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Clinical Trials/NCT04512183
NCT04512183
Unknown
Not Applicable

Effectiveness of Simulation in the Cognitive, Physiological and Emotional Sphere of Nursing Students in Caring for Patients With Signs of Sepsis: Crossover Clinical Trial

University of Brasilia0 sites60 target enrollmentSeptember 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Learning Process in Nursing Graduation
Sponsor
University of Brasilia
Enrollment
60
Primary Endpoint
Cognitive Performance (Retention)
Last Updated
5 years ago

Overview

Brief Summary

Simulation is an active teaching strategy capable of reproducing real situations and allowing practical experiences, in which the student is the protagonist of his own knowledge. Scientific evidence highlights, that exposure to the unknown or new can generate stress to the individual, but when dosed, to a certain extent it can increase the level of knowledge. Not infrequently, the lack of stress control can trigger physiological and subjective changes resulting from the increase in its level, such as situations that include the implementation of simulation scenarios in pedagogical teaching models.

Detailed Description

Objective: To evaluate the effect of simulation (high and low fidelity) on the cognitive, physiological and emotional sphere of nursing students in caring for patients with signs of sepsis. Hypothesis of the study: Null hypothesis: Students undergoing high-fidelity simulation will show similar levels of stress, cognitive performance and retention of knowledge in relation to those who will perform low-fidelity simulation in patients with signs of sepsis. Alternative hypothesis: The cognitive performance and stress will be higher in students who experience high fidelity simulation when compared to students who experience low fidelity simulation.

Registry
clinicaltrials.gov
Start Date
September 1, 2020
End Date
August 31, 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
University of Brasilia
Responsible Party
Principal Investigator
Principal Investigator

Marcia Cristina da Silva Magro

Principal Investigator; PhD

University of Brasilia

Eligibility Criteria

Inclusion Criteria

  • Students approved in the discipline related to nursing care for adult and elderly patients;
  • Aged over 18 years.

Exclusion Criteria

  • Who have experience in the health field (firefighters and nursing technicians, among others);
  • Members of the Health Simulation League;
  • Those who do not complete all stages of the research.

Outcomes

Primary Outcomes

Cognitive Performance (Retention)

Time Frame: Applied thirty days after the intervention

Students' knowledge about nursing care in sepsis measured using a structured questionnaire with six multiple-choice questions

Cognitive Performance (Baseline)

Time Frame: Applied before the intervention

Students' knowledge about nursing care in sepsis measured using a structured questionnaire with six multiple-choice questions

Cognitive Performance (Post-test)

Time Frame: Applied immediately after the intervention

Students' knowledge about nursing care in sepsis measured using a structured questionnaire with six multiple-choice questions

Secondary Outcomes

  • Student stress (Post-test)(Immediately after the intervention)
  • Student stress (Baseline)(Before the intervention)

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