- ICH GCP
- US Clinical Trials Registry
- Clinical Trial 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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Liège, Belgium, 4000
- CHU de Liège - Sart-Tilman
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Internship in the ambulatory surgery unit
Exclusion Criteria:
- Refusal to participate
Study Plan
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
|
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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
|
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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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