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    Dementia Knowledge Assessment Tool Version Two: Development of a tool to inform preparation for care planning and delivery in families and care staff

    189096_189096abs.pdf (1.108Mb)
    Access Status
    Open access
    Authors
    Toye, Christine
    Lester, Leanne
    Popescu, Aurora
    McInerney, Fran
    Andrews, S.
    Robinson, Andrew
    Date
    2013
    Type
    Journal Article
    
    Metadata
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    Citation
    Toye, Christine and Lester, Leanne and Popescu, Aurora and McInerney, Fran and Andrews, Sharon and Robinson, Andrew L. 2013. Dementia Knowledge Assessment Tool Version Two: Development of a tool to inform preparation for care planning and delivery in families and care staff. Dementia: The International Journal of Social Research and Practice. 13 (2): pp. 248-256.
    Source Title
    Dementia: The International Journal of Social Research
    DOI
    10.1177/1471301212471960
    ISSN
    1471-3012
    Remarks

    http://online.sagepub.com

    URI
    http://hdl.handle.net/20.500.11937/25222
    Collection
    • Curtin Research Publications
    Abstract

    Care for the person with dementia requires understanding of the person’s perspective and preferences, integrated with knowledge of dementia’s trajectory and appropriate care. Version One of the Dementia Knowledge Assessment Tool addressed such knowledge in care workers; Version Two is for families as well as staff. Content validity was established during development. Revisions addressed clarity, time for completion, and reliability. When 671 staff completed Version One before an education intervention, internal consistency reliability estimates exceeded 0.70. Validity was supported by higher scores in professional versus nonprofessional staff and following the education. Version Two was used with 34 family carers and 70 staff members. Internal consistency reliability (Cronbach’s alpha coefficient) was promising (0.79, both groups). Completion was within 15 minutes. Median correct responses (from 21) were 14 for families (range 4–20) and 16 for the staff (range 3–21). Eighteen staff members (26%) and two family carers (6%) reported substantive dementia education. Inclusion of the person with dementia in care planning is often limited because of a late diagnosis and the progressive impacts of the condition. Establishing a shared staff–family understanding of the dementia trajectory and care strategies likely to be helpful is therefore critical to embarking upon the development and implementation of collaborative long term and end-of-life care plans. Version Two can help establish needs for, and outcomes of, education programs and informational resources in a way that is feasible, minimises burden, and facilitates comparisons across family and staff carer groups.

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