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An exploration of the sociodemographic and health conditions associated with self-rated wellbeing for Aboriginal and Torres Strait Islander adults
BMC Research Notes volume 14, Article number: 386 (2021)
To identify sociodemographic factors and health conditions associated with self-rated wellbeing for Aboriginal and Torres Strait Islander adults. Participants were recruited via investigator networks and an online panel provider with an established nationwide panel of Aboriginal and Torres Strait Islander adults. Those interested were invited to complete a survey that included an assessment of wellbeing using a visual analogue scale. Data was collected from October–November 2019 and August–September 2020. Exploratory analyses were conducted to ascertain factors associated with self-rated wellbeing for Aboriginal and Torres Strait Islander adults.
Having more than enough money to last until next pay day, full-time employment, completion of grade 12, having a partner, and living with others were significantly associated with higher wellbeing among Aboriginal and Torres Strait Islander adults. A self-reported history of depression, anxiety, other mental health conditions, heart disease, or disability were associated with lower self-rated wellbeing scores. Our findings indicate a need for further investigation among these socioeconomic and patient groups to identify how to improve and support the wellbeing of Aboriginal and Torres Strait Islander adults.
There has been increased attention on understanding, defining and measuring wellbeing for populations worldwide, including the perspectives and considerations of cultural groups [1,2,3]. Understanding wellbeing from an Aboriginal and Torres Strait Islander perspective (herein respectfully referred to as Indigenous Australians) has received recent attention due to the imperative for Australian governments to improve Indigenous Australians’ health and wellbeing. Indigenous Australians understanding of wellbeing is holistic and includes physical, emotional, spiritual, cultural, and socio-political aspects of life of the individual and their community [4,5,6]. While no nationally relevant measure of wellbeing for Indigenous Australians is currently available , gaining an understanding of groups who are at risk of poor wellbeing is clinically pertinent. Such information may inform the provision of targeted programs and services to better support the wellbeing of Indigenous Australians.
The current study, part of the larger What Matters 2Adults Study , aims to identify sociodemographic factors and health conditions associated with self-rated wellbeing for Indigenous Australian adults.
This exploratory study recruited Indigenous Australian adults (≥ 18 years) via investigator networks and an online panel provider (Dynata) with an established nationwide panel of Indigenous Australian adults. Potential participants received study information and those interested completed an online consent form before completing the online survey. Survey data was collected during October–November 2019 (n = 309) and August–September 2020 (n = 354). There were 42 respondents who completed the survey at both times. A sensitivity analysis was conducted removing the data collected from the first round of the survey for the 42 participants who completed the survey at both rounds. The direction and size of between-group differences in self-rated wellbeing scores did not materially change with the exclusion of these data. As such, all 663 responses were treated as independent observations of wellbeing.
Data collection, measures and analysis
Participants were asked to self-rate their “…overall wellbeing at the moment” using a 100-point visual analogue scale, with zero indicating the worst wellbeing they could imagine and 100 indicating the best wellbeing they could imagine (see Additional file 1). Self-reported sociodemographic, socioeconomic and health conditions were collected, including: age, gender, Indigenous status, main language spoken at home, residential area, relationship status, household size, highest level of education, employment status, financial situation and comorbid conditions (see Table 1). Composite variables were created to measure the number of physical comorbidities, and the presence/absence of any mental health comorbidity.
Differences in mean wellbeing scores were tested using t-tests and ANOVA. Variables not statistically significantly associated with wellbeing at univariate level (using cut-off p < 0.1) were excluded in subsequent multivariable analyses. Two multiple linear regression models were conducted to produce adjusted estimates of the differences in wellbeing scores. Model 1 included sociodemographic and socioeconomic variables and composite measures relating to comorbidities (number of physical conditions participants reported having and presence of any mental health comorbidity). Model 2 included individual comorbidities eligible for inclusion based on univariate analyses. Both models were adjusted for age and calendar period at time of survey completion. As age did not have a linear relationship with wellbeing, it was modelled as a categorical variable. There were no missing values, however, one extreme outlier in household size was excluded in the multivariable analyses. All analyses were conducted in Stata v15 .
A total of 663 Indigenous Australian adults (60% female), with median age of 45 years (median; IQR 35–56), completed the online survey (47% in the first round). Participants from all mainland Australian states and territories were included, with 41% of the sample from New South Wales and 2% from the Australian Capital Territory. The distribution of participants across the states and territories was broadly reflective of the distribution of the national Indigenous Australian population. Participant characteristics and mean self-rated wellbeing scores are described in Table 1. Overall, the unadjusted mean wellbeing score was 66.1 (SD 24.5). There were significant differences in the unadjusted scores based on age group, relationship status, household size, highest education, employment, financial situation and comorbidities (p < 0.05).
