NCT03370900

Brief Summary

Learning retention after the deliberate practice of radiograph interpretation may be challenging for image types which are common enough to be clinically relevant but not so common that proficiency can be sustained through clinical practice. This is especially relevant for radiographs such as paediatric elbow films (EXR) that carry high risks for the patient if pathology is missed. Building on prior research in this area, this study will develop an innovative computer learning application for paediatric EXR interpretation. After an initial learning period, this study will quantitatively determine the rate of skill decay and the optimal timing for refresher-education.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
233

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2014

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2014

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2016

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

December 2, 2017

Completed
11 days until next milestone

First Posted

Study publicly available on registry

December 13, 2017

Completed
Last Updated

November 22, 2023

Status Verified

December 1, 2017

Enrollment Period

1.6 years

First QC Date

December 2, 2017

Last Update Submit

November 21, 2023

Conditions

Keywords

Education (Medical); Retention;

Outcome Measures

Primary Outcomes (1)

  • Accuray

    The percent of cases that were diagnosed correctly by the study participants

    12 months after learning intervention

Secondary Outcomes (2)

  • Accuracy

    2, 4, 6, 8, 10 months

  • Experience Curve

    12 months

Study Arms (4)

Learning and Assessment at 12 months

NO INTERVENTION

Study participants will complete an 80 case learning set followed by a 20-case post test. The study intervention in this group is a 20-case test at 12 months.

Testing Every Two Months

EXPERIMENTAL

Study participants will complete an 80 case learning set followed by a 20-case post test. Study participants in this group will receive the following study interventions: 20-case post tests without any feedback at 2, 4, 6, 8, 10, 12 months.

Other: Testing

Low Bolus Feedback

EXPERIMENTAL

Study participants will complete an 80 case learning set followed by a 20-case post test. Study participants in this group will receive the following study interventions: 20-case post tests at 2, 4, 6, 8, 10, 12 months. At 6 months, the 20-case post-test will be delivered with feedback.

Other: Testing

High Bolus Feedback

EXPERIMENTAL

Study participants will complete an 80 case learning set followed by a 20-case post test. Study participants in this group will receive the following study interventions: 20-case post tests at 2, 4, 6, 8, 10, 12 months. At 4, 8, and 12 months, the 20-case post-test will be delivered with feedback.

Other: Testing

Interventions

TestingOTHER

Participants either received 20 case testing with or without feedback

High Bolus FeedbackLow Bolus FeedbackTesting Every Two Months

Eligibility Criteria

AgeUp to 70 Minutes
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • Pediatric and emergency medicine residents enrolled in an accredited residency in Canada and the United States

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Fractures, Bone

Condition Hierarchy (Ancestors)

Wounds and Injuries

Study Officials

  • Kathy Boutis

    The Hospital for Sick Children

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
All analyses were blinded to group assignment
Purpose
DIAGNOSTIC
Intervention Model
PARALLEL
Model Details: This was a four arm randomized control trial. All participants completed an 80-case deliberately practiced learning set of pediatric elbow radiographs followed by an immediate 20-case post-test. Following this, Group 1 had no testing until 12 months; Groups 2, 3, and 4 had testing (20 cases without feedback) every 2 months until 12 months, but Group 3 also had refresher education (20 cases with feedback) at six months while Group 4 had refresher education at two, six, and ten months.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physician and Senior Associate Scientist

Study Record Dates

First Submitted

December 2, 2017

First Posted

December 13, 2017

Study Start

November 1, 2014

Primary Completion

June 15, 2016

Study Completion

June 15, 2016

Last Updated

November 22, 2023

Record last verified: 2017-12

Data Sharing

IPD Sharing
Will not share