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Workshop on Improving Disability Data for Policy Use
23-26 September 2003, Bangkok, Thailand

UN ESCAP Statistics Division
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Documentation for the Workshop / Country Papers : Australia

Survey and census sources of national disability data

Country: Australia

1. Overview of survey or census

  1. Title of survey or census
    Survey of Disability, Ageing and Carers
  2. Date of latest data collection
    1998 and currently being collected in 2003. Previous surveys have been conducted in 1981, 1988, and 1993.
  3. Periodicity of survey or census (continuous, annual, ad hoc, 10 or 5 yearly in case of census etc.)
    Planned to be 6 yearly from 2003 onwards.
  4. Contact person(s) for the survey/census (include title, office mail address, phone, fax, email, website, etc.)
    Ken Black
    Assistant Director
    Family and Community Statistics section
    ABS, Locked Bag 10
    Belconnen ACT 2616
    Ph 02 6262 7430
    Fax 02 6252 8007
    e-mail ken.black @ abs.gov.au
    Website http://www.abs.gov.au

2. Brief summary of survey or census

  1. Describe what information on disability is collected
    The survey of Disability, Ageing and Carers is the principle source of information on people with disabilities, older persons, and those who provide care to people because of their disability. It collects information on 3 population groups: people aged 60 and over, people with disabilities and their carers. There are other sources of information about services provided to these groups, but this survey is the only source of information on the assistance requirements of those groups, the extent to which these requirements are met, and the characteristics of those with unmet need. It also provides information on participation in economic and community activities. The survey is the major source of national statistics on carers and primary carers: numbers and characteristics of carers, care relationships, activities for which informal care is provided, and, for primary carers, support available and required, and the effects of the caring role on their lives.
  2. What uses are made of the data and who are the users?
    The data are needed for policy development and review, service planning and implementation, and general research. The key users are the Commonwealth and State Governments. The size and distribution of groups eligible for assistance under different program legislation is used by the Commonwealth Departments of Health and Ageing, and Family and Community Services as the basis for allocating and distributing program funds to State governments, and by State and Territory departments for service planning and fund distribution.
  3. Were users involved in deciding what information to collect?
    Yes, there is a User Advisory Group which includes representatives from all levels of government, service providers, peak body representatives, disability advocacy groups, people with disabilities and academics.
    A key role of the Advisory group is to advise the ABS on the needs for information about people with a disability, and priorities for data content in the collections.
  4. What definition of disability was used?
    A person has a disability if he/she has one of the following, that has lasted or is likely to last for 6 months or more:
    • Loss of sight (not corrected by glasses);
    • Loss of hearing (with difficulty communicating or use of aids);
    • Loss of speech;
    • Chronic or recurring pain that restricts everyday activities;
    • Breathing difficulties that restrict everyday activities;
    • Blackouts, fits or loss of consciousness;
    • Difficulty learning or understanding;
    • Incomplete use of arms or fingers;
    • Difficulty gripping;
    • Incomplete use of feet or legs;
    • A nervous or emotional condition that restricts everyday activities;
    • Restriction in physical activities or physical work;
    • Disfigurement or deformity;
    • Needing help or supervision because of a mental illness or condition;
    • Head injury, stroke or other brain damage, with long-term effects that restrict everyday activities;
    • Treatment for any other long-term condition, and still restricted in everyday activities; or
    • Any other long-term condition that restricts everyday activities.
  5. Were data collected and compiled according to international
    standards or national classifications and definitions? (e.g.ICIDH or ICF)
    The first collection in 1981 used the draft of the ICIDH as a conceptual framework. The more recent collections are consistent with and can be mapped to the ICF.

3. Scope of survey or census

  1. Describe the population covered in the survey (age, private dwelling population, institutionalised population, etc.)
    All persons, of all ages in both private dwellings and institutions with the following exceptions:
    • overseas visitors (usually resident outside Australia);
    • members of non-Australian defence forces (and their dependents);
    • non-Australian diplomats (including diplomatic staff and non-Australian members of their household;
    • inmates of gaols and reformatories
    • people in sparse and indigenous strata in the Northern Territory

4. Coverage and sampling

  1. Coverage of survey or census (how well was the scope achieved)
    Household component
    Usual residents of private dwellings excluding those who had been away or were likely to be away for three months.
    Residents of special dwellings (other than Health Establishments) who had been or were likely to be there for three months.
    Cared accommodation component
    Usual residents of selected Health Establishments who had been or were likely to be there for three months.
  2. Sample frame(s) (sample size? Sample frame based on lists, area, register, etc.)
    An area sample of private dwellings, covering both urban and rural areas in all States and Territories (except for those living in remote and sparsely settled parts of Australia) was used. The Census non-private dwelling list was used to identify selected special dwellings (that is, hospitals, nursing homes, retirement villages, homes for the aged, children's homes, and aged care hostels) to be sampled in the cared accommodation component of the survey. Most other non-private dwellings (eg. hotels, motels, guesthouses etc) were also included in the household (interviewer-based) component.
    The final sample of the 1998 survey comprised 36,951 persons for the household component and 5,716 persons for the cared accommodation component.

5. Are there other data sources which you use to benchmark your survey results? (e.g. previous surveys to compare with? what evaluations did you make of the results?)

Validation of the final estimates was based on comparisons with data from previous disability surveys (1981, 1988 and 1993), the Estimated Resident Population for March 1998, the 1996 Census of Population and Housing, the 1995 National Health Survey, and with administrative data relevant to the Disability Support Pension and other pensions and benefits, and Workcover.

