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Clinical Trials/NCT06533488
NCT06533488RecruitingNot Applicable

Evaluation of the Impact of a Perceptual Learning Module (PLM) on the Sonographic Identification of Spinal Structures by Novice Anesthesiology Residents. A Randomized Controlled Study

Maisonneuve-Rosemont Hospital1 site in 1 country20 target enrollmentStarted: March 26, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
20
Locations
1
Primary Endpoint
Improvement in the concordance of identifying the best image on the video within the interval specified by the expert in seconds, between the pre-test and the post-test.

Study Overview

Brief Summary

This medical education research project aims to evaluate the impact of a directed perceptual learning module (PLM) on spinal sonoanatomy. Following a demographic questionnaire, participants will be exposed to a tutorial explaining the necessary theoretical foundations for the PLM as well as the functioning of the PLM interface. A pre-test involving selecting the best image from a video sequence depicting spinal sonoanatomy will be administered to all participants. Participants will then be randomized into two groups and exposed to video sequences in the same manner as during the pre-test, with immediate feedback in the intervention group and no feedback in the control group. The video sequences presented will be the same between the two groups. Finally, a post-test will be administered immediately and remotely after exposure to the PLM. The time window corresponding to the best image will be predefined by an expert and compared to the resident's value. The difference in feedback exposure between the two groups will not be revealed to limit biases.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Participant)

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •(participants) :
  • •To be a first, second, third, or fourth-year resident in the anesthesiology program at the Université de Montréal.
  • •Not having experience in spinal ultrasound (defined as not having performed more than 5 spinal ultrasounds, whether accompanied or not).
  • •To be familiar with ultrasound.
  • •Consenting to participate in the study.
  • •Inclusion Criteria (experts) :
  • •- Having used spinal ultrasound in clinical practice or taught it within the last year.

Exclusion Criteria

  • •(participants) :
  • •Refusal to consent
  • •Not meeting the inclusion criteria.

Arms & Interventions

Feedback group

Experimental

This group will receive feedback upon completion of the task.

Intervention: Perceptual learning module (Other)

Control group

Placebo Comparator

This group will not receive any feedback

Intervention: Control (Other)

Outcomes

Primary Outcomes

Improvement in the concordance of identifying the best image on the video within the interval specified by the expert in seconds, between the pre-test and the post-test.

Time Frame: Between the pre-test and the immediate post-test, as well as the post-test at 1 month.

Secondary Outcomes

  • Improvement over time in the concordance of identifying the best image on the video within the interval specified by the expert in seconds(During the intervention phase)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Issam TANOUBI

MD, MA (Ed), DESAR

Maisonneuve-Rosemont Hospital

Study Sites (1)

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