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Menopause Knowledge Level and Myth Beliefs (Menopause)

28 de maio de 2026 atualizado por: Abdurrahim UYANIK, Tokat Gaziosmanpasa University

The Effect of Pecha Kucha and Traditional Education on Menopause Knowledge Level and Myth Beliefs: Randomized Controlled Trial

This study aims to compare the effects of the Pecha Kucha and PowerPoint presentation methods on menopause knowledge and beliefs in menopause-related myths. By introducing an innovative, concise, focused, and visually based approach to menopause education, this research is expected to strengthen health literacy, reduce myths, and contribute to the development of more positive attitudes toward menopause among women. Furthermore, by evaluating both menopause myths and different educational techniques together, this study is anticipated to be the first in the literature and to serve as a reference for future research.

Research questions:

  1. Does menopause-related knowledge increase among women who receive education using the Pecha Kucha technique and the PowerPoint method?
  2. Do beliefs in menopause-related myths decrease among women who receive education using the Pecha Kucha technique and the PowerPoint method?
  3. Is there a difference between the Pecha Kucha technique and the PowerPoint method in terms of women's menopause-related knowledge levels and their beliefs in menopause-related myths?

Visão geral do estudo

Descrição detalhada

Study Type

This study is designed as a randomized controlled trial.

Aim of the Study

This study aims to compare the effects of traditional PowerPoint and Pecha Kucha presentation methods on menopause knowledge and awareness of menopause myths among women in Türkiye.

Study Population and Sample

The study will be conducted online across Türkiye. Participants will be recruited via an Instagram announcement, and educational sessions will be delivered through Google Meet. Women who voluntarily apply through the online registration form and meet the eligibility criteria will be included.

Sample size was calculated using G*Power version 3.1.9.3. Since no similar study examining the effects of PowerPoint and Pecha Kucha presentation methods on menopause knowledge and awareness of menopause myths was identified in the literature, a large effect size was assumed (Cohen's d = 0.70) (Cohen, 1992). Based on a significance level of α = 0.05 and statistical power of 80% (1-β = 0.80), the minimum sample size was calculated as 72 participants, with 36 participants allocated to each group.

Randomization and Blinding

Eligible participants will be assigned independent identification codes by a researcher not involved in data analysis. Randomization will be performed using the "List Randomizer" tool on Random.org with a 1:1 allocation ratio. Participants will be randomly assigned to either the Pecha Kucha (P-K) group or the PowerPoint (PPT) group.

Participants will be informed that a menopause-related educational study is being conducted but will not be informed about the Pecha Kucha method before allocation. Outcome data will be analyzed by an independent statistician blinded to group assignments.

Intervention Pecha Kucha Group (P-K)

Participants in the P-K group will receive menopause education through the Pecha Kucha presentation format consisting of 20 slides displayed for 20 seconds each (total duration: 6 minutes and 40 seconds). The presentation will include highly visual materials with minimal text.

PowerPoint Group (PPT)

Participants in the PPT group will receive the same educational content using a traditional PowerPoint presentation format. The session will consist of approximately 30 slides and last 30-35 minutes.

Both groups will be trained by the same educator in separate online sessions. Educational content will include:

Definition and physiology of menopause Hormonal changes during menopause Vasomotor, urogenital, and psychosocial symptoms Common menopause myths and misconceptions Effects of myths on women's health and quality of life Evidence-based menopause information Healthy lifestyle behaviors during menopause Data Collection Procedure

Online questionnaires will be completed immediately before and after the educational intervention. Data collection will be conducted via Google Meet in a single-session format, and completion of the forms will require approximately 10-15 minutes.

Statistical Analysis

Data will be analyzed using IBM SPSS Statistics version 25.0. Descriptive statistics will be presented as frequencies, percentages, mean, and standard deviation. Normality will be assessed using the Kolmogorov-Smirnov test. Within-group pretest-posttest comparisons will be analyzed using paired samples t-tests, while between-group differences will be assessed using independent samples t-tests. Non-parametric equivalents (Wilcoxon signed-rank test and Mann-Whitney U test) will be used for non-normally distributed data. Statistical significance will be accepted at p < 0.05.

