- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06470269
Examining Clinical Reasoning With Eye-tracking
Examining Clinical Reasoning With Eye Tracking
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Objective:
In this project, the investigators plan to apply the eye-tracking technology to medical education with a specific goal of examining cognitive processing during clinical reasoning (CR). The investigators expect that by checking the eye movements of medical trainees during case and image reading, a list of valid behavioral markers could be created, to quantitatively classify the expertise, identify the moment of decision-making difficulty, and decode the source of the judgement errors. To examine differences in CR processes across varying levels of expertise, three categories of participants (novice, intermediate, and expert) will be recruited. While participants' eye motions are tracked, participants will read a trauma case, provide a diagnosis and propose a suitable treatment plan. The investigators postulate that 1) different participant groups will produce significantly different CR outcomes, measured by their score on diagnostic judgement and treatment plan; 2) participants will display different gaze fixation patterns; and 3) combining evidence from clinical judgement and eye behavior analysis will provide useful information regarding the source of judgment errors.
Research Method/Procedures:
Staff and students in the SSRL (Surgical Simulation Research Lab) with a difficulty level of health training background will be enrolled as participants in the study. A trauma case with complex life-threatening situations will be presented. The case is a trauma cases with multiple internal injuries. The case will be summarized into a one-page description and 3 x-ray films. Our participants will need to make a diagnosis and give a treatment plan based on case information displayed on a screen. The total reading time will be 4 minutes. During the case reading, the Tobii X2-60, a high-resolution remote eye-tracker, will be used to capture the participant's eye movements. In addition, the investigators will develop a 15-20 quiz regarding the patient's condition and the participant's final diagnosis. The total score and errors in the quiz will be used to describe participants' overall quality of their clinical reasoning.
The investigators will carefully examine participants' eye motions and report their scanning patterns during case reading. Specifically, the investigators will look for moments when participants rapidly move their eyes (saccade) over a sentence before fixating on a particular word (fixation). These eye behavior parameters have previous associations with mental workload and reasoning processing methods, which can be used to further analyze results.
Plan for Data Analysis:
The investigators will firstly compare quiz scores and eye behaviors variables across the three participant groups with different clinical experience levels. The investigators will then analyze eye-scanning patterns on case readings across the three different groups. Specifically, The investigators predict that experts will achieve the highest score in quiz. The investigators therefore will examine the expert's short and long fixation locations over the case reading. The assumption is that experts know where to find key information in the case description and mentally connect separate information together to generate an correct judgement in the short period of time. Fixation spots recorded from the novice and intermediate groups will be compared with experts'. Differences will help us identify different visual searching strategies over different stages in the development of clinical reasoning skills. Lastly, the investigators will examine clinical judgement errors and check the root cause by connecting quiz errors with eye behaviors. If a participant failed to give a long fixation to key case features in the case description, the clinical decision error may be due to a checking problem. If a participant performs a long fixation to key case features, the clinical decision error may due to recognition or decision-making problems.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Alberta
-
Edmonton, Alberta, Canada, T6G 2R3
- University of Alberta
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult
- Has normal or corrected to normal vision
- Healthcare provider
Exclusion Criteria:
-Non healthcare provider
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Expert
Physicians
|
Recording the eye movement of participants while they read medical cases.
|
|
Novice
Medical Students
|
Recording the eye movement of participants while they read medical cases.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Eye Fixation
Time Frame: During case reading (about 5 minutes)
|
Eye fixation over key reading area
|
During case reading (about 5 minutes)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Eye Saccade
Time Frame: During case reading (about 5 minutes)
|
Rapid eye shift between key reading areas
|
During case reading (about 5 minutes)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Pro00102074
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Diagnosis
-
SuperSonic ImagineTerminated
-
Umraniye Education and Research HospitalCompleted
-
European Institute of OncologyEuropean UnionRecruitingCancer DiagnosisFrance, Lithuania, Germany, Italy, Spain
-
Peking Union Medical College HospitalNot yet recruitingPrenatal Diagnosis
-
Danderyd HospitalRecruiting
-
Vrije Universiteit BrusselRecruitingPerinatal Palliative Care | Life-limiting Fetal Diagnosis | Life-limiting Neonatal DiagnosisBelgium
-
Beytepe Murat Erdi Eker State HospitalCompletedAnterior Segment Ischemia (Diagnosis)
-
Columbia UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development...RecruitingPrenatal Genetic DiagnosisUnited States
-
Identifai GeneticsRecruitingGenetics | Prenatal DiagnosisUnited States
-
Ankara Education and Research HospitalCompletedDiagnosis | Axilla; BreastTurkey
Clinical Trials on Eye tracking
-
McGill UniversityInnodem NeurosciencesRecruitingClinically Isolated Syndrome | Relapsing Remitting Multiple SclerosisCanada
-
Instituto Universitario de Oftalmobiología Aplicada...Hospital del Rio Hortega; Hospital Clínico Universitario de ValladolidCompletedMultiple Sclerosis | Eye Abnormalities | Parkinson Disease | Ataxia, Cerebellar | Injury BrainSpain
-
Innodem NeurosciencesRecruitingAlzheimer's DiseaseCanada
-
Central South UniversityUnknownBipolar Disorder | Suicide | Major Depressive DisorderChina
-
University Hospital, AngersUnknownHuntington DiseaseFrance
-
Institut National de la Santé Et de la Recherche...CompletedHealthy | Parkinson Disease | DystoniaFrance
-
Innodem NeurosciencesNovartis PharmaceuticalsRecruitingMultiple SclerosisCanada
-
Innodem NeurosciencesSyneos HealthCompleted
-
Radboud University Medical CenterLund University; Utrecht UniversityCompleted
-
University Hospitals Cleveland Medical CenterRecruitingBipolar DisorderUnited States