- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07572448
The Relationship Between Nurses' Perception Of Safety Culture And Patients' Sense Of Safety
An Investigation Of The Relationship Between Day Surgery Nurses' Perception Of Safety Culture And Patients' Level Of Feeling Safe During Surgery
This study will be conducted to determine the relationship between the perception of safety culture among healthcare professionals working in an outpatient surgical unit and the level of safety patients feel during surgery performed under local anesthesia.
The study population consists of healthcare professionals (N = 140) working in the Day Surgery Unit of Bursa Uludağ University Faculty of Medicine Hospital and patients undergoing procedures. The sample size calculation for the healthcare professionals to be included in the study was determined using the known population sampling method. Using the Raosoft sampling method, with a 5% margin of error and a 95% confidence interval, the minimum required sample size (n) was calculated to be 103. It was decided that the study would include healthcare professionals and patients in a 1:1 ratio. Therefore, the total sample size was calculated to be 206.
Data will be collected using the Hospital Survey on Patient Safety Culture (Version 2.0) and the Feeling Safe During Surgery Scale.
Descripción general del estudio
Estado
Condiciones
Tipo de estudio
Inscripción (Estimado)
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:
- Currently working as a healthcare professional in an outpatient surgical unit,
- No visual, auditory, or psychological impairments that would prevent them from completing the questionnaires and scales,
- At least a graduate of a vocational high school for healthcare professions,
- Patients scheduled for elective surgery under local anesthesia,
- Patients and nurses who voluntarily agreed to participate in the study.
Exclusion Criteria:
- Refusal to voluntarily participate in the study,
- Presence of any visual, auditory, or psychological impairments that would prevent the completion of questionnaires and scales,
- Individuals who are not healthcare professionals.
- Patients undergoing emergency surgical procedures or those under general anesthesia.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Nurses' level of patient safety culture
Periodo de tiempo: From the registration phase to the end of the approximately 52-week data collection process
|
It will be calculated using scores from the sub-dimensions of the Hospital Survey on Patient Safety Culture (Version 2.0).
|
From the registration phase to the end of the approximately 52-week data collection process
|
|
Patients' Sense of Safety
Periodo de tiempo: From the registration phase to the end of the approximately 52-week data collection process
|
The score range on the Patient Safety During Surgery Scale is 13-130 points.
|
From the registration phase to the end of the approximately 52-week data collection process
|
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
Palabras clave
Otros números de identificación del estudio
- 2026-6
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. .