Acute respiratory infection symptoms and COVID-19 testing behaviour: results based on South Australian health surveys
BMC Public Health volume 21, Article number: 2307 (2021)
Effective syndromic surveillance alongside COVID-19 testing behaviours in the population including in higher risk and hard to reach subgroups is vital to detect re-emergence of COVID-19 transmission in the community. The aim of this paper was to identify the prevalence of acute respiratory infection symptoms and coronavirus testing behaviour among South Australians using data from a population based survey.
We used cross-sectional data from the 2020 state-wide population level health survey on 6857 respondents aged 18 years and above. Descriptive statistics were used to explore the risk factors and multivariable logistic regression models were used to assess the factors associated with the acute respiratory infection symptoms and coronavirus testing behaviour after adjusting for gender, age, household size, household income, Aboriginal and/or Torres Strait Islander status, SEIFA, Country of birth, number of chronic diseases, wellbeing, psychological distress, and mental health.
We found that 19.3% of respondents reported having symptoms of acute respiratory infection and the most commonly reported symptoms were a runny nose (11.2%), coughing (9.9%) and sore throat (6.2%). Fever and cough were reported by 0.8% of participants. Of the symptomatic respondents, 32.6% reported seeking health advice from a nurse, doctor or healthcare provider. Around 18% (n = 130) of symptomatic respondents had sought testing and a further 4.3% (n = 31) reported they intended to get tested. The regression results suggest that older age, larger household size, a higher number of chronic disease, mental health condition, poor wellbeing, and psychological distress were associated with higher odds of ARI symptoms. Higher household income was associated with lower odds of being tested or intending to be tested for coronavirus after adjusting for other explanatory variables.
There were relatively high rates of self-reported acute respiratory infection during a period of very low COVID-19 prevalence and low rate of coronavirus testing among symptomatic respondents. Ongoing monitoring of testing uptake, including in higher-risk groups, and possible interventions to improve testing uptake is key to early detection of disease.
The current Coronavirus Disease 2019 (COVID-19) pandemic is presenting challenges to health and welfare systems worldwide. Prior to effective vaccine or pharmaceutical treatments, options for control are limited to traditional public health actions: primarily individual measures of early identification and isolation or quarantine of cases and controls (respectively)  and societal wide measures including social distancing and government mandated stay-at-home orders . Even once vaccines and other therapeutics become available, public health systems will continue to be critical to effective identification and management of disease.
Surveillance is a core function of a public health system and is imperative to the control of COVID-19 . Australia’s surveillance strategy is based on testing those with symptomatic disease in the community [4,5,6], and this has underpinned an effective public health response to COVID-19 to date. However, the effectiveness of this strategy relies on high uptake of testing in the community. Even with overall good availability of testing and health messaging on the public health importance of being tested, uptake may not be optimal. Various factors may contribute to non-optimal uptake, ranging from the generally mild illness caused by COVID-19 amongst young people , to social factors including lack of access to health care, inability to isolate and stay away from work whilst awaiting test results , or to limited access to mainstream health promotion messaging  due to language barriers. Such factors have the potential to have greater impact on high-risk populations, running the risk of undetected amplification within these groups [10, 11]. This undetected amplification occurred in Australia; when COVID-19 first emerged in Australia in March and April 2020, transmission was suppressed through widespread stay at home orders. However, re-emergence, initiated by failures in border quarantine measures, was sustained and amplified through generations of undetected transmission in hard-to-reach populations. This resulted in a large outbreak in the state of Victoria, which has caused more than 18,000 cases and 700 deaths as of 13 January 2021 .
Effective surveillance, including in higher-risk and hard-to-reach subgroups, is therefore crucial to detecting and controlling COVID-19, both when transmission is high and when community transmission has largely been suppressed, so that re-emergence is detected as early as possible. However, testing data alone has limitations in determining surveillance and testing coverage in the community, as total numbers of tests do not indicate the proportion of symptomatic people presenting for testing. Sentinel surveillance systems based on volunteers who self-report illness are also limited, as those who participate in such systems are likely to differ from the general community.
To determine testing coverage in those with symptoms, community-based representative data is therefore essential. Such information enables public health authorities to identify groups at risk of infection and groups unlikely to seek testing. This paper reports on a cross-sectional survey of adults in South Australia that can be weighted to give population-level estimates of acute respiratory infection (ARI) and testing uptake, including in groups potentially at higher risk of COVID-19 infection and those less likely to participate in testing.
Study design and data sources
This study used a cross-sectional survey design of South Australian adults aged 18 years and over.
