- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00690144
High-fidelity Simulation in Health Care Education
June 28, 2010 updated by: National Taiwan University Hospital
Prospective Study Focusing on Impact of High-fidelity Simulation in Health Care Education
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.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
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.
Study Type
Interventional
Enrollment (Anticipated)
500
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Taipei, Taiwan
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Chih-Wei Yang, M.D.
- Phone Number: 1426 886-2-2312-3456
- Email: cwyang100@ntu.edu.tw
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- healthcare trainees, including medical students, nursing students, residents, nursing staff and emergency medical technicians.
Exclusion Criteria:
- any trainees unwilling to receive simulation-based training
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: simulation group
the trainees in the simulation group receive simulation-based training
|
Critical care training using high-fidelity simulation.
The case scenarios were simulated by a high-fidelity mannequin simulator (SimMan, Laerdal, Stavanger, Norway).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
performance of clinical reasoning and skills in simulated settings
Time Frame: before and after the simulation-based training
|
before and after the simulation-based training
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
clinical performance of reasoning and skills
Time Frame: before and after the simulation-based training
|
before and after the simulation-based training
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Matthew Huei-Ming Ma, MD, PhD, National Taiwan University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2007
Primary Completion (Anticipated)
June 1, 2011
Study Completion (Anticipated)
June 1, 2011
Study Registration Dates
First Submitted
May 28, 2008
First Submitted That Met QC Criteria
June 3, 2008
First Posted (Estimate)
June 4, 2008
Study Record Updates
Last Update Posted (Estimate)
June 29, 2010
Last Update Submitted That Met QC Criteria
June 28, 2010
Last Verified
June 1, 2010
More Information
Terms related to this study
Other Study ID Numbers
- 200803078R
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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