SOCIAL RESEARCH PROJECTS
Research Participant Register
We are creating an important register of people living with epilepsy, and those caring for people living with epilepsy, who are willing to be occasional participants in future research projects.
This is not medical or clinical research but will likely involve surveys and group discussions designed to find out more about the social consequences of epilepsy.
All research carried out by the Epilepsy Foundation is confidential and anonymous. You can register by clicking here.
By registering you are only saying that you might be able to spend a few minutes to a couple of hours of your time over the next year or two. There is no obligation to take part in any of the research studies offered to participants.
For more information contact:
Pat McGuirk
Tel: (03) 9805 9111
Email epilepsy@epilepsy.asn.au
‘Out of the Shadows’: needs, perceptions and experiences of people living with epilepsy in Australia
Findings from Wave 2 of the Longitudinal Survey
The Epilepsy Foundation has initiated a nationwide project designed to better understand how people with epilepsy feel, what they need how well they are able to do their usual activities and how ....
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