Two surveys were used to collect data: the South Australian Population Health Survey (SAPHS) and the Population Health Survey Module System (PHSMS). The SAPHS is an ongoing state-wide population level survey which has been monitoring the health and wellbeing of South Australians since 2018. Data are collected in an ongoing way. The PHSMS utilises the same methodology and sampling frame (the South Australian population) as the SAPHS, however is a discrete survey of n = 3000 respondents, different to those who completed the SAPHS. Identical questions were asked across both surveys, and therefore the data collected have been combined.
A probability based, dual-frame sample of South Australian adults was selected using random digit dialling. Standard de-duplication and weighting procedures for the dual over-lapping frames were administered. As both surveys are population level surveys, the only inclusion criteria were that respondents be residents of South Australia with access to a telephone. The data collector was able to conduct interviews in selected languages other than English. Selected persons were non-replaceable, such that if the selected person was not available, interviews were not conducted with alternative household members (landline) or a person who was not the owner of the phone (mobile). There were no other exclusion criteria for the survey, although we additionally excluded children under 18 from our analysis.
Data were primarily collected using computer assisted telephone interviewing (CATI). To maximise participation, respondents were also offered the option of completing the survey on-line (CAWI, computer-assisted web interview) by receiving a unique hyperlink. The data presented in this paper were collected from 2 April to 28 June 2020 (SAPHS) and 14 May to 28 June 2020 (PHSMS).
In response to the COVID-19 pandemic, questions were included in both surveys to monitor symptoms of ARI in the adult population. Respondents were asked if they currently (or within the last week) had any symptoms of ARI consistent with coronavirus (fever, cough, sore throat, runny nose, shortness of breath, or a change of sense of taste or smell). Subsequent data collected in SAPHS from October 2020 suggests that 38% of symptomatic respondents have acute symptoms. All symptomatic respondents were also asked if they had sought health advice.
Finally, a subset of the sample was asked a question about testing behaviour. From 29 May 2020 (PHSMS) and 01 June 2020 (SAPHS), symptomatic respondents were asked if their symptoms were current on the day of the interview, and whether or not they had presented, or intended to present for COVID-19 testing. A sensitivity analysis showed no difference between those who had presented and those who intended to present for COVID-19 testing, and therefore these groups have been combined for analysis.
Data are presented by various demographic and population sub-groups. Socio-Economic Index For Areas (SEIFA) quintiles are presented according to the definition from the Australian Bureau of Statistics  using the respondent’s postcode and suburb. The respondent’s country of birth has been divided into two broad categories: English speaking countries and non-English speaking countries. Respondents who were born in Australia, the United Kingdom, Ireland, the United States of America, New Zealand, Canada, and South Africa are included in the English-speaking background category. All other respondents are included in the non-English speaking background category . Health outcomes presented in the inferential analyses are self-reported according to whether the respondent had even been told by a doctor or nurse they had the condition. Psychological distress was measured using the Kessler Psychological Distress Scale (K10) . Subjective wellbeing was measured using the United Kingdom Office for National Statistics 4-item questionnaire .
Data preparation and analysis were completed using SPSS 24 software. Excel 2010 was used to collate tables. Weighted data were used for the descriptive analysis and unweighted data were used for regression analysis.
Descriptive statistics were used to explore the associations between demographic and health outcome variables and ARI symptoms and testing behaviour. Counts and percentages were used to describe categorical data. Chi-square tests were applied to test the associations between the exposure variables and ARI symptoms and testing behaviour. The weighted proportions of people who respond to each category of the attribute are presented in the tables along with the 95% confidence interval. Raking  was used to weight respondents incorporating various population characteristics (gender, age, area of residence, country of birth, dwelling status, marital status, education level, employment status, household size) to more closely reflect the South Australian population using benchmarks derived from the June 2016 ABS Census data. The weighting of data can result in rounding discrepancies or totals not adding. Non-relevant responses such as ‘don’t know’ and ‘refused’ have not been included in the analysis except where stated.
Multiple logistic regression analyses using unweighted data was used to investigate the multiple factors related to ARI symptoms and testing behaviour. Potentially explanatory variables on the basis of known increased risk for respiratory viral transmission and the univariate analyses above such as gender, age, household size, household income, Aboriginal and/or Torres Strait Islanders status, SEIFA, Country of birth, number of chronic diseases, wellbeing, psychological distress, and mental health were considered in the multivariable analyses. A sub model including smoking status and private health insurance was performed using the SAPHS dataset only as these questions were not asked in the PHSMS survey.
