- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07572799
Midwives' Perspectives on Oral Health in Pregnancy and Early Childhood: A Cross-Sectional Online Survey
Perceived Role and Perspectives of Midwives in Oral Health of Pregnant Women and Young Children: A Cross-Sectional Online Survey
This study aims to explore how midwives in Germany perceive their professional role in the context of oral health of pregnant women and young children.
A nationwide, anonymous, non-interventional online survey will be conducted to assess self-perceived role, confidence in counseling, perceived barriers, information sources, and training needs.
The study is designed as an exploratory cross-sectional survey without hypothesis testing.
Descripción general del estudio
Estado
Descripción detallada
Midwives play an important role in early health promotion, including during pregnancy and early childhood. Oral health is a relevant but often underrepresented topic in this context.
This study aims to explore midwives' perspectives on their role in oral health promotion, including their perceived responsibilities, confidence in counseling, and structural conditions in their professional practice.
Data will be collected using an anonymous online questionnaire distributed via professional organizations and networks.
Tipo de estudio
Inscripción (Estimado)
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Jana Biermann, Dr. med. dent.
- Número de teléfono: 0049+5513960888
- Correo electrónico: jana.biermann@med.uni-goettingen.de
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
- Practicing midwives in Germany
- Age ≥ 18 years
- Consent to participate in the online survey
Exclusion Criteria:
- Age < 18 years
- Not currently working as a midwife
- Students without completed professional qualification
- No informed consent provided
Plan de estudios
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Detalles de diseño
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Self-perceived professional role in oral health assessed by a self-developed questionnaire using Likert-scale items (1-5)
Periodo de tiempo: Day 1
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Self-perceived professional role will be assessed using multiple items developed for this study, rated on a 5-point Likert scale (1 = strongly disagree to 5 = strongly agree).
Higher scores indicate a stronger perceived role in oral health.
|
Day 1
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Self-reported confidence in oral health-related topics assessed by Likert-scale items (1-5)
Periodo de tiempo: Day 1
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Confidence in oral health-related topics will be assessed using self-developed items rated on a 5-point Likert scale (1 = very unsure to 5 = very confident).
Higher scores indicate greater perceived confidence.
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Day 1
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Use of information sources related to oral health (self-reported questionnaire)
Periodo de tiempo: Day 1
|
Participants report their use of different information sources (e.g., training, literature, internet, professional exchange) using categorical response options.
Frequencies of use will be analyzed descriptively.
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Day 1
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Perceived barriers to addressing oral health in practice assessed by Likert-scale items (1-5)
Periodo de tiempo: Day 1
|
Perceived barriers will be assessed using self-developed Likert-scale items (1 = strongly disagree to 5 = strongly agree).
Higher scores indicate greater perceived barriers.
|
Day 1
|
|
Training needs and interests in oral health (self-reported questionnaire)
Periodo de tiempo: Day 1
|
Training needs and interests will be assessed using categorical and Likert-scale items.
Responses reflect interest in further education and preferred topics.
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Day 1
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- 39/3/26
Plan de datos de participantes individuales (IPD)
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Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .