premenstrual syndrome.
Conditions
Interventions
Intervention 1: Participants in the intervention group will receive 6 consecutive virtual group counseling sessions based on positive psychology for 60 to 90 minutes. The duration of the course is one
Sponsors
Zanjan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Be at least 18 years old Informed consent from participants Students living in dormitories Mild to moderate levels of PMS symptoms based on PSST questionnaire Regular menstruation at intervals between 21-35 days and bleeding duration 2-7 days Score less than or equal to 28 in the General Health Questionnaire Absence of physical and mental illness, using the general health questionnaire Lack of special diet Absence of stressful events such as parental separation, personal divorce, severe financial failure, accident, death of loved ones and surgery from 6 months before the study Lack of recent use of drugs affecting premenstrual syndrome
Exclusion criteria
Exclusion criteria: Unwilling to Participate in The Study Occurrence of tragic events such as death, family disputes, separation from parents, severe financial problems and death of loved ones during the research period The Absence of More Than one Sessions consultation Lack of cooperation in completing research tools
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Symptoms of premenstrual syndrome. Timepoint: Before study, one month later, two month later. Method of measurement: PSST Questionnaire.;Psychological capital. Timepoint: Before study, one month later, two month later. Method of measurement: Psychological Capital Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactParvin Mohebbi
Zanjan University of Medical Sciences
Outcome results
None listed