- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06567912
The Development of the Simulation Curriculum and AI-incorporated Assessment Tool for Transesophageal Echocardiography
September 16, 2025 updated by: National Taiwan University Hospital
The Development of the Simulation Curriculum and Artificial Intelligence-incorporated Assessment Tools for Transesophageal Echocardiography in Patients With Cardiac Arrest
This study aims to establish a novel transesophageal echocardiography (TEE) simulation curriculum based on previous research results and suggestions from the American College of Emergency Physicians.
To better evaluate the efficacy of the curriculum, an evaluation model utilizing artificial intelligence (AI) would be introduced.
The study population is at least 60 junior physicians in the emergency department or other departments interested in TEE.
After the curriculum, junior physicians could utilize TEE on cardiac arrest patients and improve diagnostic accuracy and patient outcomes.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
This study aims to establish a novel TEE simulation curriculum based on previous research results and suggestions from the American College of Emergency Physicians.
To better evaluate the efficacy of the curriculum, an evaluation model utilizing artificial intelligence (AI) would be introduced.
The study population is at least 60 junior physicians in the emergency department or other departments interested in TEE.
After the curriculum, junior physicians could utilize TEE on cardiac arrest patients and improve diagnostic accuracy and patient outcomes.
Study Type
Observational
Enrollment (Estimated)
100
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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Taipei, Taiwan
- Recruiting
- Lien
-
Contact:
- Wan-Ching Lien, MD
- Phone Number: 886-2-23223150
- Email: dtemer17@yahoo.com.tw
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
emergency physicians
Description
Inclusion Criteria:
Emergency physicians interested in TEE learning.
Exclusion Criteria:
Emergency physicians are not interested in TEE learning.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
the efficiency of AI model
Time Frame: 6 months
|
the AI model to recognize the TEE views, including sensitivity, specificity, PPV, NPV
|
6 months
|
|
learning outcomes:immediate assessment
Time Frame: 4 hours
|
image acquisition and image quality using 5-point Likert scales.
The range from 1 (the worst) to 5 (the best).
|
4 hours
|
|
learning outcomes: 3-month evaluation
Time Frame: 3 months
|
image acquisition and image quality using 5-point Likert scales.
The range from 1 (the worst) to 5 (the best).
|
3 months
|
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 (Actual)
August 1, 2023
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
August 18, 2024
First Submitted That Met QC Criteria
August 21, 2024
First Posted (Actual)
August 23, 2024
Study Record Updates
Last Update Posted (Actual)
September 22, 2025
Last Update Submitted That Met QC Criteria
September 16, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202211107RINB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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.