Terapia de atención plena en línea para la fatiga pandémica y la resiliencia en enfermeras de COVID-19
23 de mayo de 2024 actualizado por: Chimei Medical Center
Evaluación de los efectos de la terapia de atención plena en línea sobre la fatiga pandémica y la resiliencia entre enfermeras en salas de cuarentena COVID-19
Este estudio evalúa el impacto de la terapia de atención plena en línea sobre la fatiga pandémica y la resiliencia en enfermeras de la sala de cuarentena de COVID-19.
Sesenta enfermeras se dividieron en grupos experimental y de control, y el grupo experimental recibió un curso de atención plena en línea de 6 semanas.
Descripción general del estudio
Estado
Terminado
Intervención / Tratamiento
Descripción detallada
Este estudio evalúa la eficacia de la terapia de atención plena en línea para reducir la fatiga pandémica y mejorar la resiliencia entre las enfermeras en las salas de cuarentena de COVID-19.
Utilizando un diseño cuasiexperimental de medidas repetidas, 60 enfermeras se dividieron en grupos experimentales y de control.
El grupo experimental participó en un curso de mindfulness online de 6 semanas de duración.
Los resultados se midieron mediante cuestionarios de resiliencia y fatiga pandémica en la prueba previa, tres semanas y después de seis semanas.
Tipo de estudio
Intervencionista
Inscripción (Actual)
60
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
-
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其他（非美國）
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Tainan City, 其他（非美國）, Taiwán, 71004
- Chi Mei Medical Center
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
Criterios de inclusión:
- Más de 20 años.
- Enfermeros de salas y unidades de cuidados intensivos dedicadas a la COVID-19.
Criterio de exclusión:
- dificultad para asistir
- menos del 80% del número total de sesiones de terapia de atención plena en línea
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: El grupo experimental se someterá a un curso de mindfulness online de 6 semanas de duración
El grupo experimental recibió un curso de mindfulness online de 6 semanas de duración, una vez a la semana durante 90 minutos cada sesión.
Los participantes completaron cuestionarios antes del curso, en la semana 3 y en la semana 6.
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El grupo experimental recibió un curso de mindfulness online de 6 semanas de duración, una vez a la semana durante 90 minutos cada sesión.
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Sin intervención: Grupo de control
Atención general de rutina
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Fatiga pandémica
Periodo de tiempo: 6 semanas
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Utilice la Escala de fatiga pandémica/bloqueo (LFS) para medir la fatiga pandémica.
La escala con un total de 10 ítems mide la fatiga pandémica.
El rango de puntuaciones totales de la escala es de 10 a 50.
Muestra que la fatiga pandémica aumenta a medida que aumentan los puntos totales de la escala.
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6 semanas
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Resiliencia
Periodo de tiempo: 6 semanas
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Utilice la Escala de Resiliencia de Connor-Davidson (CD-RISC) para medir la resiliencia individual.
La escala con un total de 25 ítems mide la resiliencia.
El rango de puntuaciones totales de la escala es de 0 a 100.
Muestra que la resiliencia aumenta a medida que aumentan los puntos totales de la escala.
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6 semanas
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Publicaciones y enlaces útiles
La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.
Publicaciones Generales
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Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
1 de octubre de 2022
Finalización primaria (Actual)
31 de mayo de 2023
Finalización del estudio (Actual)
31 de mayo de 2023
Fechas de registro del estudio
Enviado por primera vez
23 de mayo de 2024
Primero enviado que cumplió con los criterios de control de calidad
23 de mayo de 2024
Publicado por primera vez (Actual)
29 de mayo de 2024
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
29 de mayo de 2024
Última actualización enviada que cumplió con los criterios de control de calidad
23 de mayo de 2024
Última verificación
1 de mayo de 2024
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 11112-001
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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. .