- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02289911
FAST Learning Methods (FAST)
November 10, 2014 updated by: Lukasz Szarpak, International Institute of Rescue Research and Education
Comparison of Two Learning Methods in Focused Assessment With Sonography for Trauma (FAST) Training Among Paramedics
Training paramedics in new skills via classroom-based teaching has inherent costs and time constraints.
The investigators sought to evaluate whether web-based didactics result in similar knowledge improvement and retention of FAST (Focused Assessment with Sonography for Trauma) compared with the traditional method.
Study Overview
Detailed Description
Paramedics 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 four weeks later.
Both groups underwent hands-on training after the first post-test.
A control group completed the two initial tests without didactic intervention.
Study Type
Interventional
Enrollment (Anticipated)
100
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
-
-
Masovia
-
Warsaw, Masovia, Poland, 03-122
- Recruiting
- International Institute of Rescue Research and Education
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- give voluntary consent to participate in the study emergency medical professionals (paramedics, nurses, physicians)
Exclusion Criteria:
- not meet the above criteria
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Class
Traditional learning form
|
Participants 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.
|
|
Active Comparator: Web
Didactic training using internet
|
Participants 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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge (Mean test scores by didactic group for three consecutive multiple choice tests)
Time Frame: 1 MONTH
|
Mean test scores by didactic group for three consecutive multiple choice tests
|
1 MONTH
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self reported satisfaction
Time Frame: 1 MONTH
|
Participant satisfaction with training and reported comfort with ultrasound use after training
|
1 MONTH
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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
November 1, 2014
Primary Completion (Anticipated)
December 1, 2014
Study Completion (Anticipated)
December 1, 2014
Study Registration Dates
First Submitted
November 7, 2014
First Submitted That Met QC Criteria
November 10, 2014
First Posted (Estimate)
November 13, 2014
Study Record Updates
Last Update Posted (Estimate)
November 13, 2014
Last Update Submitted That Met QC Criteria
November 10, 2014
Last Verified
November 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- FAST/2014/03
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.