National Disability Agreement: PI h-Proportion of carers of people with disability who report their health and wellbeing as positive, 2013 QS
Identifying and definitional attributes
|Metadata item type:||Quality Statement|
|Registration status:||Disability, Standard 13/08/2015|
Community Services (retired), Standard 23/05/2013
|Indicators linked to this Quality statement:|
National Disability Agreement: h(1)-Proportion of primary carers of people with disability who feel satisfied with their caring role, 2013 Disability, Standard 13/08/2015
National Disability Agreement: h(2)-Proportion of primary carers of people with disability who do not experience negative impacts on their wellbeing due to their caring role, 2013 Disability, Standard 13/08/2015
The SDAC is collected, processed, and published by the Australian Bureau of Statistics (ABS). The ABS operates within the framework of the Census and Statistics Act 1905 and the Australian Bureau of Statistics Act 1975. These ensure the independence and impartiality of the ABS, and the confidentiality of respondents.
For more information on the institutional environment of the ABS, including legislative obligations, financing and governance arrangements, and mechanisms for scrutiny of ABS operations, please see ABS Institutional Environment.
|Timeliness:||The SDAC is currently conducted every three years. Results from the 2009 survey were released in April 2011.|
|Accessibility:||See Disability, Ageing and Carers, Australia: Summary of Findings, 2009 (cat. no. 4430.0) for an overview of results from the SDAC. Other information from the survey is available on request.|
|Interpretability:||Information is available to aid interpretation of SDAC data - see the Disability, Ageing and Carers User Guide, on the ABS website.|
The SDAC collects information about primary carers and non-primary carers of people with disabilities.
A primary carer is a person who provides the most informal assistance, in terms of help or supervision, to a person with one or more disabilities. The assistance has to be ongoing, or likely to be ongoing, for at least six months and be provided for one or more of the core activities (communication, mobility and self-care). In this survey, primary carers only include persons aged 15 years and over for whom a personal interview was conducted.
Persons who confirm they are the primary carer of a person with disability are asked about the assistance they provide, the assistance they can call on, and their employment experience. They are also asked to complete a self-enumeration form which collects information about their attitudes to, and experience of, their caring role. Where the carer has more than one recipient of care, the information collected in the personal interview and self-enumeration form is in regard to the person who the carer considers receives the most care and attention from him/her (the main recipient of care).
The denominator for this indicator relates to a subpopulation of primary carers identified in the SDAC. This consists of primary carers with main recipient of care aged:
As age and disability status are collected or derived from information provided in interviews with the responsible adult and/or the recipient of care, these data items are only available for recipients of care (other than the main recipient of care) where the recipient lives with the carer. Therefore, the data may exclude some primary carers who would otherwise be in-scope if age and disability status information was available for all their recipients of care.
Data for this indicator are available for primary carers only.
In the SDAC carer self-enumeration form, primary carers are asked whether they have experienced a number of specific physical or emotional effects as a result of their caring role:
The numerator for measure h.i relates to those primary carers who answered positively to category 2 above (i.e. reported feeling satisfied as a result of their caring role).
The numerator for measure h.ii relates to those primary carers who did not answer positively to at least one of categories 3-6 above (i.e. did not report frequently feeling worried, depressed, angry or resentful; did not report feeling weary or lacking energy; and did not report having been diagnosed with a stress related illness due to their caring role).
The 2009 SDAC response rate for private dwellings was 89.9 per cent, and for establishments was 90.9 per cent. SDAC data are weighted to account for non-response.
The SDAC is conducted in all states and territories including people in both private and non-private dwellings (including cared-accommodation establishments) but excluding those in gaols and correctional institutions and very remote areas. The exclusion of persons usually resident in very remote areas has a small impact on estimates, except for the Northern Territory, where such persons make up a relatively large proportion of the population. For more information on SDAC scope and coverage, see the Disability, Ageing and Carers User Guide on the ABS website.
Being drawn from sample surveys, data for this indicator is subject to sampling error. Sampling error occurs because a proportion of the population is used to produce estimates that represent the whole population. Sampling error can be reliably estimated as it is calculated based on the statistical methods used to design surveys.
This indicator has varied levels of sampling error, and in some cases data are not able to be provided for confidentiality and unreliability reasons. This particularly affects data for the Australian Capital Territory (ACT) and the Northern Territory (NT), and age/sex disaggregations for all states and territories. The SDAC sample in 2009 was double compared to 2003, and therefore data for 2003 may be subject to higher levels of sampling error than corresponding data in 2009.
Tables for measure h.i have relative standard errors (RSEs) for the numerator consistently 25 per cent or greater, with much of the data for the smaller states and territories having RSEs of 50 per cent or greater.
Tables for measure h.ii tend to have lower levels of sampling error.
Data with RSEs of 25 per cent to 50 per cent should be used with caution, and data with RSEs of 50 per cent or greater are considered too unreliable for general use.
The SDAC carer self-enumeration form is subject to an element of non-response, both to individual questions and to the questionnaire as a whole. For 2009, exclusion due to non-response accounted for 9.5 per cent of the in-scope population of primary carers for this indicator. The numerator and denominator for this indicator, and consequently the proportion, both exclude primary carers who did not provide any response to the question on physical or emotional effects of the caring role but who would otherwise have been in-scope.
Disability status is derived from information provided in interviews with the responsible adult and/or the recipient of care. In a small number of cases (about 1 per cent in 2009), the primary carer indicated that he/she provided assistance with core activities because of the main recipient’s condition(s), however the recipient did not have a reported disability (was either not identified in the disability screening questions answered by the responsible adult or, in the personal interview, stated that he/she did not need assistance with core activities). These primary carers remain in the data.
Both the numerator and the denominator are drawn from the same dataset, with the numerator being a subset of the denominator population. The denominator population is the same in all tables.
Estimates of primary carers in a particular population group presented in these tables will not match estimates for primary carers in the same population group presented in other NDA indicators due to the exclusion from this indicator of carers where effects of caring role were not stated.
The particular specification of the in-scope primary carer population for this indicator represents only 55 per cent of the primary carer population identified in the SDAC, and therefore comparisons with other published information on primary carers sourced from the SDAC should be made with caution. Mostly, the primary carers that are out-of-scope are not included because they are not caring for someone aged 0-64 years.
In 2009, the identification process for primary carers in the SDAC was expanded to include members of the household who the recipient of care identified as their main care provider. Therefore, comparisons between 2009 data and previous years cannot be made. For some tables presented for this indicator, a primary carer definition based on the 2003 identification process is also included for the purposes of comparison with 2003 data. For further details on the methodology change see explanatory notes in Disability, Ageing and Carers, Australia: Summary of Findings, 2009 (cat. no. 4430.0).
|Implementation start date:||28/06/2009|
Source and reference attributes
|Submitting organisation:||The Australian Bureau of Statistics|
|Steward:||Disability Policy and Research Working Group (DPRWG)|
|Origin:||SCRGSP (Steering Committee for the Review of Government Service Provision) 2012, National Agreement Performance Information 2011-12: National Disability Agreement, Productivity Commission, Canberra.|