Effect of peer education on premenstrual syndrome

Not Applicable

• Conditions: Premenstrual syndrome.; Premenstrual tension syndrome; N94.3

• Registration Number: IRCT20150608022609N5
• Lead Sponsor: Mazandaran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 October 2020

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 100

Inclusion Criteria

single
satisfaction of students and their parents attending the study,
, regular period of menstruation from 21 to 35 days
moderate to severe PMS according to the Premenstrual Syndrome Screening Tool (PSST)
not a professional athlete

Exclusion Criteria

use of therapies due to PMS, at baseline and during the study
hormonal or psychiatric drug intake affecting PMS, at baseline and during the study
diagnosis of a chronic disease
occurrence of unfortunate/stressful events for adolescents or their family in the last six months and during the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Severity of premenstrual syndrome. Timepoint: Daily record of severity of premenstrual syndrome's problems within 2 consecutive months ( 2menstrual cycles)before intervention and within 2 consecutive months( 2menstrual cycles) after the end of the intervention. Method of measurement: Premenstrual Symptoms Screening Tool (PSST) AND Daily Record of Severity of Problems Chart (DRSP).

Secondary Outcome Measures

Name	Time	Method
Frequency of PMDD. Timepoint: At the baseline and after the intervention. Method of measurement: PSST questionnaire.;General Health score. Timepoint: At the baseline and after the intervention. Method of measurement: General Health Questionnaire- 28 Items (GHQ-28).