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Sleep problems during the COVID-19 pandemic by population: a systematic review and meta-analysis

Published Online:https://doi.org/10.5664/jcsm.8930Cited by:506

ABSTRACT

Study Objectives:

No systematic review or meta-analysis has yet been conducted to examine the impact of the pandemic on the prevalence of sleep problems among the general population, health care workers, or patients with COVID-19. Therefore, this systematic review was conducted to assess the impact and prevalence of sleep problems among those categories.

Methods:

American Psychological Association PsycINFO, Cochrane, Cumulative Index to Nursing and Allied Health Literature (CINAHL), EBSCOhost, EMBASE, Google Scholar, MEDLINE, ProQuest Medical, ScienceDirect, Scopus, and Web of Science from November 1, 2019 to July 5, 2020 were used. Additionally, 5 preprints servers (medRxiv.org; preprints.org; psyarxiv.com; arXiv.org; biorxiv.org) were also searched for papers accepted after peer review but not yet published and indexed. There was no language restriction. The random-effect models meta-analysis model was used with the DerSimonian and Laird methodology.

Results:

Forty-four papers, involving a total of 54,231 participants from 13 countries, were judged relevant and contributed to the systematic review and meta-analysis of sleep problems during COVID-19. The global pooled prevalence rate of sleep problems among all populations was 35.7% (95% confidence interval, 29.4–42.4%). Patients with COVID-19 appeared to be the most affected group, with a pooled rate of 74.8% (95% confidence interval, 28.7–95.6%). Health care workers and the general population had comparative rates of sleep problems, with rates of 36.0% (95% confidence interval, 21.1–54.2%) and 32.3% (95% confidence interval, 25.3–40.2%), respectively.

Conclusions:

The prevalence of sleep problems during the COVID-19 pandemic is high and affects approximately 40% of people from the general and health care populations. Patients with active COVID-19 appeared to have a higher prevalence rates of sleep problems.

Citation:

Jahrami H, BaHammam AS, Bragazzi NL, Saif Z, Faris M, Vitiello MV. Sleep problems during the COVID-19 pandemic by population: a systematic review and meta-analysis. J Clin Sleep Med. 2021;17(2):299–313.

INTRODUCTION

In late December of 2019, a series of cases of a novel virus, eventually named “2019 novel coronavirus (2019-nCoV/SARS-CoV-2),” causing respiratory infections in humans, was observed in the Chinese city of Wuhan.1 The virus causes the coronavirus disease 2019 (COVID-19) and spread rapidly worldwide. On January 30, 2020, the World Health Organization declared COVID-19 a Public Health Emergency of International Concern, and on March 11, 2020, a pandemic.2 COVID-19 has infected 14,832,283 patients globally, causing 612,266 deaths as of July 21, 2020.3

The COVID-19 pandemic is a considerable challenge to governments, health care systems, educational institutions, and the general public. In the absence of successful treatments or vaccines, measures to manage the spread of the virus were mainly social distancing, wearing masks, frequent hand hygiene and other measures to neutralize the virus if exposure has occurred, and quarantine.4 Outbreaks of infectious diseases, combined with measures to control the outbreaks, are associated with major psychologic distress and significant symptoms, including poor sleep quality.5,6 Data from an ongoing longitudinal study of a large representative sample of UK households indicated that 1 month after the World Health Organization’s declaration, the percentage of adults categorized as having mental health problems increased from approximately 23% in 2017–2019 to approximately 37% in late April 2020.7 This increase was particularly striking in young adults and females, an intersection where the risks of anxiety symptoms, depressive symptoms, and sleep problems are high.7

When facing the COVID-19 pandemic, sleep becomes essential because of its many benefits for mental and physical health. Lack of sleep can impair psychologic functioning and decision making, jeopardize immune response, increase accidents, lead to mood changes, increase medical expenditures, and render individuals more susceptible to contracting the virus because of poor concentration.8

No systematic review or meta-analysis has yet been conducted to examine the impact of the pandemic on the prevalence of sleep problems among the general population, health care workers, or patients with COVID-19; therefore, the prevalence and severity of sleep problems in different populations remains unknown. To address this knowledge gap, we conducted a comprehensive systematic review and meta-analysis of the prevalence of sleep problems in the face of the pandemic in different populations. These findings may prove helpful in developing effective strategies for screening and providing interventions to lower the negative outcome related to sleep problems.