In multivariable analyses, the adjusted mean wellbeing score among participants was 70.3 and, on average, 3.4 points higher in the second-round of the survey compared to the first (Table 2). On average, participants aged 30–44 years and 60 + years had wellbeing scores that were 5.2 (p = 0.02) and 11.0 points (p < 0.001) higher than those aged 45–59 years. Those who reported being single rated their wellbeing, on average, 4.6 points lower than those who were partnered (p = 0.03). The mean wellbeing score was 8.9 points and 7.5 points higher, on average, for those living in households of four people (p = 0.01) and five or more people (p = 0.02) compared to sole occupiers. Participants with Grade 12 completion had wellbeing 8.1 points higher, on average, than those who completed grade 10 or below (p = 0.01). Compared to those in full-time employment, those who reported not working, or having part-time or other employment, rated their wellbeing significantly lower on average (6.8, 6.2 and 10.2 points lower, p = < 0.01, 0.04 and 0.05, respectively). Participants who indicated having more than enough money to last until their next payday had significantly higher wellbeing, on average, compared to those who did not have enough, or had just enough money (7.6, 5.3 points lower, p = < 0.01, 0.02, respectively). Participants with seven or more physical comorbidities had wellbeing scores 8.2 points lower, on average, than those who reported having no physical comorbidities (p = 0.03), while those with fewer physical comorbidities did not have a significantly different wellbeing score than those without physical comorbidity. Participants reporting any mental health condition experienced 11.9 points lower wellbeing, on average, than those who had none (p = < 0.001).
After mutual adjustment for comorbid conditions in model 2, having heart disease, a disability, depression, anxiety and other mental health conditions were statistically significantly associated with lower wellbeing (Table 3).
In a large sample of Indigenous Australian adults, we identified several socioeconomic and sociodemographic factors and health conditions associated with wellbeing. Having more than enough money to last until next pay day, full-time employment, and completion of grade 12 were all associated with higher levels of wellbeing. Other studies identifying aspects of life that are important to the wellbeing of Indigenous Australians also found that employment, education and money are needed to achieve good wellbeing [6, 10, 11]. Our results are consistent with previous studies in other populations that identified important socioeconomic impacts on wellbeing or quality-of-life, including financial stability for respondents in China, Ghana, India, South Africa, Russia and the United States [12, 13], employment in the general Australian population , and higher education in the United States . Socioeconomic disadvantage is consistently associated with poorer health outcomes for Indigenous Australians with cancer , cardiovascular disease [16, 17], psychological distress , and liver cirrhosis , and have been associated with potentially preventable hospital admissions . The effect of socioeconomic disadvantage on health and wellbeing is likely to explain only some of the observed health disparities for Indigenous Australians compared to non-Indigenous Australians, with other factors, including systemic racism, contributing to inequalities across socioeconomic strata [16, 18].
Family, kinships and community connections are important to the wellbeing of Indigenous peoples in Australia [6, 10, 11], and globally . In this study, wellbeing was lowest among those without partners or living on their own. This was consistent with a study of Indigenous Australians with cancer where health related quality-of-life was higher for those who were married . Having a partner and/or living with others helps maintain social connections, which may mitigate the impact of social determinants of poor wellbeing [23, 24]. More work is needed to understand the role of loneliness, social connection and social isolation in wellbeing for Indigenous Australians. These factors are particularly relevant during this COVID-19 era, where public health restrictions [25,26,27] have limited opportunities for social interaction and connection.
Indigenous Australians have higher incidence of many common chronic diseases and are more likely to be diagnosed at a younger age and living with multiple chronic conditions . Half of the participants in the current study reported having at least one mental health condition and 17% had a very high burden of physical comorbidity (≥ 7 conditions). We found participants with at least one mental health condition and/or a very high burden of physical comorbidities rated their wellbeing significantly lower than those without those comorbidities. However, there did not appear to be a linear relationship between wellbeing and number of diagnosed physical conditions reported. This finding suggests the relationship between physical comorbidity and wellbeing goes beyond the number of conditions a person has. This survey did not collect information on the management or severity of comorbid conditions, nor how they impacted on daily activities, which has previously been shown to be pertinent for wellbeing and quality-of-life [29,30,31]. The findings may also suggest that socioeconomic and social connection factors may be more important than health state, emphasising the holistic nature of wellbeing for Indigenous peoples .
