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Tracking Information | |||||
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First Received Date † | May 28, 2008 | ||||
Last Updated Date | June 3, 2008 | ||||
Start Date † | July 2007 | ||||
Current Primary Outcome Measures † |
performance of clinical reasoning and skills in simulated settings [ Time Frame: before and after the simulation-based training ] [ Designated as safety issue: No ] | ||||
Original Primary Outcome Measures † | Same as current | ||||
Change History | Complete list of historical versions of study NCT00690144 on ClinicalTrials.gov Archive Site | ||||
Current Secondary Outcome Measures † |
clinical performance of reasoning and skills [ Time Frame: before and after the simulation-based training ] [ Designated as safety issue: No ] | ||||
Original Secondary Outcome Measures † | Same as current | ||||
Descriptive Information | |||||
Brief Title † | High-Fidelity Simulation in Health Care Education | ||||
Official Title † | Prospective Study Focusing on Impact of High-Fidelity Simulation in Health Care Education | ||||
Brief Summary | The purpose of this study is to determine whether the use of high-fidelity simulation in health care education is an effective training and evaluation model. |
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Detailed Description | High-fidelity simulation has many advantages in medical education. Simulation-based critical care training is especially valuable due to error-prone work settings and the high cost of patient adverse events. This study was conducted to assess the effectiveness of implementing the high-fidelity simulation in critical care training, and the feasibility of high-fidelity simulation as an evaluation tool. |
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Study Phase | |||||
Study Type † | Interventional | ||||
Study Design † | Prevention, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment | ||||
Condition † | Healthy | ||||
Intervention † | Device: High-fidelity high-fidelity mannequin simulator (SimMan, Laerdal, Stavanger, Norway). | ||||
Study Arms / Comparison Groups | Experimental: the trainees in the simulation group receive simulation-based training | ||||
Publications * | |||||
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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Recruitment Information | |||||
Recruitment Status † | Recruiting | ||||
Estimated Enrollment † | 500 | ||||
Estimated Completion Date | June 2011 | ||||
Estimated Primary Completion Date | June 2011 (final data collection date for primary outcome measure) | ||||
Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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Gender | Both | ||||
Ages | 18 Years to 80 Years | ||||
Accepts Healthy Volunteers | Yes | ||||
Contacts †† |
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Location Countries † | Taiwan | ||||
Expanded Access Status | |||||
Administrative Information | |||||
NCT ID † | NCT00690144 | ||||
Responsible Party | Matthew Huei-Ming Ma, MD, PhD, National Taiwan University Hospital | ||||
Secondary IDs †† | |||||
Study Sponsor † | National Taiwan University Hospital | ||||
Collaborators †† | |||||
Investigators † |
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Information Provided By | National Taiwan University Hospital | ||||
Verification Date | May 2008 | ||||
† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |