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Transfer of Non-technical Skills From Simulation to Clinical Practice

9. juni 2021 opdateret af: Jean François Brichant

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.

Studieoversigt

Status

Tilmelding efter invitation

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Forventet)

30

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Liège, Belgien, 4000
        • CHU de Liège - Sart-Tilman

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Barn
  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

- Internship in the ambulatory surgery unit

Exclusion Criteria:

- Refusal to participate

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Andet
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Ingen indgriben: Control group
Anesthesiology residents do not receive any in situ simulation sessions during the observation period
Eksperimentel: Simulation group
Anesthesiology residents receive in situ simulations sessions during the observation period
2 sessions of in situ simulation with 4 crisis scenarios and debriefing focused on non technical skills

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
ANTS (Anesthesia non technical skills) score
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Tidsramme
DOPS (Direct Observation of Procedural Skills) scale
Tidsramme: Once within the first 15 days of enrollment
Once within the first 15 days of enrollment
DOPS (Direct Observation of Procedural Skills) scale
Tidsramme: 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
Tidsramme: Once between the 3rd and the 4th month after enrollment
Once between the 3rd and the 4th month after enrollment

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

28. maj 2021

Primær færdiggørelse (Forventet)

30. september 2024

Studieafslutning (Forventet)

30. september 2024

Datoer for studieregistrering

Først indsendt

4. juni 2021

Først indsendt, der opfyldte QC-kriterier

9. juni 2021

Først opslået (Faktiske)

10. juni 2021

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

10. juni 2021

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

9. juni 2021

Sidst verificeret

1. juni 2021

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 2018-71

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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