App Teaches Doctors to Diagnose Skin Cancer

Sponsor
Herlev Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT05661370
Collaborator
(none)
117
1
2
9
13

Study Details

Study Description

Brief Summary

This study aimed to examine if self-paced learning with a novel digital patient-case-based educational platform can increase primary care physicians' diagnostic accuracy of malignant and benign skin lesions on both the level of benign/malignant and the diagnosis level. Secondarily the study aimed to investigate the time spent in reaching this change in proficiency.

Condition or Disease Intervention/Treatment Phase
  • Other: Dermloop Learn
N/A

Detailed Description

Participants were given a questionnaire and an initial Skin Cancer Multiple Choice-Questionnaire (MCQ) to test their diagnostic skills regardining skin and mole cancer and the most common differential diagnoses.

Participants in the Intervention group was then given access to an educational mobile application (App) for 8 days and asked to diagnose 500 patient cases. The participants did so at their own leisure and time.

After 8 days they were asked to abstain from using the App for another 8 days (wash out period) and were then given a Final Skin Cancer Multiple Choice-Questionnaire (MCQ).

Participants of the control group received no intervention nor education during the 16 days of waiting before they took the final Skin Cancer Multiple Choice-Questionnaire.

Study Design

Study Type:
Interventional
Actual Enrollment :
117 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Intervention and Controlgroup parallel design using sequential continues block randomization.Intervention and Controlgroup parallel design using sequential continues block randomization.
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Improving Diagnostic Accuracy in Skin Cancer Diagnostics Using Educational Mobile App: a Randomized Controlled Study
Actual Study Start Date :
Nov 15, 2021
Actual Primary Completion Date :
Jan 15, 2022
Actual Study Completion Date :
Aug 15, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Intervention

Access to educational mobile application for 8 days, diagnosing 500 digital patient-cases.

Other: Dermloop Learn
Educational Mobile Application with a library of digital patient-cases and written learning modules the user can access on 36 common skin lesions, both benign and malignant.

No Intervention: Control

Control group receiving no intervention, continuing daily practice.

Outcome Measures

Primary Outcome Measures

  1. Multiple-Choice Questionnaire (MCQ) Score [Before and immediately after intervention (On average 19 days after enrollment)]

    Participants are given a test before and after the intervention using a skin cancer MCQ test with 12 digital-patient cases. A higher score means better diagnostic proficiency. The primary outcome is the change of this score.

Secondary Outcome Measures

  1. Diagnostic proficiencies [During the 8 days of access to the educational mobile application.]

    Sensitivity, Specificity and Positive Predictive Value of the participants in the intervention group, calculated on their cases seen in the educational mobile application.

  2. Time spend [During the 8 days of access to the educational mobile application.]

    The Dermloop Learn app tracks how much time each user spends quizzing and reading.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Primary Care Physician who works in General Practice
Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 AISC Research Fascility Copenhagen Danmark Denmark 2700

Sponsors and Collaborators

  • Herlev Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gustav Gede Nervil, Medical Doctor, Herlev Hospital
ClinicalTrials.gov Identifier:
NCT05661370
Other Study ID Numbers:
  • GP-Learn
First Posted:
Dec 22, 2022
Last Update Posted:
Dec 22, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Gustav Gede Nervil, Medical Doctor, Herlev Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 22, 2022