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Effect of peer education on premenstrual syndrome

A Comparison between the Effects of School-based Education Programs provided by Peer Group versus Health Practitioners on Premenstrual Syndrome in Adolescents

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150608022609N5
Enrollment
100
Registered
2019-08-04
Start date
2020-04-04
Completion date
Unknown
Last updated
2020-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Premenstrual syndrome. Premenstrual tension syndrome

Interventions

Intervention 1: Intervention group (1): Training of peer educators: At first, ten eligible volunteer students will be selected as potential peer educators to educate their peers. They will educate abo

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
16 Years to 18 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzaneh Babapour

Mazandaran University of Medical Sciences

f.bbp1991@gmail.com+98 11 3332 5205

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026