Abstract
The COVID-19 pandemic has dramatically impacted lifestyle behaviour as public health initiatives aim to “flatten the curve”. This study examined changes in activity patterns (physical activity, sedentary time, sleep), recreational physical activities, diet, weight and wellbeing from before to during COVID-19 restrictions in Adelaide, Australia. This study used data from a prospective cohort of Australian adults (parents of primary school-aged children; n = 61, 66% female, aged 41±6 years). Participants wore a Fitbit Charge 3 activity monitor and weighed themselves daily using Wi-Fi scales. Activity and weight data were extracted for 14 days before (February 2020) and 14 days during (April 2020) COVID-19 restrictions. Participants reported their recreational physical activity, diet and wellbeing during these periods. Linear mixed effects models were used to examine change over time. Participants slept 27 minutes longer (95% CI 9–51), got up 38 minutes later (95% CI 25–50), and did 50 fewer minutes (95% CI -69–-29) of light physical activity during COVID-19 restrictions. Additionally, participants engaged in more cycling but less swimming, team sports and boating or sailing. Participants consumed a lower percentage of energy from protein (-0.8, 95% CI -1.5–-0.1) and a greater percentage of energy from alcohol (0.9, 95% CI 0.2–1.7). There were no changes in weight or wellbeing. Overall, the effects of COVID-19 restrictions on lifestyle were small; however, their impact on health and wellbeing may accumulate over time. Further research examining the effects of ongoing social distancing restrictions are needed as the pandemic continues.
Introduction
The COVID-19 pandemic has dramatically and rapidly changed the lifestyles of people around the world. Restricted freedom of movement, limited access to health services, food providers and exercise resources, changes in social dynamics due to distancing, and psychological adaptations to isolation have all changed what we eat, our mental wellbeing, and above all the way we use our time. Indeed, a recent New Zealand study [1] surveyed 2002 people about their experiences during lockdown. Among participants’ open-ended responses, the most commonly used word was “time”.
Several surveys have been conducted which have straddled the period of lockdown, trying to capture changes in behaviour. Most have found reductions in levels of physical activity. A large international analysis examined step counts for >19 million days recorded by users of a physical activity app [2], finding that steps decreased by 6% after 10 days and 27% after 30 days of restriction. Declines after 30 days varied from 7% (Sweden) to 49% (Italy), apparently associated with the severity of lockdown. Other international studies have reported similar results; an analysis of Fitbit data from 30 million adults showed declines of 7–38%, most marked in the stricter lockdown zones of the European Union [3]. Similarly, a report from wearable manufacturer Withings of 2 million users of their products found that step count decreased by between 1% (Germany) and 56% (Hubei Province, China) [4]. An Australian consultancy found that 44% of adults had reduced their levels of physical activity, compared with 23% who reported increased physical activity. The declines tended to be greater among younger adults [5]. A UK survey of 2000 adults found that step count declined by 28% [6]. The declines also affected children; a study of 41 overweight children under strict lockdown in Verona found a decline in physical activity of 2 hours per week [7], while a study of 2427 children and adolescents in China showed a reduction in moderate-to-vigorous intensity physical activity of 435 minutes per week between January and March [8].
Sleep patterns have also changed, characterised by longer duration, later rising, more dreams and changes in sleep quality. The Withings study [4] found that device-measured sleep duration increased by 8–21 min per day across 8 countries. Adults woke up –1 to +32 minutes later, and experienced far fewer heart rate anomalies—suggestive of sounder sleep. The overweight children from Verona also slept an extra 30 minutes each day [7]. In a survey of 723 UK adults, 28% reported sleeping about the same as before the COVID-19 virus crisis, 49% reported sleeping more and 23% reported sleeping less [9]. Other studies have reported more frequent and more disquieting dreams [10]. A survey by Sleep Standards of 1015 US adults [11] found that respondents—especially younger adults—generally reported poorer quality sleep. According to retrospective self-report on the Insomnia Severity Index, the incidence of clinical insomnia among Chinese adults rose from 15% in October to December 2019 (pre-COVID) to 20% in February 2020 (during COVID) [12].
Most reports of changes in screen time have focused on children, and report very large increases. For example, in a US Parents Together survey, parents reported a doubling of online time from 3 hours per day to 6 hours per day. While this was partly due to online homeschooling, the main increases were on non-educational platforms such as TikTok and Netflix [13]. Italian children increased screen time even more—by 5 hours per day [7]. In a study of 254 Canadian families, parents reported that 87% children, 74% of mothers and 61% of fathers increased screen time since COVID-19 physical distancing restrictions were implemented [14]. Research in US adults has also shown increases in screen time of 30–40% [15].
There have also been reported changes in diet. In an April 2020 survey of 1005 American adults by the food and beverage communications firm Hunter [16], 54% said they were cooking more now than before the pandemic (vs 11% who reported cooking less), and 38% were ordering less takeout and delivery (vs 30% who reported ordering more). Among Canadian families, many parents reported spending more time cooking (mothers, 70%; fathers, 68%), but also reported eating more food (mothers, 57%; fathers, 46%; children, 42%) and eating more snack foods (mothers, 67%; fathers, 59%; children, 55%) [14]. On average, French adults consumed 235 kcal per day more during the first month of lockdown as compared to the month before lockdown [17]. Similarly, Italian children consumed one extra meal per day, along with more sugar-sweetened beverages and red meat [7]. While one Australian study of 270 alcohol drinkers [18] found no appreciable change in consumption, another nationally representative survey found that while people reported decreasing their alcohol consumption during lockdown, it was actually higher than in matched periods in previous years [19].
With reduced physical activity, higher screen time, and potentially poorer diet, it is unsurprising that some studies have reported increases in weight. A UK survey of 2000 adults found that the average self-reported weight gain from pre- to during lock-down was >2.5 kg [6]. Other studies have shown more modest change. For example, a survey of 339 Chinese adults found that average self-reported weight gain from 5 weeks before to during lockdown was 2.2 kg for females with BMI < 24, 1.7 kg for males with BMI <24, and 0.9 kg for females with BMI ≥ 24; however, males with BMI ≥ 24 showed average weight loss of 0.9 kg [20]. Additionally, among 4379 Spanish citizens surveyed between 1 and 4 weeks into lockdown, most (53%) reported no weight change, while 26% and 22% reported weight gain and weight loss, respectively [21]. Data from Withings automated scales found that adults around the world gained between 0.08 and 0.25 kg over about a month of lockdown [4].
