Transfer of Non-technical Skills From Simulation to Clinical Practice

June 9, 2021 updated by: 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.

Study Overview

Status

Enrolling by invitation

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

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

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

- Internship in the ambulatory surgery unit

Exclusion Criteria:

- Refusal to participate

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control group
Anesthesiology residents do not receive any in situ simulation sessions during the observation period
Experimental: 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
ANTS (Anesthesia non technical skills) score
Time Frame: 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
Time Frame: 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
Time Frame: 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

Secondary Outcome Measures

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

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 28, 2021

Primary Completion (Anticipated)

September 30, 2024

Study Completion (Anticipated)

September 30, 2024

Study Registration Dates

First Submitted

June 4, 2021

First Submitted That Met QC Criteria

June 9, 2021

First Posted (Actual)

June 10, 2021

Study Record Updates

Last Update Posted (Actual)

June 10, 2021

Last Update Submitted That Met QC Criteria

June 9, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • 2018-71

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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