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How can dementia diagnosis and care for Aboriginal and Torres Strait Islander people be improved? Perspectives of healthcare providers providing care in Aboriginal community controlled health services

Crossref DOI link: https://doi.org/10.1186/s12913-021-06647-2

Published Online: 2021-07-16

Published Print: 2021-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Bryant, Jamie

Noble, Natasha

Freund, Megan

Rumbel, Jennifer

Eades, Sandra

Sanson-Fisher, Rob

Lowe, Michael

Walsh, Justin

Piterman, Leon

Koch, Susan

Meyer, Claudia

Todd, Elaine
Funding

Funding for this research was provided by:

National Health and Medical Research Council (APP1095078, APP1095078, APP1095078, APP1095078, APP1095078, APP1095078, APP1095078, APP1095078, APP1095078, APP1095078, APP1095078, APP1095078)
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Article History

Received: 22 February 2021

Accepted: 14 June 2021

First Online: 16 July 2021

Declarations

:

: Ethics approval was provided by the Aboriginal Health and Medical Research Council of NSW (HREC Reference: 1396/18), University of Newcastle (HREC Reference: H-2018-0362), Central Australian Human Research Ethics Committee (CAHREC Reference: CA-18-3270), Menzies School of Health Research (HREC Reference: 18-3255) and Aboriginal Health Council of South Australia (AHREC Reference: 04-18-794). Organisations provided written informed consent for participation of staff. All participants provided verbal informed consent prior to participation. All protocols were carried out in accordance with relevant guidelines and regulations.

: Not applicable.

: The authors declare that they have no competing interests.

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