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Article

Health and Wellbeing of Regional and Rural Australian Healthcare Workers during the COVID-19 Pandemic: Baseline Cross-Sectional Findings from the Loddon Mallee Healthcare Worker COVID-19 Study—A Prospective Cohort Study

1
La Trobe Rural Health School, La Trobe University, Bendigo, VIC 3550, Australia
2
Swan Hill District Health Service, Swan Hill, VIC 3585, Australia
3
Bendigo Health, Bendigo, VIC 3550, Australia
4
School of Psychology and Public Health, La Trobe University, Bendigo, VIC 3550, Australia
5
Kyabram District Health Service, Kyabram, VIC 3620, Australia
6
Department of Mathematics and Statistics, La Trobe University, Melbourne, VIC 3550, Australia
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2024, 21(5), 649; https://doi.org/10.3390/ijerph21050649
Submission received: 4 April 2024 / Revised: 13 May 2024 / Accepted: 15 May 2024 / Published: 20 May 2024
(This article belongs to the Special Issue Public Health: Rural Health Services Research)

Abstract

:
Background: Coronavirus 19 (COVID-19) has created complex pressures and challenges for healthcare systems worldwide; however, little is known about the impacts COVID-19 has had on regional/rural healthcare workers. The Loddon Mallee Healthcare Worker COVID-19 Study (LMHCWCS) cohort was established to explore and describe the immediate and long-term impacts of the COVID-19 pandemic on regional and rural healthcare workers. Methods: Eligible healthcare workers employed within 23 different healthcare organisations located in the Loddon Mallee region of Victoria, Australia, were included. In this cohort study, a total of 1313 participants were recruited from November 2020–May 2021. Symptoms of depression, anxiety, post-traumatic stress, and burnout were measured using the Patient Health Questionnaire-9 (PHQ-9), Generalised Anxiety Disorder-7 (GAD-7), Impact of Events Scale-6 (IES-6), and Copenhagen Burnout Inventory (CBI), respectively. Resilience and optimism were measured using the Brief Resilience Scale and Life Orientation Test—Revised (LOT-R), respectively. Subjective fear of COVID-19 was measured using the Fear of COVID-19 Scale. Results: These cross-sectional baseline findings demonstrate that regional/rural healthcare workers were experiencing moderate/severe depressive symptoms (n = 211, 16.1%), moderate to severe anxiety symptoms (n = 193, 14.7%), and high personal or patient/client burnout with median total scores of 46.4 (IQR = 28.6) and 25.0 (IQR = 29.2), respectively. There was a moderate degree of COVID-19-related fear. However, most participants demonstrated a normal/high degree of resilience (n = 854, 65.0%). Based on self-reporting, 15.4% had a BMI from 18.5 to 24.9 kgm2 and 37.0% have a BMI of 25 kgm2 or over. Overall, 7.3% of participants reported they were current smokers and 20.6% reported alcohol consumption that is considered moderate/high-risk drinking. Only 21.2% of the sample reported consuming four or more serves of vegetables daily and 37.8% reported consuming two or more serves of fruit daily. There were 48.0% the sample who reported having poor sleep quality measured using the Pittsburgh Sleep Quality Index (PSQI). Conclusion: Regional/rural healthcare workers in Victoria, Australia, were experiencing a moderate to high degree of psychological distress during the early stages of the pandemic. However, most participants demonstrated a normal/high degree of resilience. Findings will be used to inform policy options to support healthcare workers in responding to future pandemics.

1. Background

The highly contagious novel coronavirus 19 (COVID-19) has created extraordinary pressure and highly complex challenges for healthcare across the globe [1]. As the outbreak swiftly became a global pandemic, the narrative surrounding COVID-19 continued to evolve—shaping both the healthcare system and now the public’s ‘COVID normal’. However, throughout this evolution the research community has lagged in understanding how the health, wellbeing, and resilience of healthcare workers has been affected in the context of rurality and remoteness during a pandemic.
From the onset of the pandemic, healthcare workers have been placed at the frontline, bearing the brunt of the virus’ demands. Australian healthcare workers faced this pandemic on the back of some of the most devastating sequences of climatic disasters including drought, bushfire, and flooding [2]. Of the Australian communities affected by the consequences of these passing events, those people living in regional, rural, or remote locations are more exposed to the impacts of these events than their metropolitan counterparts.
According to the Australian Institute of Health and Welfare’s report on ‘Rural and Remote Health’ (2020) [3], 28% of Australians live in either rural or remote areas across multiple, diverse populations. These communities, even without the threat of COVID-19, are regularly faced with unique healthcare challenges and poorer health outcomes [3]. Rural and remote healthcare organisations act as the community’s largest employment provider [4], highlighting the major potential for significant impacts on the regional/rural/remote healthcare workforce when a pandemic of this scale erupts. In addition, there are limited published studies in the current literature that examine the immediate and long-term effects of COVID-19 on healthcare workers in these geographical locations. One longitudinal, mixed-methods study of Tasmania nurses by Marsden et al. (2022) described the stressors and manifestations of them in the context of home, work, and the social environment [5]. Although this was only during the first year of pandemic, it does provide a basis for comparison, as Tasmania, according to the Australian Bureau of Statistics, has a population with a similar geographic spread to the Loddon Mallee in terms of rurality.
Most published research evaluating the effects of COVID-19 on healthcare workers is cross-sectional and has focused exclusively on metropolitan populations. Additionally, study samples mainly include specialised physicians and intensive care unit (ICU) nursing staff and exclude other groups such as allied health and non-clinical healthcare workers. This arguably creates a misrepresentation of the healthcare workforce and also omits a diverse group of staff who are essential to delivering an effective health service [6]. However, there are exceptions with some longitudinal studies that include allied health and other support staff who work in the health system in their cohort, Lamb et al. (2022) being one such study [7]. Whilst this study is set in England, which had a very different pandemic experience to Australia, it does provide an indication of the impact of the pandemic across the health system as a whole and has a large sample to support their findings. This study highlights the need for support and clear guidelines to help staff navigate times of distress and suggests that this needs to be a part of planning for the future. McGuiness et al. (2023) is a longitudinal cohort study undertaken in Metropolitan Melbourne, Victoria, that looked more broadly at the health sector, and whilst they had 1667 unique responses, only 496 completed all three surveys [8]. Apart from the metropolitan context, a further confounding factor in using this study as a comparison is the number of lockdowns experienced in Melbourne compared to regional Victoria, with fewer lockdowns experienced in regional Victoria. The LMHCWCS fills an important gap in our current understanding of the effects of the COVID-19 pandemic by being conducted exclusively in a regional/rural setting and including both clinical and non-clinical healthcare workers. It also provides an opportunity for significant longitudinal research on the long-term effects of the pandemic on a uniquely regional and rural healthcare worker sample; research that to date has been scarcely reported in Australia [4]. The LMHCWCS is collecting information from healthcare workers employed within the Loddon Mallee region, Victoria, Australia.
The COVID-19 pandemic has placed more pressure on the Loddon Mallee region healthcare workforce than ever before and rural and regional health services are working through a backlog of treatment and care delayed by the pandemic [9]. It is anticipated that this cohort will provide an understanding of the protective and resilience factors that result in better health and wellbeing outcomes for healthcare workers within these regional and rural communities in the face of the mass disruption associated with the COVID-19 pandemic. In turn, this will help create evidence-based recommendations for policies and practice to better support regional and rural health workers now and when faced with other pandemics into the future [4].

2. Method

2.1. Aims

The aims of the current study are as follows:
To cross-sectionally describe the health and wellbeing of the rural/regional healthcare workforce during the early stages of the COVID-19 pandemic using baseline data from the LMHCWCS cohort.

2.2. Design and Setting

The LMHCWCS is a prospective longitudinal cohort study exploring the immediate and long-term impacts of the COVID-19 pandemic on the health and wellbeing of regional and rural healthcare workers. The findings for this current investigation pertain to cross-sectional data from a baseline survey conducted as part of the broader longitudinal study. Healthcare workers currently employed or volunteering within the Loddon Mallee region of Victoria, Australia, were recruited from 23 health organisations, including 17 regional and rural health services (16 public hospitals and 1 non-public hospital), 5 community health centres, and the Murray Primary Health Network (MPHN). Full details of the study design and methods are available in the study protocol [4].
Data were collected through self-administered online questionnaires at baseline (November 2020–May 2021). Previously validated and reliable instruments were used to measure various health, wellbeing, and resilience outcomes for participants during the COVID-19 pandemic.

2.3. Participant Eligibility

Eligible participants during the baseline recruitment period needed to provide informed consent, be aged 18 or over, have the ability to access and use an electronic device, and be currently employed in any capacity (clinical or non-clinical) or volunteering within a participating Loddon Mallee health service [4]. As it is a condition of employment that healthcare workers must be able to read/speak English and be able to use an electronic device (i.e., computer, mobile phone), all potential participants were eligible and hence no healthcare workers had to be actively excluded on this basis.

2.4. Recruitment

The sampling frame consisted of a workforce of 8107 healthcare workers in public hospitals in the Loddon Mallee region and an unknown number of healthcare workers working within non-public hospitals, community health organisations, and primary healthcare providers in the region. All eligible healthcare workers at each of the public hospitals and an unknown number of healthcare workers within the non-public hospitals, community health organisations, and primary healthcare providers were invited to participate in the study. An online link directed potential participants to a consent form and questionnaire sent via staff email systems.
Baseline recruitment commenced on 30 November 2020 and ceased on 31 May 2021. Within this time, Victorians experienced two state-wide COVID-19 lockdowns [10]. A timeline of pandemic-related events illustrating the events that occurred during the baseline data collection period is summarised in Figure 1 as a means of providing a greater understanding the specific challenges faced by regional and rural healthcare workers during the pandemic. Pre-notification and reminder emails, as well as a random draw incentive, were employed to encourage participation in the study.
Study participants were recruited through three different approaches: (1) online invitations sent through the health organisation’s direct staff emails; (2) a multimodal recruitment media campaign, including Trialfacts online recruitment targeting participating health service employees [11]; and (3) face-to-face recruitment presentations (see Figure 2).
All three recruitment approaches involved the incentive of winning a AUD 1000 grocery voucher for enrolling in the study. Where a member of the study team was present to promote the study to potential participants, for ethical reasons, no recruitment was made directly through this contact. Rather directions were given on how to access and complete the online questionnaire previously sent to them through staff email and other means.

