NCT07646769

Brief Summary

Premenstrual syndrome is a common women's health condition characterized by physical, psychological, and behavioral symptoms that may negatively affect daily life, academic functioning, and quality of life among young women. This study evaluated the effect of a Health Belief Model-based podcast education program on premenstrual symptom severity and PMS-specific quality of life among young female university students living in Istanbul, Türkiye. This single-group pretest-posttest quasi-experimental study enrolled 120 participants. The intervention consisted of an eight-episode podcast education program delivered over four weeks, with two episodes per week. Premenstrual symptom severity and PMS-specific quality of life were assessed before and after the education program using validated scales.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Dec 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 15, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

June 9, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 15, 2026

Completed
Last Updated

June 15, 2026

Status Verified

June 1, 2026

Enrollment Period

5 months

First QC Date

June 9, 2026

Last Update Submit

June 9, 2026

Conditions

Keywords

Premenstrual syndromePremenstrual symptomspodcasthealth belief modelDigital health educationUniversity studentsYoung womenQuality of life

Outcome Measures

Primary Outcomes (1)

  • Change in Premenstrual Symptom Severity

    Premenstrual symptom severity was assessed using the Premenstrual Symptoms Screening Scale. The scale consists of 30 items and five subscales: psychological status, physical status, cognitive perception and sleep status, work and social life status, and nutritional status. Total scores range from 30 to 120, with higher scores indicating more frequent and severe premenstrual symptoms.

    Baseline and post-intervention assessment, approximately eight weeks after baseline

Secondary Outcomes (1)

  • Change in PMS-Specific Quality of Life

    Baseline and post-intervention assessment, approximately eight weeks after baseline

Study Arms (1)

Health Belief Model-Based Podcast Education Program

EXPERIMENTAL

Participants received a Health Belief Model-based podcast education program for premenstrual syndrome management. The program was delivered online over four weeks and consisted of eight podcast episodes, with two episodes per week. Each episode lasted approximately 8 to 10 minutes.

Behavioral: Health Belief Model-Based Podcast Education Program

Interventions

The intervention was a structured podcast-based education program developed according to the Health Belief Model. The program included eight podcast episodes delivered over four weeks. The educational content addressed perceived susceptibility, perceived severity, perceived benefits, perceived barriers, cues to action, and self-efficacy in relation to PMS management. Podcast episodes were shared online, and participants were followed through a WhatsApp group for reminders and access to educational content.

Health Belief Model-Based Podcast Education Program

Eligibility Criteria

Age17 Years - 25 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsThis study included young female university students because the intervention focused on premenstrual syndrome and PMS-specific quality of life.
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Being a female university student
  • Living in Istanbul, Türkiye
  • Reporting premenstrual symptoms
  • Voluntarily agreeing to participate in the study
  • Having access to the technical resources required to follow the podcast-based education program

You may not qualify if:

  • Reporting a psychiatric diagnosis or receiving psychiatric treatment
  • Having previously attended an education or counseling program related to PMS
  • Studying in a directly health-related department
  • Not completing the education program
  • Not completing the posttest assessment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istanbul Medipol University

Istanbul, 34000, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Premenstrual Syndrome

Condition Hierarchy (Ancestors)

Menstruation DisturbancesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Şerife Çınar, MSc

    Medipol University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
No masking was used because all participants received the same educational intervention.
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Model Details: All participants received the same Health Belief Model-based podcast education program. Outcomes were assessed before and after the intervention using a single-group pretest-posttest design.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

June 9, 2026

First Posted

June 15, 2026

Study Start

December 15, 2025

Primary Completion

April 30, 2026

Study Completion

April 30, 2026

Last Updated

June 15, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be publicly shared due to participant confidentiality and ethical restrictions. De-identified data may be made available from the corresponding author upon reasonable request and subject to institutional and ethical approval.

Locations