Skip to main content
Clinical Trials/NCT02926599
NCT02926599CompletedNot Applicable

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

Claude Bernard University2 sites in 1 country118 target enrollmentStarted: September 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
118
Locations
2
Primary Endpoint
Performance during simulation

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Anesthesiology and Intensive care resident in the simulation education curriculum

Exclusion Criteria

  • Refusal to participate (written approval required)

Arms & Interventions

Personal Optimization Training

Experimental

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.

Intervention: Personal Optimization Training (Behavioral)

Control

No Intervention

No particular training.

Screening of normal labs results during 2 min, after briefing of the scenario and before the start of the scenario.

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)

Investigators

Sponsor
Claude Bernard University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lilot Marc

MD

Claude Bernard University

Study Sites (2)

Loading locations...

Similar Trials

Potential Optimization Training in... | Clinical Trial