2.5. Study Sample

Email invitations were sent to all employees, (n = 8107) in public hospitals in the Loddon Mallee region. An unknown number of email invitations were also extended to non-public hospitals, community health organisations, and primary healthcare providers in the region through the staff email system and staff newsletters. A total of 2735 potential participants clicked on the baseline questionnaire link: 1174 from public hospitals (14.5% of this population), 286 from non-public organisations, and 1275 from other organisations. The number who completed the consent was 1043 from public hospitals (12.9% of this population); 266 from non-public hospitals, community health organisations, or primary healthcare providers; and 4 who were missing employer information. Of the 1313 consenting participants, 97.1% provided usable complete data.

2.6. Sample Weighting

The sample consists of respondents from public hospitals (79.4%) and non-public hospitals, community health organisations, and primary healthcare providers (20.3%). Given that there were Victorian state government workplace characteristics data on the sampling frame for the public hospital participants, and that these people represent the majority of the sample, the public hospital participant part of the sample was weighted for non-response using these data. Weighting for the non-public hospitals, community health organisations, and primary healthcare provider part of the sample was not performed as no workplace data were available.
Public hospital sample weights were calculated by raking, using four known demographic factors in the public hospital population from the annual Victoria’s Health and Human Services Knowledge Bank, Information Portal, as of July 2020 [12]. The inverse probability weighting of the data was chosen instead of the multiple imputations of missing data as a means of assessing the potential effects of sampling bias and has been shown to be comparable to multiple imputations for assessing the likely impacts of missing data [13]. The four-dimensional raking residuals were calculated using age, sex-at-birth, profession, and hospital size. These variables were available for 80.5% (n = 6528) of the sampling frame. Matching public hospital participant sample weights were calculated with SPSS 28.0.0 [14] and R 4.1.2 [15].

2.7. Follow-Up Assessments

Self-administered online questionaries will be used for the follow-up of the cohort at 6, 12, and 24 months after baseline recruitment. The same/similar questionnaires (including the same psychometric scales) as used in the baseline data collection will be readministered to study participants at each follow-up timepoint. Each participant will receive their follow-up questionnaire at 6, 12, and 24 months from the time they completed their baseline questionnaire. Reminder strategies and continued participant updates through social media and participant newsletters are being used to encourage continued participation at critical time points and to reduce attrition.

2.8. Study Outcome and Outcome Measurement Instruments

To date there is no ‘core outcome set’ for examining the health and wellbeing of healthcare workers [4]. As such, an outcome taxonomy was created by the study team based on the WHO International Classification of Functioning, Disability, and Health (ICF) [16] and Williamson and Clarke taxonomies [17] and constructed according to standards developed by the Core Outcomes Measures in Effectiveness Trials (COMET) initiative [17,18].

2.9. Study Outcomes

The complete list of study outcomes has been described elsewhere [4]. For the current investigation, the primary study outcomes are grouped according to (1) emotional health and wellbeing; and (2) lifestyle and physiological outcomes.

2.9.1. Emotional Health and Wellbeing Outcomes

Emotional health and wellbeing were measured using self-reported validated measures of wellbeing, generalised anxiety, fear of COVID-19, post-traumatic stress symptoms (PTS), depressive symptoms, burnout, psychological stress, resilience, mental fatigue, isolation and loneliness, and optimism.

2.9.2. Lifestyle and Physiological Outcomes

Lifestyle and physiological outcomes include body mass index, alcohol intake, smoking, dietary intake, and sleep quality.

2.10. Outcome Measuring Instruments and Data Analysis

Subjective wellbeing was measured using the single life satisfaction question from the Personal Wellbeing Index—Adult (Cronbach’s alpha (α) = 0.80) [19]. This question asks participants to rate their level of life satisfaction with the following question “How satisfied are you with your life as a whole?” Response options range from 0–10 with zero indicating no satisfaction and 10 indicating complete satisfaction, i.e., higher scores indicate greater wellbeing. Depressive symptoms were measured using the Patient Health Questionnaire—9 (PHQ-9) (α = 0.89) [20], range 0–27, with higher scores indicating greater degree of depressive symptoms; score ≥ 10 indicating moderate-to-severe depressive symptoms. Anxiety symptoms were measured using the Generalised Anxiety Disorder—7 (GAD-7) (α = 0.92) [21], range 0–21, with higher scores indicating greater degree of anxiety symptoms and a score ≥ 10 indicating moderate-to-severe anxiety symptoms. Post-traumatic stress was measured using the Impact of Events Scale—6 (IES-6) (α = 0.80) [22], range 0–24, with higher scores indicating greater degree of post-traumatic stress and a score >9 indicating moderate-to-severe post-traumatic stress (PTS) reactions. Personal (α = 0.87) and patient/client (α = 0.74) burnout was measured using the Copenhagen Burnout Inventory (CBI) [23], range 0–100, with higher scores indicating greater burnout. Resilience was measured using the Brief Resilience Scale (α = 0.80) [24], range 1–5, with higher scores indicating greater psychological resilience; categorised as low (scores 1.00–2.99), normal (scores 3.00–4.30), and high resilience (4.31–5.00), respectively. Optimism was measured using the Life Orientation Test—Revised (LOT-R) (α = 0.78) [25], range 0–24, with higher scores indicating higher optimism; categorised as low (score < 14), moderate (scores 14–18), and high optimism (Score > 18), respectively. Subjective fear of COVID-19 was measured using the Fear of COVID-19 Scale (α = 0.82) [26], range 7–35, with higher scores indicating greater COVID-19-related fear. Fatigue was measured using the vitality question of the Short Form—12 (SF-12) (α = 0.89) [27]. This question asks participants to rate their energy levels in the last 4 weeks using the following question “How much of the time during the past 4 weeks did you have a lot of energy?” Response options were “all of the time”, “most of the time”, “a good bit of the time”, “some of the time”, “a little of the time”, and “none of the time”. Isolation and loneliness were measured using the UCLA loneliness score version 3 (α = 0.72) [28], range 3–9, with higher scores indicating greater isolation and loneliness.
A comparison of emotional health and wellbeing outcomes between four different occupational groups (medicine, nursing, allied health, and non-clinical) was made. Regression models adjusted for potential confounders (i.e., age, gender, modified Monash category, education) were used to examine differences. Age, gender, modified Monash category, and education were included as categorical predictors in each model. For continuous outcomes, linear mixed models (lmer function in R lme4 package) were developed, including random intercepts for healthcare site (20 healthcare sites and 4 individuals have missing healthcare site). Results are expressed as adjusted differences in mean outcomes and 95% confidence intervals between occupational groups, using nursing (largest sample size) as the reference category. A Type III Analysis of Variance with Satterthwaite’s method was used for fixed-effect terms tests, including occupation variables. For binary outcomes, random effects models were developed (glmer function in R) using binomial distribution with logit link to estimate adjusted risk ratios and 95% confidence intervals. Type III Wald chi-square tests were used to obtain fixed-effect terms tests.
Self-reported anthropometric and lifestyle behaviours included body mass index (BMI), dietary consumption, smoking tobacco, alcohol consumption, and sleep quality. Body mass index was calculated from self-reported height and weight and categorised according to World Health Organisation (WHO)-recommended criteria [29]. Dietary intake was measured using the Australian short diet questions [30]; fruit and vegetable consumption was measured using the following questions: “How many serves of vegetables do you usually eat each day? (a ‘serve’ = 1/2 cup cooked vegetables or 1 cup of salad vegetables)” and “How many serves of fruit do you usually eat each day? (a ‘serve’ = 1 medium piece or two small pieces of fruit or 1 cup of diced pieces)”. Response options for each question were “1 serve or less”, “2–3 serves”, “4–5 serves”, “6 serves or more”, and “Do not eat vegetables/fruit”. Tobacco intake was measured using the American Cancer Society smoking questionnaire [31] and categorised as past, current, and never smoked. Alcohol intake was measured using the three-item AUDIT questionnaire [32], range 0–12, with higher scores indicating more risky drinking behaviour; categorised as non-drinker/low-risk (0–4), moderate-risk (5–7), and high-risk (8–12). Sleep quality was measured using the Pittsburgh Sleep Quality Index (PSQI) (α = 0.83) [33], range 0–21, with higher scores indicating poorer sleep quality. Sleep quality was categorised as poor sleep quality and good sleep quality based on the following question for the instrument: “During the past month, how would you rate your sleep quality overall?”

2.11. Participant Sociodemographic Characteristics

The baseline sociodemographic characteristics of study participants are described in Table 1. Characteristics and findings are reported for participants working within public hospitals and those working in non-public hospitals, community health organisations, or primary healthcare providers separately due to the weighting applied to the public healthcare part of the sample, and overall sample sociodemographic and occupational characteristics are reported for the total unweighted sample. Sociodemographic characteristics are also compared between four different occupations (medicine, nursing, allied health, and non-clinical) (Table 2). Overall, 80.5% (n = 1057) of the participants are female, with nursing employing the largest proportion of female workers (88.6%). Participants range in age from 18–79 years, mean age of 44.9 years (SD. 12.8), with medicine employing the largest proportion of workers under 45 years of age (61.0%). Most participants live in a MM 2 location (n = 566, 43.1%) with non-clinical workers having the largest proportion of workers living in an MM 3–7 location (53.1%). Approximately 75.0% (n = 988) live in their own home. Less than 1.0% (n = 8) identify as being of Aboriginal and/or Torres Strait Islander origin. Almost 73.0% (n = 957) reported completing a university degree and 2.4% (n = 32) did not complete secondary school level of education. Non-clinical workers were the smallest proportion of workers without a university/other tertiary education (56.3%). Close to 67.0% (n = 884) of participants were either married or in a de facto relationship, 15.9% (n = 209) reported a gross annual income of less than AUD 52,000 per year, while 21.6% (n = 284) reported that they had concerns about their income. Allied health workers were the largest proportion of workers with concerns about their income (25.1%). Home schooling responsibilities were reported by 27.6% (n = 362) of participants, and 28.6% (n = 376) reported carer responsibilities. These results were similar across occupational groups.

