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E-learning for carers
Orphanet Journal of Rare Diseases volume 5, Article number: P13 (2010)
The Centre for Rare Disorders is an interdisciplinary, nationwide competence centre which offers information, counselling and seminars on a selected range of rare disorders.
The purpose of the e-learning programme in question is to improve quality of life for patients with Huntington’s disease by increasing the carer’s knowledge. E-learning and interactive sharing of information can be an effective and secure way of providing professionals with new knowledge. E-learning also functions as a tool for network-building.
Methods/techniques
The e-learning programme is organised as a module based compilation of knowledge and competence gathered by the Centre for Rare Disorders and its collaborators over the last 15 years. In addition to the modules, the users have shared information in on-line discussions. Their level of knowledge was evaluated through several tests.
Security
The participants received a password and username for logging on to the programme.
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Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Solberg, O., Miller, J.U., Heivang, S. et al. E-learning for carers. Orphanet J Rare Dis 5 (Suppl 1), P13 (2010). https://doi.org/10.1186/1750-1172-5-S1-P13
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DOI: https://doi.org/10.1186/1750-1172-5-S1-P13
Keywords
- Public Health
- Rare Disorder
- Interactive Sharing
- Competence Centre
- Base Compilation