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NCT Number: NCT06533488

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

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.

Recruiting

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Maisonneuve-Rosemont Hospital

Montreal, Quebec, H1T 2M4, Canada

Location status: Recruiting

Location contact

Issam Tanoubi, MD

CONTACT

[email protected]

514-252-3400

Tanoubi

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Perceptual learning module

Other

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

Control

Other

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

Primary outcomes

  1. 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

  1. Improvement over time in the concordance of identifying the best image on the video within the interval specified by the expert in seconds

    Time frame: During the intervention phase

Study contacts

Contact information is provided by the study sponsor or research team.

Issam Tanoubi, MD

CONTACT

[email protected]

514-252-3400

Sponsors and collaborators

Lead sponsor

Maisonneuve-Rosemont Hospital

Other

Registry information

Official study title

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

Acronym: MAP-Rachis

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Aug 1, 2024
Registry last updated
Aug 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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