METHODS

Search strategy

We conducted a scoping review of all available literature on sleep and COVID-19, followed by a systematic review and meta-analysis of original research in compliance with the recommendations and criteria described in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses checklist.9

Databases search

Two authors (HJ and ZS) conducted an electronic search in 10 electronic databases and 1 scholarly search engine: American Psychological Association PsycINFO; Cochrane; Cumulative Index to Nursing and Allied Health Literature (CINAHL); EBSCOhost; EMBASE; Google Scholar; MEDLINE; ProQuest Medical; ScienceDirect; Scopus; and Web of Science from November 1, 2019 to July 5, 2020. Additionally, 5 preprints servers (medRxiv.org; Preprints.org; psyarxiv.com; arXiv.org; biorxiv.org) were also searched for papers accepted after peer-review but not yet published and indexed. There was no language restriction.

The search strategy involved the crosschecking of keywords selected based on the Medical Subjects Headings and Boolean logic operators. The following keywords were used in an [All Fields] search:

“COVID-19” OR “2019-nCoV” OR “2019 coronavirus” OR “Wuhan coronavirus” OR “2019 novel coronavirus” OR “SARS-CoV-2” AND “sleep” OR “sleep medicine” OR “sleep disturbances” OR “sleep disorders” OR “sleep problems” OR “polysomnography” OR “sleep quality” OR “PSQI” OR “Pittsburg Sleep Quality Index” OR “insomnia” OR “circadian rhythm” OR “restless leg syndrome” OR “sleep apnea” OR “narcolepsy” OR “daytime dysfunction” OR “daytime sleepiness” OR “ESS” or “Epworth Sleepiness Scale” AND “prevalence” OR “incidence” OR “epidemiology” OR “rate” OR “frequency” OR “risk factors” OR “interventions” OR “treatment” OR “therapy” OR “management”.

Reference lists of the obtained studies were searched to find relevant articles and reviews and to make sure that all related publications were included in the current analysis.

The full-text versions of the obtained literature were screened, extracted, and analyzed for methodologic quality by 2 researchers (HJ and ZS). The processes were performed independently, and disagreements between reviewers were resolved by discussion and consensus with a third member of the research team (AB).

Selection criteria and outcomes

The primary outcome of the meta-analysis is the magnitude of sleep problems during the COVID-19 pandemic. Thus, we screened all observational and intervention clinical studies that studied the effect of COVD-19 on the sleep quantity and quality of different populations (eg, patients infected with COVID-19, health care workers, and the general population). Specific inclusion criteria for study selection were as follows: (1) publication date between November 1, 2019 and July 5, 2020; (2) original research articles published in the English, Spanish, German, Portuguese, French, Italian, and Arabic languages; and (3) studies that reported numerical values (eg, arithmetic mean with/without standard deviation or prevalence rate) for sleep problems. The following exclusion criteria were applied to retrieved articles to eliminate factors that may incur potential methodologic and quality issues: abstracts, infographics, letters, editorials, narrative reviews, opinions, and position statements. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses flow diagram of study selection is presented in Figure 1.

Figure 1: Preferred Reporting Items for Systematic Reviews and Meta-Analyses flow diagram of study inclusion.

Data extraction

Data extraction for complex meta-analysis guidelines10 were used to plan data extracting for this review. Data extraction involved “study details”, “epidemiological findings”, and “citation of the article”. Study details included: “last author”, “time of publication MM/YYYY”, “country of origin”, “type of study”, “objectives of the study”, “sample size”, “recruitment strategy”, “basic sample characteristics including age and %male”. Epidemiologic findings included the following: arithmetic mean with/without standard deviation or prevalence rate for “sleep quality” and “other significant findings.” The citation included the full citation details of the article, including the digital object identifier. We contacted the corresponding authors when needed for clarifications and to request more information.

