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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 novembro de 2021 atualizado 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

Visão geral do estudo

Status

Ainda não está recrutando

Condições

Descrição detalhada

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 estudo

Observacional

Inscrição (Antecipado)

60

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

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

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Método de amostragem

Amostra Não Probabilística

População do estudo

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

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

Coortes e Intervenções

Grupo / Coorte
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)

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Residents' non technical skills after a night shift
Prazo: 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 resultados secundários

Medida de resultado
Descrição da medida
Prazo
Residents' non technical skill before a night shift
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Antecipado)

1 de dezembro de 2021

Conclusão Primária (Antecipado)

1 de junho de 2023

Conclusão do estudo (Antecipado)

1 de setembro de 2023

Datas de inscrição no estudo

Enviado pela primeira vez

18 de outubro de 2021

Enviado pela primeira vez que atendeu aos critérios de CQ

23 de novembro de 2021

Primeira postagem (Real)

7 de dezembro de 2021

Atualizações de registro de estudo

Última Atualização Postada (Real)

7 de dezembro de 2021

Última atualização enviada que atendeu aos critérios de controle de qualidade

23 de novembro de 2021

Última verificação

1 de outubro de 2021

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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