2.12. Occupational and Workplace-Related Characteristics

The occupational and workplace-related characteristics of study participants and between four different occupations (medicine, nursing, allied health, and non-clinical) are described in Table 2 and Table 3. Most participants were nurses (n = 499, 38.0%), followed by non-clinical staff (n = 435, 33.1%), allied health staff (n = 219, 16.7%), and then medical staff (n = 59, 4.5%). Participants were in part-time (n = 649, 49.4%), full-time (n = 436, 33.2%), casual (n = 72, 5.5%), volunteer (n = 32, 2.4%), retired (n = 11, 0.8%), or other (n = 12, 0.9%) employment. Only 11.7% (n = 153) of participants reported taking direct care of COVID-19 patients with those employed in medicine (54.2%) and nursing (43.3%) having the largest proportion of workers in direct contact with COVID-19 patients.
Half the sample (n = 668, 50.9%) reported that their workplace was very or moderately prepared for the COVID-19 pandemic, while 7.6% (n = 100) reported that their workplace was not prepared at all. There was 64.0% (N = 840) of the sample that were very or moderately confident that the training they received would protect them during the pandemic. Allied health workers had the greatest confidence in infection control training with 72.1% (N = 158) of workers reporting that they were very or moderately confident that the training they received would protect them during the pandemic. Most participants (n = 780, 59.4%) reported that they often or very often had access to the right amount of personal protective equipment (PPE) with 7.1% (n = 92) reporting that they rarely or never had access to PPE. Most had confidence in the PPE training they received (n = 945, 72.0%) and were moderately or very confident in the infection control training (n = 840, 63.7%) that they received. Interestingly, a little more than half of participants (n = 677, 51.6%) were unsure if their workplace had a policy for breaks for those working in full PPE, 7.1% (n = 93), indicated that there was no policy, while almost three-quarters (n = 945, 72.0%) of participants felt that their concerns about PPE were supported by their workplace. Sixteen percent (n = 210) of participants reported that they had been deployed to a new area of work at the start of the pandemic; however, the majority of these participants were confident or very confident in their new role (n = 130, 61.9%). Nursing and allied health workers were more likely to be redeployed. Importantly, most participants did not intend to change their career due to the COVID-19 pandemic (n = 1013, 77.2%). This was similar across occupational groups.

3. Results

3.1. Emotional Health and Wellbeing

The emotional health and wellbeing attributes of study participants are described in Table 4 and Table 5. Symptoms of psychological distress measured by objective and validated scales indicated that participants were experiencing moderate to severe depressive symptoms (n = 211, 16.1%), moderate to severe anxiety symptoms (n = 193, 14.7%), and high personal or patient/client burnout with median total scores of 46.4 (IQR = 28.6) and 25.0 (IQR = 29.2), respectively. Those employed in nursing had the largest proportion of workers experiencing moderate/severe symptoms of depression (21.0%) and anxiety (19.0%), while medical workers reported the largest level of personal or patient/client burnout with median total scores of 64.3 (IQR 16.0) and 29.2 (IQR 26.6), respectively (Table 5). Many participants also reported feeling fatigued a good bit of the time, most of the time, or all the time (n = 543, 41.4%). This was similar across occupational groups. Surprisingly, 17.5% (n = 230) participants were already experiencing symptoms associated with moderate-to-severe post-traumatic stress (PTS) and this was similar across occupational groups. Despite the relatively high level of symptoms of psychological distress, most participants demonstrated a normal or high degree of resilience (n = 854, 65.0%). Workers employed in medicine had the largest proportion of workers with normal/high resilience (90.0%), while allied health workers had the lowest (78.0%). However, only 20.1% (n = 264) of participants reported a moderate or high degree of optimism, with those employed in medicine reporting the lowest (10.2%). Participants had a high degree of personal wellbeing with a mean life satisfaction score of 7.2 (SD. 1.8) and a range of 0–10. Those employed in medicine had the highest mean level of life satisfaction of 7.7 (SD. 1.4), while those in nursing experienced the lowest with a mean score of 7.2 (SD. 1.9). Despite this, many participants reported feeling isolation or loneliness with a median total score of 5.0 (IQR = 3.0) and a range of 3–9. This was similar across occupational groups. Participants also reported a moderate degree of COVID-19-related fear with a mean of 13.1 (SD. 5.1) and a range of 7–34. Allied health workers experienced the highest level of fear with a mean score of 13.6 (SD. 5.3), while those in medicine experienced the lowest with a mean score of 11.2 (SD. 4.0). All psychometric instrument scales had acceptable internal consistency (α > 0.70).
Occupational group differences in mean scores and the proportions of emotional health and wellbeing outcomes are described in Table 6. Statistically significant adjusted differences between groups were only observed for life satisfaction, fear of COVID-19, and optimism. The largest difference in life satisfaction was observed between medicine and nursing workers. The largest differences in fear and optimism were observed between medicine and nursing workers and medicine and allied health workers. Important, but not statistically significant, differences were also observed for burnout, with those working in medicine generally experiencing higher levels of burnout but, surprisingly, higher levels of life satisfaction.
The comparison of HCWs working within the private hospital or community health services settings with those working within the public hospital setting indicates that those in private hospital or community health services were marginally older, allied health or non-clinical workers, in full-time employment, and were less likely to have access to PPE, less confident in infection control training, and less likely to have direct care of COVID-19 patients. These HCWs were less likely to be experiencing moderate/severe symptoms of depression, anxiety, fatigue, or burnout and were less likely to be experiencing poor sleep but had higher levels of psychological resilience. However, these workers were also more likely to be current smokers and report high-risk alcohol drinking behaviour.

3.2. Lifestyle and Physiological Characteristics

The lifestyle behaviours of healthcare workers are described in Table 7. Based on self-reported height and weight, 0.8% (n = 10) of participants have a body mass index (BMI) of <18.5 kgm2, 15.4% (n = 202) have a BMI from 18.5 to 24.9 kgm2, and 37.0% (n = 486) have a BMI of 25 kgm2 or over, indicating overweight or obesity. Overall, 7.3% (n = 96) of participants reported they are current smokers and 20.6% (n = 271) reported alcohol consumption that is considered moderate- to high-risk drinking. Only 21.2% (n = 278) of the sample reported consuming four or more serves of vegetables daily and 37.7% (n = 496) reported consuming two or more serves of fruit daily. Almost half the sample reported having poor sleep quality (n = 631, 48.0%).