Demographic profile of survey respondents
The weighted and unweighted sample of the SAPHS and PHSMS 2020 surveys in this study are presented in (Table 1). The population groups underrepresented by the survey include adults aged 18–29 years and people from non-English speaking backgrounds, while there was overrepresentation of adults 50 to 69 years, people with a degree or higher education level, people who earn over $150,000, and people who are retired.
Of the 6857 respondents included in this study, 48.4% were male and 51.6% were female, most resided in metropolitan areas (72.4%), were from an English-speaking background (83.3%), spoke English at home (91.5%), had less than four people living in their household (81.7%), and were employed (50.0%).
Descriptive analysis results
Across both surveys, 6833 respondents were asked if they had any symptoms of ARI, with the majority (80.7%) not reporting any symptoms. Of those who reported symptoms (n = 1318, 19.3%) the most commonly reported symptoms were a runny nose (11.2%), coughing (9.9%), sore throat (6.2%), and shortness of breath (6.0%). Less than one percent % (0.8%) of respondents reported having fever and cough in the past week. Weekly estimates of symptomatic respondents ranged from 9.9 to 22.7% over the 13-week study period. Symptomatic respondents were then asked if they had sought health advice from a nurse, doctor, or other health care provider. Of the 1312 people who responded to this question, 32.6% reported seeking health advice from a nurse, doctor or other healthcare provider.
The proportions of respondents reporting ARI symptoms by selected demographic and health outcome measures are presented in (Table 2). Females were more likely to report ARI symptoms than males. The likelihood of reporting ARI symptoms tended to be higher in lower household income groups and in Aboriginal and/or Torres Strait Islander respondents compared with non-Aboriginal and/or Torres Strait Islander respondents. The symptom report proportion increased with increasing household members, although this was not statistically significant.
Respondents who had at least three chronic conditions were more likely to report ARI symptoms than who did not have these conditions. Respondents who had poor overall wellbeing, mental health conditions (including anxiety, depression, stress related problem, and other mental health conditions), and psychological distress were also more likely to report ARI (Table 2).
A subset of symptomatic respondents (n = 722/3544) were further asked if their symptoms were present on the day of interview and whether they had presented, or intend to, for COVID-19 testing. Around half (n = 365) of symptomatic respondents reported ARI symptoms on the day of the interview, representing 10.3% of all respondents. Most symptomatic respondents (n = 562, 78%) had not presented for tested nor planned to do so. Around 18% (n = 130) had sought testing and a further 4.3% (n = 31) said they intended to get tested.
The proportions of symptomatic respondents reporting being tested or intending to be tested for COVID-19 by selected demographic measures and health outcome measures are presented in (Table 3). The likelihood of reporting COVID-19 testing was significantly higher in the highest SEIFA group and those with an English speaking background. The proportion of respondents reporting COVID-19 testing was lower among respondents who had household income of $100,001- $150,000 and more than $150,000.
Symptomatic respondents who had and at least three chronic conditions were more likely to report being tested or the intent to be tested for COVID-19. Respondents who had poor overall wellbeing, mental health conditions (includes anxiety, depression, stress related problem, and other mental health conditions), and psychological distress were also more likely to report for being tested for COVID-19 (Table 3).
Regression analysis results
The multivariate logistic regression analysis in Table 4 provides odds ratios (OR) for respondents reporting ARI symptoms compared to those not having ARI symptoms after adjusting for other explanatory variables in the model. The regression results suggest that older age (OR 0.99, 95% CI 0.98–0.99) larger household size (OR 1.06, 95% CI 1.01–1.12), and a higher number of chronic health conditions (OR 1.31, 95% CI 1.22–1.40) were associated with higher odds of ARI symptoms. Respondents who had a mental health condition (OR 1.27, 95% CI 1.06–1.53), poor wellbeing (OR 1.83, 95% CI 1.54–2.17) and those with psychological distress (OR 1.69, 95% CI 1.37–2.07) had higher odds of ARI symptoms. Aboriginal and/or Torres Strait Islander participants had an odds of reporting ARI of 1.46 (95% CI 0.86–2.49) compared to non-Aboriginal and/or Torres Strait Islander participants, estimated on a small number of participants and so with low precision.
