Health Belief Model-Based Podcast Education for Premenstrual Symptoms in University Students
HBM-PMS-POD
Effect of a Health Belief Model-Based Podcast Education Program on Premenstrual Symptom Severity and PMS-Specific Quality of Life in University Students: A Single-Group Pretest-Posttest Quasi-Experimental Study
2 other identifiers
interventional
120
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedFirst Submitted
Initial submission to the registry
June 9, 2026
CompletedFirst Posted
Study publicly available on registry
June 15, 2026
CompletedJune 15, 2026
June 1, 2026
5 months
June 9, 2026
June 9, 2026
Conditions
Keywords
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
EXPERIMENTALParticipants 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.
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.
Eligibility Criteria
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)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Şerife Çınar, MSc
Medipol University
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
- 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.