None listed
Conditions
Interventions
All participants perform the first simulation without cognitive aids. For the second simulation,
they are randomized into three groups with stratification on their status:
Group A is the control group without cognitive aids,All participants perform the first simulation without cognitive aids. Fo
they are randomized into three groups with stratification on their status:
Group B is the group with the « CPR form » as a cognitive aid available throughout CPR
,All participants perform the first
they are randomized into three groups with stratification on their status:
Group C is the group with visualization in real-
time of their CPR activity on the QCPRTM screen
Other,Other,Other
Sponsors
None
Eligibility
Sex/Gender
All
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: Doctors and registered nurses carrying out the University Diploma in Emergency Pediatrics (Faculty of Medicine of Poitiers) (13,14) Pediatric residents from the Poitiers University Hospital who received theoretical and practical training in infant CPR Participants who agreed to participate
Exclusion criteria
Exclusion criteria: existence of physical constraints preventing participants from performing CPR or ventilation Participants who did not follow up all the steps of the intervention
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| global performance score of CPR Initial simulation and repeated simulation after 4 weeks score of CPR displayed on the QCPR screen | — |
Secondary
| Measure | Time frame |
|---|---|
| self-assessment of the simulation training after the second simulation self-assessment questionnaire,evolution of specific respiratory and circulatory performance scores between 1st and 2nd sim Initial and after 4 weeks score of CPR displayed on the QCPR screen | — |
Countries
France
Contacts
Public ContactDenis Oriot
University of Poitiers
Outcome results
None listed