6. Response and non-response

  1. What was the response rate?
    • Household component:
      Household non-response rates
      fully responding 83.8%
      partial non-response 9.3% (mainly income questions)
      full non-response 6.9% (refusal 1.8%, non-contact 3%, other 2.1%)
    • Cared accommodation component
      fully responding 93.4%
  2. Did you evaluate the non-response? (e.g. break it up into full and partial? impact of non-response? follow-up studies? imputations for missing items?)
    No follow-up studies of the non-responding population have been conducted, but the impact of case non-response is expected to be very small.
    There was very little item non-response to disability items, mostly in regard to income questions. Records with item non-response were not included in final survey estimates. No imputation for income or any other item was conducted.

7. Data collection (Attach or mail us a copy of your questionnaire)

  1. Manner of collection (face-to-face interviews, self-administered questionnaire, telephone, other?)
    Household interview conducted by ABS interviewers, in-person or proxy for initial screening question set, then personal interview for all people identified as having a disability, all carers, and all people aged 60 years and over.
    The cared accommodation component used a mail-back questionnaire.
  2. Type of respondent (who replied? The disabled person or proxy for the person?)
    Household component:
    Personal interview for all people identified as having a disability, all carers, and all people aged 60 years and over. Proxy interview utilised where selected respondents could not answer on their own behalf. (Foreign language interviewers were available to overcome difficulties due to language other than English, including signing.
    Cared accommodation component:
    Mail-back forms completed by staff at the selected establishments.
  3. Format of questions (how many questions? pre-coded standardised?)
    Questions are standardised with computer assisted interviewing (CAI) in the household component, and form based mailback methodology for the cared accommodation component. There are 17 screening questions which determine disability status. Depending on disability status, age and carer status, respondents are sequenced through different question structures and modules. The variation is reflected in the range of interview times from 12 minutes to just under 5 hours. The average interview time for all fully responding households was 47 minutes.
  4. List the languages used in the survey or census
    In English, with specialist interviewers available for languages commonly encountered. Interpreters employed if necessary, and initial contact letters and explanatory brochures available in a range of languages.

8. Measurement error

  1. Which special data collection procedures were undertaken to reduce measurement error (e.g. pilot testing of questions and questionnaire? training of interviewers? detailed coding instructions? follow-up of non response by specialist staff?)
    Measurement error is reduced through:
    • thorough testing of individual questions and the overall questionnaire before being used in the final survey to minimise problems caused by misleading or ambiguous questions, inadequate or inconsistent definitions of terminology used or by poor layout of the questionnaires. Testing for the 1998 survey included the conduct of two pilot tests and a dress rehearsal;
    • training and supervision of interviewers to ensure uniform interviewing practices and a high level of accuracy in recording answers;
    • the development of detailed coding instructions and regular checking for coding accuracy;
    • application of computer edits to ensure that logical sequences were followed;
    • validation of tabulation of the file content and identification of unusual values;
    • contact letters sent to all selected dwellings prior to interviewer contact;
    • probity checks undertaken on a small sample of interviews; and
    • follow-up of non response by specialist staff, including reference to the survey being conducted under the Census and Statistics Act, and it being compulsory to respond.

9. Highlights of the strengths and limitations of survey or census Strengths: (e.g. a very detailed survey; sound sample design; use of international standard concept and classifications, etc.)

The key strengths of the survey include:

  • A very detailed survey focussed specifically on disability issues, using a large nationally representative sample.
  • The survey was originally designed using the ICIDH as a conceptual framework.
  • Interviewers are drawn from the existing household survey interviewer panel, and provided with intensive training specific to the SDAC survey.
  • Sound sample design.
  • Inclusion of cared accommodation component.
  • Inclusion of carer questions, including a self-completion form for questions seen as particularly sensitive.
  • Inclusion of questions on unmet need for assistance across a range of activity areas.

Limitations: (e.g. high relative standard error for small population groups/geographic areas; respondent overload due to length of questionnaire; lack of consistency or survey items across surveys, etc.)
Main limitations relate to:

  • high relative standard error for small population groups/geographic areas, this mainly impacts on small geographic area data needed for service planning at a local level, and the lack of an Indigenous identifier due to small population constraints.
  • expense of the survey.
  • lack currently of test-retest data and detailed understanding of the reliability of the survey.
  • time constraints on the interview to avoid respondent overload (average interview time for 1998 was 47 minutes, with some household taking up to 5 hours).
  • lack of consistent time-series data, or change in the disability population over time, as the survey items have changed across surveys.

10. List published sources on disability statistics

Disability, Ageing & Carers: Summary of findings, Australia 1998 (ABS Cat. No. 4430.0)
Disability, Ageing & Carers: User Guide, Australia 1998 (ABS Cat. No. 4431.0)
Disability, Ageing & Carers: Caring in the Community, Australia 1998 (ABS Cat. No. 4436.0)
Disability, Ageing & Carers: Disability and Long-Term Health Conditions, Australia 1998 (ABS Cat. No. 4433.0)
Disability, Ageing and Carers: Unit Record File on Magnetic Media:
- Compact disk (ABS Cat. No. 4430.0.30.001) available in Australia only.
State and Territory standard tables as above
Small Area Predictor standard tables, 1998 survey/1996 Census

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