Abstract
Background and aims: Family members often become the primary caregiver
following brain injury and experience significant unmet information needs regarding behavioural changes. The level of information provided is often not understood or relevant to families’ individual situations. This emphasises the need for accessible information provided to families in layperson language, which is relevant to individualised and community-based contexts.
following brain injury and experience significant unmet information needs regarding behavioural changes. The level of information provided is often not understood or relevant to families’ individual situations. This emphasises the need for accessible information provided to families in layperson language, which is relevant to individualised and community-based contexts.
Original language | English |
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Pages (from-to) | 326 |
Number of pages | 1 |
Journal | BRAIN IMPAIRMENT |
Volume | 19 |
Issue number | 3 |
DOIs | |
Publication status | Published - 21 Dec 2018 |
Event | Australasian Society for the Study of Brain Impairment 2018 - Adelaide, Australia Duration: 3 May 2018 → 5 May 2018 Conference number: 41st |
Keywords
- Conference abstract