In the current study, depression, anxiety, other mental health conditions, heart disease, and disability were associated with wellbeing. Recent national estimates suggest 25% of Indigenous Australian females and 23% of Indigenous Australian males have a mental illness or behavioural condition, with anxiety (17%) and depression (13%) the most common conditions . The relationship between mental health and wellbeing has previously been demonstrated for the general Australian population [34, 35] and other Indigenous populations worldwide , highlighting the need for increased investment in preventive mental health programs. Indigenous Australians have higher rates of heart disease than non-Indigenous Australians (27% and 21%, respectively) , and 38% of Indigenous Australians have a disability that restricts their everyday lives, at a rate of 1.8 times that of non-Indigenous Australians . Heart disease is commonly associated with disability and poor quality-of-life, however the link between disability and wellbeing is poorly understood [38, 39]. Previous reports have shown a link between chronic health conditions and their impact on wellbeing long-term . Further investigation among these patient groups may provide critical information about how to improve and maintain good wellbeing for Indigenous Australians.
This study explored the relationship between wellbeing and downstream social determinants of health for Indigenous Australians. Our findings suggest those with a history of mental illness, heart disease, a disability, as well as those without partners, living on their own, and who have not completed high school, are in precarious or under employment, and have financial instability are at risk of poor wellbeing. The identification of these factors may offer health and social services a way to identify Indigenous Australians at risk and provide opportunities for individual intervention. Prospective studies are needed to gain deeper understanding of the dynamic and intersectional nature of the relationships between socioeconomic wellbeing, social connection, and physical and mental health for Indigenous Australians.
This is one of the largest studies investigating factors associated with self-rated wellbeing among a geographically diverse respondent sample of Indigenous Australian adults. However, we were limited by a self-reported single global measure of wellbeing. In studies with non-Indigenous populations the visual analogue scale was found to measure quality-of-life comparably with multi-item questionnaires . However, the use of a visual analogue scale to measure overall wellbeing has not been validated with Indigenous Australians [41,42,43] limiting our ability to examine specific dimensions of wellbeing. This study explored downstream social determinants of wellbeing. However, we recognise the importance of midstream determinants, such as the characteristics and accessibility of health and social services that may support or hinder wellbeing of individuals and communities, and upstream determinants, such as the political, education and justice systems of society and the structural racism that is pervasive within these systems and known to be critical for wellbeing [16, 18]. While this cross-sectional study limited our ability to infer causality, findings may inform the direction of future research to understand the nature of these relationships and develop ways to improve clinical, public health and social services capabilities to support wellbeing among Indigenous Australian adults and their communities.
Availability of data and materials
The datasets generated and analysed during the current study are not publicly available but may be available from the authors on request.
Maggino F. Challenges, needs and risks in defining wellbeing indicators. In: Maggino F, editor. A life devoted to quality of life. Cham: Springer; 2016. p. 209–33.
Dodge R, Daly AP, Huyton J, Sanders LD. The challenge of defining wellbeing. Int J Wellbeing. 2012. https://doi.org/10.5502/ijw.v2i3.4.
Cooke PJ, Melchert TP, Connor K. Measuring well-being: a review of instruments. Couns Psychol. 2016;44(5):730–57.
King M, Smith A, Gracey M. Indigenous health part 2: the underlying causes of the health gap. Lancet. 2009;374(9683):76–85.
Kite E, Davy C, Gibson O, McBride K, Brown A. Aboriginal and Torres Strait Islander peoples’ perceptions of quality of life and wellbeing and how they are measured: a systematic review protocol. JBI Evid Synth. 2014;12(7):138–47.
Butler TL, Anderson K, Garvey G, Cunningham J, Ratcliffe J, Tong A, et al. Aboriginal and Torres Strait Islander people’s domains of wellbeing: a comprehensive literature review. Soc Sci Med. 2019;233:138–57.
Howard K, Anderson K, Cunningham J, Cass A, Ratcliffe J, Whop LJ, et al. What Matters 2 Adults: a study protocol to develop a new preference-based wellbeing measure with Aboriginal and Torres Strait Islander adults (WM2Adults). BMC Public Health. 2020;20(1):1739.
StataCorp. Stata Statistical Software: Release 15. In: Station C, editor.: TX: Stata Corp LLC.; 2017.
Australian Bureau of Statistics. Estimates of Aboriginal and Torres Strait Islander Australians Canberra: Australian Bureau of Statistics; 2018 [cat. no. 3238.0.55.001].
Garvey G, Anderson K, Gall A, Butler TL, Whop LJ, Arley B, et al. The fabric of Aboriginal and Torres Strait Islander wellbeing: a conceptual model. Int J Environ Res Public Health. 2021;18(15):7745.