Mental health also appears to have suffered under lockdown. A large Australian study of 15,000 respondents [22] found that reports of depressive symptoms had doubled or trebled, most markedly in younger adults. There were similar patterns for symptoms of anxiety [22]. In the UK, a study of 600 adults also found abnormally high levels of depression and anxiety, which were more pronounced amongst those who were more isolated [23]. Patterns were similar in New Zealand [24], Italy [25], Spain [26], the USA [27] and China [28]. Unsurprisingly, those with pre-existing conditions found that their mental health deteriorated under lockdown. A UK study by the charity Rethink Mental Illness found that 80% of people living with serious mental illnesses such as borderline personality disorder and psychosis thought that their mental health had become worse due to the impact of COVID-19 [29].
The ensemble of these studies reports decreases in physical activity, increases in screen time and sleep, later bedtimes, increases in weight, and poorer mental health. However, most of these reports come from the grey literature, based on retrospective self-report, or else derived from big data analytics with little individualised demographic information. The aim of the present study was to examine changes in 24-h activity patterns (physical activity, sedentary time, sleep), recreational physical activities, diet, weight and wellbeing in a group of adults who were intensively tracked both before and during the social distancing and lockdown periods of the COVID-19 response in Adelaide, Australia.
Methods
Study design
This study used data from the prospective cohort study “Annual Rhythms In Adults’ lifestyle and health” (ARIA). ARIA is an ongoing study that is following participants over a 13-month period, measuring daily activity, dietary intake, weight and wellbeing. The study was approved by the University of South Australia Human Research Ethics committee (Protocol number: 201901) and participants provided informed, written consent prior to commencing participation. The study has been registered on the Australian New Zealand Clinical Trial Registry (Trial ID: ACTRN12619001430123).
Participants and procedure
A community-based sample of 64 healthy adults was recruited from greater metropolitan Adelaide, South Australia between September and November 2019. Parents and guardians of children enrolled in a separate three-year cohort study “Life on Holidays” [30] were invited to participate via email or postal invitation. Inclusion criteria were 18 to 65 years old, residing in greater metropolitan Adelaide, having access to a Bluetooth-enabled mobile device or computer and home internet, proficiency in English, and ambulant. Exclusion criteria were pregnancy, having an implanted electronic medical device, or experiencing or receiving treatment for any life-threatening condition impacting daily lifestyle and health. A baseline face-to-face home visit was conducted between October and November 2019 where participants were provided with a Fitbit Charge 3 activity monitor and Aria 2 body weight scale (Fitbit Inc, San Francisco, CA, USA), had their height measured, and completed a baseline survey about their demographics, health and lifestyle. Participants were asked to wear the activity monitor and weigh themselves daily, and to complete eight online surveys on dietary intake, work status, recreational activities, and wellbeing between December 2019 and December 2020.
This study used data from 61 participants who remained enrolled in April 2020. Survey data were timepoint 3 of the larger study, assessing behaviour and experiences in February 2020 prior to COVID-19 related restrictions in Australia, and timepoint 4, assessing behaviour and experiences in April when the most rigorous COVID-19 related restrictions were in place. Fitbit data were extracted for 14 days before (February 10–23 2020) and 14 days during (April 14–27 2020) the COVID-19 restrictions. In the latter period, restrictions included enforced social distancing, closure of cinemas and food venues, a ban on large gatherings, and widespread working from home and school closures, but did not involve shelter-in-place orders.
Variables
Demographics
At baseline, participants reported their date of birth, sex, country of birth, marital status (never married, widowed, divorced, separated but not divorced, married or de facto), number of children at home, highest education level (below year 10, year 10, year 11, year 12 or equivalent, certificate III/IV, advanced diploma/diploma, bachelor degree, postgraduate or higher degree), combined gross household income (AU$; <$50,000, $50,000-$99,999, $100,000-$199,999, ≥$200,000), occupation (open-ended response classified according to the Australian and New Zealand Standard Classification of Occupations [31]), hours worked per week (none, <15, 15–35, 36+) and smoking status (yes, no). Height was measured at the baseline home visit (Leister Height Measure MKII).
Daily activity composition
Activity composition was measured using Fitbit Charge 3 activity monitors (Fitbit Inc, San Francisco, CA, USA) worn on participants’ non-dominant wrist 24 hours a day, except during water activities and device charging. Fitbit activity monitors are commonly used in biomedical research [32, 33] and have acceptable validity for moderate-to-vigorous physical activity (MVPA) [34], sleep [35] and total daily energy expenditure [36]. Each minute in every 24-h period was classified as sleep, sedentary, light, moderate or vigorous physical activity according to Fitbit’s proprietary algorithms, which also provided bedtime and get up time. Data were synced to participants’ Fitbit account and collected remotely via bespoke software called “Fitnesslink”, developed for the ARIA study. Minutes classified as sedentary (recorded when no other activities are detected) AND with missing heart rate data were classified as non-wear. Valid days were defined as a minimum of 18 hours wear time and overnight wear. Only records that contained at least 1 valid weekday and 1 valid weekend day during each 14-day period were used for analysis. Daily MVPA was calculated as the sum of minutes spent in moderate and vigorous activity. Daily activities (sleep, sedentary, light and MVPA) were calculated as the mean over each 14-day period, weighted 5:2 for weekdays and weekend days. Fifty-five participants were included in the analysis; on average they had 12 valid days in each period (Mdn = 12, IQR = 10–14 both timepoints) and 23 hours of wear time per day (before COVID-19 Mdn = 23.2, IQR = 22.8–23.5; during COVID-19 Mdn = 23.4, IQR = 22.9–23.6).
Recreational physical activity
Recreational physical activity was assessed using items from the How Areas in Brisbane Influence Health and Activity (HABITAT) study [37] which were modified to reflect recreational activity over the previous month. Participants rated how often they did 15 activities (e.g. running or jogging, team sports, water activities) on a 5-point scale (1 = never, 2 = once a month, 3 = once every 2 weeks, 4 = once a week, 5 = more than once a week).
Dietary intake
Dietary intake (energy including fibre, percentage of energy from protein, total fat, saturated fat, carbohydrate, alcohol and fibre) was assessed using the online Dietary Questionnaire for Epidemiological Studies (DQES v3.2; Cancer Council Victoria), which was modified to reflect diet over the previous month. The DQES v3.2 is a self-administered questionnaire that estimates nutritional intake based on 144 foods and beverages across five groups, including: cereal foods; sweets and snacks; dairy products, meats and fish; fruit; vegetables; and alcoholic beverages [38]. The DQES has been demonstrated to have good reproducibility and has good agreement with weighed food records [39].