4. Discussion

There are several studies describing the impacts of the COVID-19 pandemic on the mental health and wellbeing of healthcare workers within different professional groups and settings from within Australia [34,35,36,37,38] and many more internationally [39]. This study provides a unique perspective into the impacts of the pandemic on over 1300 clinical and non-clinical healthcare workers working within a regional and rural setting during the early stages of the pandemic in Australia. Findings from within a regional or rural setting have been scarcely reported in the literature, either in Australia or internationally. Furthermore, this study offers comprehensive findings on health and wellbeing, including lifestyle behaviours, which are seldom collected and reported together.
The proportions of moderate to severe degrees of anxiety symptoms, depressive symptoms, symptoms of PTS, and burnout within regional and rural healthcare workers during the COVID-19 pandemic in Victoria are concerning; however, the proportions of workers with these symptoms were generally lower that those reported by other Australian studies [35]. Furthermore, the higher levels of anxiety and depressive symptoms experienced by nursing workers are in line with findings from other studies [39]. The higher levels of personal or patient/client burnout in medical workers has also been commonly reported [40]. These levels of burnout in medical staff might be due to staff shortages in regional/rural Australia, with these staff having longer travel times to work, greater workloads, longer working hours, and additional responsibilities compared with their metropolitan counterparts [41].
These differences between studies are likely attributable to different data collection times during the pandemic, measurement tools, and population structures, with the current study consisting of approximately one-third non-clinical healthcare workers who may not be at high risk of occupational COVID-19 exposure. Most participants were recruited and completed their questionnaires between the second and third public health state lockdowns at a time when healthcare workers may have been experiencing less concerns about COVID-19 infection (Figure 1). However, the third and fourth public health state lockdowns occurred in February and May 2021, respectively, with a noticeable decline in recruitment numbers during this timeperiod. Victoria’s vaccine rollout in February 2021, during the recruitment period, may have also contributed to the lower levels of psychological distress reported in this study. Finally, although Victoria experienced significant bushfire and flooding events in 2019–20 and 2021, the Loddon Mallee region was not directly impacted. Moreover, none of these natural disasters occurred during the data collection period. Therefore, it is unlikely that the study findings have been impacted by these events.
The lower prevalence of distress and lower burnout scores in healthcare workers within the private hospital and community health settings compared with public hospital healthcare workers may be due to a lower perceived risk of a COVID-19 infection as COVID-19 patients only initially presented to public hospitals during the pandemic in Australia. These findings might also be influenced by different working conditions such as reduced overall caseloads and higher quality working environment due to fewer working hours and better working conditions [42,43].
Workplace pandemic preparedness and the availability of appropriate PPE are also associated with lower degrees of psychological distress [44], with almost 70% healthcare workers in this study reporting that their workplace was somewhat to very prepared and less than 20% of workers reporting an insufficient supply of PPE. Furthermore, the risk of infection in this study was lower than that reported in large tertiary hospitals in the state capital, Melbourne [34], as only 11.7% of healthcare workers reported taking direct care of COVID-19 patients.
A key finding of this study is that 65.0% of healthcare workers considered themselves to have a normal or high level of psychological resilience, with medical workers having the greatest level of resilience. This suggests that the relatively high level of resilience within the study population may be an additional reason for the lower degree of psychological distress compared with other studies. This relatively high level of psychological resilience has also been reported in other Australian studies [34,35,36,37,45]; however, it did not always correspond with low levels of psychological distress [34]. By comparison, a recent meta-review of 40 systematic reviews (1828 primary studies) of the mental health of healthcare workers globally, during the COVID-19 pandemic, reported a pooled prevalence for anxiety, depression, stress/post-traumatic stress symptoms, and burnout of 16–41%, 14–37%, 18.6–56.5%, and 12–36%, respectively [39]. The prevalence of the corresponding measures of psychological distress in the current study are at the lower end of the prevalence range reported in this meta-review.
Social support is an important component of overall wellbeing and a lack of social support and isolation/loneliness are well-known risk factors for psychological distress [46] [47]. The moderate to high degree of loneliness observed in the current study during the COVID-19 pandemic has also previously been reported in Australia [35] and internationally [48,49]. This may have been the result of the severe public health restrictions experienced by residents of Victoria during the pandemic, as well as an increased need to quarantine from family and friends to prevent the transmission of the virus. Given the impact that loneliness can have on the wellbeing of healthcare workers, interventions, such as peer-support programs, aimed at improving social support (especially during a pandemic) may be helpful for reducing the degree of psychological distress and improve the quality of life of healthcare workers during times of crises.
Of note is the relatively low level of optimism reported by healthcare workers in this study with only one-fifth of participants reporting high feelings of optimism about the future. Medical workers were the least optimistic. This is surprising considering that this occupation group had the highest level of resilience and life satisfaction. By comparison, a higher proportion of optimism was reported by another Australian study conducted within Melbourne metropolitan healthcare workers around the same time as the current study, with one-third of healthcare workers experiencing high feelings of optimism about the future [35]. However, in the study by McGuiness et al. (2021), those working in medicine reported higher levels of optimism than nursing and allied health workers. The differences between studies in the proportion of healthcare workers experiencing high feelings of optimism, especially in medical workers, are likely to be attributable to different measuring instruments, with McGuinness, S., et al. (2021) [35] using a visual analogue scale to measure optimism about the future. However, the low level of optimism reported by medical workers in this study may also be due to the corresponding high burnout observed, possibly due to increased workload and demands due to under resourcing in regional/rural areas.
Moderate to high degrees of COVID-19-related fear have been reported across the world during the pandemic [50]. In Australia, several studies have measured and reported COVID-19-related fear in healthcare workers [45,51,52,53,54]. All studies, except one [54], included healthcare workers and the general public/patients in the study population, with mean COVID-19-related fear scores, measured with the Fear of COVID-19 Scale, ranging from 15.0 to 18.4. The total Fear of COVID-19 Score of 13.1 observed in the current study is less than that reported by previous studies and may be one explanation for the lower prevalence of psychological distress observed in this study. The lower prevalence of COVID-19-related fear may be due to the regional/rural locations of the health services where COVID-19 cases were lower and the high level of health service preparedness perceived by healthcare workers. The relatively lower level of COVID-19-related fear was also observed in healthcare workers residing in south–west Victoria around the same time as the current study [45]. The differences in the fear of COVID-19 scores observed between medicine and nursing workers and medicine and allied health workers observed in this study has been reported in previous studies [55,56]; however, only a few studies used the validated Fear of COVID-19 Scale used in this study.
There are scarce data on lifestyle and physiological characteristics of Australian healthcare workers during the COVID-19 pandemic. Overweight and obesity are highly prevalent in the Australian general population with a prevalence of overweight and obesity of 36.0% and 31.0%, respectively, in 2017–18 [57]. To the best of the author’s knowledge, until now, the prevalence of overweight and obesity in Australian healthcare workers during the COVID-19 pandemic has not been reported. However, a 2020 nationally represented study of Australian workers across multiple industries (including healthcare) reported that 59.0% of Australian employees were either overweight or obese [58]. The proportion of overweight or obesity of 37.0% observed in the current study is lower than the Australian general population and that of Australian workers in general. This is also lower than that reported by international studies [59], except for studies conducted in some Asian populations, where the prevalence of overweight or obesity is quite low [60]. One explanation for the lower prevalence of overweight or obesity in the current study is that BMI was a self-reported measure. It is well known that individuals under-report weight status [61], and this is unlikely to differ among healthcare workers. Another explanation is that regional/rural healthcare workers might have greater access to outdoor recreational activities such as hiking, gardening, or other physical pursuits due to the natural surroundings of rural areas.
Several studies in Australia and internationally have reported an increase in alcohol consumption or high prevalence of alcohol use disorder during the COVID-19 pandemic [62,63,64,65]. This is important to examine, as alcohol use is associated with psychological distress and poor personal relationships [66,67]. Smallwood, N., et al. (2021) reported that 26.3% of Australian healthcare workers increased alcohol use during the second wave of the COVID-19 pandemic, and this was associated with a history of poor mental health and worse personal relationships [62]. The proportion of moderate or high-risk drinking behaviour observed in this study of 20.6% is difficult to compare with the study by Smallwood, N., et al. (2021) as they asked participants whether they increased alcohol consumption or not, and the current study measured this using the AUDIT-3, a validated instrument for quantifying alcohol use and the risk associated with this. However, the proportion of moderate- or high-risk alcohol consumption observed in this study is lower than that reported by studies conducted in the USA around the same time, with Hennein, R., et al. (2020) reporting that 42.6% of health workers had probable alcohol use disorder [63]. The lower proportion of moderate alcohol consumption observed during the pandemic could be due to sampling bias in which more healthy people agreed to complete the study questionnaires or the result of under reporting due to social desirability bias. It might also be the result of limited access to alcohol due to the severe public health restrictions imposed in Victoria or due to greater emphasis on preventive health behaviours because of limited access to services in regional/rural areas. The longitudinal data collection of the current study will examine whether there was an increase in alcohol use over the first two years of the COVID-19 pandemic and, if so, the factors associated with this.
The prevalence of tobacco smoking in healthcare workers during the pandemic has been reported by several studies. In Australia, Stubbs, J.M., et al. (2021) reported that 11.1% of metropolitan hospital healthcare workers were smokers [68], while Rahman, M., et al. (2020) reported a prevalence of smoking of 13.4% [52]. However, the latter study included patients, frontline health and other essential service workers, and community members. Marsden et al. (2022) reported a current smoking prevalence of 8.1% in a sample of public hospital nurses and midwives in the southern region of Tasmania, Australia, in April 2020 [5]. The proportion of tobacco smokers observed in our study of regional/rural healthcare workers of 7.3% is slightly lower than some of the Australian studies but similar to that in Marsden et al. (2022) and may be related to the lower degree of psychological distress observed in this study. Although smoking prevalence is generally higher in adults in outer rural and remote communities, the relatively low prevalence observed in this study might also be due to the healthcare worker study population who may be more aware of the risk of tobacco use and to the low proportion of healthcare worker study participants residing in outer rural and remote communities, with only 17.5% of the study population designated as residing in modified Monash 5–7 categories. Finally, as suggested for alcohol use, the low proportion of current smokers observed in this study might also be due to sampling bias and/or social desirability bias.
To the best of the author’s knowledge, there are no Australian studies that have reported on the eating behaviours of Australian healthcare workers during the COVID-19 pandemic. The low proportion of adequate vegetable and fruit consumption observed in this study is concerning given the growing body of research linking high diet quality with better mental health [69]. These current findings are similar to that reported in the Australian general population in 2020–21, in which only around 6.0% of Australians consume the recommended daily intakes of fruits and vegetables [70]. The low proportion of adequate vegetable and fruit consumption observed is in contrast with the other ‘healthy’ lifestyle behaviours observed in this study and might be the result of demanding schedules with long hours and irregular shifts, leaving many healthcare workers with limited time to prepare or consume healthy meals.
The high proportion of healthcare workers experiencing poor sleep quality (i.e., 48.0%) observed in the current study is similar to that reported by other Australian [68] and international studies [71,72,73,74]. This is also similar to the pooled prevalence of sleep disturbance of 43% (95% CI 36–50) reported by a recent meta-analysis of 18 studies involving nurses [75]. Although stressful events and psychological distress are known to be associated with sleep disturbance [76,77], the high proportion of healthcare workers experiencing poor sleep quality observed in the current study is somewhat surprising given the relatively lower degree of psychological distress in this study population. Previous studies have reported that factors associated with reduced sleep quality included changes in sleeping habits, shift work, anxiety, fear driven by COVID-19 news and lack of treatment knowledge, female gender, monthly income, isolation [78], perceived income, hours spent outdoors, the number of family/friends with COVID-19, and history of depression [79]. Further research is needed to determine which factors have had the greatest impact on sleep quality in this study population.
Although the proportion of HCWs experiencing clinically significant mental health issues was relatively low in this cohort at the time of recruitment, prolonged work stress, isolation, and lockdowns might cause further deterioration in mental health over time. It is therefore important for governments and healthcare services to consider ways of supporting HCWs and preventing further declines in mental health. A recent systematic review on interventions shown to be effective for dealing with mental health issues of HCWs during infectious disease outbreaks reported that interventions could be grouped into four categories: (1) informational support (training, guidelines, prevention programs); (2) instrumental support (personal protective equipment, protection protocols); (3) organisational support (manpower allocation, working hours, re-organization of facilities/structures, provision of rest areas); and (4) emotional and psychological support (psychoeducation and training, mental health support team, peer-support and counselling, therapy, digital platforms and tele-support) [80]. Based on these findings, one explanation for the low prevalence of fear and distress in this cohort may relate to the high degree of informational and instrumental support provided by Loddon Mallee healthcare service leaders during the early stages of the pandemic. This is evidenced by the high proportion of HCWs who reported that their workplace was very or moderately prepared for the COVID-19 pandemic, and that they often or very often had access to the right amount of PPE. Most HCWs also had confidence in the PPE training they received and were moderately or very confident in the infection control training that they received and felt that their concerns about PPE were supported by their workplace.
This study has several strengths and some limitations. Strengths include the prospective cohort study design which will provide a detailed longitudinal understanding of the impact of the COVID-19 pandemic on the health and wellbeing of clinical and non-clinical healthcare workers in regional and rural Victoria, Australia, which to date has been largely unexplored. This will allow changes in mental health and wellbeing over time to be measured, defining the temporal sequence of events, and providing stronger evidence for a causal association with risk factors. Validated and reliable survey instruments were used for the majority of survey items, and these were selected based on robust evidence available from recent systematic reviews. Finally, response bias was evaluated by weighting study findings using workforce data which were available for approximately 80% of the study population, and the impact of this was minimal for most study measures. The main limitations of this research are that only healthy employed healthcare workers were included in this study; thus study findings may be impacted by healthy worker effects. Missing data may have introduced some sampling bias; however, the comparison of the total sample with the part of the sample weighted for non-response did not identify major differences in prevalence estimates. There were marginal differences observed for some variables. That is, the study sample had marginally fewer female, University educated, and married healthcare workers than the weighted sample, which is representative of the Loddon Mallee region sampling frame. The sample also had marginally fewer healthcare workers in part-time employment, medicine and nursing workers, healthcare workers engaging in moderate risk alcohol consumption, and workers experiencing poor-quality sleep than the sampling frame. It is also well known that female healthcare workers were more likely to be exposed to the COVID-19 virus and experienced greater levels of psychological distress during the COVID-19 pandemic compared with their male counterparts [81]. However, we did not undertake gender subgroup analyses as there was insufficient statistical power to examine differences across the large number of outcomes reported in this study due to the relatively small proportion of male healthcare workers. Finally, the sample’s representativeness may be limited to the Loddon Mallee region of regional and rural Victoria, Australia.

