Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
118 participants
INTERVENTIONAL
2016-09-30
2017-10-31
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
DOUBLE
Study Groups
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Personal Optimization Training
Personal Optimization Training such as positive reinforcement, personalized psycho-physiological relaxation and mental rehearsal (total 5 hours a few weeks before the simulation).
Having 2 min to focus on techniques they were trained, after briefing of the scenario and before the start of the scenario.
Personal Optimization Training
Control
No particular training.
Screening of normal labs results during 2 min, after briefing of the scenario and before the start of the scenario.
No interventions assigned to this group
Interventions
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Personal Optimization Training
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
Yes
Sponsors
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Claude Bernard University
OTHER
Responsible Party
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Lilot Marc
MD
Principal Investigators
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Jean-Jacques, Lehot, PHD
Role: STUDY_CHAIR
CLESS
Locations
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CLESS
Lyon, Auvergne-Rhône-Alpes, France
Countries
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Other Identifiers
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TOPCLESS
Identifier Type: -
Identifier Source: org_study_id
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