The multivariate logistic regression analysis in Table 5 provides odds ratios (OR) for respondents reporting being tested or intending to be tested for COVID-19 compared to those not tested for COVID-19 after adjusting for other explanatory variables in the model. The regression results suggest that respondents who had household income of $100,001- $150,000 (OR 0.40, 95% CI 0.16–0.98) and more than $150,000 (OR 0.32, 95% CI 0.12–0.86) were associated with lower odds of COVID testing. Aboriginal and/or Torres Strait Islander participants had an odds of reporting COVID-19 testing of 2.42 (95% CI 0.59–9.88) compared to non-Aboriginal and/or Torres Strait Islander participants, estimated on a small number of participants and so with low precision.
This paper reports on a community-based population level representative survey of ARI and testing patterns among adults in South Australia with good coverage of population sub-groups by rurality, education level, household income and country of birth. We found that 19.3% of respondents reported ARI symptoms at the time of interview or within the week prior to being interviewed (weekly estimates ranging from 9.9 to 22.7% over the 13 weeks), and that less than a third had sought medical advice for their symptoms. The most common symptoms reported were runny nose and cough. Less than one percent (0.8%) reported fever and cough. These surveys took place during a period of very low COVID-19 activity in the South Australian community where there were 443 confirmed cases (to 30 June 2020), of which 304 were acquired overseas. Therefore, it is assumed that the vast majority of those reporting ARI had illness in the surveys were caused by a non-COVID-19 respiratory pathogen, or from another cause (e.g. allergies). However public health messaging at the time strongly encouraged anyone with even mild respiratory symptoms to seek medical care and be tested for COVID-19. This was also during a period when there were relatively few restrictions on social interaction and mobility in South Australia . In Victoria, levels of ARI were lower , and this may be due to higher levels of restrictions impacting on non-COVID-19 respiratory illness in Victoria due to an active outbreak at that time.
In both the univariate and multivariate analysis, older age, larger household size, more chronic conditions, poor or neutral wellbeing, any mental health condition, and psychological distress were risk factors for self-report of ARI symptoms. While some of these factors, such as larger household size, have previously been established as risk factors for ARI, older age is generally protective against ARI . We believe that the association we found may be due to the lack of ability within our study to differentiate chronic from acute ARI symptoms, as well as younger respondents (18–29 years) being underrepresented and those aged 50–69 years overrepresented (unweighted data).
There are relatively few other studies on community prevalence of ARI during the COVID-19 pandemic. In Australia, the only national source of community prevalence for ARI is ‘Flutracker’ ; an online community influenza-like illness (ILI) surveillance system. Over the same period as our survey, the Flutracker weekly incidence of self-reported fever and cough was less than 1%, while afebrile illness (with runny nose and sore throat) ARI was between 0.5 to 1.5%; this is considerably lower than the prevalence found in this survey. This difference may be due to varying case definitions, with this survey reporting current symptoms rather than new symptoms. Subsequently, from October 2020, the SAPHS collected information from symptomatic respondents to determine those with acute or chronic symptoms. The proportion of symptomatic respondents reporting acute symptoms (aligning closer to the Flutracker definition) in the SAPHS was 38%, in addition to only having fever and cough (0.8%). To retrospectively apply this proportion over the sample in this study, gives an average of 7.3% with acute ARI symptoms. Those with acute symptoms tended to be younger, and as such the analyses presented here are considered to reflect both those presenting acutely or also with chronic ARI symptoms. The difference between the two surveillance systems could be partly explained by biases generally found in online participatory surveillance systems such as ‘Flutracker’  including over-representation of those in higher socio-economic groups and older ages. These differences emphasise the value of representative surveys to support COVID-19 surveillance and response.
There are significant public health implications to our finding that, within the subgroup with ARI, when asked whether they had had a COVID-19 test, only 18% had already taken a test, with a further 4.3% intending to. COVID-19 testing rates in Australia are high by international standards, and there is strong public health messaging on the importance of getting tested with even minor symptoms. However, our findings indicate that the majority of the population are not being tested when they experience ARI symptoms. The only other relevant Australian data we are aware of comes from Flutracker and shows a similarly low rate of testing uptake. Another Australian study using survey data collected between April to June 2020 has also found that only 49% of people strongly agreed they would get tested if they had COVID-19 symptoms . However, the study participants for this study were recruited online via social media platforms and therefore may not be representative to the general population as compared to our study. This is further borne out by considering absolute testing rates; over the time of the study, South Australia had a crude rate of 1.2 tests per 1000 population per day which is much lower than the community prevalence of ARI found by our survey. Given that this number of tests is likely to include some asymptomatic people, this indicates the relatively low testing uptake amongst those with ARI. Our descriptive and regression analyses suggested lower testing rates in the highest income group ($100,000 and above). It is possible this reflects workers being less likely to present for testing due to the need to self-isolate until test results are returned. However, given how few participants were in the highest income group, the finding should be interpreted cautiously. Population surveys of ARI, such as that presented here, are crucial for public health to monitor, on an ongoing basis, the proportion of symptomatic people being tested. This group should be the main focus of testing, except in the event of an outbreak when testing contacts of cases.
