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Clinical Trials/NCT02483546
NCT02483546
Completed
Not Applicable

High Fidelity Simulation In Medecine Education

University of Monastir1 site in 1 country181 target enrollmentJanuary 2014
ConditionsCardiac Arrest

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Arrest
Sponsor
University of Monastir
Enrollment
181
Locations
1
Primary Endpoint
better acquisition of cognitive skills for students
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

High fidelity Simulation has spread from anesthesiology to other disciplines such as internal medicine, pediatrics, and emergency medicine . Over the past decade, the use of simulation in medical education has increased exponentially. The term ''simulation'' spans a wide variety of formats, from the low-tech actor portraying a standardized patient to high-fidelity mannequin-based human patient simulation (HPS). HPS is able of both simulating realistic patient encounters and giving real-time, physiologically accurate feedback. Studies thus far show that use of simulation in training medical students and residents is helpful in strengthening students' knowledge and in evaluating their performance. Students appreciate simulation-based education as ''an opportunity to learn new skills in a safe environment .

Detailed Description

This was a randomized, controlled trial of a simulation- based educational intervention designed to increase medicine student's clinical skills in cardiac arrest procedures .The investigators included 181 fifth-year medical students rotating in the emergency department of Fattouma Bourguiba University hospital of Monastir (Tunisia) during the period from January 2013 to January 2014.Students were randomized into two groups using a random number generator to an intervention group (simulatortrained, n = 99) or a control group (traditionally teaching, n =82). The investigators conducted a prospective, randomized, non-blinded study to determine whether simulation based training is superior to traditional teaching in the assessment and management of simulated patients presenting with myocardial infarction (MI) complicated by ventricular fibrillation.

Registry
clinicaltrials.gov
Start Date
January 2014
End Date
September 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Pr. Semir Nouira

professor

University of Monastir

Eligibility Criteria

Inclusion Criteria

  • Medecine students

Exclusion Criteria

  • Non Medecine students

Outcomes

Primary Outcomes

better acquisition of cognitive skills for students

Time Frame: just after randomisation (one day)

Pretest using 20 multiple choice questions after randomization. A second round of the same testing was then conducted for both groups just after the course (posttest). The test score range from 0 to 20 (maximum). The difference between the rating of the post-test and pre-test identifies the delta score of the student.

Secondary Outcomes

  • Satisfaction 5 point likert scale(just after randomisation (one day))

Study Sites (1)

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