NCT04221100

Brief Summary

xrAI (pronounced "X-ray") serves as a clinical assistance tool for trained clinical professionals who are interpreting chest radiographs. The tool is designed as a quality control and adjunct, limited, clinical decision support tool, and does not replace the role of clinical professionals. It highlights areas on chest radiographs for review by an interpreting clinician. The objective of this study is to utilize machine learning and artificial intelligence algorithms (xrAI) to improve the quality and efficiency in the interpretation of chest radiographs by radiologists. The hypothesis is that the addition of xrAI's analysis will reduce inter-observer variability in the interpretation of chest radiographs and increase participants' sensitivity, recall, and accuracy in pulmonary abnormality screening.

Trial Health

15
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Timeline
Completed

Started Mar 2021

Shorter than P25 for not_applicable

Status
withdrawn

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

First Submitted

Initial submission to the registry

January 6, 2020

Completed
3 days until next milestone

First Posted

Study publicly available on registry

January 9, 2020

Completed
1.1 years until next milestone

Study Start

First participant enrolled

March 1, 2021

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2021

Completed
Last Updated

February 23, 2021

Status Verified

February 1, 2021

Enrollment Period

2 months

First QC Date

January 6, 2020

Last Update Submit

February 21, 2021

Conditions

Outcome Measures

Primary Outcomes (3)

  • Number of abnormalities identified divided by number of total of images analyzed (accuracy)

    Accuracy is defined as the ratio of the images where the physician's prediction matched the labels of the dataset. Accuracy= (TP+FP) / (TP+FP+TN+FN) TP (true positives) = cases interpreted as abnormal that are abnormal; FP (false positives) = cases wrongly interpreted to be abnormal; TN (true negatives) = cases correctly interpreted to be normal; FN (false negatives) = abnormal cases wrongly interpreted as normal.

    Time needed to analyze 500 images. Participants will be asked to completed the exercise within 2 weeks.

  • Number of true abnormalities identified divided by the total of abnormalities identified (precision)

    Precision is defined as the probability of a radiograph being abnormal if a physician makes the determination that it is abnormal. Precision= TP / (TP+FP) TP (true positives) = cases interpreted as abnormal that are abnormal; FP (false positives) = cases wrongly interpreted to be abnormal; TN (true negatives) = cases correctly interpreted to be normal; FN (false negatives) = abnormal cases wrongly interpreted as normal.

    Time needed to analyze 500 images. Participants will be asked to completed the exercise within 2 weeks.

  • Number of true abnormalities identified divided by the sum of true abnormalities identified and abnormalities missed (recall)

    Recall is defined as the probability of a physician catching an abnormality in an image if one exists (based on the labels of the dataset). Recall= TP / (TP+FN) TP (true positives) = cases interpreted as abnormal that are abnormal; FP (false positives) = cases wrongly interpreted to be abnormal; TN (true negatives) = cases correctly interpreted to be normal; FN (false negatives) = abnormal cases wrongly interpreted as normal.

    Time needed to analyze 500 images. Participants will be asked to completed the exercise within 2 weeks.

Secondary Outcomes (3)

  • Mean of radiologist accuracy (as defined in outcome 1)

    Time needed to analyze 500 images. Participants will be asked to completed the exercise within 2 weeks.

  • Mean of radiologist precision (as defined in outcome 2)

    Time needed to analyze 500 images. Participants will be asked to completed the exercise within 2 weeks.

  • Mean of radiologist recall (as defined in outcome 3)

    Time needed to analyze 500 images. Participants will be asked to completed the exercise within 2 weeks.

Study Arms (2)

Control

PLACEBO COMPARATOR

Participants will review the 500 chest radiographs without the assistance of xrAI

Device: Radiograph interpretation for pulmonary abnormalities

Treatment

EXPERIMENTAL

Participants will review the 500 chest radiographs with the assistance of xrAI

Device: Radiograph interpretation for pulmonary abnormalities

Interventions

The pulmonary abnormalities detected by xrAI and included in the definition of abnormality are as follows: any linear scar or fibrosis, atelectasis, consolidation, abscess or cavity, nodule, pleural effusion, severe cases of emphysema and COPD (mild cases with hyperinflation but not significant emphysema are not flagged), pneumothorax. Participants in the treatment group will interpret 500 images presented alongside the results of xrAI's processing in a dark room and asked to categorize each image into one of the following categories: lungs are clear, at least one pulmonary abnormality is present, not sure. Participants in the control group will be asked to interpret the same 500 images as the treatment group but without xrAI's analysis.

ControlTreatment

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Radiologist currently practicing at a Pureform Radiology clinic in Calgary, Canada.

You may not qualify if:

  • Radiologists not currently practicing at a Pureform Radiology clinic in Calgary, Canada.
  • Physicians currently practicing at a Pureform Radiology clinic in Calgary, Canada, but that are not radiologists by training.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Lung Diseases

Condition Hierarchy (Ancestors)

Respiratory Tract Diseases
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
DIAGNOSTIC
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 6, 2020

First Posted

January 9, 2020

Study Start

March 1, 2021

Primary Completion

May 1, 2021

Study Completion

May 1, 2021

Last Updated

February 23, 2021

Record last verified: 2021-02