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Health Belief Model-Based Podcast Education for Premenstrual Symptoms in University Students (HBM-PMS-POD)

9. juni 2026 oppdatert av: Şerife Çınar, Medipol University

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.

Studieoversikt

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Faktiske)

120

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen

Tar imot friske frivillige

Ja

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Støttende omsorg
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Premenstrual Symptom Severity
Tidsramme: Baseline and post-intervention assessment, approximately eight weeks after baseline
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

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in PMS-Specific Quality of Life
Tidsramme: Baseline and post-intervention assessment, approximately eight weeks after baseline
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.
Baseline and post-intervention assessment, approximately eight weeks after baseline

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Şerife Çınar, MSc, Medipol University

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

15. desember 2025

Primær fullføring (Faktiske)

30. april 2026

Studiet fullført (Faktiske)

30. april 2026

Datoer for studieregistrering

Først innsendt

9. juni 2026

Først innsendt som oppfylte QC-kriteriene

9. juni 2026

Først lagt ut (Faktiske)

15. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

15. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

9. juni 2026

Sist bekreftet

1. juni 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • PMS-POD-HBM-2026
  • 1919B012554344 (Annet stipend/finansieringsnummer: TÜBİTAK 2209 University Students Research Projects Support Program)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

IPD-planbeskrivelse

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.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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