Body weight
Body weight was measured using Fitbit Aria 2 smart scales (Fitbit Inc, San Francisco, CA, USA) [40, 41]. Participants were advised to weigh themselves daily in the morning, whilst wearing minimal clothing, prior to meals and after voiding. Body weight data was collected remotely via our Fitnesslink software. Weight was calculated as the mean of all measures taken over each 14-day period.
Wellbeing
Quality of life was assessed using the World Health Organization Quality of Life assessment 26-item version (WHOQOL-BREF) [42]. WHOQOL-BREF is a self-report questionnaire which measures four broad domains: physical health, psychological health, social relationships and environment. The WHOQOL-BREF has good discriminant validity, content validity and test-retest reliability and internal consistency [42, 43]. Internal consistency in the current sample pre-COVID was high (physical health r = .84; psychological health r = .82; social relationships r = .72; environment r = .76). Symptoms of depression, anxiety and stress were assessed using the 21-item short-form Depression Anxiety Stress Scale (DASS-21) [44]. The DASS-21 has good convergent and discriminant validity, adequate construct validity, and high reliability [44–46]. Internal consistency in the current sample pre-COVID was excellent (depression r = .94; anxiety r = .80; stress r = .92).
Statistical analysis
Analyses used random intercept mixed effects models with family and individual IDs as the random effects to account for the structure of the data (repeated measures nested within individuals, nested within 45 families). Change over time in daily activity composition (expressed as isometric logratios) was examined using a multivariate linear mixed effects model, following recommendations by Baldwin et al [47] using the packages compositions [48] and lme4 [49] in R version 3.5.0 (R Foundation for Statistical Computing, Vienna, Austria). Changes over time in sleep timing, recreational physical activities, dietary intake, weight and wellbeing were analysed using linear mixed effects models using Stata 16 (StataCorp, College Station, TX, USA).
Results
Participants were predominantly female, overweight, born in Australia, married and well-educated (Table 1). The sample was broadly representative of middle-aged Australian adults in terms of BMI (66% overweight or obese vs 66% of 35- to 44-year-old Australian adults [50]), smoking status (16% smokers vs 15% of Australian adults aged 18 and over [50]), whether they were born in Australia (72% vs 67% of 30- to 49-year-old Australian adults [51]), and marital status (79% married or defacto vs 74% of 34- to 44-year-old Australian adults [51]). However, the sample was overrepresented by women, parents (100% were parents whereas 77% of Australian women aged 30 to 49 years report having children [51]), and employed persons (84% reported working vs 75% of 35- to 45-year-old Australian adults [51]). The sample was also slightly more highly educated; although the sample had similar rates of non-school education (79% with a non-school qualification vs approximately 75% of 30- to 50-year-old Australian adults [52]), rates of University education were slightly higher (54% with a university degree vs approximately 40% of 30- to 50-year-old Australian adults [52]).
Table 1. Sociodemographic characteristics of the participants at baseline (n = 61).
Variable | N | (%) | Mean | (SD) |
---|---|---|---|---|
Age (years) | 41.3 | (5.8) | ||
Female | 40 | (65.6) | ||
Male | 21 | (34.4) | ||
Weight (kg) | 80.8 | (18.6) | ||
Height (cm) | 169.6 | (9.3) | ||
BMI | ||||
Underweight | 1 | (1.6) | ||
Normal | 20 | (32.8) | ||
Overweight | 21 | (34.4) | ||
Obese | 19 | (31.1) | ||
Current Smoker | 10 | (16.4) | ||
Born in Australia | 44 | (72.1) | ||
Marital Status | ||||
Never married | 7 | (11.5) | ||
Married/defacto | 48 | (78.7) | ||
Separated, divorced or widowed | 6 | (9.8) | ||
Number of children at home | ||||
One | 4 | (6.6) | ||
Two | 29 | (47.5) | ||
Three | 21 | (34.4) | ||
Four or more | 7 | (11.5) | ||
Education | ||||
Year 10 or less | 4 | (6.6) | ||
Year 11–12 | 9 | (14.8) | ||
Certificate/diploma | 15 | (24.6) | ||
University degree | 33 | (54.1) | ||
Household income (AU$) | ||||
<$50,000 | 9 | (14.8) | ||
$50,000 - $99,999 | 21 | (34.4) | ||
$100,000-$199,999 | 22 | (36.1) | ||
≥$200,000 | 9 | (14.8) | ||
Occupation | ||||
Managerial and professional | 19 | (31.1) | ||
Technical and clerical | 13 | (21.3) | ||
Community, personal service and sales | 15 | (24.6) | ||
Machinery operators, drivers, and labourers | 3 | (4.9) | ||
No job/other | 11 | (18.0) | ||
Hours worked per week | ||||
None | 10 | (16.4) | ||
<15 | 3 | (4.9) | ||
15–35 | 25 | (41.0) | ||
36+ | 23 | (37.7) |
Table 2 shows changes over time in daily activity composition, sleep timing, recreational physical activity, dietary intake, weight and wellbeing. There was a significant change in daily activity composition (χ2(3) = 8.931, p = 0.030). On average participants slept longer, got up later, and did less light physical activity during COVID-19 restrictions than before COVID-19 restrictions. Additionally, participants engaged in more cycling but less swimming, team sports and boating or sailing. Total energy intake did not change but participants consumed a slightly lower percentage of energy from protein and a greater percentage of energy from alcohol during COVID-19 restrictions. There were no changes in weight or wellbeing.
Table 2. Changes over time in daily activity composition, sleep timing, recreational physical activity, dietary intake, weight and wellbeing during COVID-19 restrictions (n = 61).
