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Clinical Trials/NCT06080711
NCT06080711
Enrolling By Invitation
Not Applicable

AI-Augmented Skin Cancer Diagnosis in Teledermatoscopy: A Prospective Randomized Study

Karolinska University Hospital1 site in 1 country30 target enrollmentFebruary 15, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Skin Cancer
Sponsor
Karolinska University Hospital
Enrollment
30
Locations
1
Primary Endpoint
Diagnostic accuracy
Status
Enrolling By Invitation
Last Updated
2 years ago

Overview

Brief Summary

In this study an artificial intelligence (AI) tool for skin cancer diagnosis is implemented in a teleldermatoscopy platform. The aim is to study the effects on clinician diagnostic accuracy, management decisions, and confidence. Furthermore, this prospective randomized study investigates the role of human factors in determining clinician reliance on AI tools and the consequent accuracy in a real-world setting.

Detailed Description

Deep-learning algorithms can potentially benefit many areas in healthcare, including the diagnosis of skin cancer using teledermatoscopy. However, there is a dearth of clinical, prospective research on human-AI interaction in diagnostic tasks that take human factors into account. In this study we will examine the impact of such factors in a real-world setting where we integrate an algorithm in an existing teledermatoscopy platform that is used clinically at a tertiary hospital in Sweden. We will investigate what impact various implementations of AI tool output in relation to human factors have on diagnostic accuracy and management decisions. Study subjects are recruited at the Department of Dermatology at Karolinska University Hospital and will be asked to rate prospective teledermatoscopic consults with and without AI-support. Each consult will be randomized into one of three workflows with or without one pre-defined implementation of the AI tool. Study subjects are also asked to complete two surveys with demographic information and questions relating to various human factors. Patients participating in the study will be diagnosed outside the study prior to inclusion without any involvement of an AI tool, notably by two experienced dermatologists who do not participate as study subjects.

Registry
clinicaltrials.gov
Start Date
February 15, 2023
End Date
October 30, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Karolinska University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Jan Lapins

MD, PhD

Karolinska University Hospital

Eligibility Criteria

Inclusion Criteria

  • Licensed physician
  • Working at a dermatology clinic
  • Sufficient knowledge in Swedish
  • Written consent to participate

Exclusion Criteria

  • No experience of using dermatoscopy
  • Does not wish to participate
  • Incomplete answers
  • Physicians that are involved in the patients' clinical care relating to the teledermoscopical consult

Outcomes

Primary Outcomes

Diagnostic accuracy

Time Frame: 1 year

Determine sensitivity, specificity, accuracy and AUROC in terms of diagnostic accuracy for dermatologists with vs without AI advice. Further, to investigate the role of the different workflows (diagnosis with or without AI with varying sequencing) and the influence of demographics and human factors (e.g. level of experience) on diagnostic accuracy

Self-reported confidence in diagnosis and management decisions

Time Frame: 1 year

Investigate whether AI or other factors affect the physician's confidence in their diagnosis and management decisions

Tendency to change initial diagnosis or management decision

Time Frame: 1 year

Evaluate which factors affect the likelihood of a physician changing their evaluation after receiving algorithmic input

Accuracy of management decisions

Time Frame: 1 year

Determine sensitivity, specificity, accuracy and AUROC in terms of accuracy for management decisions for dermatologists with vs without AI and investigate the role of the different workflows (with or without AI with varying sequencing) and the influence of demographics and human factors (e.g. level of experience) on management decisions (biopsy/surgery, no intervention, or follow-up)

Study Sites (1)

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