- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04834700
Comparison of Hands-on Versus Online Learning About Ocular Ultrasound
Comparison of Hands-on Versus Online Learning in Teaching Ultrasound Skills for Eye
Study Overview
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Seoul, Korea, Republic of, 06351
- Recruiting
- Samsung Medical Center
-
Contact:
- Hee Yoon, PhD., MD.
- Phone Number: 81-02-3410-2053
- Email: wildhi.yoon@samsung.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria for doctors:
- Those who have received basic ultrasound education but have not received ocular ultrasound education
- Residents and interns working in the emergency room
- Those who voluntarily agree to participate in the research through the recruitment announcement
Inclusion Criteria for standard patients:
- Adults over 18 years of age without eye-related symptoms
- Those who do not have unusual findings in the eye when scanning by ultrasound
- Those who voluntarily agree to participate in the research through the recruitment announcement
Exclusion Criteria for standard patients:
- Those with a history of ophthalmic diseases
- Those who have a history of ophthalmic surgery such as lens implantation
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: hands-on group
The doctors who participated in the study will be educated ocular ultrasound scanning method by hands-on about 20 minutes, and perform ocular ultrasound scans on two standard patients.
|
|
|
Other: online group
The doctors who participated in the study will be educated ocular ultrasound scanning method by online lecture about 20 minutes, and perform ocular ultrasound scans on two standard patients.
|
In terms of teaching ultrasound, video lectures will be conducted rather than hands-on, which is the traditional method.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
scan score
Time Frame: through study completion, an average of 1 year
|
We make our own guideline to evaluate ocular ultrasound scans. The ocular ultrasound images performed participants are evaluated according to the guideline. We compare the scores of the hands-on group and the online group to see if there is a significant difference between the two groups. |
through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Optic nerve sheath diameter (ONSD)
Time Frame: through study completion, an average of 1 year
|
Two ultrasound experts measure the standard patient's ONSD and use it as a reference value. The course of ocular ultrasound scanning involves measuring ONSD. We compare the measured ONSD of the hands-on group and the online group to see if there is a significant difference between the two groups. |
through study completion, an average of 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Hee Yoon, MD., PhD., Samsung medical center, Emergency department
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-09-174
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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