- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05297877
Use of Artificial Intelligence Cardiac Ultrasound Technology in Teaching Point of Care Cardiac Ultrasound
March 23, 2023 updated by: NUS Anaesthesia, National University of Singapore
Use of Artificial Intelligence Cardiac Ultrasound Technology in Teaching Point of Care Cardiac Ultrasound - a Randomised Controlled Trial
The aim of the study is to evaluate the effectiveness of artificial intelligence (A.I.) cardiac ultrasound technology in teaching point of care cardiac ultrasound (POCUS Cardiac).
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
50
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 Contact
- Name: Suresh Paranjothy
- Phone Number: 6772 6897
- Email: anasp@nus.edu.sg
Study Contact Backup
- Name: Vanessa Chua
- Phone Number: 6772 6897
- Email: anactyv@nus.edu.sg
Study Locations
-
-
-
Singapore, Singapore
- Recruiting
- National University of Singapore
-
Contact:
- Suresh Paranjothy
- Phone Number: 6772 6897
-
Contact:
- Vanessa Chua
- Phone Number: 6772 6897
-
Sub-Investigator:
- Zheng Ning Koh
-
Sub-Investigator:
- Ashokka Balakrishnan
-
Sub-Investigator:
- Fun Gee Chen
-
Sub-Investigator:
- Siaw May Leong
-
Sub-Investigator:
- Rohit Vijay Agrawal
-
Sub-Investigator:
- Donald Peng Xiang Foo
-
Sub-Investigator:
- Tze Yuh Vanessa Chua
-
Sub-Investigator:
- Xin Yan Tan
-
-
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
19 years to 30 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Medical students with no prior training in point of care cardiac ultrasound
Exclusion Criteria:
- Medical students who have received prior training in point of care cardiac ultrasound
- Participants who are unable to complete the entire training programme (pre-training MCQ, simulation session, post-training MCQ, practical evaluation, follow up practical evaluation one month later)
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: AI Machine
All study participants will undergo a full day (roughly 8 hours) training programme consisting of a pre-test MCQ, a didactic lecture, hands-on training session, a post-test MCQ, and a practical evaluation.
They will be randomised to using an A.I. ultrasound machine for teaching.
|
Participants will go through the training programme using an AI machine for learning.
|
|
Other: Conventional Machine
All study participants will undergo a full day (roughly 8 hours) training programme consisting of a pre-test MCQ, a didactic lecture, hands-on training session, a post-test MCQ, and a practical evaluation.
They will be randomised to using a conventional ultrasound machine for teaching.
|
Participants will go through the training programme using a conventional machine for learning.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Effectiveness of artificial intelligence (A.I.) cardiac ultrasound technology in teaching point of care cardiac ultrasound vs conventional echo machine
Time Frame: Study till 1 month post-study
|
Evaluate the effectiveness between AI and conventional echo machine by pre and post-session MCQs, and post intervention evaluation of practical skills using echo machine
|
Study till 1 month post-study
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Suresh Paranjothy, National University Health System
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)
January 14, 2022
Primary Completion (Anticipated)
December 1, 2024
Study Completion (Anticipated)
December 1, 2024
Study Registration Dates
First Submitted
March 7, 2022
First Submitted That Met QC Criteria
March 16, 2022
First Posted (Actual)
March 28, 2022
Study Record Updates
Last Update Posted (Actual)
March 24, 2023
Last Update Submitted That Met QC Criteria
March 23, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- NUS-IRB-2021-484
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
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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