Action 6: Support dementia carers

Where do we want to be in 10 years?

Carers have the information, training and support they need to undertake their supporting role and maintain their own health and wellbeing.

Outcome statement for people living with dementia

My carers are well supported and able to maintain their own health and wellbeing. My carers and I are able to maintain a meaningful and mutually beneficial relationship.

How will we know if the National Dementia Action Plan has made a difference?

This web report presents specific metrics, called indicators, to track change over time, under each of the measures of progress (see Table 6). Measures of progress are part of the Action Plan and are broad statements on how governments will assess if the Action Plan is meeting its objectives.

Baseline values below represent the situation at the start of the Action Plan. In future years, data will be updated to assess if indicators are improving over time. More information about each indicator is presented in the next pages.

Table 6: Summary of indicators for Action 6 measures of progress

Measure of progress

Indicator

Baseline value

Baseline timepoint

Data source

6.1 Carer satisfaction with support services1

Proportion of carers of people living with dementia who connected with other carers to share experiences and advice in the past year.

36%*

2024

Carer Wellbeing Survey

6.1 Carer satisfaction with support services1

Proportion of carers of people living with dementia who had accessed carer training and skills courses in the past year.

23%*

2024

Carer Wellbeing Survey

6.1 Carer satisfaction with support services1

Number of family and carers who receive support through Dementia Australia.

10,163*

2023-24

Dementia Australia

6.2 First Nations carer supports

Data not currently available, development needed

6.3 Respite services1

Proportion of carers of people living with dementia who had accessed respite care services in the past year.

40%*

2024

Carer Wellbeing Survey

6.3 Respite services1

Proportion of the National Health Data Hub (NHDH) dementia cohort who accessed respite care services.

13%^

2021–22

National Health Data Hub

6.4 Culturally appropriate respite care

Data not currently available, development needed

6.5 Younger onset dementia carer support

Data not currently available, development needed

6.6 Carer self-reported wellbeing1

Proportion of carers of people living with dementia who were socially connected.

25%*

2024

National Carer Survey

6.6 Carer self-reported wellbeing1

Proportion of carers of people living with dementia who experienced high personal wellbeing.

16%*

2024

Carer Wellbeing Survey

Notes on data availability and completeness:

  1. Some data available, development underway.

For more information, see how data availability and completeness are assessed.

Notes on data status for this release: 
    *   Updated data
    ^   New data.