Despite relatively small demonstrable achievements more recently, there still remains concerns that Indigenous Australians have been over-researched without corresponding improvements in health outcomes: “despite all the research and medical interventions spaning decades, improvements – where they occur – are incremental and trend up at a slower rate than for non-Indigenous Australians”. Historically however, health research has not served Indigenous Australians well this has generally been the case for Indigenous people in colonised nations globally. In Aboriginal and Torres Strait Islander health research, research benefit is broadly defined as any elements of research that are advantageous or good such as strengthening capacities, opening opportunities or improving health outcomes that progress the interests that are valued by Aboriginal and Torres Strait Islander (respectfully hereafter Indigenous) people. As a point of departure to improving impact and reaching mutually beneficial outcomes for researchers and partners in Indigenous health research, we need to routinise the assessment of benefit from outset of research as one of the standards toward which we work. In Indigenous health research, this will often mean adopting a benefit-led approach by changing the way research is done and preferencing alternative research methodologies. The authors conclude that as an imperative, a systematic benefit assessment strategy that includes identification of research priorities and planning, monitoring and evaluation components needs to be developed and implemented across research projects. We need to work collaboratively and listen more closely to the voice of Indigenous Australians to better understand, demonstrate and measure health research benefits. Different research stakeholders have different conceptions of the value and nature of research, its conduct, what it should achieve and the kinds of benefits expected. The research impact debate must take account of the various standards of accountability (to whom), impact priorities (for whom), positive and negative impacts, and biases that operate in describing impact and measuring benefit.Ī perennial question in Indigenous research discourse is whether the abundance of research conducted purportedly to improve health, is justified and benefits Indigenous people in ways that are meaningful and valued by them. Research reform has only focussed on research translation in more recent years. Assessing societal and other non-academic impacts and benefits however, has not been accorded corresponding attention. Increasingly, more sophisticated performance measures have been implemented to ensure academic impact and benefits are captured. Because research practices come from Western knowledge bases, attaining such positions in research means reconciling both Indigenous and Western knowledge systems to produce new methodologies that guide planning, evaluating and monitoring of research practices as necessary. Capturing the meaning of research benefit takes the form of ethical value-oriented methodological considerations in the decision-making processes of Indigenous research endeavours.
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