5. Conclusions

Regional and rural healthcare workers in Victoria, Australia, were experiencing a moderate to high degree of psychological distress and COVID-19-related fear during the early stages of the pandemic; however, the proportion of workers experiencing moderate to high degrees of distress was generally lower than that reported by other Australian studies and international studies. The high proportion of workers with a normal/high level of resilience, as well as the high perception of workplace pandemic preparedness and managerial support offer plausible explanations for the observed findings. Future research should examine the effects of resilience and workplace pandemic preparedness on mental health outcomes in healthcare workers, especially in the context of infectious disease outbreaks or a pandemic. The collection of the same health measures at several time-points during the first two years of the pandemic will allow us to determine whether mental health outcomes remained the same or deteriorated as the pandemic evolved and the determinants of these trends. Findings will be used to inform policy options to support healthcare workers in responding to future pandemics.

Author Contributions

A.C. (Angela Crombie) and M.M. initially designed the study with input from P.F., A.M., S.J.B., and T.S.; M.M. coordinated the study set-up and finalisation of study questionnaire with C.P., L.B., G.C., M.M., A.C. (Angela Crombie), C.P., L.B., G.C., P.F., A.M. and S.J.B. and T.S. contributed to questionnaire development and study design. All authors (M.M., A.C. (Angela Crombie), C.P., L.B., G.C., P.F., A.M., S.J.B., T.S., K.M., E.S., A.C. (Amanda Collings) and X.L.) contributed to editing and critiquing the final manuscript for intellectual content. K.M. also contributed to data management and analysis. X.L. contributed to data analysis. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by a COVID-19 research grant provided by the Victoria Government Department of Jobs, Precincts and Regions.

Institutional Review Board Statement

The LMHCWCS was approved by the Bendigo Health (ID: 68671), La-Trobe University, and the St John of God Human Research Ethics Committees. All methods were carried out according to the Declaration of Helsinki. Informed consent to participate was taken from all participants to participate in the study.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Due to privacy reasons, subsets of non-identifiable data may be made available to collaborating researchers where there is a formal request (i.e., expression of interest research proposal) to make use of the data. Collaborators may request to either analyse LMHCWCS questionnaire data and/or conduct a substudy of the LMHCWCS participants. For both, permission must be first obtained from the Data Access Committee of LMHCWCS, or in the case of substudies, the Investigator Committee. All future collaborators will be linked to the project through a Human Research Ethics Committee amendment that outlines who will be using the data and the purpose of the project [4]. Shared data cannot be shared with any third party and may only be used for the purposes approved by the study’s Data Access Committee. Researchers wishing to access data should contact the Principal Investigator using the corresponding author contact details or the Study Coordinator at [email protected].

Acknowledgments

The authors would like to thank participating Loddon Mallee healthcare workers and volunteers for their support of this study. The authors thank the members of the Study Scientific Steering Committee who provided guidance and support for this study.

Conflicts of Interest

The authors declare no conflicts of interest.

List of Abbreviations

BMIBody Mass Index
BRSBrief Resilience Scale
COVID-19Coronavirus 19
GAD-7Generalised Anxiety Disorder—7 items
IES-6Impact of Events Scale—6 items
IQRInterquartile Range
LOT-RLife Orientation Test—Revised
LMHCWCSLoddon Mallee Healthcare Worker COVID-19 Study
MMMModified Monash Model classification
PHQ-9Patient Health Questionnaire—9 items
PPEPersonal Protective Equipment
PSQIPittsburgh Sleep Quality Index
PTSPost-Traumatic Stress
PWI-APersonal Wellbeing Index—Adult
SDStandard Deviation

