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
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.
Przegląd badań
Status
Interwencja / Leczenie
Szczegółowy opis
This study was designed as a single-group pretest-posttest quasi-experimental study to evaluate a Health Belief Model-based podcast education program for premenstrual syndrome management among university students. The study was conducted online with young female university students living in Istanbul, Türkiye.
The educational intervention was structured according to the Health Belief Model components, including perceived susceptibility, perceived severity, perceived benefits, perceived barriers, cues to action, and self-efficacy. The program aimed to help participants recognize PMS and PMDD symptoms, monitor their symptoms, understand the effects of PMS on quality of life and academic functioning, recognize the role of healthy lifestyle behaviors in symptom management, and develop PMS-related self-management skills.
The podcast education program lasted four weeks and included eight episodes in total. Two podcast episodes were shared each week. Each episode lasted approximately 8 to 10 minutes. Podcast episodes were shared online, and reminder messages were sent before each episode. A WhatsApp group was used to facilitate access to the podcast episodes, share educational announcements, and monitor the education process.
Data were collected using a Personal Information Form, the Premenstrual Symptoms Screening Scale, and the PMS-Specific Quality of Life Scale. The primary outcome was change in premenstrual symptom severity from baseline to posttest. The secondary outcome was change in PMS-specific quality of life from baseline to posttest.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
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Istanbul, Turcja (Türkiye), 34000
- Istanbul Medipol University
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dziecko
- Dorosły
Akceptuje zdrowych ochotników
Opis
Inclusion Criteria:
- 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
Exclusion Criteria:
- 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
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie podtrzymujące
- Przydział: Nie dotyczy
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
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Eksperymentalny: Health Belief Model-Based Podcast Education Program
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.
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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.
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Change in Premenstrual Symptom Severity
Ramy czasowe: Baseline and post-intervention assessment, approximately eight weeks after baseline
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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.
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Baseline and post-intervention assessment, approximately eight weeks after baseline
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Change in PMS-Specific Quality of Life
Ramy czasowe: Baseline and post-intervention assessment, approximately eight weeks after baseline
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PMS-specific quality of life was assessed using the PMS-Specific Quality of Life Scale.
The scale consists of 22 items and three subscales: social well-being, emotional well-being, and physical well-being.
Total scores range from 22 to 110, with higher scores indicating a greater negative impact of PMS on quality of life.
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Baseline and post-intervention assessment, approximately eight weeks after baseline
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Współpracownicy i badacze
Sponsor
Śledczy
- Główny śledczy: Şerife Çınar, MSc, Medipol University
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- PMS-POD-HBM-2026
- 1919B012554344 (Inny numer grantu/finansowania: TÜBİTAK 2209 University Students Research Projects Support Program)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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