Data
Actioning Indigenous Data Sovereignty: Aboriginal and Torres Strait Islander consent and data sharing priorities to guide community-controlled health service best practice
Aboriginal and Torres Strait Islander people have the right to access culturally safe information and health and wellbeing services to empower their participation in informed…
View researchResearch Our Way: Closing the gap in Aboriginal and Torres Strait Islander health human research
This project aims to answer the following research questions: What are the strengths and/or limitations of existing human research ethics committee structures for Aboriginal and…
View researchVictorian Aboriginal Health Research Ethics Committee: Steps to Establishment
Victoria’s health, medical and wellbeing research sector is one of the state’s most significant and productive industries, yet we are one of the few states…
View researchA national approach to improving cancer outcomes
Towards a national approach to improving cancer outcomes for Aboriginal and Torres Strait Islander people Little is known about the availability of Indigenous-specific cancer support…
View researchUptake of evidence to policy: The Indigenous Burden of Disease case study
Uptake of evidence to policy: The Indigenous Burden of Disease case study Using the Indigenous Burden of Disease (BOD) study (Vos, et al. 2009) as…
View researchDiscourse, Data and Deficit: Deconstructing the ‘Indigenous Health’ paradigm and its effects on Aboriginal and Torres Strait Islander peoples
Project aims To conduct field-based research among Aboriginal and Torres Strait Islander communities on how local community discourses impact on health service provision by demonstrating…
View researchData resource on key influences on health in the Northern Territory
A longitudinal data resource on key influences on health in the Northern Territory: Opportunities and obstacles The role of social factors in contributing to the…
View researchThe burden of disease and injury in Indigenous Australians
The Indigenous Burden of Disease Study is a component of the Australian Burden of Disease Study, which described the health status of Australians in the…
View researchVictorian Aboriginal Child Mortality Study (VACMS): Phase 2
The Victorian Aboriginal Child Mortality Study (VACMS): Phase 2 – analysis of mortality and disparities for Aboriginal compared to non-Aboriginal infants, children and young people…
View researchValuing Aboriginal and Torres Strait Islander Young Men
Valuing Aboriginal and Torres Strait Islander young men Project Aim: This project aimed to identify how Aboriginal and Torres Strait Islander young men remain strong…
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