Volume 5 Supplement 1

5th European Conference on Rare Diseases (ECRD 2010)

Open Access

E-learning for carers

  • Olga Solberg1Email author,
  • Jeanette Ullmann Miller1,
  • Synne Heivang1 and
  • Mads Bjerke1
Orphanet Journal of Rare Diseases20105(Suppl 1):P13

https://doi.org/10.1186/1750-1172-5-S1-P13

Published: 19 October 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.

Authors’ Affiliations

(1)
Centre for Rare Disorders – Rikshospitalet, Oslo University Hospital

Copyright

© Solberg et al; licensee BioMed Central Ltd. 2010

This article is published under license to BioMed Central Ltd.

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