Variable | Before COVID-19 | During COVID-19 | Change | [95% CI] | Sig.a | ||
---|---|---|---|---|---|---|---|
Daily activity composition, min(%)b | 0.03 | ||||||
Sleep | 497 | (35) | 523 | (36) | 27 | [9, 51] | |
Sedentary | 601 | (43) | 623 | (43) | 22 | [-4, 40] | |
Light PA | 318 | (22) | 269 | (19) | -50 | [-69, -29] | |
MVPA | 25 | (2) | 25 | (2) | 1 | [-7, 8] | |
Sleep timing, M(SD) | |||||||
Bedtime | 22:52 | (0:59) | 22:48 | (1:18) | -2 | [-24, 19] | 0.835 |
Get up time | 07:04 | (0:42) | 07:40 | (1:09) | 38 | [25, 50] | <0.001 |
Recreational PA, M(SD)c | |||||||
PA with others in a park | 2.7 | (1.4) | 2.4 | (1.6) | -0.32 | [-0.71, 0.07] | 0.105 |
Running | 2.2 | (1.5) | 1.9 | (1.4) | -0.28 | [-0.58, 0.02] | 0.064 |
Weights | 1.8 | (1.5) | 1.5 | (1.1) | -0.31 | [-0.66, 0.04] | 0.083 |
Cycling | 1.6 | (1.0) | 1.9 | (1.4) | 0.35 | [0.01, 0.69] | 0.047 |
Exercise class | 1.5 | (1.2) | 1.4 | (0.9) | -0.13 | [-0.49, 0.24] | 0.497 |
Golf | 1.0 | (0.3) | 1.0 | (0.1) | -0.03 | [-0.10, 0.03] | 0.324 |
Swimming | 1.6 | (1.0) | 1.1 | (0.3) | -0.64 | [-0.81, -0.27] | <0.001 |
Tennis | 1.1 | (0.5) | 1.2 | (0.6) | 0.04 | [-0.13, 0.21] | 0.621 |
Team sports | 1.6 | (1.1) | 1.2 | (0.7) | -0.36 | [-0.68, -0.05] | 0.025 |
Yoga, pilates, tai chi or qigong | 1.4 | (1.0) | 1.4 | (1.0) | 0.05 | [-0.15, 0.26] | 0.601 |
Home-based exercises | 2.3 | (1.6) | 2.6 | (1.7) | 0.32 | [-0.11, 0.75] | 0.147 |
Boating or sailing | 1.1 | (0.5) | 1.0 | (0.1) | -0.13 | [-0.24, -0.03] | 0.015 |
Water activities | 1.0 | (0.3) | 1.0 | (0.3) | -0.03 | [-0.12, 0.06] | 0.479 |
PA with others on a beach | 1.5 | (0.8) | 1.4 | (0.9) | -0.11 | [-0.39, 0.18] | 0.468 |
Dietary intake, M(SD) | |||||||
Energy including fibre (kj) | 7048 | (2107) | 7091 | (2080) | 59 | [-417, 536] | 0.807 |
Energy from protein (%) | 19.5 | (4.3) | 18.8 | (3.5) | -0.8 | [-1.5, -0.1] | 0.036 |
Energy from total fat (%) | 36.7 | (5.3) | 35.7 | (4.7) | -1.0 | [-2.1, 0.1] | 0.085 |
Energy from saturated fat (%) | 12.7 | (2.8) | 12.7 | (2.7) | 0.1 | [-0.4, 0.6] | 0.729 |
Energy from carbohydrate (%) | 41.0 | (6.4) | 42.0 | (5.6) | 0.9 | [-0.6, 2.5] | 0.217 |
Energy from alcohol (%) | 2.8 | (5.6) | 3.7 | (5.9) | 0.9 | [0.2, 1.7] | 0.018 |
Energy from fibre (%) | 2.5 | (0.8) | 2.5 | (0.7) | -0.1 | [-0.2, 0.1] | 0.248 |
Weight (kg), M(SD) | 80.8 | (18.6) | 80.7 | (18.6) | -0.0 | [-0.4, 0.3] | 0.906 |
Wellbeing, M(SD) | |||||||
WHOQOL physical health | 16.2 | (2.1) | 15.9 | (2.1) | -0.29 | [-0.77, 0.18] | 0.230 |
WHOQOL psychological | 14.8 | (2.3) | 14.6 | (2.5) | -0.17 | [-0.61, 0.27] | 0.453 |
WHOQOL social relationships | 15.2 | (2.9) | 15.1 | (2.9) | 0.03 | [-0.43, 0.48] | 0.910 |
WHOQOL environment | 15.8 | (1.7) | 15.6 | (2.1) | -0.15 | [-0.52, 0.22] | 0.425 |
DASS depression | 6.1 | (7.7) | 6.2 | (8.0) | 0.00 | [-1.23, 1.23] | 1.000 |
DASS anxiety | 4.2 | (5.7) | 3.9 | (5.8) | -0.26 | [-1.19, 0.67] | 0.584 |
DASS stress | 9.3 | (8.2) | 10.0 | (8.5) | 0.53 | [-1.02, 2.09] | 0.510 |
aBased on linear mixed effects models adjusting for clustering of individual within family. The p value for the activity composition relates to the multiple correlation coefficient (Wald Chi-squared) for set of isometric log ratios (i.e., the change in overall composition).
bTime-use composition is presented as geometric means, adjusted to a sum of 1440 minutes and 100%. Bootstrapped 95% confidence intervals are presented for predicted change in time-use components.
cRecreational PA calculated based on 5-point ordinal scale where 1 = never, 2 = once a month, 3 = once every 2 weeks, 4 = once a week, 5 = more than once a week.
Note: Significant results are shown in boldface. PA = physical activity MVPA = moderate-to-vigorous physical activity, DASS = 21-item short form Depression, anxiety, stress scale; WHOQOL = World Health Organization Quality of Life assessment 26-item version.
Discussion
The aim of the study was to comprehensively examine changes in daily activity patterns, diet, weight and wellbeing in a natural setting during an early period of COVID-19 restrictions in Adelaide, Australia. Small changes were identified in some aspects of diet (increased alcohol consumption and reduced energy from protein), and daily activity patterns (increased sleep duration, later get up time, and reduced light physical activity). Whilst participants reported some changes in recreational activities (namely, an increase in cycling, and a reduction in swimming, sport and boating), there were no overall changes in device-measured MVPA, body weight or measures of psychological wellbeing.
Before considering the implications of these findings, the strengths and limitations of our study must be acknowledged. Firstly, to our knowledge, this is the first study to examine numerous aspects of lifestyle (physical activity, sedentary time, sleep and diet), weight and wellbeing, in concert, during the COVID-19 pandemic. Fortuitously, we were already collecting high fidelity lifestyle and wellbeing data in a cohort study which commenced in late 2019, prior to the COVID-19 pandemic. Our data were collected prospectively with repeated within-person assessments, and used high-quality measurement methods, including device-measured weight and 24-h movement activities, meaning that we have excellent comparison data from before the COVID-19 pandemic. This is an important advantage over much of the research on lifestyle changes across the COVID-19 period, which has tended to rely on retrospective comparisons of lifestyle and psychological factors and is therefore highly susceptible to selection and recall bias.
