Comparison of Web- Versus Classroom-based Basic Ultrasound and Extended Focused Assessment With Sonography for Trauma (EFAST) Training in Two European Hospitals
NCT ID: NCT01040767
Last Updated: 2009-12-30
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
55 participants
INTERVENTIONAL
2008-11-30
2009-02-28
Brief Summary
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Methods: Physicians from two German emergency departments were randomized into a classroom group with traditional lectures and a web group that watched narrated lectures online. All participants completed a pre- and post-test, and a second post-test eight weeks later. Both groups underwent hands-on training after the first post-test. A control group completed the two initial tests without didactic intervention.
Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
NONE
Study Groups
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Class
Didactic training in basic ultrasound and the EFAST
Physicians in the classroom group (class) listened to traditional lectures, while the web group (web) watched narrated lectures online. All participants completed a pre- and post-test, and a second post-test eight weeks later. Both groups underwent hands-on training after the first post-test.
Web
Didactic training in basic ultrasound and the EFAST
Physicians in the classroom group (class) listened to traditional lectures, while the web group (web) watched narrated lectures online. All participants completed a pre- and post-test, and a second post-test eight weeks later. Both groups underwent hands-on training after the first post-test.
Control
No interventions assigned to this group
Interventions
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Didactic training in basic ultrasound and the EFAST
Physicians in the classroom group (class) listened to traditional lectures, while the web group (web) watched narrated lectures online. All participants completed a pre- and post-test, and a second post-test eight weeks later. Both groups underwent hands-on training after the first post-test.
Eligibility Criteria
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Inclusion Criteria
* Age ≥ 18 years
Exclusion Criteria
* Control group: Subjects who did not complete the pre-test
18 Years
ALL
Yes
Sponsors
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Klinikum Nürnberg
OTHER
Institut fuer Notfallmedizin Kempten e.V., Germany
UNKNOWN
Brigham and Women's Hospital
OTHER
Responsible Party
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Department of Emergency Medicine, Brigham and Women's Hospital, Boston, USA
Principal Investigators
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Elke Platz, MD, RDMS
Role: PRINCIPAL_INVESTIGATOR
Brigham and Women's Hospital, Boston USA
Locations
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Institut fuer Notfallmedizin e.V.
Kempten (Allgäu), Bavaria, Germany
Klinikum Nuernberg
Nuremberg, Bavaria, Germany
Countries
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Other Identifiers
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2008-P-002019/1
Identifier Type: -
Identifier Source: org_study_id