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Impact of a Day Without Clinical Activity Before Night Shift on Non-technical Skills of Intensive Care Residents (REPOPREGARD)

23 de noviembre de 2021 actualizado por: University Hospital, Clermont-Ferrand

Impact of a Modified Schedule Including a Day Without Clinical Activity Before Night Shift on Non-technical Skills of French Residents in Intensive Care Unit, a Prospective Randomized Multi Center Study: REPOPREGARD Protocol Study

In this proposal, investigators seek to address conclusively two knowledge gaps: 1) the lack of data on the impact of a schedule including a day off clinic before night shift on performances of residents in anesthesia or critical care medicine and 2) the lack of data on the relationship between resident sleep deprivation and their non technical skills impairment. Investigators designed a prospective, randomized, blinded in cross over evaluation of medical pratices. Investigators will compare resident's performance during a high fidelity simulation session, on crisis managment in intensive care unit, after a night shift in intensive care unit, of residents who work on an intervention schedule with no clinical activity before night shift, with resident's performance of residents who had a traditionnal schedule including an usual clinical day before night shift. Investigators also assess cognitive performances, sleepiness and self esteem before and after night shift. Investigators specific aims will be:

To test the hypothesis that residents working on an intervention schedule will have non technical skills, assessed by Ottawa GRS global score, significantly less impaired after a night shift, than those on traditionnal schedule

To test the hypothesis that residents working on an interveniton schedule will have cognitive performances, sleepiness and self esteem less impaired after night shift than those on a traditionnal schedule

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Descripción detallada

Main objective of this study is to compare the non-technical skills after night shift, of anaesthesia and critical care residents who did not have clinical activity before the night shift with those who had at least 8 hours of clinical activity before. The workforce is constrained by the number of residents in training at Clermont-Ferrand and Lyon University Public Hospital. Thus, it is possible to consider the inclusion of 60 residents for 55 evaluable. With such numbers, the clinically relevant difference of 6 points for the Ottawa GRS score (for a standard deviation of 11) can be demonstrated with an alpha risk of bilateral error of 5% and a power of 80%. Two interim analyzes will be carried out including the first 20 interns and then 20 additional interns (therefore for 40 interns) with the aim of stopping the study for "effectiveness", more precisely stopping the study for evidence of a statistically significant difference for the primary outcome measure, with risks of first error observed respectively at 0.0005 and 0.014 comparisons (correction due to multiples). A simulation of the statistical power will also be proposed during the performance of these analyzes; if necessary, a new estimation of the workforce will be proposed to the competent authorities. Investigators do not plan loss of follow up.

Tipo de estudio

De observación

Inscripción (Anticipado)

60

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

      • Clermont-Ferrand, Francia, 63000
        • Clermont-Ferrand University Hospital
        • Investigador principal:
          • Alexandre LAUTRETTE

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

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

The investigators will include volunteer residents in anesthesia of critical care medicine of Gabriel Montpied university hospital of Clermont Ferrand.

Descripción

Inclusion Criteria:

  • residents in Anesthesia or Critical care medicine
  • Who effect night shift in intensive care unit
  • Able to take a day off clinic before night shift
  • Able to give consent

Exclusion Criteria:

  • Refusal of participation

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

Cohortes e Intervenciones

Grupo / Cohorte
Control
Residents in control group have a usual day with clinical activity before night shift
Intervention
Residents in intervention group have a day off clinic before night shift (i.e day off or day with university activity)

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Residents' non technical skills after a night shift
Periodo de tiempo: Immediatly after the end of the night shift
Measured by Ottawa Global Rated Scale global score assessed during a high fidelity simulation session of crisis managment. Global score is comprise between 7 for a performance expected from a beginner and 42 for a performance expeted from an expert.
Immediatly after the end of the night shift

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Residents' non technical skill before a night shift
Periodo de tiempo: Baseline, before the night shift
Measured by Ottawa Global Rated Scale global score assessed during a high fidelity simulation session of crisis managment. Global score is comprise between 7 for a performance expected from a beginner and 42 for a performance expeted from an expert.
Baseline, before the night shift
Cognitive performances : Phasic alert test
Periodo de tiempo: Before the night shift
refers to the notion of general wakefulness allowing to react quickly and appropriately to requests, score obtained from computer tool
Before the night shift
Cognitive performances : Phasic alert test
Periodo de tiempo: After the night shift up to 12 hours
refers to the notion of general wakefulness allowing to react quickly and appropriately to requests, score obtained from computer tool
After the night shift up to 12 hours
Cognitive performances : Divided attention test
Periodo de tiempo: Before the night shift
refers to the notion of paying attention to several things at the same time, score obtained from computer tool
Before the night shift
Cognitive performances : Divided attention test
Periodo de tiempo: After the night shift up to 12 hours
refers to the notion of paying attention to several things at the same time, score obtained from computer tool
After the night shift up to 12 hours
Cognitive performances : Flexibility test with alternation
Periodo de tiempo: Before the night shift
refers to the notion of displacement of the attentional focus, score obtained from computer tool
Before the night shift
Cognitive performances : Flexibility test with alternation
Periodo de tiempo: After the night shift up to 12 hours
refers to the notion of displacement of the attentional focus, score obtained from computer tool
After the night shift up to 12 hours
Cognitive performances : Working memory test
Periodo de tiempo: Before the night shift
refers to the notion of maintaining and updating when carrying out complex problems, score obtained from computer tool
Before the night shift
Cognitive performances : Working memory test
Periodo de tiempo: After the night shift up to 12 hours
refers to the notion of maintaining and updating when carrying out complex problems, score obtained from computer tool
After the night shift up to 12 hours
Cognitive performances : Computerized Speed Cognitive Test
Periodo de tiempo: Before the night shift
refers to the notion of the speed of information processing, score obtained from computer tool
Before the night shift
Cognitive performances : Computerized Speed Cognitive Test
Periodo de tiempo: After the night shift up to 12 hours
refers to the notion of the speed of information processing, score obtained from computer tool
After the night shift up to 12 hours
Sleepiness
Periodo de tiempo: Before the night shift
Measured by Karolinska Sleepiness scale, a score of 1 for a great tiredness to 9 for a very well awake state.
Before the night shift
Sleepiness
Periodo de tiempo: After the night shift up to 12 hours
Measured by Karolinska Sleepiness scale, a score of 1 for a great tiredness to 9 for a very well awake state.
After the night shift up to 12 hours
Self esteem
Periodo de tiempo: Before the night shift
Measured by Rosenberg Self Esteem scale, a score lower than 25 indicates a low self esteem and a score higher than 39 indicates a high self esteem.
Before the night shift
Self esteem
Periodo de tiempo: After the night shift up to 12 hours
Measured by Rosenberg Self Esteem scale, a score lower than 25 indicates a low self esteem and a score higher than 39 indicates a high self esteem.
After the night shift up to 12 hours

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

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 (Anticipado)

1 de diciembre de 2021

Finalización primaria (Anticipado)

1 de junio de 2023

Finalización del estudio (Anticipado)

1 de septiembre de 2023

Fechas de registro del estudio

Enviado por primera vez

18 de octubre de 2021

Primero enviado que cumplió con los criterios de control de calidad

23 de noviembre de 2021

Publicado por primera vez (Actual)

7 de diciembre de 2021

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

7 de diciembre de 2021

Última actualización enviada que cumplió con los criterios de control de calidad

23 de noviembre de 2021

Última verificación

1 de octubre de 2021

Más información

Términos relacionados con este estudio

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. .

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