The key limitation to our study is the relatively small sample size. Given this, we focused our interpretation on overall patterns, bearing in mind clinical significance. We also acknowledge that the small sample increases the likelihood that our participants may not be representative of the population of adults in Adelaide. A further limitation is that participants were middle-aged adults from one Australian city, who were predominantly female, though otherwise broadly similar to the general middle-aged Australian population in terms of demographic characteristics and weight status. One exception was that the participants were all parents of school age children, when about one quarter of Australian adults this age do not have children at home. It is unclear how our results might apply to adults without children. It is also unclear to what extent our results may be generalised to the other geographical areas, given differences in contextual factors within states of Australia and internationally (such as local COVID-19 social distancing restrictions, economic impacts and infection rates). For context, our COVID-19 data were collected approximately 1 month after the introduction of strict COVID-19 social distancing restrictions. At the time of data collection, restaurants, cafes, cinemas and playgrounds were closed, public and in-home gatherings were banned, some schools were closed (and where they were open, many families chose to keep their children home), and people were encouraged to work from home wherever possible. Whilst shops were allowed to remain open, many opted to close. The Australian government had announced financial assistance for people experiencing financial hardship related to COVID-19. Research with a larger and more diverse sample of adults in Adelaide is needed to confirm our findings, while broader research is needed to understand how conditions during lockdown affected adults in various Australian contexts.
In terms of people’s daily lifestyle activities, the largest changes were in participants’ sleep and sedentary patterns; around 30 minutes extra sleep and 20 minutes extra sedentary time each day, offset by a 50-minute reduction in daily light physical activity. The later get up time suggests that those who began working from home or had children learning from home during school closures may have replaced commuting time with sleep. Amongst adults, both long and short sleep durations are associated with detriments in health [53]. In our study, mean sleep duration both pre- and during COVID-19 was within healthy sleep guidelines (7–9 hours) [54] suggesting the changes we observed may not have either positive or negative health impacts. The reduction in light activity may reflect reduced active transport or a lack of incidental activity at work when people started working from home. On the other hand, the increase in cycling could be explained by attempts to avoid public transport among those who continued to travel to work. These changes in daily activities from pre- to during COVID-19 lockdown appear to mirror the differences in daily activities typically seen on weekday and weekend days; the latter are characterised by longer sleep durations, later wake-up times, and more sedentary time [55]. The changes we observed across the COVID-19 transition also resemble the differences between pre- and post-retirement, which in an Australian sample were characterised by 30 min longer sleep duration, and correspondingly later get up times, with no change in physical activity [56]. Although we saw few changes in participants’ recreational physical activities, we note that there was a floor effect for many activities. At both timepoints, over 80% of participants reported never doing exercise classes or yoga, and over 90% reported never doing golf, tennis, lawn bowls, boating or water activities. Therefore, little change would be expected in these activities.
Generally speaking, there were few changes in dietary intake. Overall energy intake did not change significantly, either statistically, or meaningfully based on absolute values (which suggested that energy intake was approximately 1% higher during lockdown than before). This contrasts with previous studies suggesting increased food intake in Canadian families [14] and increased energy intake in French adults during COVID-19 [17]. During lockdown, alcohol consumption increased. This is consistent with findings reported in another recent study [19]. However, even allowing for under-reporting, the increase amounted to less than half a glass of wine. With the increase in the percentage of energy from alcohol, there was a decrease in energy from protein, and there was a trend for percentage energy from fat to decrease (p = 0.07), though all these changes were fairly small.
Sleep aside, the changes in lifestyle patterns that we detected were generally in a direction associated with negative health impacts. It is possible that this suite of lifestyle changes, though small in magnitude, may have harmful impacts if sustained over a long period. This is particularly important when considered in the broader context of COVID-19. We are writing this study at a time that Australia, and many other countries around the world, is reinstating restrictions due to a second rise in infections. COVID-19 restrictions, in one form or another, are likely to remain for many months, and the impact of them on people’s health and wellbeing is likely to accumulate over time.
Somewhat surprisingly, there was no change in any of the measures of psychological wellbeing, either based on statistical results, or based on effect sizes. Effect sizes for change in WHOQOL-BREF scores from pre- to during lockdown ranged from Cohen’s d = -0.14 to 0.01. A previous study examining the WHOQOL-BREF’s responsiveness to change in 14 different patient populations reported that intervention effect sizes >0.2 were considered “small”, >0.5 “moderate” and >0.80 “large” [57], suggesting that the magnitude of changes seen in the current study were negligible. Similarly, effect sizes for change in the DASS-21 subscales ranged between d = -0.05 and 0.06, again suggesting negligible change. Ronk et al. (2013) [58] suggested that a change of approximately 4 points is considered meaningful change, whereas in our sample, the average change was less than a point. Average scores for depression, anxiety and stress were within the normal ranges at both pre- and during lockdown.
Our findings contrast with scientific discourse, with peer-reviewed commentaries predicting dire mental health sequelae [59, 60], such as a looming mental health “pandemic” [60], and with empirical studies showing high levels of distress during COVID-19 [25, 26, 28]. It also contrasts with empirical studies which have examined mental health in volunteer samples during COVID-19 and compared them with population norms [22–24, 27]. It is possible that selection bias may explain the difference in findings between those studies and ours–i.e. while people with heightened mental health symptoms volunteer for surveys on COVID-19 and mental health, our participants tended to have relatively good mental health (e.g., the majority of scores on the DASS-21 were in the normal range [44]). Our findings also differ markedly from two US studies that found that symptoms of depression and mental distress were significantly higher in nationally representative samples measured in April 2020 during the pandemic than those measured in 2018 [61, 62]. They also contrast with findings from a longitudinal probability sample of UK adults which showed a significant increase in mental distress between 2018–19 and April 2020 (1 month into UK lock-down) [63]. Our findings are perhaps even more surprising when considering that our sample was parents of primary-school aged children, who may have been contending with having children at home rather than at school. However, relative to many other countries, Australia had lower infection and mortality rates at the time of this study. Mental health would likely be more affected when the risk of catching the virus and becoming ill is greater, and when faced with critically ill family and friends. Additionally, lock-down was less strict in Adelaide as compared to the UK and many US states where non-essential stores were closed, and stay-at-home orders meant that people were likely to be more isolated from family, friends and colleagues. Furthermore, our study assessed only a short period of time. The effects of lock-down on well-being may become greater as lock-down extends. We also acknowledge that our sample was slightly more highly educated than population norms and may have experienced greater income security than other populations during this time. Participants were also middle-aged adults; a demographic that has reported enjoying the slower pace of life under COVID-19 restrictions [64].
