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

Sponsor
University Health Network, Toronto (Other)
Overall Status
Unknown status
CT.gov ID
NCT03262532
Collaborator
(none)
20
1
17.6
1.1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Web-base simulator
  • Other: No web-base simulator

Study Design

Study Type:
Observational
Anticipated Enrollment :
20 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Assessment of a Web-Based Simulation Module to Improve Performance in Obtaining Standard Transesophageal Echocardiography (TEE) Views
Actual Study Start Date :
Mar 13, 2017
Anticipated Primary Completion Date :
Jul 1, 2018
Anticipated Study Completion Date :
Sep 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental

Learning TEE manipulation with a Web-based TEE simulation module

Other: Web-base simulator
Training manipulation of TEE using a Web-based simulator

Control

Learning a TEE manipulation without the Web-based TEE simulation

Other: No web-base simulator
Training manipulation of TEE with out a web-base simulator

Outcome Measures

Primary Outcome Measures

  1. TEE simulation model decreases time to select image acquisition in trainee participant vs. participants trained by reading material only [2 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 Outcome Measures

  1. 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 cardiographers [2 week review 1 session for assessment- time required to acquire 10 views]

    Each image will be captured by the model and graded according to a 5 point scale.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Toronto General Hospital Toronto Ontario Canada M5G 2C4

Sponsors and Collaborators

  • University Health Network, Toronto

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Health Network, Toronto
ClinicalTrials.gov Identifier:
NCT03262532
Other Study ID Numbers:
  • REB 15-9547
First Posted:
Aug 25, 2017
Last Update Posted:
Feb 20, 2018
Last Verified:
Nov 1, 2017
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Keywords provided by University Health Network, Toronto

Study Results

No Results Posted as of Feb 20, 2018