Garvey G, Anderson K, Gall A, Butler TL, Cunningham J, Whop LJ, et al. What Matters 2 Adults (WM2Adults): understanding the foundations of Aboriginal and Torres Strait Islander wellbeing. Int J Environ Res Public Health. 2021;18(12):6193.
Huang R, Ghose B, Tang S. Effect of financial stress on self-rereported health and quality of life among older adults in five developing countries: a cross sectional analysis of WHO-SAGE survey. BMC Geriatr. 2020;20(1):288.
Kobau R, Sniezek J, Zack MM, Lucas RE, Burns A. Well-being assessment: an evaluation of well-being scales for public health and population estimates of well-being among US adults. Appl Psychol Health Well Being. 2010;2(3):272–97.
Dockery M. The subjective wellbeing of Indigenous Australians. Perth: Centre for Labour Market Research; 2010. Report No.: 1329–2676.
Dasgupta P, Baade PD, Youlden DR, Garvey G, Aitken JF, Wallington I, et al. Variations in outcomes for Indigenous women with breast cancer in Australia: a systematic review. Eur J Cancer Care. 2017;26(6):e12662.
Cunningham J. Socioeconomic disparities in self-reported cardiovascular disease for Indigenous and non-Indigenous Australian adults: analysis of national survey data. Popul Health Metrics. 2010;8(1):31.
Brown A, Carrington MJ, McGrady M, Lee G, Zeitz C, Krum H, et al. Cardiometabolic risk and disease in Indigenous Australians: the heart of the heart study. Int J Cardiol. 2014;171(3):377–83.
Cunningham J, Paradies YC. Socio-demographic factors and psychological distress in Indigenous and non-Indigenous Australian adults aged 18–64 years: analysis of national survey data. BMC Public Health. 2012;12(1):95.
Powell EE, Skoien R, Rahman T, Clark PJ, O’Beirne J, Hartel G, et al. Increasing hospitalization rates for cirrhosis: overrepresentation of disadvantaged Australians. EClinicalMedicine. 2019;11:44–53.
Banham D, Chen T, Karnon J, Brown A, Lynch J. Sociodemographic variations in the amount, duration and cost of potentially preventable hospitalisation for chronic conditions among Aboriginal and non-Aboriginal Australians: a period prevalence study of linked public hospital data. BMJ Open. 2017;7(10):e017331.
Gall A, Anderson K, Howard K, Diaz A, King A, Willing E, et al. Wellbeing of Indigenous Peoples in Canada, Aotearoa (New Zealand) and the United States: a systematic review. Int J Environ Res Public Health. 2021;18(11):5832.
Garvey G, Cunningham J, He VY, Janda M, Baade P, Sabesan S, et al. Health-related quality of life among Indigenous Australians diagnosed with cancer. Qual Life Res. 2016;25(8):1999–2008.
Ziersch A, Miller E, Baak M, Mwanri L. Integration and social determinants of health and wellbeing for people from refugee backgrounds resettled in a rural town in South Australia: a qualitative study. BMC Public Health. 2020;20(1):1700.
Eckermann E. Living alone and living together—their significance for wellbeing. In: Glatzer W, Camfield L, Møller V, Rojas M, editors. Global handbook of quality of life: exploration of well-being of nations and continents. Dordrecht: Springer; 2015. p. 435–44.
Storen R, Corrigan N. COVID-19: a chronology of state and territory government announcements (up until 30 June 2020). In: Department of Parliamentary Services, editor. Canberra: Parliament of Australia,; 2020.
Smith JA, Judd J. COVID-19: Vulnerability and the power of privilege in a pandemic. Health Promot J Austr. 2020;31(2):158–60.
Australian Bureau of Statistics. One year of COVID-19: Aussie jobs, business and the economy: Australian Bureau of Statistics; 2021. https://www.abs.gov.au/articles/one-year-covid-19-aussie-jobs-business-and-economy. Accessed 16 July 2021.
Australian Institute of Health and Welfare. Contribution of chronic disease to the gap in adult mortality between Aboriginal and Torres Strait Islander and other Australians. Canberra: Australian Institute of Health and Welfare; 2010.
Bayliss EA, Ellis JL, Steiner JF. Subjective assessments of comorbidity correlate with quality of life health outcomes: initial validation of a comorbidity assessment instrument. Health Qual Life Outcomes. 2005;3:51.
John R, Kerby DS, Hagan HC. Patterns and impact of comorbidity and multimorbidity among community-resident American Indian elders. Gerontologist. 2003;43(5):649–60.
