Implementation of Teledermoscopy and Artificial Intelligence
Condition(s) studied
Investigational drug(s) / intervention(s)
Diagnostic algorithms: Assessors of teledermoscopy will be randomly assigned to use the results of artificial intelligence when the assess a teledermoscopic case.
Study summary
The study has 2 parts. Part 1 will investigate the effects of introducing teledermoscopy in clinical practice, more specifically the change in referral patterns, the risk of undetected skin cancers and the effect on diagnostic accuracy in general practitioners.
Part 2 will investigate how to introduce artificial intelligence (AI) within teledermocsopy. In this study the investigators will measure the diagnostic accuracy of teledermoscopic assessors that had access to the results of artificial intelligence algorithm compared to those who did not.
Data will be collected through teledermoscopic referrals, patient records, national registries and questionnairs.
Eligibility
Primary outcome measure(s)
- Effect on referral patterns — 2 years
Measure how referral patterns are affected by the introduction of teledermoscopy - Effect on diagnostic accuracy due to availability of artificial intelligence — 8 years
Measuring if the diagnostic accurcy differs depending on if physician can see the results of the artificial intelligence. - Risk of undetected skin cancer — 2 years
Measuring if the risk of undetected skin cancer increases with the use of teledermoscopy - Artificial intelligence timing and effect on diagnostic accuracy and willingness to rethink the preliminary diagnosis — 8 years
Measuring if the diagnostic accuracy and the willingness to reconsider the preliminary diagnosis differs according to when in the process a physician is presented with the results of the artificial intelligence
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Department of dermatology, Skane University Hospital | Lund | Sweden | Recruiting |
More Region Skane trials in Sweden
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05033678 on ClinicalTrials.gov ↗ ← All trials in Sweden