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Assessment of a Web-Based Simulation in Transesophageal Echocardiography (TEE) Views

Assessment of a Web-Based Simulation Module to Improve Performance in Obtaining Standard Transesophageal Echocardiography (TEE) Views

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03262532
Acronym
Web-SimTEE
Enrollment
20
Registered
2017-08-25
Start date
2017-03-13
Completion date
2018-09-01
Last updated
2018-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Education, Training

Keywords

Interactive web-base simulation

Brief summary

Transesophageal echocardiography (TEE) is often used by anesthesiologists during cardiac surgery, as a monitoring tool in non-cardiac surgery, and as a point of care diagnostic tool in the intensive care unit (ICU). Furthermore, TEE is becoming a core skill in many specialties to facilitate focused cardiovascular assessment in hemodynamically compromised patients in various settings. Educators must determine how to best instruct current and future trainees to achieve clinical competence in TEE within a time limited and constantly expanding medical curriculum. In this study the investigators will evaluate a new online TEE Simulation module as a learning tool to accelerate and enhance traditional clinical teaching. This project will evaluate a new online TEE Simulation module that replicates the actions required to adjust TEE probe position and the ultrasound plane in relation to a 3D heart model. The investigators hypothesize that experience with the online TEE simulation module will improve the ability of trainees to independently perform TEE probe manipulations necessary to obtain standard TEE views. The proposed study will answer this question by measuring the performance of trainees in obtaining 10 of the 25 standard TEE views using the Vimedix mannequin-based ultrasonography simulator following an hour of review of the online TEE Simulation module. The educational benefit of the Web-based TEE simulation module, will be evaluated by 20 novices randomly assigned to two groups, a control group of 10 subjects without exposure to the Web-based simulation, and an experimental group of 10 subjects with exposure to the Web-based simulation. Both groups will be assessed on their performance in attaining the 10 standard TEE views with the Vimedix simulator.

Interventions

OTHERWeb-base simulator

Training manipulation of TEE using a Web-based simulator

OTHERNo web-base simulator

Training manipulation of TEE with out a web-base simulator

Sponsors

University Health Network, Toronto
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Residents or fellows in anesthesia, cardiology and critical care enrolled at the Toronto General Hospital

Exclusion criteria

* Residents or fellows in anesthesia, cardiology and critical care with prior experience with TEE probe manipulation

Design outcomes

Primary

MeasureTime frameDescription
TEE simulation model decreases time to select image acquisition in trainee participant vs. participants trained by reading material only2 week review 1 session for assessment (Control: time required to acquire 10 views, Intervention: I hour session with online simulator plus time required to acquire 10 views)The metrics for acquiring each image will be recorded by the model, the primary measurement will be time in seconds per view acquired.

Secondary

MeasureTime frameDescription
TEE simulation model improves select image quality in trainee participants vs. participants trained by reading material only as assessed by a expert review panel of echo cardiographers2 week review 1 session for assessment- time required to acquire 10 viewsEach image will be captured by the model and graded according to a 5 point scale.

Countries

Canada

Contacts

Primary ContactAnnette Vegas, MD
annette.vegas@uhn.ca416-340-4800

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026