Effective surveillance for COVID-19 requires representative community prevalence data on ARI paired with data on uptake of testing to understand disease patterns and testing rates among different groups. As mentioned above, Flutracker is the only long-term national source of community surveillance for ILI and ARI in Australia and whilst valuable, should be supported by surveys that capture the wider population, along with a range of other demographic, health and wellbeing data. Several syndromic systems in Australia report on ARI presentations  however these are all healthcare based, and so inherently biased towards those more likely to seek healthcare. Undertaking regular, representative community-based surveys allows validation of systems such as Flutracker and sentinel surveillance and qualification of potential bias, and in addition, the opportunity to obtain insights into the reasons for testing- related behaviours. As was done in South Australia, adaptation of existing population survey chronic disease surveillance systems is an efficient and effective way to do this.
Like any self-reported system, there is the potential for inherent measurement bias in the reporting of both symptoms and comorbidities. Additionally, our questions on respiratory symptoms did not differentiate between acute versus chronic symptoms. However, we have rectified this in our ongoing ARI syndromic surveillance and commenced collecting this data from October 2020. While we used weighting to account for differences between our sample and target population, we did not collect data on non-respondents. The combined cooperation rate  of both surveys was 80.4%. Reporting of both respiratory symptoms and presentation to a health care provider may also have been influenced by the changing context of COVID-19 in the South Australian and broader Australian community during the time period in which these surveys took place. Telephone-based surveys may also under-represent key groups of interest, and this has the potential to bias our results.
This paper shows the relatively high rates of self-reported ARI found in a usual community setting during a period of very low COVID-19 prevalence, and the relatively low percentage of this group who sought health advice or testing for their symptoms despite consistent public health messaging around this. Ongoing monitoring of testing uptake, including in higher-risk groups, and interventions for understating and improving uptake are key to early detection of disease. Our results demonstrate the feasibility and utility of ongoing community-based representative surveys in addressing these goals.
Availability of data and materials
The datasets generated and/or analysed during the current study are available from the corresponding author on reasonable request.
Acute Respiratory Infection
Computer assisted telephone interviewing
Computer-assisted web interview
Coronavirus Disease 2019
Population Health Survey Module System
South Australian Population Health Survey
Socio-Economic Index For Areas
World Health Organisation. Contact tracing in the context of COVID-19 2020 [Available from: https://www.who.int/publications/i/item/contact-tracing-in-the-context-of-covid-19.
World Health Organisation. Critical preparedness, readiness and response actions for COVID-19 2020 [Available from: https://www.who.int/publications/i/item/critical-preparedness-readiness-and-response-actions-for-covid-19.
World Health Organisation. Public health surveillance for COVID-19: interim guidance 2020 [Available from: https://www.who.int/publications/i/item/who-2019-nCoV-surveillanceguidance-2020.7.
Lokuge K, Banks E, Davis S, Roberts L, Street T, O’Donovan D, et al.. Exit strategies: optimising feasible surveillance for detection, elimination and ongoing prevention of COVID-19 community transmission. 2020:2020.04.19.20071217.
Department of Health. Australian national disease surveillance plan for COVID-19 2020 [Available from: https://www.health.gov.au/resources/publications/australian-national-disease-surveillance-plan-for-covid-19.
Department of Health. Coronavirus (COVID-19) in Australia – Pandemic Health Intelligence Plan 2020 [Available from: https://www.health.gov.au/resources/publications/coronavirus-covid-19-in-australia-pandemic-health-intelligence-plan.
Sinha IP, Harwood R, Semple MG, Hawcutt DB, Thursfield R, Narayan O, et al. COVID-19 infection in children. Lancet Respir Med. 2020;8(5):446–7.
Bonner C, Batcup C, Ayre J, Pickles K, Dodd R, Copp T, et al. Behavioural barriers to COVID-19 testing in Australia. 2020:2020.09.24.20201236.
Piller I, Zhang J, Li J. Linguistic diversity in a time of crisis: language challenges of the COVID-19 pandemic. Multilingua. 2020;39(5):503–15.
