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Accepted for/Published in: JMIR Research Protocols

Date Submitted: Jun 10, 2021
Date Accepted: Oct 20, 2021
Date Submitted to PubMed: Jan 4, 2022
(closed for review but you can still tweet)

The final, peer-reviewed published version of this preprint can be found here:

The Future of Disability Research in Australia: Protocol for a Multiphase Research Agenda–Setting Study

Smith-Merry J, O'Donovan MA, Dew A, Hemsley B, Imms C, Carey G, Darcy S, Ellem K, Gallego G, Gilroy J, Guastella A, Marella M, McVilly K, Plumb J

The Future of Disability Research in Australia: Protocol for a Multiphase Research Agenda–Setting Study

JMIR Res Protoc 2022;11(1):e31126

DOI: 10.2196/31126

PMID: 34706859

PMCID: 8764607

The future of disability research in Australia: protocol for a multi-phase research agenda-setting exercise.

  • Jennifer Smith-Merry; 
  • Mary-Ann O'Donovan; 
  • Angela Dew; 
  • Bronwyn Hemsley; 
  • Christine Imms; 
  • Gemma Carey; 
  • Simon Darcy; 
  • Kathy Ellem; 
  • Gisselle Gallego; 
  • John Gilroy; 
  • Adam Guastella; 
  • Manjula Marella; 
  • Keith McVilly; 
  • Jenny Plumb

ABSTRACT

Background:

For people with disability to live a good life it is essential that funded research in health and social care addresses their interests, meets their needs and fills gaps in our understanding of the impact services, systems and policies may have on them. Decisions about research funding should be based on a clear understanding of the research priorities of people with disability, their supporters and allies, disability researchers, service providers, and policy makers working in the field.

Objective:

The aim of this protocol is to describe the research design and methods of a large-scale disability research agenda-setting exercise in Australia, conducted in 2021.

Methods:

The research agenda-setting exercise involves 3 integrated phases of work. In the first phase, a previous Audit of Disability Research in Australia is updated to understand prior research and continuing gaps in the research. Building on this, the second phase involves a consultation with stakeholders: people with disability and their supporters and family members, the disability workforce, services and connected sectors (e.g., ageing, employment, education, housing), academia, and public policy. Data for the second phase will be gathered via: i) a national online survey, ii) a consultation process undertaken through the government and non-government sector, and iii) targeted consultation with Aboriginal and Torres Strait Islander people, children with disabilities and their families, people with cognitive disability, and people with complex communication needs. The last phase involves an online survey to develop a research agenda based on the outcomes of all phases.

Results:

TBC

Conclusions:

This multi-method research agenda-setting study will be the first to provide an indication of the areas of health and social research people across the Australian disability community consider should be prioritised in disability research funding decisions. Project results from all phases will be made publicly available through reports, open access journal publications, and easy-read documents.


 Citation

Please cite as:

Smith-Merry J, O'Donovan MA, Dew A, Hemsley B, Imms C, Carey G, Darcy S, Ellem K, Gallego G, Gilroy J, Guastella A, Marella M, McVilly K, Plumb J

The Future of Disability Research in Australia: Protocol for a Multiphase Research Agenda–Setting Study

JMIR Res Protoc 2022;11(1):e31126

DOI: 10.2196/31126

PMID: 34706859

PMCID: 8764607

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