- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01883570
Improving Search Strategy for Identifying Urgent Conditions on the Chest X-ray
Improving Search Strategy for Identifying Urgent Conditions on the Chest X-ray. (Original Title in French: Améliorer la stratégie de Recherche et l'Identification Des Conditions Urgentes Sur Une Radiographie Pulmonaire: Impact de l'Utilisation d'un Logiciel Interactif de Lecture systématique)
Currently, teaching X-ray interpretation to medical students is not standardized, and is generally not very effective.
Objective: The goal of our study is to evaluate whether directly teaching an expert search strategy for x-ray interpretation to 3d year medical students is effective.
Methods:
- An expert's visual search strategy was recorded using a gaze-tracking device. The search strategy was then reproduced using a dynamic cursor moving across the corresponding chest x-ray, and incorporated into a teaching program accessible via the internet.
- Participants are 3rd year medical students who will be randomized into two groups. The experimental group will have access to the teaching program as described. The control group will have access to the same x-rays but not the expert's search strategy.
- At the end of the study period the investigators will collect performance data (the participants' accuracy at reading a series of chest x-rays) and process data (using gaze-tracking to evaluate the participants' search strategies); the experimental and control groups will be compared.
Expected results:
The investigators expect the group trained in expert search strategy to show improved accuracy at reading chest x-rays, and an improvement in their visual search strategy
Study Overview
Status
Study Type
Enrollment (Anticipated)
Phase
- Phase 3
Contacts and Locations
Study Locations
-
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Quebec
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Montreal, Quebec, Canada, H1T 2M4
- Recruiting
- Hopital Maisonneuve-Rosemont
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Contact:
- George Rakovich, MD
- Phone Number: 4558 514-252-3400
- Email: george.rakovich@umontreal.ca
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 3rd year medical students enrolled in medicine or surgery rotations during the planned study period
Study Plan
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: trained visual search strategy
An expert's visual search strategy for reading the chest x-ray was recorded using a gaze tracking device.
This strategy was reproduced using a dynamic cursor and will be made available to participants in the experimental group using an interactive website.
|
|
Active Comparator: not trained in visual search strategy
Participants will learn to read chest x-rays by having access to a library of chest x-rays identical to the one used by the experimental arm, but without the search strategy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Improvement in medical student's visual search strategy at reading a chest x-ray
Time Frame: 2 months
|
participants enrolled in the experimental group will be trained to learn the expert's search strategy for reading a chest x-ray.
We hypothesize that by the end of the study period they will show an improved visual search strategy over students who were not trained in visual search but were taught through standard methods (interaction with clinician-educators during their clerkship rotations)
|
2 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CPER-11-120-D(1)
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.
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