Evaluation of Simulator Training on TEE Performance in Residents (TEESimulation)
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ClinicalTrials.gov Identifier: NCT02842632 |
Recruitment Status :
Completed
First Posted : July 25, 2016
Last Update Posted : October 20, 2017
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Training in TEE is based on hands-on training in the operation room which is time consuming and therefore its use and experience is limited among anesthesiologists.
Recent studies demonstrate that simulation-based education is also superior to a conventional didactic system and superior to hands-on teaching in the OR in terms of theoretical knowledge in echocardiography. So far there is no study evaluating the study effect in obtaining the 11 basic TEE views as recommended by the American Society of Echocardiography (ASE) and the Society of Cardiovascular Anesthesiologists (SCA) between simulator training and training in the operation room in residents with no prior knowledge of echocardiography. The basic TEE examination focus on the 11 most relevant views.
Therefore the investigators want to assess if there is a difference in the study effect in obtaining the 11 basic TEE views and also in theoretical knowledge in 3 groups of residents with no prior knowledge of echocardiography:
the simulation group (CAE Vimedix Simulator), the hands-on OR group and the online group (http://pie.med.utoronto.ca/TEE/).
prospective randomized single-center study. The investigators want to include 51 anaesthesia residents (17 per group) in their first or second year of training with no prior knowledge of echocardiography in this randomized, Controlled single-centre study.
The investigators want to assess the pre- and post training scores of the theoretical multiple choice test and the practical test in all 3 groups. The multiple choice test consists of 50 questions with 1 point per question (max. 50 points) and the practical test is an evaluation of 11 basic perioperative TEE examination on the simulator (CAE Vimedix Simulator). Each view is evaluated on a scale of 0 to 10 according to predetermined criteria including image angle, overall clarity and visualization of 3 major anatomic structures pertinent to each view. Each view can receive a maximum score of 10 and each study a maximum of 109 (ME asc. aortic LAX has only 2 main structures). Further the time to adjust each view and the time to complete the basic TEE Examination will be assessed.
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Satisfaction | Other: theoretical test Other: practical test | Not Applicable |

Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 54 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Health Services Research |
Official Title: | Evaluation of Simulator Training on Transesophageal Echocardiography (TEE) Performance in Anaesthesia Residents |
Actual Study Start Date : | April 2016 |
Actual Primary Completion Date : | May 2017 |
Actual Study Completion Date : | September 2017 |
Arm | Intervention/treatment |
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A virtual teaching
Group A will be introduced to the virtual TEE online (http://pie.med.utoronto.ca/TEE/)
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Other: theoretical test
The theoretical test is a multiple choice test which consists of 50 questions with 1 point per question (max. 50 points). It will be done before the teaching, after the 2 teaching sessions and 3 Months after the study Other: practical test The practical test is an evaluation of 11 basic perioperative TEE examination on the simulator (CAE Vimedix Simulator). Each view is evaluated on a scale of 0 to 10 according to predetermined criteria including image angle, overall clarity and visualization of 3 major anatomic structures pertinent to each view. Each view can receive a maximum score of 10 and each study a maximum of 109 (ME asc. aortic LAX has only 2 main structures). It will be done after the first and second teaching session, and 3 Months after the study. |
B simulator
Group B will be introduced to the simulator (CAE Vimedix Simulator)
|
Other: theoretical test
The theoretical test is a multiple choice test which consists of 50 questions with 1 point per question (max. 50 points). It will be done before the teaching, after the 2 teaching sessions and 3 Months after the study Other: practical test The practical test is an evaluation of 11 basic perioperative TEE examination on the simulator (CAE Vimedix Simulator). Each view is evaluated on a scale of 0 to 10 according to predetermined criteria including image angle, overall clarity and visualization of 3 major anatomic structures pertinent to each view. Each view can receive a maximum score of 10 and each study a maximum of 109 (ME asc. aortic LAX has only 2 main structures). It will be done after the first and second teaching session, and 3 Months after the study. |
C hands on OR
group C will be introduced to the TEE training in the operation room.
|
Other: theoretical test
The theoretical test is a multiple choice test which consists of 50 questions with 1 point per question (max. 50 points). It will be done before the teaching, after the 2 teaching sessions and 3 Months after the study Other: practical test The practical test is an evaluation of 11 basic perioperative TEE examination on the simulator (CAE Vimedix Simulator). Each view is evaluated on a scale of 0 to 10 according to predetermined criteria including image angle, overall clarity and visualization of 3 major anatomic structures pertinent to each view. Each view can receive a maximum score of 10 and each study a maximum of 109 (ME asc. aortic LAX has only 2 main structures). It will be done after the first and second teaching session, and 3 Months after the study. |
- Change in Score from the theoretical test [ Time Frame: change from baseline to 1 day after training ]Change from Baseline test score at 1 day after training
- Change in score from practical test [ Time Frame: change from baseline to 1 day after training ]Change from Baseline test score at 1 day after training

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- anaesthesia residents in their first or second year of clinical training
Exclusion Criteria:
- prior knowledge of echocardiography

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02842632
Austria | |
Medical university of vienna, General hospital of Vienna | |
Vienna, Austria, 1090 |
Principal Investigator: | Ulrike Weber, MD, PhD | Medical University of Vienna |
Responsible Party: | Ulrike Weber, Dr. Ulrike Weber, Medical University of Vienna |
ClinicalTrials.gov Identifier: | NCT02842632 |
Other Study ID Numbers: |
1057/2016 |
First Posted: | July 25, 2016 Key Record Dates |
Last Update Posted: | October 20, 2017 |
Last Verified: | October 2017 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |