Voluntary assisted dying views and experiences of Australians living with dementia: a qualitative study

This study explored the views and experiences of Australians living with dementia relating to voluntary assisted dying (VAD) as an end-of-life care option. Semi-structured interviews were conducted online with 12 Australians living with dementia. The findings of this study identified that participants wanted VAD as an end-of-life care option to achieve improved quality of life, a good death, and to control their end-of-life care. Without this option, participants feared they are at risk of a poor dying experience, including potential abuse if they require residential care. The participants felt their living experiences of stigma and discrimination presented significant barriers to realising what they viewed as their right to VAD access. These findings highlight the importance of capturing the views of people living with dementia relating to VAD as an end-of-life care option, as without an in-depth understanding of their experiences, future end-of-life policy and practice may not reflect their end-of-life care preferences.

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Publication Details

Journal
Mortality
Published
2026-07-23
DOI
https://doi.org/10.1080/13576275.2026.2704548
Primary Topic
Palliative Care and End-of-Life Issues
Type
article
Field-Weighted Citation Impact
0.00

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article

Voluntary assisted dying views and experiences of Australians living with dementia: a qualitative study

Bernadette Moorhead, Belinda Cash, Adrienne Matthys
Mortality
Palliative Care and End-of-Life Issues
article

Voluntary assisted dying views and experiences of Australians living with dementia: a qualitative study

Bernadette Moorhead, Belinda Cash, Adrienne Matthys
article en

Abstract

This study explored the views and experiences of Australians living with dementia relating to voluntary assisted dying (VAD) as an end-of-life care option. Semi-structured interviews were conducted online with 12 Australians living with dementia. The findings of this study identified that participants wanted VAD as an end-of-life care option to achieve improved quality of life, a good death, and to control their end-of-life care. Without this option, participants feared they are at risk of a poor dying experience, including potential abuse if they require residential care. The participants felt their living experiences of stigma and discrimination presented significant barriers to realising what they viewed as their right to VAD access. These findings highlight the importance of capturing the views of people living with dementia relating to VAD as an end-of-life care option, as without an in-depth understanding of their experiences, future end-of-life policy and practice may not reflect their end-of-life care preferences.

Mortality
Charles Sturt University (AU)
Australian Government
Gender equality
Openalex Percentile: Top 7%
Palliative Care and End-of-Life Issues
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Voluntary assisted dying views and experiences of Australians living with dementia: a qualitative study — Bernadette Moorhead, Belinda Cash, et al. · Mortality (2026) | TGRS Research Map | TGRS