Cummings A, Grimmett C, Calman L, Patel M, Permyakova NV, Winter J, et al. Comorbidities are associated with poorer quality of life and functioning and worse symptoms in the 5 years following colorectal cancer surgery: results from the ColoREctal Well-being (CREW) cohort study. Psychooncology. 2018;27(10):2427–35.
Kingsley J, Townsend M, Henderson-Wilson C, Bolam B. Developing an exploratory framework linking Australian Aboriginal peoples’ connection to country and concepts of wellbeing. Int J Environ Res Public Health. 2013;10(2):678–98.
Australian Institute of Health and Welfare. Indigenous health and wellbeing. Canberra: Australian Institute of Health and Welfare; 2020.
Rossell SL, Neill E, Phillipou A, Tan EJ, Toh WL, Van Rheenen TE, et al. An overview of current mental health in the general population of Australia during the COVID-19 pandemic: results from the COLLATE project. Psychiatry Res. 2021;296:113660.
Rahman MA, Hoque N, Alif SM, Salehin M, Islam SMS, Banik B, et al. Factors associated with psychological distress, fear and coping strategies during the COVID-19 pandemic in Australia. Glob Health. 2020;16(1):95.
Kant S, Vertinsky I, Zheng B, Smith PM. Social, cultural, and land use determinants of the health and well-being of Aboriginal peoples of Canada: a path analysis. J Public Health Policy. 2013;34(3):462–76.
Australian Institute of Health and Welfare. Cardiovascular disease, diabetes and chronic kidney disease—Australian facts: Aboriginal and Torres Strait Islander people. Canberra: Australian Institute of Health and Welfare; 2015.
Fortune N, Badland H, Clifton S, Emerson E, Rachele J, Stancliffe RJ, et al. The disability and wellbeing monitoring framework: data, data gaps, and policy implications. Aust NZ J Public Health. 2020;44(3):227–32.
Gao L, Moodie M, Chen G. Measuring subjective wellbeing in patients with heart disease: relationship and comparison between health-related quality of life instruments. Qual Life Res. 2019;28(4):1017–28.
de Boer AGEM, van Lanschot JJB, Stalmeier PFM, van Sandick JW, Hulscher JBF, de Haes JCJM, et al. Is a single-item visual analogue scale as valid, reliable and responsive as multi-item scales in measuring quality of life? Qual Life Res. 2004;13(2):311–20.
Gilchrist L, Bessarab D, Douglas H, LoGiudice D, Ratcliffe J, Flicker L, et al. The validity of the good spirit, good quality-of-life tool for older Aboriginal Australians: development and validation of cognitive and quality of life assessments for older indigenous peoples internationally. Alzheimers Dement. 2020;16:e040108.
Nagel T, Sweet M, Dingwall KM, Puszka S, Hughes JT, Kavanagh DJ, et al. Adapting wellbeing research tools for Aboriginal and Torres Strait Islander people with chronic kidney disease. BMC Nephrol. 2020;21:1–8.
Le Grande M, Ski C, Thompson D, Scuffham P, Kularatna S, Jackson A, et al. Social and emotional wellbeing assessment instruments for use with Indigenous Australians: a critical review. Soc Sci Med. 2017;187:164–73.
The What Matters study is funded by a National Health and Medical Research Council (NHMRC) Project grant (#1125434). This study was also supported by the NHMRC funded Centre of Research Excellence (CRE) in Targeted Approaches To Improve Cancer Services for Indigenous Australian Australians (TACTICS; #1153027). KA salary was supported by the NHMRC funded What Matters study (#1125434). GG salary was supported by an NHMRC Investigator Grant (#1176651). AD receives salary from the TACTICS CRE (#1153027). AG is supported by a NHMRC Postgraduate Scholarship (APP1168150) and a TACTICS Postgraduate Scholarship top-up. The views expressed in this publication are those of the authors and do not necessarily reflect the views of the funding agencies.
Ethics approval and consent to participate
Ethics approval for this study was granted by the Human Research and Ethics Committee of the Northern Territory Department of Health and Menzies School of Health Research (NHMRC Reg No. EC00153), The University of Sydney Human Research Ethics Committee (CRICOS Number: 00026A), and the University of Technology Sydney (UTS) Human Research Ethics Committee (TRIM No. RES20/234). Potential participants received study information and those interested completed an online consent form before completing the online survey.
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Gall, A., Diaz, A., Garvey, G. et al. An exploration of the sociodemographic and health conditions associated with self-rated wellbeing for Aboriginal and Torres Strait Islander adults. BMC Res Notes 14, 386 (2021). https://doi.org/10.1186/s13104-021-05794-3
- Quality of life
- Indigenous peoples
- Visual analogue scale
- Aboriginal and Torres Strait Islander people
- Mental health