Two independent researchers (HJ and ZS) used a Microsoft Excel Spreadsheet to extract the data independently; this was confirmed by a third member (NB).

Quality assessment of the studies

We used the Newcastle–Ottawa Scale adapted for cross-sectional studies by Herzog et al11 to assess the quality of the included studies. The Newcastle–Ottawa Scale for cross-sectional studies checklist contains 7 questions, which we divided into 3 domains: participants selection (questions 1–4), comparability (question 5), and outcome and statistics (questions 6 and 7). Scores range from 0 to 10. Details of the items used in Newcastle–Ottawa Scale and score interpretations are presented in Supplemental Table S1. Quality assessment was also performed in parallel with data extraction by the same researchers (HJ and ZS), and a consensus approach was used to determine the quality score for each study.

Data analysis

Random-effect models meta-analysis model were used with the DerSimonian and Laird methodology,12 assuming that the effect of interest is not the same in all studies and that the differences observed between them are only caused by sampling errors (variability within the studies). The heterogeneity of the estimates of the sample size effect throughout these studies was quantified by the I2 statistic. The heterogeneity between the studies was assessed by Cochran's Q test and τ2 statistics. As the estimates of the prevalence of sleep problems can vary according to the types of populations involved, subgroup meta-analyses were used to assess whether the sleep problems in each of the populations influenced the joint estimate. The results are presented in a forest plot as a point estimate with 95% confidence intervals (95% CIs). A leave-one-out sensitivity analysis was performed by iteratively removing 1 study at a time to confirm that any single study did not drive our findings. Subgroup analysis was performed to examine differences between groups based on categorical variables (eg, research population, research measure). Subgroup analysis was only reported if there were 3 or more studies available for analysis. Meta-regression techniques were applied to analyze for continuous covariates of sleep problems; we used 2 covariates, mean age, and proportion of male sex. Publication bias was assessed using funnel plots to visually assess publication bias. For robust assessment of publication bias, Kendall’s tau rank order correlations and Egger's regression were computed.13 It was planned a priori that when needed, Duval and Tweedie’s trim and fill procedure was used to calculate adjusted point estimates to correct for funnel plot asymmetry arising from potential publication bias.14 Data analyses were performed using Comprehensive Meta-Analysis version 3.0, and visualizations were made using R software for statistical computing version 4.0.2 using the package metafor.

RESULTS

Characteristics of included literature

The initial search was conducted up to June 10, 2020 and was updated to July 5, 2020. A total of 1273 records were identified through database searching and other sources. When duplicates were removed, 371 records remained. A total of 178 potential papers were full text screened. Of these, 134 papers were excluded including narrative and systematic reviews, editorials, commentaries, letters to the editor, position statements irrelevant literature, duplicates, or wrongly classified papers.

Three major themes were identified in the excluded literature; the impact of COVID-19 on the practice of sleep medicine; the importance of prioritization the services for individuals with sleep disorders (especially breathing-related sleep disorders) during the pandemic; and the role of melatonin and other supplements on regulating sleep-wake rhythm.

Forty-four papers,6,1557 involving a total of 54,231 participants from 13 countries, were judged relevant and contributed to the systematic review and meta-analysis of sleep problems during COVID-19 (Table 1; Supplemental Table S1). Thirty-seven papers (84%)6,15,17,1922,2427,2940,4246,4853,55,57 were published in peer-reviewed journals, and the remaining 7 (16%)16,18,23,28,41,47,56 were either accepted or provisionally accepted for publication and were available from a preprint server.

Table 1 Selected characteristics, methods, and major findings of the included studies in this review about sleep problems during COVID-19.

