This article presents the findings from a study that gives voice to older Aboriginal Australians’ perspectives culturally-appropriate programs to assist with healthy ageing.
The impact of hearing impairment on early academic achievement in Aboriginal children living in remote Australia: a data linkage study
This study aimed to investigate prevalence of otitis media (OM) and related hearing loss in Aboriginal children living in the Northern Territory (NT) of Australia.
Quantitative evaluation of an outreach case management model of care for urban Aboriginal and Torres Strait Islander adults living with complex chronic disease: a longitudinal study
This article aims to determine the impact of the Home-based Outreach case Management of chronic disease Exploratory (HOME) Study model of care on participants’ health and wellbeing at 12 months.
The recommendations in this paper are aimed at enabling health services to maximise their effectiveness in providing services to Aboriginal and Torres Strait Islander women, babies and their families during pregnancy and childbirth.
Mobile primary health care clinics for Indigenous populations in Australia, Canada, New Zealand and the United States: a systematic scoping review
This review identifies geographical gaps in the implementation of primary health care mobile clinics for Indigenous populations in Australia, Canada, New Zealand, and the United States.
This research presents client and staff perspectives of a model of clinical genetics services provided by the MJD Foundation (MJDF) in geographically and culturally complex contexts within the Northern Territory of Australia.
This report is an evaluation of the development and implementation of the National Indigenous Crisis Response Service, providing support for individuals and families who have experienced a suicide or other traumatic event in their family network.
Voluntary Indigenous identifier (VII) Framework: a framework for the collection, release, use and publication of VII data
This draft document is intended for data users and potential data users to set out the rules and principles used by the Department of Health when making decisions about the collection, release, use and publication of Voluntary Indigenous Identifier (VII) data. It also sets out...
This report provides an evidence base for monitoring changes in Indigenous eye health over time, access to and use of eye health services, and for identifying gaps in service delivery.
The authors of this report were commissioned by the National Health Leadership Forum to investigate approaches to workforce planning based on the healthcare needs of Aboriginal and Torres Strait Islander people.