---|---|
| Severity and duration of menstruation. Timepoint: Before Intervention- 1,2,3,4,5,6hours after intervention. Method of measurement: Self reported Quastionare. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam Maddineshat
North Khorasan University of Medical Science
Outcome results
None listed