Simulation training
Conditions
Interventions
This is a methodological study followed by an experimental study of the controlled and randomized clinical trial (CRCT) type, whose main purpose is to create situations to analyze effects on the parti
s variables of interest that simulate natural environmental conditions. In the present study, a pre-test and post-test design will be used in both groups. Therefore, the experimental method with a par
s Health,” with a workload of 30 hours. The course will be conducted in the practice laboratories of both institutions in five stages: lecture-based theoretical class, simulation scenario 1, 2
Sponsors
Universidade Federal do Rio Grande do Norte - Lagoa Nova Campus Central - UFRN
Pós-Graduação em Enfermagem
Eligibility
Inclusion criteria
Inclusion criteria: Students enrolled in the undergraduate Nursing program; with regular attendance in the women's health course; with 100% attendance in the experiment
Exclusion criteria
Exclusion criteria: Students who have failed the course and are therefore retaking it
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| A significant improvement in the correct answer score is expected on the post-test compared to the pre-test for the experimental group that experienced the clinical simulation, compared to the control group that did not | — |
Secondary
| Measure | Time frame |
|---|---|
| Does not have a secondary outcome | — |
Countries
Brazil
Contacts
Public ContactRichardson Silva
Richardson Augusto Rosendo da Silva
Outcome results
None listed