How Does Task Loading in PICU Impact on Clinician Situational Awareness and Awareness of the Passage of Time?
How Does Task Loading in a PICU Environment Impact on Clinician Situational Awareness and Awareness of the Passage of Time?
1 other identifier
interventional
30
1 country
1
Brief Summary
There is little published literature on the subject of clinician perception of trends in patient observations on PICUs (Paediatric Intensive Care Units) and how this situational awareness is impacted on by clinical tasks. Human factors training cautions against the loss of situational awareness and time perception but there is no supporting observational data in the IC (Paediatric Intensive Care) setting. Perceptual loading theory hypothesises that, under low load situations, awareness extends to environmental features not directly related to the task at hand. However in high load situations awareness is restricted to the object of focused attention. Individuals experience different load from a given task depending on their skills and experience. Our pilot project intends to examine how clinician perception is affected by task loading. In our protocol two tasks are undertaken. The administrative task involves requesting a list of investigations from a clinical guideline. The technical task is the uncomplicated insertion of a central venous catheter (CVC) into a simulated vein. In each case the investigators will record proxies for perception: awareness of the passage of time, the time point at which monitoring changes are noted and retrospective recall of observation trends. Our protocol was designed with psychology input from Prof. Nilli Lavie, group leader of the UCL Attention \& Cognitive Control laboratory. Passage of time is measured by the participant pressing a foot pedal linked to timing software at every perceived 10 second interval of elapsed time. A retrospective estimate of total elapsed time will also be recorded. After the second task, immediate verbal questions are asked followed by a written questionnaire which contains questions targeting the participant's awareness of monitoring changes. Analysis will involve paired t testing of the timing interval and observation trend data to see if task loading significantly impacts accuracy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2022
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 1, 2021
CompletedFirst Posted
Study publicly available on registry
May 20, 2022
CompletedStudy Start
First participant enrolled
September 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2022
CompletedMay 20, 2022
May 1, 2022
Same day
December 1, 2021
May 16, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Prospective identification of monitoring trends
Proportion (%) of clinicians who correctly identify any change in the monitored parameters during the tasks. Measured through post task questionnaire
Following recruitment of the 30th participant- expected 3 months after starting recruitment
Retrospective identification of monitoring trends
Proportion (%) of clinicians who correctly identify any change in the monitored parameters following the tasks. Measured through post task questionnaire
Following recruitment of the 30th participant- expected 3 months after starting recruitment
Retrospective identification of the magnitude of the change in monitoring
Percentage error in the retrospectively recalled magnitude of the change in monitored parameters, compared to the actual change in value. Measured through comparison of the post task questionnaire answers to the actual change.
Following recruitment of the 30th participant- expected 3 months after starting recruitment
Accuracy of clinician time perception
As compared to the actual 10s elapsed time interval. Measured through the computer logging timestamps of foot pedal presses vs computed measured 10s interval
Following recruitment of the 30th participant- expected 3 months after starting recruitment
Study Arms (2)
ICU clinicians- technical first
EXPERIMENTALStaff working on the Great Ormond Street ICUs Completing technical task first
ICU clinicians- administrative first
EXPERIMENTALStaff working on the Great Ormond Street ICUs Completing administrative task first
Interventions
Simulated insertion of a central venous catheter
Requesting a battery of investigations on the EPR
Eligibility Criteria
You may qualify if:
- \. Medical staff working on the Great Ormond Street ICUs
You may not qualify if:
- \. Staff identifying as unable to insert central venous catheters
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Great Ormond Street PICU
London, WC1N 3JH, United Kingdom
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- Participants
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 1, 2021
First Posted
May 20, 2022
Study Start
September 1, 2022
Primary Completion
September 1, 2022
Study Completion
November 1, 2022
Last Updated
May 20, 2022
Record last verified: 2022-05
Data Sharing
- IPD Sharing
- Will not share
Nil shared