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Evaluation of a Perceptual Learning Module on Spinal Ultrasound Among Residents.

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06533488
Acronym
MAP-Rachis
Enrollment
20
Registered
2024-08-01
Start date
2024-03-26
Completion date
2025-04-30
Last updated
2024-08-01

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

Conditions

Medical Education, Spinal Anesthesia Skill, Ultrasound Imaging of Anatomical Structures

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.

Interventions

OTHERPerceptual learning module

Perceptual learning module providing feedback on the most relevant image for clinical practice in a spinal ultrasound video.

OTHERControl

Participants in the control group will view the same videos as participants in the intervention group without feedback on the best image.

Sponsors

Maisonneuve-Rosemont Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
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.

Design outcomes

Primary

MeasureTime frame
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.Between the pre-test and the immediate post-test, as well as the post-test at 1 month.

Secondary

MeasureTime frame
Improvement over time in the concordance of identifying the best image on the video within the interval specified by the expert in secondsDuring the intervention phase

Countries

Canada

Contacts

Primary ContactIssam Tanoubi, MD
i.tanoubi@umontreal.ca514-252-3400

Outcome results

None listed

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