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Figure 1. Timeline of recruitment and corresponding external COVID-19-related events for the Loddon Mallee Healthcare Worker COVID-19 Study.
Figure 1. Timeline of recruitment and corresponding external COVID-19-related events for the Loddon Mallee Healthcare Worker COVID-19 Study.
Ijerph 21 00649 g001
Figure 2. Loddon Mallee Healthcare Worker COVID-19 Study recruitment strategy and study sample.
Figure 2. Loddon Mallee Healthcare Worker COVID-19 Study recruitment strategy and study sample.
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Table 1. Sociodemographic characteristics of Loddon Mallee Healthcare Worker COVID-19 Study sample recruited during the COVID-19 pandemic.
Table 1. Sociodemographic characteristics of Loddon Mallee Healthcare Worker COVID-19 Study sample recruited during the COVID-19 pandemic.
VariablesUnit of MeasurementPublic Health ServicesPrivate Health and Community Health ServicesTotal
Sample
(Unweighted)
Sample Weighted for
Non-Response #
Sample
(Unweighted)
Sample
(Unweighted) *
N = 1043N = 6528N = 266N = 1313
Age
Mean (SD) (years)44.7 (12.8)44.3 (13.1)45.6 (12.9)44.9 (12.8)
Median (IQR)46.0 (21.0)45.0 (22.0)46.0 (22.0)46.0 (21.0)
Missing3115940
Freq.%Freq.%Freq.%Freq.%
Sex at birth
Female84681.1547783.920878.2105780.5
Male14013.4105116.13513.217613.4
Missing575.500238.6806.1
Geographic location, MMM classification
MM 1151.41141.7102.0262.0
MM 249247.2286443.97343.156643.1
MM 3686.54747.39112.216012.2
MM 418317.5121118.62415.820815.8
MM 518517.7128219.64117.222617.2
MM 630.3160.30030.2
MM 710.170.10010.1
Missing969.25588.62710.21239.4
Household income
<AUD 52,000/year16315.6100215.44416.520915.9
≥AUD 52,000/year77269.2479673.516762.889167.9
Missing15815.172911.25520.721316.2
Concerns about income
Yes22221.3143121.96022.628421.6
No76573.3507077.718368.895072.4
Missing565.4270.4238.6796.0
Education
Secondary Schooling Not Completed252.41482.362.3322.4
Secondary Schooling Completed555.33164.8166.0715.4
Trade Qualification or TAFE13012.584312.92710.215712.0
University or Other Tertiary Study76173.0507077.719372.695772.9
Missing726.91522.3249.0967.3
Marital status
Married54252.0345753.012446.666750.8
De Facto/Living with Partner17316.6116517.84416.521716.5
Widowed212.01402.262.3272.1
Divorced/Separated11711.282812.73613.515611.9
Never Married12011.585013.03011.315011.4
Missing706.7881.4269.8967.3
Identify as Indigenous
Aboriginal60.6270.420.880.6
Non-Aboriginal 97793.7642498.424090.2122193.0
Missing605.8771.2249.0846.4
Type of Household
Own House76773.5495575.919372.696273.3
Own Flat/Unit222.11392.131.1251.9
Rented House12411.988613.63312.415912.2
Rented Flat/Unit353.42423.751.9403.0
Own Mobile Home10.1000010.1
With Family/Relatives343.32343.641.5382.9
With Friends10.1100.141.550.4
Other60.6520.810.470.5
Missing535.1100.1238.6765.8
Home schooling
Yes29628.4187428.76524.436227.6
No11310.876911.82810.514210.8
Missing63460.8388559.517365.080961.6
Carer responsibilities
Yes30629.3195229.96725.237628.6
No67865.0453469.517465.485365.0
Missing595.7420.6259.4846.4
# Sample characteristics weighted for baseline non-participation is the pseudo-population sample characteristics from the public hospital sample frame had the allocated number of participants responded. * Note—four participants did not provide information on whether they work within a public or private health service, thus the public and private health service subtotals do not add up to the sample total.
Table 2. Sociodemographic and occupational characteristics of Loddon Mallee Healthcare Worker COVID-19 Study sample recruited during the COVID-19 pandemic according to occupational group.
Table 2. Sociodemographic and occupational characteristics of Loddon Mallee Healthcare Worker COVID-19 Study sample recruited during the COVID-19 pandemic according to occupational group.
MedicineNursingAllied HealthNon-ClinicalOverall Sample #
(N = 59)(N = 499)(N = 219)(N = 435)(N = 1313)
Age (years)
>4523 (39.0%)259 (51.9%)89 (40.6%)236 (54.3%)650 (49.5%)
≤4536 (61.0%)227 (45.5%)128 (58.4%)181 (41.6%)623 (47.4%)
Missing0 (0%)13 (2.6%)2 (0.9%)18 (4.1%)40 (3.0%)
Sex at birth
Male20 (33.9%)49
(9.8%)
37 (16.9%)67 (15.4%)176 (13.4%)
Female38 (64.4%)442 (88.6%)181 (82.6%)366 (84.1%)1057 (80.5%)
Missing1 (1.7%)8 (1.6%)1 (0.5%)2 (0.5%)80 (6.1%)
Geographic location, MMM classification
MM 1–245 (76.3%)238 (47.7%)102 (46.6%)168 (38.6%)592 (45.1%)
MM 3–712 (20.3%)215 (43.1%)96 (43.8%)231 (53.1%)598 (45.5%)
Missing2 (3.4%)46 (9.2%)21 (9.6%)36 (8.3%)123 (9.4%)
Household income
<AUD 52000/year2
(3.4%)
70 (14.0%)34 (15.5%)100 (23.0%)209 (15.9%)
≥AUD 52000/year54 (91.5%)368 (73.7%)165 (75.3%)286 (65.7%)891 (67.9%)
Missing3
(5.1%)
61 (12.2%)20
(9.1%)
49 (11.3%)213 (16.2%)
Concern about income
No52 (88.1%)386 (77.4%)164 (74.9%)333 (76.6%)950 (72.4%)
Yes6
(10.2%)
111 (22.2%)55 (25.1%)101 (23.2%)284 (21.6%)
Missing1 (1.7%)2 (0.4%)0 (0%)1 (0.2%)79 (6.0%)
Education
Other education0
(0%)
12
(2.4%)
4
(1.8%)
12
(2.8%)
28
(2.1%)
Secondary schooling completed0 (0%)8 (1.6%)5 (2.3%)56 (12.9%)71 (5.4%)
Secondary schooling not completed0 (0%)1 (0.2%)1 (0.5%)29 (6.7%)32 (2.4%)
Trade qualification or TAFE0 (0%)49 (9.8%)11 (5.0%)93 (21.4%)157 (12.0%)
University or other tertiary study59 (100%)429 (86.0%)198 (90.4%)245 (56.3%)957 (72.9%)
Missing000068 (5.2%)
Marital status
Married39 (66.1%)255 (51.1%)115 (52.5%)246 (56.6%)667 (50.8%)
De facto/living with a partner8
(13.6%)
89 (17.8%)45 (20.5%)65 (14.9%)217 (16.5%)
Widowed0 (0%)15 (3.0%)1 (0.5%)10 (2.3%)27 (2.1%)
Divorced or separated1
(1.7%)
78 (15.6%)17
(7.8%)
60 (13.8%)156 (11.9%)
Never married11 (18.6%)54 (10.8%)35 (16.0%)48 (11.0%)150 (11.4%)
Missing0 (0%)8 (1.6%)6 (2.7%)6 (1.4%)96 (7.3%)
Home schooling
Yes18 (30.5%)150 (30.1%)61 (27.9%)131 (30.1%)362 (27.6%)
No9
(15.3%)
54 (10.8%)23 (10.5%)51 (11.7%)142 (10.8%)
Missing32 (54.2%)295 (59.1%)135 (61.6%)253 (58.2%)809 (61.6%)
Caring responsibilities
Yes16 (27.1%)150 (30.1%)71 (32.4%)131 (30.1%)376 (28.6%)
No42 (71.2%)347 (69.5%)147 (67.1%)299 (68.7%)853 (65.0%)
Missing1 (1.7%)2 (0.4%)1 (0.5%)5 (1.1%)84 (6.4%)
Confidence in infection control training
Very confident19 (32.2%)181 (36.3%)60 (27.4%)167 (38.4%)427 (32.5%)
Moderately confident15 (25.4%)183 (36.7%)98 (44.7%)117 (26.9%)413 (31.5%)
Somewhat confident10 (16.9%)71 (14.2%)31 (14.2%)41 (9.4%)153 (11.7%)
A little confident6 (10.2%)19 (3.8%)8 (3.7%)10 (2.3%)43 (3.3%)
Not confident at all0 (0%)8 (1.6%)1 (0.5%)5 (1.1%)14 (1.1%)
Missing9 (15.3%)37 (7.4%)21 (9.6%)95 (21.8%)263 (20.0%)
Redeployed to a new work area
No54 (91.5%)397 (79.6%)174 (79.5%)365 (83.9%)990 (75.4%)
Yes4
(6.8%)
99 (19.8%)41 (18.7%)66 (15.2%)210 (16.0%)
Missing1 (1.7%)3 (0.6%)4 (1.8%)4 (0.9%)113 (8.6%)
Direct contact with COVID-19 patients
No26 (44.1%)274 (54.9%)185 (84.5%)385 (88.5%)870 (66.3%)
Yes32 (54.2%)216 (43.3%)33 (15.1%)43
(9.9%)
324 (24.7%)
Missing1 (1.7%)9 (1.8%)1 (0.5%)7 (1.6%)119 (9.1%)
Considering career change due to COVID-19
Yes3 (5.1%)49 (9.8%)21 (9.6%)38 (8.7%)114 (8.7%)
No54 (91.5%)397 (79.6%)184 (84.0%)361 (83.0%)1013 (77.2%)
Unsure0 (0%)51 (10.2%)14 (6.4%)35 (8.0%)101 (7.7%)
Missing2 (3.4%)2 (0.4%)0 (0%)1 (0.2%)85 (6.5%)
# A total of 101 study participants did not indicate the type of occupation.
Table 3. Occupational characteristics of Loddon Mallee Healthcare Worker COVID-19 Study sample during the COVID-19 pandemic.
Table 3. Occupational characteristics of Loddon Mallee Healthcare Worker COVID-19 Study sample during the COVID-19 pandemic.
VariablesUnit of MeasurementPublic Health ServicesPrivate Health and Community Health ServicesTotal
Sample
(Unweighted)
Sample Weighted for
Non-Response #
Sample
(Unweighted)
Sample
(Unweighted) *
N = 1043N = 6528N = 266N = 1313
Freq.%Freq.%Freq.%Freq.%
Employment status
Full time34232.8217933.49234.643633.2
Part time 53551.3376157.611342.564949.4
Casual585.63665.6134.9725.5
Retired 90.9500.820.8110.8
Volunteer212.01171.8114.1322.4
Other80.8540.841.5120.9
Missing706.7003111.71017.7
Primary Profession
Medicine464.44396.7124.5594.5
Nursing43541.7366356.16424.149938.0
Allied Health16215.55999.25621.121916.7
Non-clinical33031.6182728.010338.743533.1
Missing706.7003111.71017.7
Workplace preparedness
Very prepared31229.9200730.75219.536527.8
