High Fidelity Simulation Training
Conditions
Interventions
Open-label, parallel, randomized, and controlled clinical trial with nursing students from two universities in the Federal District. The participants will be divided into two groups: the traditional s
the difference lies in the scenario development methodology. The participants will immerse themselves in the simulation practice, and each group will have a maximum of 20 minutes for performance.
I02.903.847
Sponsors
UNB Ceilândia - Faculdade de Ciências e Tecnologias em Saúde
UNICEPLAC - Centro Universitário do Planalto Central Apparecido dos Santos
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Volunteer students aged 18 or over and regularly enrolled in courses dealing with Perioperative Nursing.
Exclusion criteria
Exclusion criteria: Student volunteers who are nursing technicians or first responders, or those on sick leave.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to observe improvements in cognitive skills (knowledge) and behavioral/affective skills (attitudes, behaviors and feelings), measured through satisfaction/self-confidence scales and the learner's experience with the adopted debriefing technique. | — |
Secondary
| Measure | Time frame |
|---|---|
| Participants are expected to improve their performance in clinical settings in the prevention, identification, and treatment of opioid-induced sedation and respiratory depression. Comparisons will be made using a checklist of expected behaviors to assess performance. | — |
Countries
Brazil
Contacts
Public Contactkarina ogliari
UNB Ceilândia - Faculdade de Ciências e Tecnologias em Saúde
Outcome results
None listed