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Personalised versus non-individualised case-based CME: A randomised pilot study
The PinPoint Case Platform (PPCP) offers independent online case-based CME. To align with personal learning needs, a functionality of needs assessments (“QuickScan”) was developed, directing users to follow personalised case journeys. A randomised study was conducted, comparing its effectiveness, ti...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718550/ https://www.ncbi.nlm.nih.gov/pubmed/36465494 http://dx.doi.org/10.1080/21614083.2022.2153438 |
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author | Stoevelaar, Herman Bahl, Amit Helsen, Nicky Michels, Nele R.M. Smets, Louis Speakman, Mark J. Stranne, Johan Toelen, Jaan Van der Aa, Frank Van Ruysevelt, Luc Yperman, Jessa Zilli, Thomas Tombal, Bertrand F. Michel, Martin C. |
author_facet | Stoevelaar, Herman Bahl, Amit Helsen, Nicky Michels, Nele R.M. Smets, Louis Speakman, Mark J. Stranne, Johan Toelen, Jaan Van der Aa, Frank Van Ruysevelt, Luc Yperman, Jessa Zilli, Thomas Tombal, Bertrand F. Michel, Martin C. |
author_sort | Stoevelaar, Herman |
collection | PubMed |
description | The PinPoint Case Platform (PPCP) offers independent online case-based CME. To align with personal learning needs, a functionality of needs assessments (“QuickScan”) was developed, directing users to follow personalised case journeys. A randomised study was conducted, comparing its effectiveness, time efficiency and user experience with a format of non-individualised case-based learning. Forty-two residents in urology from five European countries were randomly assigned to follow non-individualised case-based learning (control group) or a needs assessment plus personalised case journeys on different topics in prostate cancer. After performing a pre- and post-assessment, both groups showed a similar increase in test scores (Mann-Whitney U = 247; p = .113), but the time needed for completing the learning exercise was significantly lower in the group with the personalised approach (median: 45 vs 90 minutes; Mann-Whitney U = 97.5; p = .0141). The quality of the two learning methods was similarly well received by both groups. In conclusion, learners who followed personalised case journeys learned similarly effective but more time efficient than non-individualised case-based learners. Future studies should determine if these findings can be extrapolated to board-certified physicians following CME activities. |
format | Online Article Text |
id | pubmed-9718550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-97185502022-12-03 Personalised versus non-individualised case-based CME: A randomised pilot study Stoevelaar, Herman Bahl, Amit Helsen, Nicky Michels, Nele R.M. Smets, Louis Speakman, Mark J. Stranne, Johan Toelen, Jaan Van der Aa, Frank Van Ruysevelt, Luc Yperman, Jessa Zilli, Thomas Tombal, Bertrand F. Michel, Martin C. J Eur CME Research Article The PinPoint Case Platform (PPCP) offers independent online case-based CME. To align with personal learning needs, a functionality of needs assessments (“QuickScan”) was developed, directing users to follow personalised case journeys. A randomised study was conducted, comparing its effectiveness, time efficiency and user experience with a format of non-individualised case-based learning. Forty-two residents in urology from five European countries were randomly assigned to follow non-individualised case-based learning (control group) or a needs assessment plus personalised case journeys on different topics in prostate cancer. After performing a pre- and post-assessment, both groups showed a similar increase in test scores (Mann-Whitney U = 247; p = .113), but the time needed for completing the learning exercise was significantly lower in the group with the personalised approach (median: 45 vs 90 minutes; Mann-Whitney U = 97.5; p = .0141). The quality of the two learning methods was similarly well received by both groups. In conclusion, learners who followed personalised case journeys learned similarly effective but more time efficient than non-individualised case-based learners. Future studies should determine if these findings can be extrapolated to board-certified physicians following CME activities. Taylor & Francis 2022-11-29 /pmc/articles/PMC9718550/ /pubmed/36465494 http://dx.doi.org/10.1080/21614083.2022.2153438 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Stoevelaar, Herman Bahl, Amit Helsen, Nicky Michels, Nele R.M. Smets, Louis Speakman, Mark J. Stranne, Johan Toelen, Jaan Van der Aa, Frank Van Ruysevelt, Luc Yperman, Jessa Zilli, Thomas Tombal, Bertrand F. Michel, Martin C. Personalised versus non-individualised case-based CME: A randomised pilot study |
title | Personalised versus non-individualised case-based CME: A randomised pilot study |
title_full | Personalised versus non-individualised case-based CME: A randomised pilot study |
title_fullStr | Personalised versus non-individualised case-based CME: A randomised pilot study |
title_full_unstemmed | Personalised versus non-individualised case-based CME: A randomised pilot study |
title_short | Personalised versus non-individualised case-based CME: A randomised pilot study |
title_sort | personalised versus non-individualised case-based cme: a randomised pilot study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718550/ https://www.ncbi.nlm.nih.gov/pubmed/36465494 http://dx.doi.org/10.1080/21614083.2022.2153438 |
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