Moderately prepared25024.0167225.65319.930323.1
Somewhat prepared18918.1130219.94918.424018.3
A little prepared1039.970410.83011.313310.1
Not prepared at all656.24006.13412.81007.6
Unsure636.04236.5207.5836.3
Missing615.8210.32810.5896.8
Sufficient PPE for staff
Never201.91261.972.6272.1
Rarely474.53375.2176.4655.0
Sometimes10710.375511.62710.213410.2
Often23022.1158724.36424.129522.5
Very often40538.8278842.77929.748536.9
Not applicable to my role16315.688013.54215.820615.7
Missing716.8550.83011.31017.7
Confidence in PPE training
Yes76473.3530181.217967.394572.0
No666.34717.2145.3806.1
Not applicable to my role13412.869910.74015.017513.3
Missing797.6570.93312.41138.6
Workplace supported concerns about PPE
Yes76173.0526180.617866.994171.7
No767.35358.2186.8957.2
Not applicable to my role12812.367410.33513.216412.5
Missing787.5580.93513.21138.6
Policy for breaks while working in full PPE
Yes35433.9238036.57929.743433.1
No615.84837.43011.3937.1
Unsure55353.0363755.712346.267751.6
Missing757.2280.43412.81098.3
Redeployed to a new area of work
Yes 16816.1114317.54115.421016.0
No79776.4534081.819071.499075.4
Missing787.5440.73513.21138.6
Confidence in new area of work (those redeployed)
Not confident at all50.5290.40050.4
A little confident191.81322.051.9241.8
Someday confident403.83014.6114.1513.9
Confident636.04066.2166.0806.1
Very confident413.92754.293.4503.8
Missing87583.9538482.522584.6110384.0
Direct care of COVID-19 patients
Yes13012.590613.9238.615311.7
No60457.9418364.113952.374756.9
Not applicable to my role23322.3140121.57227.130523.2
Missing 767.3380.63212.01088.2
Confidence in infection control training
Not confident at all101.0691.141.5141.1
A little confident383.62914.55 1.9433.3
Somewhat confident12812.389313.7259.415311.7
Moderately confident33331.9220933.88030.141331.3
Very confident34433.0235436.18030.142732.4
Missing19018.271210.97227.126320.0
Considering career change due to COVID-19
Yes838.05458.43011.31148.7
No81978.5540282.819171.8101377.2
Unsure817.85598.6207.51017.7
Missing605.8220.3259.4856.5
# Sample characteristics weighted for baseline non-participation is the pseudo-population sample characteristics from the public hospital sample frame had the allocated number of participants responded. * Note—four participants did not provide information on whether they work within a public or private health service, thus the public and private health service subtotals do not add to the sample total.
Table 4. Emotional health/wellbeing of Loddon Mallee Healthcare Worker COVID-19 Study sample during the COVID-19 pandemic.
Table 4. Emotional health/wellbeing of Loddon Mallee Healthcare Worker COVID-19 Study sample during the COVID-19 pandemic.
VariablesUnit of MeasurementPublic Health ServicesPrivate Health and Community Health ServicesTotal
Sample
(Unweighted)
Sample Weighted for
Non-Response #
Sample
(Unweighted)
Sample
(Unweighted) *
N = 1043N = 6528N = 266N = 1313
Wellbeing (life satisfaction)
(PWI-A) (α = 1.0 (single question))
Mean (SD)7.2 (1.8)7.2 (1.7)7.2 (1.8)7.2 (1.8)
Median (IQR)8.0 (2.0)7.3 (2.0)8.0 (2.0)8.0 (2.0)
Missing172111345217
Burnout
(client/patient-based) (α = 0.89, 0.87–0.90)
Mean (SD)24.8 (19.4)24.8 (19.4)24.8 (20.7)24.9 (19.7)
Median (IQR)25.0 (29.2)25.0 (29.2)20.8 (29.2)25.0 (29.2)
Missing3371571103441
Burnout
(work/personal) (α = 0.91, 0.89–0.92)
Mean (SD)46.3 (19.2)46.6 (18.8)44.6 (17.6)45.9 (18.8)
Median (IQR)46.4 (28.6)46.4 (28.6)42.9 (32.1)46.4 (28.6)
Missing80551611971005
Isolation and loneliness
(UCLA Loneliness Scale Version 3) (α = 0.87, 0.85–0.88)
Mean (SD)5.0 (1.9)5.0 (4.9)4.8 (1.8)4.9 (1.9)
Median (IQR)5.0 (3.0)5.0 (3.0)4.0 (3)5.0 (3.0)
Missing224108657282
Fear of COVID-19 scale (α = 0.89, 0.87–0.90)
Mean (SD)13.05 (5.1)12.9 (5.1)13.26 (4.9)13.1 (5.1)
Median (IQR)13.0 (7.0)13.0 (7.0)13.0 (7.0)13.0 (7.0)
Missing253 (24.3%)1247 (19.1%)64 (24.1%)319 (24.3%)
Depressive symptoms
(PHQ-9) (α = 0.99, 0.99–0.99)
Mean (SD)5.8 (5.5)5.7 (5.5)5.8 (5.5)5.9 (5.6)
Median (IQR)4.0 (6.0)4.0 (6.0)5.0 (6.0)4.0 (6.0)
Freq%Freq%Freq%Freq%
Moderate–severe
score ≥ 1017216.5115417.73613.521116.1
Negligible–low score < 1066363.6443868.017264.783563.6
Missing20819.993614.35821.826720.3
Anxiety symptoms
(GAD-7) (α = 0.93, 0.92–0.94)
Mean (SD)5.5 (5.1)5.4 (5.0)5.5 (5.1)5.6 (5.1)
Median (IQR)5.0 (7.0)5.0 (6.0)4.0 (6.0)5.0 (7.0)
Freq%Freq%Freq%Freq%
Moderate–severe
Score ≥ 1015514.9102115.63613.519314.7
Negligible–low score < 1069466.5466871.518268.487866.9
Missing19418.683812.84818.024218.4
Resilience
(BRS) (α = 0.90, 0.89–0.91)
Mean (SD)3.5 (0.8)3.5 (0.8)3.6 (0.8)3.5 (0.8)
Median (IQR)3.7 (1.0)3.7 (1.0)3.7 (1.0)3.7 (1.0)
Freq%Freq%Freq%Freq%
Low
(1.00–2.99)
16916.2113117.33814.321016.0
Normal
(3.00–4.30)
56153.8374657.413550.869653.0
High
(4.31–5.00)
11511.077511.94316.215812.0
Missing19819.087513.45018.824919.0
Optimism
(LOT-R) (α = 0.73, 0.69–0.76)
Mean (SD)12.4 (2.5)12.5 (2.5)12.2 (2.1)12.4 (2.4)
Median (IQR)12.0 (3.0)12.0 (3.0)12.0 (2.0)12.0 (3.0)
Freq%Freq%Freq%Freq%
Low optimism (<14)60958.4402861.717063.978159.5
Moderate optimism (14–18)20419.6139221.34115.424618.7
High optimism (>18)161.51121.720.8181.4
Missing21420.599615.35319.926820.4
Post-traumatic stress
(IES-6) (α = 0.94, 0.93–0.95)
Freq%Freq%Freq%Freq%
None to minimal PTS (≤9) 65662.9434366.517365.083063.2
Moderate to severe PTS (>9)18117.4122618.84617.323017.5
Missing20619.895914.74717.725319.3
Fatigue
Freq%Freq%Freq%Freq%
All the time222.11422.251.9272.1
Most of the time20219.4140121.54516.924818.9
A good bit of the time20819.9139021.36022.626820.4
Some of the time26525.4173226.55721.432224.5
A little of the time14213.695314.63814.318213.7
None of the time343.32213.4145.3493.7
Missing17016.368910.54717.721716.5
# Sample characteristics weighted for baseline non-participation is the pseudo-population sample characteristics from the public hospital sample frame had the allocated number of participants responded. * Note—four participants did not provide information on whether they work within the public or private health service, thus the public and private health service subtotals do not add to the sample total. α = Cronbach’s alpha and 95% confidence interval (internal consistency)).
Table 5. Emotional health and wellbeing of Loddon Mallee Healthcare Worker COVID-19 Study sample recruited during the COVID-19 pandemic according to occupational group.
Table 5. Emotional health and wellbeing of Loddon Mallee Healthcare Worker COVID-19 Study sample recruited during the COVID-19 pandemic according to occupational group.
CharacteristicMedicine
N = 59
Nursing
N = 499
Allied Health
N = 219
Non-Clinical
N = 435
p-Value $N = 1313 #
Wellbeing (life satisfaction) (PWI-A Queston 1) 0.1
Mean (SD)7.7 (1.4)7.2 (1.9)7.2 (1.7)7.2 (1.8) 7.2 (1.8)
Median (IQR)8.0 (1.5)8.0 (2.0)8.0 (2.0)8.0 (2.0) 8.0 (2.0)
Missing8601632 217
Burnout (client/patient-based) <0.001
Mean (SD)31.4 (20.3)24.7 (19.4)27.3 (19.8)21.1 (19.4) 24.9 (19.7)
Median (IQR)29.2 (26.6)25.0 (29.2)25.0 (25.0)16.7 (29.1) 25.0 (29.2)
Missing46631239 441
Burnout (work/personal) 0.084
Mean (SD)60.7 (16.4)48.8 (17.5)51.4 (22.1)44.5 (18.6) 45.9 (18.8)
Median (IQR)64.3 (16.0)50.0 (28.6)53.6 (25.0)42.9 (28.5) 46.4 (28.6)
Missing56450194204 1005
Isolation and loneliness (UCLA Loneliness Scale Version 3) 0.61
Mean (SD)5.0
(1.9)
5.0
(1.9)
4.9
(1.8)
5.0
(1.9)
4.9
(1.9)
Median (IQR)5.0 (3.0)5.0 (3.0)4.0 (3.0)5.0 (3.0) 5.0 (3.0)
Missing13952449 282
Fear of COVID-19 Scale 0.039
Mean (SD)11.2 (4.0)13.3 (5.1)13.6 (5.3)12.9 (5.1) 13.1 (5.1)
Median (IQR)10.0 (6.0)13.0 (7.0)13.0 (8.0)12.0 (7.0) 13.0 (7.0)
Missing151033367 319
Depressive symptoms (PHQ-9) 0.66
Mean (SD)5.3 (5.6)5.8 (5.7)6.0 (5.7)5.9 (5.5) 5.9 (5.6)
Median (IQR)4.0 (5.0)4.0 (6.0)4.0 (7.0)5.0 (6.0) 4.0 (6.0)
Missing8782654 267
Depressive symptoms group (PHQ-9) 0.78
Negligible–low score < 1043 (73.0%)331 (63.3%)155 (70.8%)306 (70.3%) 835 (63.6%)
Moderate–severe ≥ 108 (13.5%)90 (18.0%)38 (17.3%)75 (17.2%) 211 (16.1%)
Missing8782654 267
Anxiety symptoms (GAD-7) 0.39
Mean (SD)4.6 (5.1)5.6 (5.05)5.7 (5.3)5.5 (5.1) 5.6 (5.1)
Median (IQR)3.0 (5.0)5.0 (7.0)5.0 (5.0)5.0 (7.0) 5.0 (7.0)
Missing10672242 242
Anxiety symptoms group 0.94
Negligible–low score < 1041 (69.5%)352 (70.5%)164 (74.9%)321 (73.8%) 878 (66.9%)
