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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04235790
Enrollment
10
Registered
2020-01-22
Start date
2020-10-30
Completion date
2021-08-18
Last updated
2021-08-20

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

Conditions

Procedural Complication

Brief 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).

Interventions

Eye tracking glasses

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Fixation FrequencyDuration of procedure (approximately 4 hours)Number of fixations within an area of interest. Higher values indicate focused attention.
Visit FrequencyDuration of procedure (approximately 4 hours)Number of times an area of interest is entered and left. Indexes which areas repeatedly attracted participant's attention.
Dwell TimeDuration of procedure (approximately 4 hours)Total fixation duration measured in seconds

Countries

United States

Outcome results

None listed

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