A Musculoskeletal Ultrasound Course for Orthopedic Surgery Residents

Sponsor
Université de Sherbrooke (Other)
Overall Status
Completed
CT.gov ID
NCT04204369
Collaborator
(none)
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Study Details

Study Description

Brief Summary

A group of orthopedic surgery residents underwent a structured online and practical musculoskeletal ultrasound course. Their proficiency on a written and practical exam, as well as frequency and comfort when using was recorded prior to the course, immediately after, and 6 months after the course.

Condition or Disease Intervention/Treatment Phase
  • Other: Ultrasound education curriculum
N/A

Detailed Description

Musculoskeletal ultrasound (MSK-US) can have many uses for orthopedic surgeons, such as assisting in clinical diagnosis for muscle, tendon and ligament injuries, providing direct guidance for joint injections, or assessing the adequacy of a reduction in the emergency department. However, proficiency in sonography is not a requirement for certification in orthopedic surgery in Canada, and orthopedic trainees are rarely exposed to the subject. This project aims assess the usefulness in clinical education of a newly implemented MSK-US course in an orthopedic surgery program.

An MSK-US course for orthopedic surgery residents has been developed. An online survey covering the level of training of the resident, their prior experience with ultrasound (number of times used by month) and their comfort level with different parts of the examination (numeric analog scale - NAS), was filled by the participants prior to the course. A pre-course written and practical test was also given to the residents. Following the course, the participants were reassessed with the same tests and surveys on the same day as the course, and at 6 months post. Change in frequency of use, comfort level and test scores were assessed using a Kruskal-Wallis ANOVA and post-hoc Wilcoxon tests.

It was expected that residents' frequency of use, comfort level and tests scores would improve following the implementation of the course. The results were expected to be maintained at the 6 months endpoint.

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
One group receiving intervention. Assessement prior to intervention, immediately after, and at 6 months.One group receiving intervention. Assessement prior to intervention, immediately after, and at 6 months.
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Usefulness of a Musculoskeletal Ultrasound Course in an Orthopedic Surgery Residency Training Program
Actual Study Start Date :
Nov 6, 2017
Actual Primary Completion Date :
Jul 6, 2018
Actual Study Completion Date :
Jul 6, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Teaching arm

This group received the teaching intervention and was evaluated before and after the intervention. Improvement was compared to their performance prior to the intervention.

Other: Ultrasound education curriculum
Participants were enrolled in a musculoskeletal ultrasound course including 2 components: An online course (1-2 hours) to be done before the practical session. The videos were made available one (1) month prior to the practical course. This component reviewed the basics of ultrasonography, as well as the normal and abnormal appearance of relevant musculoskeletal structures (bone, tendon, ligaments, muscles, bursas, and nerves), and the ultrasound anatomy of high yield regions of the musculoskeletal system (shoulder, elbow, knee, ankle) A practical session (4-6 hours) done during one of the usual academic days of the orthopedic residency program. This session covered the use of the ultrasound; the examination of the shoulder, elbow, knee, and ankle; ultrasound-guided musculoskeletal injections and aspirations; and ultrasound-guided distal radius fracture reductions. Ample practice time was given to the residents using means such as phantom models, cadavers, and real patients.

Outcome Measures

Primary Outcome Measures

  1. Change in Musculoskeletal ultrasound knowledge after the course [Before the course (within a month), immediately after the course (same day)]

    A 13 questions written examination was given to the residents using an online platform at each endpoint. The exam covered the basics of ultrasound physics; how to use the machine; the normal and pathologic appearance of tendons, ligaments, and muscles; and ultrasound appearance of the musculoskeletal anatomy described in the course. The score was reported on a scale from 0 to 100, with 100 being the best score.

  2. Change in Musculoskeletal ultrasound knowledge at 6 months [Before the course (within a month), 6 months after the course]

    A 13 questions written examination was given to the residents using an online platform at each endpoint. The exam covered the basics of ultrasound physics; how to use the machine; the normal and pathologic appearance of tendons, ligaments, and muscles; and ultrasound appearance of the musculoskeletal anatomy described in the course. The score was reported on a scale from 0 to 100, with 100 being the best score.

Secondary Outcome Measures

  1. Practical shoulder ultrasound exam [Immediately after the course (same day), 6 months after the course]

    Each participant underwent a practical examination assessing ultrasound proficiency at each endpoint. The residents were assessed by one of the author of the study on their ability to perform a shoulder ultrasound exam as well as the different tasks related to the MSK-US. For each task, the assessor rated the participant on a scale of 0 to 2, where : 0 means an inability to perform the task, 1 means the task is only partially completed, 2 means that the task that is performed correctly. The final score was then be calculated and reported in percentage (with 100 being a perfect score) for the analysis.

  2. Ultrasound comfort in clinical setting [Before the course (within a month), 6 months after the course]

    A questionnaire covering different aspect of ultrasound use by the residents was given using the online platform at each endpoint. The questionnaire inquired about the comfort level when using MSK-US for different examinations and procedure (Numeric Analog Scale from 0 to 10, with 0 being very uncomfortable and 10 being very comfortable). Each numeric analog scale was reported independently and not compound score was created: Setting up the ultrasound machine Choosing the appropriate probe Adjusting the depth and contrast Diagnosing a ligament, tendon, muscle, nerve, or bone injury Performing a joint injection or aspiration Performing an injection or aspiration in any other region than a joint Guiding the reduction of a fracture in the forearm Guiding the reduction of any other fracture than the forearm Performing ultrasound in general

  3. Ultrasound use in clinical setting [Before the course (within a month), 6 months after the course]

    The questionnaire inquired about the number of time ultrasound was used in the last 6 months for different examinations and procedures. This was reported as an absolute number for each aspect of ultrasound use: Diagnosing a ligament, tendon, muscle, nerve, or bone injury Performing a joint injection or aspiration Performing an injection or aspiration of any other region than a joint Guiding the reduction of a fracture in the adult patient Guiding the reduction of a pediatric fracture

Other Outcome Measures

  1. Socio-demographic questionnaire [Before the course (within a month)]

    This questionnaire was presented to participants once at the moment of their inclusion in the study. It covered the residents' level of training (post-graduate year), age, sex, the amount of prior exposure to ultrasound (in approximate hours), and the different settings in which the residents have been exposed to MSK-US.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Be an orthopedic surgery resident

  • Training at the University of Manitoba

  • Post-graduate year (PGY) one to five

Exclusion Criteria:
  • Residents having less than six months of training left before graduation

  • Residents on extended leave (for example: completing graduate studies abroad, parental leave, and sabbatical)

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Manitoba Winnipeg Manitoba Canada R3A1R9

Sponsors and Collaborators

  • Université de Sherbrooke

Investigators

  • Principal Investigator: Samuel Larrivee, MD-MSc, University of Manitoba

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Université de Sherbrooke
ClinicalTrials.gov Identifier:
NCT04204369
Other Study ID Numbers:
  • H2017:227 (HS20921)
First Posted:
Dec 19, 2019
Last Update Posted:
Dec 19, 2019
Last Verified:
Dec 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Université de Sherbrooke
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 19, 2019