Moderate–severe ≥ 108 (13.6%)80 (16.0%)33 (15.1%)72 (16.5%) 193 (14.7%)
Missing10672242 242
Resilience (BRS) 0.13
Mean (SD)3.8 (0.82)3.5 (0.8)3.5 (0.8)3.5 (0.8) 3.5 (0.8)
Median (IQR)3.8 (1.0)3.7 (1.0)3.7 (1.0)3.7 (1.0) 3.7 (1.0)
Missing10742341 249
Resilience group 0.069
Low (1.00–2.99)5 (8.5%)86 (17.2%)42 (19.2%)77 (17.7%) 210 (16.0%)
Normal (3.00–4.30)29 (49.1%)280 (56.1%)128 (58.5%)259 (59.5%) 696 (53.0%)
High (4.31–5.00)15 (25.4%)59 (11.8%)26 (11.9%)58 (13.3%) 158 (12.0%)
Missing10742341 249
Optimism (LOT-R) 0.002
Mean (SD)11.5 (2.2)12.5 (2.4)11.9 (2.0)12.6 (2.6) 12.4 (2.4)
Median (IQR)12.0 (3.0)12.0 (3.0)12.0 (2.0)12.0 (3.0) 12.0 (3.0)
Missing13842050 268
Optimism group
Low optimism (<14)40 (67.8%)304 (60.9%)160 (73.1%)277 (63.7%) 781 (59.5%)
Moderate optimism (14–18)6 (10.2%)103 (20.6%)38 (17.3%)99 (22.8%) 246 (18.7%)
High optimism (>18)0 (0%)8 (1.6%)1 (0.5%)9 (3.8%) 18 (1.4%)
Missing13842050 268
Post-traumatic stress (IES-6) 0.71
Mean (SD)4.8 (5.1)5.0 (5.2)4.6 (5.4)5.2 (5.9) 5.0 (5.5)
Median (IQR)4.0 (8.0)3.0 (8.0)3.0 (6.0)3.0 (8.0) 3.0 (8.0)
Missing9781748 253
Post-traumatic stress group (IES-6) 0.14
None to minimal PTS (≤9)39 (66.1%)327 (65.5%)170 (77.6%)294 (67.6%) 830 (63.2%)
Moderate to severe PTS (>9)11 (18.6%)94 (18.8%)32 (14.6%)93 (21.4%) 230 (17.5%)
Missing9781748 253
Fatigue 0.86
All of the time1 (2.0%)8 (1.8%)6 (2.9%)12 (3.0%) 27 (2.5%)
Most of the time14 (27%)96 (22%)39 (19%)99 (25%) 248 (23%)
A good bit of the time11 (22%)113 (26%)55 (27%)89 (22%) 268 (24%)
Some of the time14 (27%)128 (29%)60 (29%)120 (30%) 322 (29%)
A little of the time9 (18%)75 (17%)35 (17%)63 (16%) 182 (17%)
None of the time2 (3.9%)17 (3.9%)10 (4.9%)20 (5.0%) 49 (4.5%)
Missing8621432 217
# A total of 101 study participants did not indicate the type of occupation. $ Kruskal–Wallis rank sum test; Pearson’s chi-squared test.
Table 6. Comparison * of continuous and binary outcomes for measures of emotional health and wellbeing across occupations.
Table 6. Comparison * of continuous and binary outcomes for measures of emotional health and wellbeing across occupations.
VariablesMedicine vs. Nursing Mean DifferenceAllied vs. Nursing Mean Difference Non-Clinical/
Administration vs. Nursing Mean Difference
Medicine vs. Allied # Mean Differencep-ValueMedicine vs.
Nursing Difference
Allied vs.
Nursing Difference
Non-Clinical/
Administration vs. Nursing Difference
Medicine vs. Allied # Differencep-Value **
Comparison of Continuous OutcomesComparison of Binary Outcomes
Wellbeing (life satisfaction (PWI-A—Q1)0.7 (0.1, 1.3)0.2 (−0.2, 0.5)0.1 (−0.2, 0.5)0.5 (−0.1, 1.2)0.037NANANANANA
Burnout (client/patient-based)5.0 (−2.6, 12.6)2.2 (−2.5, 6.9)−1.7 (−6.9, 3.5)2.8 (−5.3, 10.9)0.144NANANANANA
Burnout (work/personal)17.8 (−17.3, 52.9)−2.8 (−15.9, 10.3)−6.9 (−15.8, 1.9)20.6 (−15.2, 56.4)0.055NANANANANA
Isolation and loneliness (UCLA Loneliness Scale Version 3)0.1 (−0.7, 0.9)−0.2 (−0.6, 0.2)0.01 (−0.4, 0.4)0.3 (−0.5, 1.1)0.611−0.05 (−0.9, 0.8)0.3 (−0.2, 0.8)−0.1 (−0.5, 0.3)−0.3 (−1.2, 0.6)0.345
Fear of COVID−19 Scale−1.6 (−3.7, 0.6)0.5 (−0.7,1.7)−0.5 (−1.5, 0.6)−2.1 (−4.4, 0.1)0.047NANANANANA
Depressive symptoms (PHQ−9)−1.2 (−3.4, 1.0)−0.2 (−1.5, 1.1)0.01 (−1.1, 1.1)−0.97 (−3.3, 1.3)0.5448−0.8 (−2.0, 0.4)−0.4 (−1.0, 0.2)−0.2 (−0.8, 0.3)−0.4 (−1.7, 0.8)0.165
Anxiety symptoms (GAD−7)−1.4 (−3.5, 0.6)−0.2 (−1.4, 1.0)−0.1 (−1.1, 0.9)−1.2 (−3.4, 0.9)0.355−0.4 (−1.6, 0.8)−0.4 (−1.0, 0.3)−0.1 (−0.7, 0.4)−0.04 (−1.3, 1.2)0.468
Post-traumatic stress (IES−6)−0.4 (−2.5, 1.8)−0.6 (−1.9, 0.6)0.2 (−0.9, 1.3)0.3 (−2.0, 2.6)0.457−0.2 (−1.2, 0.8)−0.6 (−1.2, 0.03)−0.0 (−0.5, 0.5)0.4 (−0.7, 1.5)0.084
Resilience (BRS)0.3 (−0.03, 0.6)−0.05 (−0.2, 0.1)0.04 (−0.1, 0.2)0.3 (−0.0, 0.7)0.0691.0 (−0.4, 2.4)0.01 (−0.6, 0.6)0.14 (−0.4, 0.7)0.97 (−0.5, 2.4)0.313
Optimism (LOT-R)−0.9 (−1.9, 0.1)−0.7 (−1.2, −0.1)−0.03 (−0.5, 0.5)−0.2 (−1.3, 0.8)0.0040.9 (−0.3, 2.2)0.5 (−0.1, 1.1)0.0 (−0.5, 0.5)0.4 (−0.9, 1.8)0.048
# With Tukey’s adjustment. The binary differences are given on the log odds ratio (not the response) scale. * The models used to estimate differences between means or relative risks are adjusted for age, gender, modified Monash category, and education. Relative risks correspond to the risk of having the poorer psychological outcome category. ** p-values correspond to the test of the global null hypothesis of no difference between occupations.
Table 7. Lifestyle characteristics of Loddon Mallee Healthcare Worker COVID-19 Study sample during the COVID-19 pandemic.
Table 7. Lifestyle characteristics of Loddon Mallee Healthcare Worker COVID-19 Study sample during the COVID-19 pandemic.
VariablesUnit of MeasurementPublic Health ServicesPrivate Health and community Health ServicesTotal
Sample
(Unweighted)
Sample Weighted for
Non-Response #
Sample
(Unweighted)
Sample
(Unweighted) *
N = 1043N = 6528N = 266N = 1313
Freq%Freq.%Freq.%Freq.%
Body mass index (BMI) kgm2
<18.580.8621.020.8100.8
18.5–24.915815.199415.24416.520215.4
25.0–29.917316.6113717.43914.721316.2
30.0–39.917216.5122118.74717.722016.8
≥40403.82563.9124.5534.0
Missing49247.2285743.812245.961546.8
Alcohol intake (standard drinks/day)
Non-drinker/
low-risk drinker
(0–4)
45043.1287044.012346.257443.7
Moderate-risk
drinker
(5–7)
16015.3113717.43212.019214.6
High-risk drinker
(8–12)
605.83906.0186.8796.0
Missing37335.8213232.79335.046835.6
Smoking
Never50448.3326450.012948.563448.2
Ex-smoker20519.7140721.64918.425419.3
Current696.64877.5259.4967.3
Missing26525.4137021.06323.732925.0
Dietary intake
No. serves of vegetables/day
1 serve or less949.06399.8249.01189.0
2–3 serves 39838.2265840.711041.451038.8
4–5 serves 18117.4114817.65119.223217.7
6 serves or more403.82674.162.3463.5
Do not eat vegetables50.5450.7 50.4
Missing32568.8177127.17528.240230.6
Dietary intake
No. serves of fruit/day
1 serve or less31229.9205731.57929.739129.8
2–3 serves 34433.0229535.29435.344033.5
4–5 serves 343.32243.4124.5463.5
6 serves or more80.8661.020.8100.8
Do not eat fruit191.81191.841.5231.8
Missing32631.3176727.17528.240330.7
Sleep (PSQI) (α = 0.81, 0.74–0.85)
Poor sleep quality51649.5342952.511342.563148.0
Good sleep quality20119.3133720.57327.427420.9
Missing32531.2175026.88030.140731.0
# Sample characteristics weighted for baseline non-participation is the pseudo-population sample characteristics from the public hospital sample frame had the allocated number of participants responded. * Note—four participants did not provide information on whether they work within a public or private health service, thus the public and private health service subtotals do not add to the sample total. α = Cronbach’s alpha and 95% confidence interval (internal consistency)).
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McEvoy, M.; Caccaviello, G.; Crombie, A.; Skinner, T.; Begg, S.J.; Faulkner, P.; McEvoy, A.; Masman, K.; Bamforth, L.; Parker, C.; et al. Health and Wellbeing of Regional and Rural Australian Healthcare Workers during the COVID-19 Pandemic: Baseline Cross-Sectional Findings from the Loddon Mallee Healthcare Worker COVID-19 Study—A Prospective Cohort Study. Int. J. Environ. Res. Public Health 2024, 21, 649. https://doi.org/10.3390/ijerph21050649

AMA Style

McEvoy M, Caccaviello G, Crombie A, Skinner T, Begg SJ, Faulkner P, McEvoy A, Masman K, Bamforth L, Parker C, et al. Health and Wellbeing of Regional and Rural Australian Healthcare Workers during the COVID-19 Pandemic: Baseline Cross-Sectional Findings from the Loddon Mallee Healthcare Worker COVID-19 Study—A Prospective Cohort Study. International Journal of Environmental Research and Public Health. 2024; 21(5):649. https://doi.org/10.3390/ijerph21050649

Chicago/Turabian Style

McEvoy, Mark, Gabriel Caccaviello, Angela Crombie, Timothy Skinner, Stephen J. Begg, Peter Faulkner, Anne McEvoy, Kevin Masman, Laura Bamforth, Carol Parker, and et al. 2024. "Health and Wellbeing of Regional and Rural Australian Healthcare Workers during the COVID-19 Pandemic: Baseline Cross-Sectional Findings from the Loddon Mallee Healthcare Worker COVID-19 Study—A Prospective Cohort Study" International Journal of Environmental Research and Public Health 21, no. 5: 649. https://doi.org/10.3390/ijerph21050649

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