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Clinical Trials/NCT02926599
NCT02926599
Completed
Not Applicable

High Fidelity Simulation Performance After a Potential Optimization Training for Anesthesiologist Resident: a Randomized Controlled Trial.

Claude Bernard University1 site in 1 country118 target enrollmentSeptember 2016
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
Claude Bernard University
Enrollment
118
Locations
1
Primary Endpoint
Performance during simulation
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Simulated environment allowed safe learning of critical events and knowledge of appropriate response and treatment. Anesthesiology resident education curriculum in Lyon plans several high fidelity simulation session with a large panel of critical events. Anticipation of critical events before they may occur and planification of team resources and priority in the treatment strategy may help to improve team performance during the scenario. The investigators' goal is to compare individual and team performances with or without an optimization personal potential training.

Detailed Description

The investigators aim to compare the individual and team performances for resident who were taught personal optimization skills (positive reinforcement, personalized psycho-physiological relaxation, mental rehearsal) and those who didn't. The investigators are going to compare groups of anesthesiology residents going through same scenarios of simulated critical events in high fidelity simulation session. Scenarios will be recorded to be analyzed by 2 reviewers independently. A specific checklist of appropriate treatment and a non technical skill checklist will be use to cote team performance (OTTAWA and TEAM scales). Stress of the participants will be assessed by visual analogic scale of participants anxiety and stress. The two groups will be compare to see if improvement in team performance is associated with the intervention.

Registry
clinicaltrials.gov
Start Date
September 2016
End Date
October 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Claude Bernard University
Responsible Party
Principal Investigator
Principal Investigator

Lilot Marc

MD

Claude Bernard University

Eligibility Criteria

Inclusion Criteria

  • Anesthesiology and Intensive care resident in the simulation education curriculum

Exclusion Criteria

  • Refusal to participate (written approval required)

Outcomes

Primary Outcomes

Performance during simulation

Time Frame: day 1

Performance will be assessed by the sum of 3 assessment: Ottawa non technical skill scale, team scanle and specific technical skill scale Total will be a number from 0 to 100.

Secondary Outcomes

  • Visual analogic scales of confidence(day 1)
  • visual analogic scale of anxiety(day 1)

Study Sites (1)

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