BehaviourWorks. Australia Monash Sustainable Development Institute. SCRUB COVID-19 findings round 8: Australians are still complying but testing remains a challenge Monash University. 2020 [Available from: https://www.behaviourworksaustralia.org/scrub-covid-19-findings-round-8-australians-are-still-complying-but-testing-remains-a-challenge/.
McCaffery KJ, Dodd RH, Cvejic E, Ayrek J, Batcup C, Isautier JM, et al. Health literacy and disparities in COVID-19-related knowledge, attitudes, beliefs and behaviours in Australia. Public Health Res Pract. 2020;30(4).
Department of Health and Human Services. Victorian coronavirus (COVID-19) data: State Government of Victoria, Australia; 2020. Available from: https://www.dhhs.vic.gov.au/victorian-coronavirus-covid-19-data.
Australian Bureau of Statistics. 2033.0.55.001 -Census of Population and Housing: Socio-Economic Indexes for Areas (SEIFA), Australia, 2016 2018 [Available from: https://www.abs.gov.au/ausstats/abs@.nsf/Lookup/by%20Subject/2033.0.55.001~2016~Main%20Features~FAQs%20-%20SEIFA%202016~4.
Australian bureau of statistics. 1200055004 - Country of Birth Standard, 2012, Version 1.0 2012 [Available from: https://www.google.com/search?q=1200.0.55.004+-+Country+of+Birth+Standard%2C+2012%2C+Version+1.0&rlz=1C1GCEB_enAU873AU873&oq=1200.0.55.004+-+Country+of+Birth+Standard%2C+2012%2C+Version+1.0&aqs=chrome.0.69i59j69i60j69i61.1019j0j7&sourceid=chrome&ie=UTF-8.
Kessler RC, Barker PR, Colpe LJ, Epstein JF, Gfroerer JC, Hiripi E, et al. Screening for serious mental illness in the general population. Arch Gen Psychiatry. 2003;60(2):184–9.
Randall C, Corp A, Self A. Measuring National Well-being: life in the UK. London: Office for National Statistics; 2014.
Dal Grande E, Chittleborough CR, Campostrini S, Tucker G, Taylor AW. Health estimates using survey raked-weighting techniques in an Australian population health surveillance system. Am J Epidemiol. 2015;182(6):544–56.
Government of South Australia. Activities and gatherings South Australia. 2020. Available from: https://www.covid-19.sa.gov.au/restrictions-and-responsibilities/activities-and-gatherings.
BehaviourWorks. Australia Monash Sustainable Development Institute. SCRUB project wave 4: Australians’ views on private gatherings, remote working and getting tested Monash University: Monash University; 2020. Available from: https://www.behaviourworksaustralia.org/scrub-project-wave-4-australians-views-on-private-gatherings-remote-working-and-getting-tested/.
Chen Y, Williams E, Kirk M. Risk factors for acute respiratory infection in the Australian community. PLoS One. 2014;9(7):e101440.
Moberley S, Carlson S, Durrheim D, Dalton C. Flutracking: weekly online community-based surveillance of influenza-like illness in Australia, 2017 annual report. Commun Dis Intell. 2018;2019:43.
Cantarelli P, Debin M, Turbelin C, Poletto C, Blanchon T, Falchi A, et al. The representativeness of a European multi-center network for influenza-like-illness participatory surveillance. BMC Public Health. 2014;14(1):984.
Communicable Diseases Intelligence. COVID-19, Australia: Epidemiology Report 24 (Fortnightly reporting period ending 30 August 2020). 2020 Sep 9. Report No.: 2209–6051.
American Association for Public Opinion Research. Standard definitions: final dispositions of case codes and outcome rates for surveys. 2016.
The authors thank Holly Vuong (Senior Research Project Officer, The Australian National University) for her assistance in preparing the manuscript document ready for submission.
No specific funding was received for this project beyond the salary support the authors receive from their institutions and elsewhere.
Ethics approval and consent to participate
The collection and reporting of COVID-19 related data was approved by the Department for Health and Wellbeing Human Research Ethics Committee (SAPHS: HREC/18/SAH/11/AM04, PHSMS:HREC/18/SAH/78/AM06). Informed consent was verbally obtained from all participants. The study was performed in accordance with the Declaration of Helsinki.
Consent for publication
The authors declare no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Joshi, S., D’Onise, K., Nolan, R. et al. Acute respiratory infection symptoms and COVID-19 testing behaviour: results based on South Australian health surveys. BMC Public Health 21, 2307 (2021). https://doi.org/10.1186/s12889-021-12359-3