Cancer Data and Aboriginal Disparities (CanDAD)—developing an Advanced Cancer Data System for Aboriginal people in South Australia: a mixed methods research protocol. Issue 12 (23rd December 2016)

• Record Type: Journal Article
• Authors: Yerrell, Paul Henry; Roder, David; Cargo, Margaret; Reilly, Rachel; Banham, David; Micklem, Jasmine May; Morey, Kim; Stewart, Harold Bundamurra; Stajic, Janet; Norris, Michael; Brown, Alex
• Other Names: author non-byline.; Weetra Aunty Roslyn author non-byline.; Weetra Aunty Cynthia author non-byline.; Miller Sandra author non-byline.; Burgoyne Arlene author non-byline.; Fazulla Neville author non-byline.; Kenmore George author non-byline.; Mitchell Amanda author non-byline.; Keefe Dorothy author non-byline.; Eckert Marion author non-byline.; Farshid Gelareh author non-byline.
• Is Part Of: BMJ open. Volume 6:Issue 12(2016)
• Publication Date: 2016-12-23
• Subjects: Indigenous Health -- ONCOLOGY -- QUALITATIVE RESEARCH -- Data linkage; Medicine -- Research -- Periodicals; 610.72
• DOI: 10.1136/bmjopen-2016-012505
• Languages: English
• ISSNs: 2044-6055

Abstract

Abstract : Introduction: In Australia, Aboriginal and Torres Strait Islander People carry a greater burden of cancer-related mortality than non-Aboriginal Australians. The Cancer Data and Aboriginal Disparities Project aims to develop and test an integrated, comprehensive cancer monitoring and surveillance system capable of incorporating epidemiological and narrative data to address disparities and advocate for clinical system change. Methods and analysis: The Advanced Cancer Data System will integrate routinely collected unit record data from the South Australian Population Cancer Registry and a range of other data sources for a retrospective cohort of indigenous people with cancers diagnosed from 1990 to 2010. A randomly drawn non-Aboriginal cohort will be matched by primary cancer site, sex, age and year at diagnosis. Cross-tabulations and regression analyses will examine the extent to which demographic attributes, cancer stage and survival vary between the cohorts. Narratives from Aboriginal people with cancer, their families, carers and service providers will be collected and analysed using patient pathway mapping and thematic analysis. Statements from the narratives will structure both a concept mapping process of rating, sorting and prioritising issues, focusing on issues of importance and feasibility, and the development of a real-time Aboriginal Cancer Measure of Experience for ongoing linkage with epidemiological data in the Advanced Cancer Data System. Aboriginal Community engagement underpins this Project. Ethics and dissemination: The research has been approved by relevant local and national ethics committees. Findings will be disseminated in local and international peer-reviewed journals and conference presentations. In addition, the research will provide data for knowledge translation activities across the partner organisations and feed directly into the Statewide Cancer Control Plan. It will provide a mechanism for monitoring and evaluating the implementation of the recommendations in these documents.