- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02289885
FAST Examination During Emergency Practice (FAST)
November 10, 2014 updated by: Lukasz Szarpak, International Institute of Rescue Research and Education
Knowledge, Attitude and Practice About Focused Assessment With Sonography in Trauma Among Paramedics. Randomized Crossover Manikin Trial
The study evaluates the knowledge, attitude and practice about Focused Assessment with Sonography in Trauma among emergency medicine practitioners in Poland.
Study Overview
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
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-
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Warsaw, Poland, 04-628
- Recruiting
- International Institute of Rescue Research and Education
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-
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:
- Paramedics currently practicing in a Polish emergency department units and emergency medical services
- Age ≥ 18 years
Exclusion Criteria:
- Inability to participate in all aspects of the study prior to study begin
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: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: normal model patient
Images of the ultrasound window were captured to disk and later evaluated by an expert in emergency medicine.
In this study, the FAST examination was measured to the perihepatic space (also called Morison's pouch or the hepatorenal recess), perisplenic space, pericardium, and the pelvis.
|
Ultrasonography device
Other Names:
|
|
Experimental: ascites positive model patient
Images of the ultrasound window were captured to disk and later evaluated by an expert in emergency medicine.
In this study, the FAST examination was measured to the perihepatic space (also called Morison's pouch or the hepatorenal recess), perisplenic space, pericardium, and the pelvis.
|
Ultrasonography device
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Tests of Knowledge of the FAST Examination
Time Frame: 1 day
|
knowledge-based measures used to evaluate participants' knowledge of FAST-examination-related concepts (Survey)
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
FAST Performance Test
Time Frame: 1 day
|
The performance test required participants to conduct a FAST examination on two model patients (one normal, one ascites positive).
No help or feedback was given to the participants.
|
1 day
|
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Window acquisition time
Time Frame: 1 day
|
Identification of FAST Window Quadrants and Diagnostic Interpretation of FAST Windows. The window acquisition time was measured with a stopwatch and represented the period between first contact of the probe with the model patient's body and when the participant said "stop" to indicate an adequate window or the participant's judgment that he or she could not acquire the window. |
1 day
|
|
Window quality
Time Frame: 1 day
|
For each acquired window, an expert evaluated the quality of the window.
The window was rated as "excellent, fair, poor, or other."
"Other" captured situations where the window acquired was nondiagnostic.
Window quality was dichotomized into two categories, "excellent or not excellent," and subsequent analyses examined the number of participants that acquired "excellent" windows by quadrant (perihepatic space (also called Morison's pouch or the hepatorenal recess), perisplenic space, pericardium, and the pelvis and suprapubic quadrant) and patient type (normal, positive).
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1 day
|
|
Diagnostic accuracy
Time Frame: 1 day
|
For each acquired window, the participant rendered a diagnosis of that window.
An expert evaluated the quality of the diagnosis.
The diagnosis was rated as "correct, incorrect, or other."
"Other" captured situations where the window acquired was nondiagnostic.
For analysis purposes, diagnostic accuracy was dichotomized into two categories, "correct or not correct," and subsequent analyses examined the number of participants that interpreted the window correctly by quadrant (perihepatic space (also called Morison's pouch or the hepatorenal recess), perisplenic space, pericardium, and the pelvis and suprapubic quadrant) and patient type (normal, positive).
|
1 day
|
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/2014/02
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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