In conclusion, this study comprehensively examined prospective changes in a small sample of middle-aged adults’ lifestyle behaviours and wellbeing across the early COVID-19 lockdown in Adelaide. It identified small dietary changes (increased alcohol consumption and reduced energy from protein), and modest changes in daily activity patterns (increased sleep duration and reduced light physical activity). No changes in MVPA, weight or psychological wellbeing were observed. Overall, results were more positive than might have been expected, however further rigorous research examining the health and lifestyle impacts of social distancing restrictions, particularly if they are ongoing, will be needed as the COVID-19 pandemic unfolds.
Data Availability
Data cannot be shared publicly because participants did not provide informed consent for their data to be shared publicly. Data is available on request to the University of South Australia Human Ethics Officer humanethics@unisa.edu.au for researchers who meet the criteria for access to confidential data.
Funding Statement
This research was supported by the Australian National Health and Medical Research Council (APP1163338). CM is supported by a Career Development Fellowship from the National Health and Medical Research Council (APP1125913). DD is supported by a National Health and Medical Research Council (APP1162166) and Heart Foundation (APP102084) Early Career Fellowship. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
References
- 1.Prickett KC, Fletcher M, Chapple S, Doan N, Smith C. Life in lock-down: the economic and social effect of lock-down during Alert Level 4 in New Zealand. Working Paper. 2020. Wellington, New Zealand: Victoria University of Wellington. [cited October 23 2020]. Available from: https://www.wgtn.ac.nz/__data/assets/pdf_file/0010/1865512/WP-20-03-covid-19-life-in-lockdown.pdf
- 2.Tison G, Avram R, Kuhar P, Abreau S, Marcus G, Pletcher M, et al. Worldwide effect of COVID-19 on physical activity: a descriptive study. Ann Intern Med. 2020. 10.7326/M20-2665 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Fitbit staff. The impact of coronavirus on global activity. Fitbit. 2020. [cited October 23, 2020]. Available from: https://blog.fitbit.com/covid-19-global-activity/
- 4.Felber S. Data: Quarantine isn’t making us gain weight or slow down. Withings. 2020. [cited October 23, 2020]. Available from: https://blog.withings.com/2020/05/01/data-quarantine-isnt-making-us-gain-weight-or-slow-down/
- 5.Gemba. Physical activity during COVID-19 lock-down. Insights into Australians’ physical activity and fitness during the covid-19 shut-down. 2020. Gemba Insights. [cited October 23 2020]. Available from: http://thegembagroup.com/wp-content/uploads/2020/04/GEMBA_COVID-19_Insights_Sports-and-Physical-Activity-Participation__290420.pdf
- 6.Yorkshire Cancer Research. Physical activity among adults has fallen by a quarter since the lock-down–national. 2020 [cited October 23 2020]. Available from: https://yorkshirecancerresearch.org.uk/news/physical-activity-among-adults-has-fallen-by-a-quarter-since-the-lockdown-national
- 7.Pietrobelli A, Pecoraro L, Ferruzzi A, Heo M, Faith M, Zoller T, et al. Effects of COVID‐19 lock-down on lifestyle behaviors in children with obesity living in Verona, Italy: a longitudinal study. Obesity. 2020;28: 1382–1385. 10.1002/oby.22861 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Xiang M, Zhang Z, Kuwahara K. Impact of COVID-19 pandemic on children and adolescents’ lifestyle behavior larger than expected. Prog Cardiovas Dis. 2020;63: 531–532. 10.1016/j.pcad.2020.04.013 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Robinson E, Gillespie S, Jones A. Weight-related lifestyle behaviours and the COVID-19 crisis: an online survey study of UK adults during social lockdown. Obes Sci Pract. 2020;6(6): 735–740. 10.1002/osp4.442 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Hooper R. How the coronavirus crisis is affecting your dreams. New Sci. 2020;246(3281): 11. 10.1016/S0262-4079(20)30878-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Sleep Standards. Sleep habits post lockdown in the U.S. (2020). 2020. [cited November 27, 2020]. Available from: https://sleepstandards.com/sleep-habits-post-quarantine/#Demographics
- 12.Lin L-y, Wang J, Ou-yang X-y, Miao Q, Chen R, Liang F-x, et al. The immediate impact of the 2019 novel coronavirus (COVID-19) outbreak on subjective sleep status. Sleep Med. 2020;Advance online access. 10.1016/j.sleep.2020.05.018 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Parents Together Foundation. Survey shows parents alarmed as kids’ screen time skyrockets during COVID-19 crisis. New York, NY: Parents Together Foundation. 2020. [cited July 12, 2020]. Available from: https://parents-together.org/survey-shows-parents-alarmed-as-kids-388 screen-time-skyrockets-during-covid-19-crisis/ [Google Scholar]
- 14.Carroll N, Sadowski A, Laila A, Hruska V, Nixon M, Ma DWL, et al. The impact of COVID-19 on health behavior, stress, financial and food security among middle to high income Canadian families with young children. Nutrients. 2020;12(8): 2352. 10.3390/nu12082352 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Meyer J, McDowell C, Lansing J, Brower C, Smith L, Tully MA, et al. Changes in physical activity and sedentary behavior in response to COVID-19 and their associations with mental health in 3,052 US adults. Int J Environ Res Public Health. 2020;17: 6469. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.HUNTER. America Gets Cooking: The Impact of COVID-19 on Americans’ food habits. LinkedIn Corporation. 2020 [cited July 12, 2020]. Available from: https://www.slideshare.net/HUNTERNY/hunter-food-study-special-report-america-gets-cooking-231713331
- 17.Marty L, de Lauzon-Guillain B, Labesse M, Nicklaus S. Food choice motives and the nutritional quality of diet during the COVID-19 lockdown in France. Appetite. 2020;157: 105005. 10.1016/j.appet.2020.105005 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Lockshin L, Corsi A, Bruwer J. How wine and alcohol purchasing and consumption changed during COVID-19 isolation in Australia. Australian and New Zealand Grapegrower and Winemaker. 2020;680: 112–114. [Google Scholar]
