Examining Behaviors of Teachers of Invasive Bedside Procedures Using an Eye Tracking Device

Procedural Complication Clinical Trial

Official title:

Examining Behaviors of Teachers of Invasive Bedside Procedures Using an Eye Tracking Device: Towards Improving Supervisor Expertise and Decreasing Complications in the Intensive Care Unit

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04235790
• Other study ID #: 19-003774
• Status: Completed
• Phase: N/A
• Start date: October 30, 2020
• Est. completion date: August 18, 2021

Study information

• Verified date: August 2021
• Source: Mayo Clinic
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Researchers are studying the behaviors in teachers of invasive bedside procedures to improve the safety of invasive bedside procedure in the Intensive Care Unit (ICU).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: August 18, 2021
• Est. primary completion date: August 18, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Novice and expert Invasive bedside procedure (IBP) teachers from Pulmonary Critical Care Medicine and Anesthesia-Critical Care at Mayo Clinic Rochester
• Expert teachers will be identified based on years as faculty, number of supervised procedures, prior teacher awards, and participation in IBP teaching at international conferences
• Novice teachers will include those that have performed less than 50 CVCs
• Medical student or resident

Exclusion Criteria:

• <25% FTE in the ICU

Related Conditions & MeSH terms

• Procedural Complication

Intervention

Device:
• Eye Tracking Device
Eye tracking glasses

Locations

Country	Name	City	State
United States	Mayo Clinic	Rochester	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Fixation Frequency	Number of fixations within an area of interest. Higher values indicate focused attention.	Duration of procedure (approximately 4 hours)
Primary	Visit Frequency	Number of times an area of interest is entered and left. Indexes which areas repeatedly attracted participant's attention.	Duration of procedure (approximately 4 hours)
Primary	Dwell Time	Total fixation duration measured in seconds	Duration of procedure (approximately 4 hours)

External Links

•   Mayo Clinic Clinical Trials