Instructor-led Simulation Training Versus Self-directed Simulator Training During Simulated Neonatal Resuscitation
NCT ID: NCT01875900
Last Updated: 2018-07-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
38 participants
INTERVENTIONAL
2013-06-30
2014-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
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Video-assisted learning and self-directed training
The Neonatal Resuscitation Program (NRP) digital video disc (DVD) will be provided for video study and a low-fidelity newborn manikin for self-directed resuscitation training (90 minutes training time, six students per group).
Video-assisted learning and self-directed training
The Neonatal Resuscitation Program (NRP) DVD will be provided for video study and a low-fidelity newborn manikin for self-directed resuscitation training (90 minutes training time, six students per group).
Simulation-based neonatal resuscitation training
Students will learn initial assessment of newborns and basic resuscitation skills and actively apply these skills during simulated clinical scenarios both with a low- and high-fidelity manikin (90 minutes training time, six students per group).
Simulation-based neonatal resuscitation training
Students will learn initial assessment of newborns and basic resuscitation skills and actively apply these skills during simulated clinical scenarios both with a low- and high-fidelity manikin (90 minutes training time, six students per group).
Interventions
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Video-assisted learning and self-directed training
The Neonatal Resuscitation Program (NRP) DVD will be provided for video study and a low-fidelity newborn manikin for self-directed resuscitation training (90 minutes training time, six students per group).
Simulation-based neonatal resuscitation training
Students will learn initial assessment of newborns and basic resuscitation skills and actively apply these skills during simulated clinical scenarios both with a low- and high-fidelity manikin (90 minutes training time, six students per group).
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Signing of informed consent
Exclusion Criteria
The first two OSCEs in July and August will be part of a pilot study. The combined results of both examinations will be used for a sample size calculation.
18 Years
70 Years
ALL
Yes
Sponsors
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Medical University of Graz
OTHER
Responsible Party
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Lukas P Mileder, MD
cand.med.
Principal Investigators
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Georg Schmölzer, M.D., Ph.D.
Role: STUDY_CHAIR
Division of Neonatology, Department of Pediatrics, Medical University of Graz, Austria; Department of Pediatrics, University of Alberta, Edmonton, Canada
Berndt Urlesberger, M.D.
Role: STUDY_CHAIR
Division of Neonatology, Department of Pediatrics, Medical University of Graz, Austria
Ernst Eber, M.D.
Role: STUDY_CHAIR
Respiratory and Allergic Disease Division , Department of Pediatrics, Medical University of Graz, Austria
Albrecht Schmidt, M.D.
Role: STUDY_CHAIR
Division of Cardiology, Department of Internal Medicine, Medical University of Graz, Austria; Clinical Skills Center, Medical University of Graz, Austria
Locations
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Clinical Skills Center, Medical University of Graz
Graz, Styria, Austria
Countries
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Other Identifiers
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25-399 ex 12/13
Identifier Type: -
Identifier Source: org_study_id
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