Simulation Training
Conditions
Interventions
A non-blinded randomized clinical trial was conducted based on two training strategies: with or without the use of a feedback device. It was carried out between 2019 and 2021 at the University Hospita
(2) debriefing of the results obtained in the previous phase and theoretical training in basic life support, followed by a post-test
(3) a second simulation of a cardiac arrest scenario, with randomized use of the feedback device by participants. The participants were divided into four groups: (1) nurses from critical care units wh
(2) nurses from critical care units who did not use the feedback device
(3) nurses from non-critical care units who used the feedback device
(4) nurses from non-critical care units who did not use the feedback device. Randomization was stratified using random distribution lists generated in Microsoft® Excel® by an external member of the st
Sponsors
Hospital Universitário da Universidade de São Paulo
Escola de Enfermagem da Universidade de São Paulo
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Active healthcare nurses; aged 18 years or older; of both sexes; from critical and non-critical adult patient units; working across all three shifts (morning, afternoon, and night)
Exclusion criteria
Exclusion criteria: Working in administrative areas of the hospital; being an instructor of Basic or Advanced Life Support courses; having completed another Basic or Advanced Life Support course between the first and second stages of the study; having health issues that impair CPR skills performance or being pregnant at the time of data collection
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome1: to evaluate whether the use of the cardiopulmonary resuscitation feedback device by nurses contributes to improving the quality of cardiopulmonary resuscitation, regardless of the professional's work unit;Found outcome 1: An improvement in cardiopulmonaru resuscitation metrics and learning was observed among nurses from both critical and non-critical units who used the feedback device during the simulation, regardless of the unit in which they work | — |
Secondary
| Measure | Time frame |
|---|---|
| The scope of this study was limited to primary outcome and no secondary outcome were assessed | — |
Countries
Brazil
Contacts
Public ContactThatiane Polastri
Escola de Enfermagem da Universidade de São Paulo
Outcome results
None listed