- 19.Biddle N, Edwards B, Gray M, Sollis K. Alcohol consumption during the COVID19 period: May 2020. ANU Centre for Social Research and Methods. 2020. [cited July 12, 2020]. Available from: https://csrm.cass.anu.edu.au/sites/default/files/docs/2020/6/Alcohol_consumption_during_the_COVID-19_period.pdf [Google Scholar]
- 20.He M, Xian Y, Lv X, He J, Ren Y. Changes in body weight, physical activity, and lifestyle during the semi-lockdown period after the outbreak of COVID-19 in China: an online survey. Disaster Med Public Health Preparedness. 2020;Advance online access. 10.1017/dmp.2020.237 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Fernandez-Rio J, Cecchini JA, Mendez-Gimenez A, Carriedo A. Weight changes during the COVID-19 home confinement. Effects on psychosocial variables. Obes Res Clin Pract. 2020;14: 383–385. 10.1016/j.orcp.2020.07.006 [DOI] [PubMed] [Google Scholar]
- 22.Fisher JRW, Tran TD, Hammarberg K, Sastry J, Nguyen H, Rowe H, et al. Mental health of people in Australia in the first month of COVID-19 restrictions: A national survey. Med J Aust. 2020;213(10): 458–464. 10.5694/mja2.50831 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.White RG, Van Der Boor C. Impact of the COVID-19 pandemic and initial period of lock-down on the mental health and well-being of adults in the UK. BJ Psych Open. 2020;6(5): e90. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Sibley CG, Greaves LM, Satherley N, Wilson MS, Overall NC, Lee CHJ, et al. Effects of the COVID-19 pandemic and nationwide lock-down on trust, attitudes toward government, and well-being. Am Psychol. 2020;75(5): 618–630. 10.1037/amp0000662 [DOI] [PubMed] [Google Scholar]
- 25.Rossi R, Socci V, Talevi D, Mensi S, Niolu C, Pacitti F, et al. COVID-19 pandemic and lockdown measures impact on mental health among the general population in Italy. Front Psychiatry. 2020;11: 790. 10.3389/fpsyt.2020.00790 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Rodríguez-Rey R, Garrido-Hernansaiz H, Collado S. Psychological impact and associated factors during the initial stage of the Coronavirus (COVID-19) pandemic among the general population in Spain. Front Psychol. 2020; Advance online access. 10.3389/fpsyg.2020.01540 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Czeisler MÉ, Lane RI, Petrosky E, Wiley JF, Christensen A, Njai R, et al. (2020). Mental health, substance use, and suicidal ideation during the COVID-19 pandemic—United States. MMWR Morb Mortal Wkly Rep. 2020;69(32): 1049–1057. 10.15585/mmwr.mm6932a1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Wang C, Pan R, Wan X, Tan Y, Xu L, Ho CS, et al. Immediate psychological responses and associated factors during the initial stage of the 2019 Coronavirus Disease (COVID-19) epidemic among the general population in China. Int J Environ Res Public Health. 2020;17(5): 1729. 10.3390/ijerph17051729 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Hamm D. Mental health suffers under the lock-down. The Guardian. 2020. [cited October 23, 2020]. Available from: https://www.theguardian.com/world/2020/apr/30/mental-health-suffers-under-the-lockdown
- 30.Watson A, Maher C, Tomkinson GR, Golley R, Fraysse F, Dumuid D, 412 et al. Life on holidays: study protocol for a 3-year longitudinal study tracking changes in children’s fitness and fatness during the in school versus summer holiday period. BMC Public Health. 2019;19(1): 1353. 10.1186/s12889-019-7671-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Australian Bureau of Statistics. 1220.0 –ANZSCO–Australian and New Zealand Standard Classification of Occupations, Version 1.3. Canberra; Commonwealth of Australia, 2019. [cited July 12, 2020] Available from: https://www.abs.gov.au/AUSSTATS/abs@.nsf/DetailsPage/1220.02013,%20Version%201.3?OpenDocument
- 32.Wright SP, Collier SR, Brown TS, Sandberg K. An analysis of how consumer physical activity monitors are used in biomedical research. The FASEB Journal. 2017;31(1_supplement): 1020. [Google Scholar]
- 33.Henriksen A, Haugen Mikalsen M, Woldaregay AZ, Muzny M, Hartvigsen G, Hopstock LA, et al. Using fitness trackers and smartwatches to measure physical activity in research: analysis of consumer wrist-worn wearables. J Med Internet Res. 2018;20(3): e110. 10.2196/jmir.9157 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Reid RER, Insogna JA, Carver TE, Comptour AM, Bewski NA, Sciortino C, et al. Validity and reliability of Fitbit activity monitors compared to ActiGraph GT3X+ with female adults in a free-living-environment. J Sci Med Sport. 2017;20(6): 578–82. 10.1016/j.jsams.2016.10.015 [DOI] [PubMed] [Google Scholar]
- 35.de Zambotti M, Goldstone A, Claudatos S, Colrain IM, Baker FC. A validation study of Fitbit Charge 2™ compared with polysomnography in adults. Chronobiol Int. 2018;35(4): 465–76. 10.1080/07420528.2017.1413578 [DOI] [PubMed] [Google Scholar]
- 36.Murakami H, Kawakami R, Nakae S, Nakata Y, Ishikawa-Takata K, Tanaka S, et al. Accuracy of wearable devices for estimating total energy expenditure: Comparison with metabolic chamber and doubly labeled water method. JAMA Intern Med. 2016;176(5): 702–3. 10.1001/jamainternmed.2016.0152 [DOI] [PubMed] [Google Scholar]
- 37.Burton NW, Haynes M, Wilson L-AM, Giles-Corti B, Oldenburg BF, Brown WJ, et al. HABITAT: a longitudinal multilevel study of physical activity change in mid-aged adults. BMC Public Health. 2009;9: 429 76. 10.1186/1471-2458-9-429 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Milne RL, Fletcher AS, MacInnis RJ, Hodge AM, Hopkins AH, Bassett JK, et al. Cohort profile: The Melbourne Collaborative Cohort Study (Health 2020). Int J Epidemiol. 2017;46(6): 1757–i. 10.1093/ije/dyx085 [DOI] [PubMed] [Google Scholar]
