Resilience and Acute Stress in Simulation (SimStress)
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About
The objective is to study an association between the resilience developed by anesthesia professionals and the level of acute stress during a simulation session.
Full description
This trial will take place at the Grenoble Alpes University Hospital. Volunteer anaesthetists, nurse anaesthetists, professionals or students will perform a simulation scenario. This scenario generates a high level of stress and focuses on medication errors, which is a good educational tool for the participants.
The simulation is performed in an available operating room with a dedicated anesthesia cart. In this environment, 17 error opportunities were created, i.e., factors that could contribute to the occurrence of a medication error. A person playing the role of the anesthesiologist will give instructions, leave the room, and return to interrupt the participant several times, which will contribute to the intensity of the stressor. The simulation will proceed as follows:
Briefing:
Welcome and explanation of the session. Collection of age, gender, number of years in anesthesia, number of previous simulation sessions, participation or not in stress management training. Presentation of the context and the anesthesiologist, then the participants evaluate their stress using the VAS (visual analog scale) Stress, which triggers the beginning of the scenario. Introduction of the setting and the anesthesiologist, then participants rate their stress using the VAS Stress scale, triggering the start of the scenario.
Scenario:
10 minutes in length. After the briefing, the anesthesiologist announces the imminent arrival of a patient with a suspected abdominal aortic aneurysm. The participant must quickly prepare a tray of medications. The scenario ends just prior to the patient's arrival, with the anesthesiologist presenting the stress VAS again for further evaluation.
Debriefing:
The participant completes a questionnaire about opportunities for detected errors, followed by a 15-minute debriefing after the simulation session.
For each participant, data regarding stress VAS, CD-RISC, PSS-10 and number of errors detected will be compared.
The primary objective is to analyze an association between resilience developed by anesthesia professionals and acute stress level.
The secondary objectives are to study the association between the resilience developed by the anesthesia professionals and the level of acute stress present immediately at the end of the simulation.
immediately at the end of the simulation. Measure the association between resilience (CDRISC 10) and performance (number of potential errors detected). Compare resilience and acute stress between different statuses (anesthesiologist, intern, nurse anesthetist, student nurse anesthetist).
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Inclusion criteria
- Accepts Healthy Volunteers
Exclusion criteria
- Participants who object to the use of their data for research purposes.
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Data sourced from clinicaltrials.gov
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