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.
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
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.
Tipo de estudo
Inscrição (Real)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
-
-
-
Istanbul, Turquia (Türkiye), 34000
- Istanbul Medipol University
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Filho
- Adulto
Aceita Voluntários Saudáveis
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Cuidados de suporte
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: 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.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change in Premenstrual Symptom Severity
Prazo: 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
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change in PMS-Specific Quality of Life
Prazo: 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
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Şerife Çınar, MSc, Medipol University
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- PMS-POD-HBM-2026
- 1919B012554344 (Número de outro subsídio/financiamento: TÜBİTAK 2209 University Students Research Projects Support Program)
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .