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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03049098
Other study ID # MMT-2016
Secondary ID
Status Completed
Phase N/A
First received February 7, 2017
Last updated February 7, 2017
Start date July 14, 2016
Est. completion date January 25, 2017

Study information

Verified date February 2017
Source Université de Montréal
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this observational study is to compare the visual interests between residents in high-fidelity simulation practice


Description:

Eighteen first year residents were asked to take part in a nine-minute scenario based on an ACLS bradycardia algorithm in which a high-fidelity mannequin required external pacing. The scenario was considered a success if the material was correctly set by the participant to obtain electrical and mechanical pacing in nine minutes. All participants were wearing Tobii Glasses® which is a mobile eye-tracking system that automatically aggregates gaze data. Infrared markers were placed in the simulation room to create Area of Interest (AOI), from which results were obtained. Three AOI were created: the vital signs monitor, the defibrillator/pacing unit and the head of the patient. Eye-tracking data were analyzed using the Tobii Studio® program.


Recruitment information / eligibility

Status Completed
Enrollment 21
Est. completion date January 25, 2017
Est. primary completion date July 18, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- First-year residents from various specialties in their first three weeks of training

Exclusion Criteria:

- Underwent a previous residency

- Attending physicians in another country

Study Design


Intervention

Behavioral:
Simulation
A 9-minute scenario based on an ACLS bradycardia algorithm in which a high-fidelity mannequin requires external pacing

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Issam Tanoubi

References & Publications (5)

Browning M, Cooper S, Cant R, Sparkes L, Bogossian F, Williams B, O'Meara P, Ross L, Munro G, Black B. The use and limits of eye-tracking in high-fidelity clinical scenarios: A pilot study. Int Emerg Nurs. 2016 Mar;25:43-7. doi: 10.1016/j.ienj.2015.08.002. — View Citation

Duchowski AT. A breadth-first survey of eye-tracking applications. Behav Res Methods Instrum Comput. 2002 Nov;34(4):455-70. — View Citation

Schulz CM, Schneider E, Fritz L, Vockeroth J, Hapfelmeier A, Wasmaier M, Kochs EF, Schneider G. Eye tracking for assessment of workload: a pilot study in an anaesthesia simulator environment. Br J Anaesth. 2011 Jan;106(1):44-50. doi: 10.1093/bja/aeq307. — View Citation

Turgeon DP, Lam EW. Influence of Experience and Training on Dental Students' Examination Performance Regarding Panoramic Images. J Dent Educ. 2016 Feb;80(2):156-64. — View Citation

Wilson MR, McGrath JS, Vine SJ, Brewer J, Defriend D, Masters RS. Perceptual impairment and psychomotor control in virtual laparoscopic surgery. Surg Endosc. 2011 Jul;25(7):2268-74. doi: 10.1007/s00464-010-1546-4. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Time to first fixation, Total visit time Using eye-tracking technology, gaze date can be aggregate onto Areas of interest where data can be extrapolated. During the scenario
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