The Influence of an E-learning Program on Recognition of Actinic Keratosis

April 2, 2025 updated by: Maastricht University Medical Center

The Influence of an E-learning Program on Recognition of Actinic Keratosis by General Practitioners). Implementation of Actinic Keratosis Guidelines Among General Practitioners.

The evaluation on the diagnostic accuracy of actinic keratosis recognition by general practitioners before and after participation on an e-learning program.

Study Overview

Status

Active, not recruiting

Intervention / Treatment

Detailed Description

Actinic keratosis is defined as the most frequent common intra-epithelial neoplasm in the Caucasian population, with an increasing prevalence. If left untreated, actinic keratosis has the potency to develop into a cutaneous squamous-cell carcinoma. Treatment of actinic keratosis is aimed at both lesion reduction and to prevent malignant transformation. To achieve treatment adherence for patients, it is necessary to raise physician awareness about actinic keratosis.

This study primarily aimed to investigate whether the sensitivity of establishing a correct actinic keratosis diagnosis by general practitioners (in training) would increase after participating in an e-learning program about the recognition of actinic keratosis. This was achieved by comparing the results of a pre- and post-test completed by general practitioners which was incorporated in the e-learning program.

Study Type

Observational

Enrollment (Actual)

32

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Data from general practitioners who

Description

Inclusion Criteria:

  • general practitioner in the Netherlands
  • access to e-learning module via phone/computer/tablet
  • knowledge of the Dutch language

Exclusion Criteria:

  • no knowledge of the Dutch language
  • different specialists than general practitioner

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
General practitioners
All participants were general practitioners (in training).
All participants participate in this intervention: an e-learning program about the recognition of actinic keratosis. The program exists of 30 cases. Each case exists of a question and thorough explanation including references to various sources.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difference in sensitivity
Time Frame: Measurement by baseline and after finalising the e-learning program (same day up until 30 days)
Difference in sensitivity of participants in the recognition of actinic keratosis, before and after the use of an e-learning program (paired).
Measurement by baseline and after finalising the e-learning program (same day up until 30 days)
Difference in specificity
Time Frame: Measurement by baseline and after finalising the e-learning program (same day up until 30 days)
Difference in specificity of participants in the recognition of actinic keratosis, before and after the use of an e-learning program (paired).
Measurement by baseline and after finalising the e-learning program (same day up until 30 days)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difference in area under the receiver operating characteristic (ROC) curve
Time Frame: Measurement by baseline and after finalising the e-learning program (same day up until 30 days)
Difference in area under the curve of participants in the recognition of actinic keratosis, before and after the use of an e-learning program.
Measurement by baseline and after finalising the e-learning program (same day up until 30 days)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Klara Mosterd, prof.dr., Maastricht UMC+

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2021

Primary Completion (Actual)

January 1, 2024

Study Completion (Estimated)

December 1, 2025

Study Registration Dates

First Submitted

July 20, 2023

First Submitted That Met QC Criteria

August 3, 2023

First Posted (Actual)

August 14, 2023

Study Record Updates

Last Update Posted (Actual)

April 4, 2025

Last Update Submitted That Met QC Criteria

April 2, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 2020-1334

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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