SNFirst AuthorYear/MonthCountryThemePopulationMethodsMeasuresQuality*
1Abdulah2020/05IraqQuantifying the severity of sleep difficulty and its association with duration of dealing with suspected/confirmed cases of (COVID-19) in physicians.268 physicians. Age: 35.06 ± 7.61 Male: 188 (70.1%)Cross-sectional, convenience samplingAIS PSS8
2Ahmad2020/05IndiaExamining the correlation between anxiety and socio-demographic factors during Covid19 lockdown among the general Indian population.398 general population. Age: 30.3 ± 9.28Cross-sectional, convenience samplingGAD-78
3Ammar2020/05GermanyCreating scientific data to analyzing risk-factors for the psychosocial strain during the COVID-191047 general population. Male: 482 (46%)Cross-sectional, convenience samplingResearcher developed7
4Bai2020/04ChinaEvaluating Sleep quality and working pressure in HCWs118 healthcare workers 12 HCWs (Acquired COVID-19) 106 Healthcare workers (Healthy) Age: 30.5 ± 5.3 yearsCross-sectional, convenience samplingPSQI NSI7
5Beck2020/05FranceExamine sleep quality among 1005 general population and COVID-19 patients.1005 general population.Cross-sectional, Convenience samplingResearcher developed7
6Bohlken2020/05GermanEvaluating the effects of the COVID-19 pandemic On German psychiatrist and neurologist.396 psychiatrists and neurologists.Cross-sectional, convenience samplingResearcher developed7
7Casagrande2020/05ItalyAssessing psychological effects of the COVID-19 outbreak on aspects of sleep quality, general anxiety symptomatology, and psychological distress.2291 general population. Age: 18.89 ± 11.5 Male: 580 (25.3%)Cross-sectional, convenience samplingGAD-7 PGWB PSQI PCL-58
8Cellini2020/05ItalyInvestigating the change in digital media use before going to bed, sleep quality, and their association with depression, anxiety, and stress levels.1, 310 young adults aged 18 to 35 years Age: 23.91 ± 3.60 yearsCross-sectional, convenience samplingPSQI DASS‐218
9Garcia-Priego2020/05MexicoEstimating the prevalence and distribution of anxiety and depression and assessing the correlation with internet addiction during the COVID-19 outbreak.561 general population Age: 30.7 ± 10.6 years Male: 163 (29%)Cross-sectional, convenience samplingHADS IAT8
10Goodman-Casanova2020/05SpainInvestigating the impact of confinement on the health status and well-being of community-dwelling and examine the consequence of a television-based assistive integrated technology during COVID-19.93 general population (older adults). Age: 73.34 ± 6.07 Male: 32 (35%)Cross-sectional, convenience samplingResearcher developed7
11Hartley2020/05FranceAnalyzing the sleep evolution of during the COVID-19 and identifying associated factors1, 777 COVID-19 patients in quarantine. Age: 25–54 years Male: 409 (23%)Cross-sectional, convenience samplingResearcher developed7
12Huang2020/04ChinaExamining the mental health burden of the public during the COVID-19 outbreak and to determining the high-risk group.7, 236 general population Age: 35.3 ± 5.6 years Male: 3284 (45.4%) were males.Cross-sectional, convenience samplingGAD-7 CES-D PSQI8
13Innocenti2020/06ItalyExamine sleep disorders in Italy amid pandemic COVID-19.1035 general population. Age: 30–50 years range Male: 177(17.1)%Cross-sectional, Convenience samplingPSQI8
14Jahrami2020/07BahrainAssess the prevalence of stress and poor sleep quality and its association with demographic among healthcare workers professionals.257 healthcare workers (129 frontline healthcare workers and 12 nonfrontline healthcare workers). Age: 40.2 ± 9.7 Male: 77 (30.0%)Cross-sectional, Simple random samplePSS PSQI8