Ethical Considerations

Ethical approval will be obtained from the Tokat Gaziosmanpaşa University Human Research Ethics Committee. Written and verbal informed consent will be obtained from all participants prior to data collection. Participant confidentiality will be maintained, and personal data will be used solely for research purposes. Participants may withdraw from the study at any stage without penalty. The study will be conducted in accordance with the principles of the Declaration of Helsinki.

Tipo de estudo

Intervencional

Inscrição (Real)

500

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Tokat Province
      • Erbaa, Tokat Province, Turquia (Türkiye), 60500
        • Tokat Gaziosmanpaşa University

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

Inclusion Criteria:

  • Being between 30 and 65 years of age (the lower age limit of 30 years was determined to establish a methodological threshold between young adulthood, in which menopause perception has not yet developed, and the menopausal transition period)
  • Being female
  • Volunteering to participate in the study
  • Not having previously received education about menopause
  • Being able to use technological devices
  • Being able to understand Turkish

Exclusion Criteria:

  • Being outside the 30-65 age range
  • Having a history of prior menopause-related education or formal training
  • Having cognitive, psychiatric, or medical conditions that could impair the ability to understand and complete the study procedures or questionnaires

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Pesquisa de serviços de saúde
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Pecha Kucha
A presentation consisting of 20 slides, supported by high-resolution visual materials and lasting 6 minutes and 40 seconds, was delivered. Each slide was displayed for 20 seconds as planned. The training included fundamental information about the menopausal period and addressed commonly encountered myths and misconceptions.
A presentation consisting of 20 slides, supported by high-resolution visual materials and lasting 6 minutes and 40 seconds, was delivered. Each slide was displayed for 20 seconds as planned. The training included fundamental information about the menopausal period and addressed commonly encountered myths and misconceptions
Comparador Ativo: PowerPoint group
Participants in this group received education on menopause and menopause-related myths using the PowerPoint presentation method. The same content was delivered by the same educator using the PowerPoint format. The presentation consisted of 30 slides and lasted approximately 35 minutes.
Participants in this group received education on menopause and menopause-related myths using the PowerPoint presentation method. The same content was delivered by the same educator using the PowerPoint format. The presentation consisted of 30 slides and lasted approximately 35 minutes.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Menopause Knowledge
Prazo: 1 hour
Menopause Knowledge Scale The scale developed by Mete et al. (2024) is a 5-point Likert-type scale. The items of the Menopause Knowledge Scale can be summed, and an increase in the score indicates increased knowledge of menopause. A minimum total score of 14 and a maximum total score of 70 can be obtained from the scale. Knowledge of Menopause Symptoms and Management (Factor 1) consists of questions 6, 7, 8, 9, 10, 11, 12, 13, and 14, with a minimum score of 9 and a maximum score of 45. General Menopause Knowledge (Factor 2) consists of questions 1, 2, 3, 4, and 5, with a minimum score of 5 and a maximum score of 25. The internal consistency Cronbach's alpha reliability coefficient of the scale is 0.917, 0.830 for Factor 1, and 0.908 for Factor 2.
1 hour

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Menopause Myths
Prazo: 1 hour
Menopause Myths Scale The Menopause Myths Scale (MMS), developed by Erol and Beydağ (2025), is a 5-point Likert-type scale designed to assess misconceptions about the menopausal process. The scale consists of 13 items and three sub-dimensions. The sub-dimensions are: "Myths regarding the impact on sexual life" (items 1-6), "Myths regarding the impact on family and social life" (items 7-10), and "Myths regarding the impact on mental health" (items 11-13). In the study where the scale was developed, the Cronbach's alpha coefficient was determined as 0.87; it was reported as 0.85 for the sub-dimensions "Myths regarding the impact on sexual life", and 0.79 for "Myths regarding the impact on family and social life" and "Myths regarding the impact on mental health". The maximum score that can be obtained from the scale is 65. The minimum score is 13. It is stated that as the score increases, the belief in myths also increases.
1 hour

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

15 de fevereiro de 2026

Conclusão Primária (Real)

16 de fevereiro de 2026

Conclusão do estudo (Real)

20 de fevereiro de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

22 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

28 de maio de 2026

Primeira postagem (Real)

3 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

3 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

28 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • Gaziosmanpasa- AUGE

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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 .

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