- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05987553
The Influence of an E-learning Program on Recognition of Actinic Keratosis
The Influence of an E-learning Program on Recognition of Actinic Keratosis by General Practitioners). Implementation of Actinic Keratosis Guidelines Among General Practitioners.
Study Overview
Status
Conditions
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
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Maastricht, Netherlands
- Ellen Oyen
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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.
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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).
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Measurement by baseline and after finalising the e-learning program (same day up until 30 days)
|
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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
Investigators
- Principal Investigator: Klara Mosterd, prof.dr., Maastricht UMC+
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-1334
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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