- 39.Hebden L, Kostan E, O’Leary F, Hodge A, Allman-Farinelli M. Validity and reproducibility of a food frequency questionnaire as a measure of recent dietary intake in young adults. PLoS One. 2013;8(9): e75156–e. 10.1371/journal.pone.0075156 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Shaffer JA, Diaz K, Alcántara C, Edmondson D, Krupka DJ, Chaplin WF, et al. An inexpensive device for monitoring patients’ weights via automated hovering. Int J Cardiol. 2014;172(2): e263–e4. 10.1016/j.ijcard.2013.12.123 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Yorkin M, Spaccarotella K, Martin-437 Biggers J, Quick V, Byrd-Bredbenner C. Accuracy and consistency of weights provided by home bathroom scales. BMC Public Health. 2013;13(1): 1194. 10.1186/1471-2458-13-1194 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Skevington SM, Lotfy M, O’Connell KA. The World Health Organization’s WHOQOL-BREF quality of life assessment: psychometric properties and results of the international field trial. A Report from the WHOQOL Group. Qual Life Res. 2004;13(2): 299–310. 10.1023/B:QURE.0000018486.91360.00 [DOI] [PubMed] [Google Scholar]
- 43.Krägeloh CU, Kersten P, Rex Billington D, Hsu PH-C, Shepherd D, Landon J, et al. Validation of the WHOQOL-BREF quality of life questionnaire for general use in New Zealand: confirmatory factor analysis and Rasch analysis. Qual Life Res. 2013;22(6): 1451–7. 10.1007/s11136-012-0265-9 [DOI] [PubMed] [Google Scholar]
- 44.Lovibond PF, Lovibond SH. Manual for the Depression Anxiety Stress Scales. 2nd ed. Sydney: Psychology Foundation; 1995. [Google Scholar]
- 45.Henry JD, Crawford JR. The short-form version of the Depression Anxiety Stress Scales (DASS-21): construct validity and normative data in a large non-clinical sample. Br J Clin Psychol. 2005;44(2): 227–39. [DOI] [PubMed] [Google Scholar]
- 46.Lovibond PF, Lovibond SH. The structure of negative emotional states: Comparison of the Depression Anxiety Stress Scales (DASS) with the Beck Depression and Anxiety Inventories. Behav Res Ther. 1995;33(3): 335–43. 10.1016/0005-7967(94)00075-u [DOI] [PubMed] [Google Scholar]
- 47.Baldwin S, Imel Z, Braithwaite S, Atkins D. Analyzing multiple outcomes in clinical research using multivariate multilevel models. J Consult Clin Psychol. 2014;82: 920–30. 10.1037/a0035628 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.van den Boogaart KG, Tolosana-Delgado RJ. “Compositions”: a unified R package to analyze compositional data. Comput Geosci. 2008;34(4): 320–38. [Google Scholar]
- 49.Bates D, Mächler M, Bolker B, Walker S. Fitting linear mixed-effects models using lme4. J Stat Softw. 2015;67: 1–48. [Google Scholar]
- 50.Australian Institute of Health and Welfare. Australia’s health 2018. Canberra: AIHW, 2018. [Google Scholar]
- 51.Australian Bureau of Statistics. Census of Population and Housing: General Community Profile, Australia, 2016. Cat. No. 2001.0. Canberra: Commonwealth of Australia, 2017.
- 52.Australian Bureau of Statistics. Education and Work, Australia, May 2019. Canberra: Commonwealth of Australia, 2019. Available from: https://www.abs.gov.au/statistics/people/education/education-and-work-australia/may-2019
- 53.Gallicchio L, Kalesan B. Sleep duration and mortality: a systematic review and meta‐analysis. J Sleep Res. 2009;18(2): 148–58. 10.1111/j.1365-2869.2008.00732.x [DOI] [PubMed] [Google Scholar]
- 54.Ferrara M, De Gennaro L. How much sleep do we need? Sleep Med Rev. 2001;5(2): 155–79. 10.1053/smrv.2000.0138 [DOI] [PubMed] [Google Scholar]
- 55.Monk TH, Buysse DJ, Rose LR, Hall JaA, Kupfer DJ. The sleep of healthy people—a diary study. Chronobiol Int. 2000;17(1): 49–60. 10.1081/cbi-100101031 [DOI] [PubMed] [Google Scholar]
- 56.Olds T, Burton N, Sprod J, Maher C, Ferrar K, Brown W, et al. One day you’ll wake up and won’t have to go to work: the impact of changes in time use on mental health following retirement. PLoS One. 2018;13(6): e0199605. 10.1371/journal.pone.0199605 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Skevington SM, McCrate FM. Expecting a good quality of life in health: assessing people with diverse diseases and conditions using the WHOQOL‐BREF. Health Expect. 2012;15: 49–62. 10.1111/j.1369-7625.2010.00650.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Ronk FR, Korman JR, Hooke GR, Page A C. Assessing clinical significance of treatment outcomes using the DASS-21. Psychol Assessment. 2013;25: 1103–1110. 10.1037/a0033100 [DOI] [PubMed] [Google Scholar]
- 59.Venkatesh A, Edirappuli S. Social distancing in COVID-19: what are the mental health implications? BMJ. 2020;369: m1379. 10.1136/bmj.m1379 [DOI] [PubMed] [Google Scholar]
- 60.Galea S, Merchant RM, Lurie N. The mental health consequences of COVID-19 and physical distancing: The need for prevention and early intervention. JAMA Intern Med. 2020;180(6): 817–8. 10.1001/jamainternmed.2020.1562 [DOI] [PubMed] [Google Scholar]
- 61.Ettman CK, Abdalla SM, Cohen GH, Sampson L, Vivier PM, Galea S. Prevalence of depression symptoms in US adults before and during the COVID-19 pandemic. JAMA Network Open. 2020;3(9): e2019686. 10.1001/jamanetworkopen.2020.19686 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Twenge JM, Joiner TE. Mental distress among U.S. adults during the COVID‐19 pandemic. J Clin Psychol. 2020;76: 2170–2182 10.1002/jclp.23064 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Pierce M, Hope H, Ford T, Hatch S, Hotopf M, John A, et al. Mental health before and during the COVID-19 pandemic: a longitudinal probability sample survey of the UK population. Lancet Psychiatry. 2020;7(10): 883–892. 10.1016/S2215-0366(20)30308-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.McCrindle M, Renton S. Recovering from COVID-19. Exploring how Australians have been impacted by and responded to COVID-19. Norwest NSW, Australia: 2020.
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Data cannot be shared publicly because participants did not provide informed consent for their data to be shared publicly. Data is available on request to the University of South Australia Human Ethics Officer humanethics@unisa.edu.au for researchers who meet the criteria for access to confidential data.