- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04922203
Transfer of Non-technical Skills From Simulation to Clinical Practice
Are the Non Technical Skills Taught to Residents in Anesthesiology During in Situ Simulation Sessions Transferred to Clinical Practice
Since 1988, simulation has been proposed as a teaching tool in Anesthesia. The simulation environment allows to teach learners non-technical skills which are a combination of cognitive, social, and personal resources complementary to procedural skills that contribute to an efficient and safe performance.
Non-technical skills traditionally used in Anesthesia are task management, situational awareness, teamwork and decision making. They can be indirectly measured with validated scales (e.g. Anesthesia Non-Technical Skills (ANTS) system). In addition to these basic skills, specific skills such as Anesthesia Crisis Resource Management (ACRM) are required when the patient presents a critical clinical situation.
Simulation, as proposed by Gaba, was initially practiced in centers specifically designed for this purpose. More recently, we have proposed the model of in situ simulation, i.e. in the usual workplace with the usual work team, as another option for the practice of simulation.
There are many theories about the transfer of learning. Transfer can be defined as what remains of the completed training that the learner actually uses, i.e. the final real effect.
Nevertheless, almost 30 years after the introduction of simulation in the training of anesthesiologists, data demonstrating the interest of this teaching in terms of transfer of learning of non-technical skills to clinical practice or benefits for patients are rare.
The main objective of this study is to evaluate the transfer of non-technical skills taught in a training program including in situ simulation to clinical practice by anesthesiology residents.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Anticipado)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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-
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Liège, Bélgica, 4000
- CHU de Liège - Sart-Tilman
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-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Internship in the ambulatory surgery unit
Exclusion Criteria:
- Refusal to participate
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Sin intervención: Control group
Anesthesiology residents do not receive any in situ simulation sessions during the observation period
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Experimental: Simulation group
Anesthesiology residents receive in situ simulations sessions during the observation period
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2 sessions of in situ simulation with 4 crisis scenarios and debriefing focused on non technical skills
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
ANTS (Anesthesia non technical skills) score
Periodo de tiempo: Once a day for 5 consecutive days between the first and the 15th day after enrollment in the study
|
15 items - From 1(poor) to 4 (good) for each item - Minimum 15 - Maximum 60
|
Once a day for 5 consecutive days between the first and the 15th day after enrollment in the study
|
|
ANTS (Anesthesia non technical skills) score
Periodo de tiempo: Once a day for 5 consecutive days between the 30th and 45th day after enrollment
|
15 items - From 1(poor) to 4 (good) for each item - Minimum 15 - Maximum 60
|
Once a day for 5 consecutive days between the 30th and 45th day after enrollment
|
|
ANTS (Anesthesia non technical skills) score
Periodo de tiempo: Once a day for 5 consecutive days between the 3rd and the 4th month after enrollment
|
15 items - From 1(poor) to 4 (good) for each item - Minimum 15 - Maximum 60
|
Once a day for 5 consecutive days between the 3rd and the 4th month after enrollment
|
Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
DOPS (Direct Observation of Procedural Skills) scale
Periodo de tiempo: Once within the first 15 days of enrollment
|
Once within the first 15 days of enrollment
|
|
DOPS (Direct Observation of Procedural Skills) scale
Periodo de tiempo: Once between the 30th and the 45th day after enrollment
|
Once between the 30th and the 45th day after enrollment
|
|
DOPS (Direct Observation of Procedural Skills) scale
Periodo de tiempo: Once between the 3rd and the 4th month after enrollment
|
Once between the 3rd and the 4th month after enrollment
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
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
- 2018-71
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. .