Ethical conduct in research with Aboriginal and Torres Strait Islander peoples and communities: guidelines for researchers and stakeholders

This guide from the National Health and Medical Research Council provides a set of principles to ensure research is safe, respectful, responsible, high quality and of benefit to Aboriginal and Torres Strait Islander people and communities.

The health, wellbeing and experiences of Aboriginal and Torres Strait Islander Peoples continue to be the focus of much research to promote positive outcomes. Over the years, research has contributed to positive outcomes and benefits in, for example, health, medicine and education, and in preserving the languages, stories and songs of Aboriginal and Torres Strait Islander Peoples and communities in culturally appropriate ways.



However, not all research has been of benefit for Aboriginal and Torres Strait Islander Peoples and communities. This absence of benefit can often be understood in the context of ethical considerations related to human research with Aboriginal and Torres Strait Islander people and communities.



Ethical research with Aboriginal and Torres Strait Islander Peoples and communities should:

  • improve the way all researchers work with Aboriginal and Torres Strait Islander people and their communities
  • develop and/or strengthen research capabilities of Aboriginal and Torres Strait Islander people and their communities
  • enhance the rights of Aboriginal and Torres Strait Islander Peoples as researchers, research partners, collaborators and participants in research

Ethical conduct in research with Aboriginal and Torres Strait Islander peoples and communities: guidelines for researchers and stakeholders

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