Funding for this research was provided by:
Ministère de la Santé et des Services sociaux (PREPS-15-0024)
Received: 29 April 2021
Accepted: 19 January 2022
First Online: 2 February 2022
: The study was approved by the ethical committee (CPP LYON SUD-EST IRB: 00009118) in line with the French law on clinical research. The patient cases used for the simulation session scenarios can only be developed after the patient has been informed of the study. An information note has been made available to the departments concerned. This document informs the patients of the implementation of the study and the use of hospitalisation data after anonymisation. Participation in the study is voluntary for wards and team members. The study, by its nature, does not present any additional risk to participants. There are no risks for wards and participants. Non-participation has no negative consequences whatsoever. Moreover, participants can withdraw from the study at any time without stating their reasons and without experiencing any associated disadvantages. Statutory data protection provisions will be adhered in the study.
: Not applicable.
: The authors declare that they have no competing interests.