- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02304133
Transfer From a Point-of-care Ultrasound Course
November 25, 2014 updated by: Tobias Todsen, Rigshospitalet, Denmark
Transfer From a Point-of-care Ultrasound Course to Diagnostic Performance on Patients - a Randomized Controlled Trial
This study explores the effect of a four-hour ultrasound course on physicians' point-of-care ultrasound performance on patients representing acute abdominal surgical conditions.
Study Overview
Detailed Description
A randomized controlled trial with physicians was conducted.
The intervention group participated in a four-hour abdominal POC US course before performing ultrasound on four patients with different abdominal surgical conditions.
The control group did not participate in a course before performing ultrasound on the patients.
Study Type
Interventional
Enrollment (Actual)
64
Phase
- Not Applicable
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Medical Doctor
- Signed up for a courses in abdominal point-of-care ultrasound
Exclusion Criteria:
- None
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
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Intervention
participating in a four-hour course in abdominal POC US
|
|
|
Placebo Comparator: Control
no training
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ultrasound performance
Time Frame: 4 ultrasound cases conducted by the study participants were assessed immediately after the intervention/control circumstances
|
An Objective Structured Assessment of Ultrasound Skills (OSAUS) scoring form was used to assess ultrasound performance
|
4 ultrasound cases conducted by the study participants were assessed immediately after the intervention/control circumstances
|
|
Diagnostic accuracy
Time Frame: 4 ultrasound cases conducted by the study participants were assessed immediately after the intervention/control circumstances
|
The ultrasound diagnoses were evaluated as "correct," "inconclusive," or "false," and the diagnostic accuracy was calculated by sensitivity and specificity
|
4 ultrasound cases conducted by the study participants were assessed immediately after the intervention/control circumstances
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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
January 1, 2012
Primary Completion (Actual)
February 1, 2013
Study Completion (Actual)
November 1, 2014
Study Registration Dates
First Submitted
November 24, 2014
First Submitted That Met QC Criteria
November 25, 2014
First Posted (Estimate)
December 1, 2014
Study Record Updates
Last Update Posted (Estimate)
December 1, 2014
Last Update Submitted That Met QC Criteria
November 25, 2014
Last Verified
November 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- H-3-2012-006
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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