15Jung2020/05GermanyExamining mental health during the lockdown.3, 545 general population. Age: 40.36 ± 11.70 Male:539 (15.2%)Cross-sectional, convenience samplin.PHQ-D/9 PHQ-4 WHO-58
16Kaparounaki2020/05GreeceExamining the impact of the lockdown on the mental health behaviors in university students.1,000 general population (university students). Age: 22.07 ± 3.3 years Male: (30.99%)Cross-sectional, convenience samplingSTAI CES-D RASS8
17Killgore2020/05USAAssessing Anxiety about COVID-19 and it’s the association with insomnia severity and suicidal ideation.1, 013 adult general population. Age: Ranging 18-35 years Male: 446 (44%)Cross-sectional, convenience samplingISI PHQ-98
18Kokou-Kpolou2020/05FranceEstimating the prevalence of clinical insomnia and its contributing factors during COVID-19.566 adult general population. Age: 30.06 years Male: 142 (25%).Cross-sectional, convenience samplingISI UCLA8
19Li2020/06ChinaExamine potential risk factors associated with sleep Disturbances during pandemic COVID-19.1970 general population. Age: 37.81 ± 11.00 years. Male: 650(33)%Cross-sectional, Convenience samplingSDST8
20Liguori2020/05ItalyExamining the sNS in patients with COVID-19 infection.103 patients with COVID-19 infection hospitalized at the University Hospital of Rome. Age: 55 ± 14.65 Male: 94 (91.5%)Cross-sectional, convenience samplingsNS7
21Lin2020/06ChinaExamine sleep disorders in China amid pandemic COVID-19.5641 general population. Age: range 18+ years Male: 1685 (29.9%)Cross-sectional, Convenience samplingISI PHQ-9 GAD-7 ASDS8
22Liu2020/05ChinaInvestigating the prevalence and predictors of posttraumatic stress symptoms (PTSS) and sleep problems during COVID-19.285 residents in Wuhan and surrounding cities age > 18 years. General population. Age: ≤ 35 = 136 (47.7%) > 35 = 149 (52.3%) Male: 118 (45.6%)Cross-sectional, convenience samplingPCL-5; PSQI8
23Liu2020/04ChinaIdentifying the clinical characteristics of suspected COVID-19 schizophrenic hospitalized patients in Hubei Province21 (infected) hospitalized patients with schizophrenia with suspected COVID-19 in the isolation ward in Wuhan. Age: 43.1 ± 2.6 Male: 9 (42.9%) 30 (not infected) hospitalized patients with schizophrenia (in the general ward in Yichang Age: 45.0 ± 9.2 Male: 15 (50%)Cross-sectional, convenience samplingPANSS PSS HAMD HAMA PSQI6
24Qi2020/05ChinaEvaluating sleep disturbances of Chinese frontline medical workers (FMW) compared to non-FMW under the outbreak of COVID-19.1,306 medical workers Age: 33.1 ± 8.4 Male: 256 (19.6%)Cross-sectional, convenience samplingPSQI AIS VAS8
25Roy2020/06IndiaStudy the knowledge, attitude, and anxiety level during the COVID-19 pandemic662 adult general population. Aged 18 years or more. Age: 29.09 ± 8.83 years Males: 332 (48.6%)Cross-sectional, observational, snowball sampling techniqueResearcher developed7
26Sheng2020/03ChinaExamining the psychological status and sleep quality during the outbreak of COVID-19.95 nursing Interns isolated a general teaching hospital Age: (21.26 ± 1.01) years Male: 6 (6.5%)Cross-sectional, convenience samplingSAS SDS PSQI8
27Stanton2020/06AustraliaChanges in physical activity, sleep, tobacco and alcohol use in Australian adults during COVID-191491 general adult population. Age: 50.5 ± 14.9 Male: 493 (33%).Cross-sectional, Convenience snowball samplingResearcher developed7
28Sun2020/03ChinaEstimating the prevalence and exploring risk factors of acute posttraumatic stress symptoms (PTSS) amid the outbreak of COVID-19.2091 general population Age: 18-60 years Male: 816 (39%)Cross-sectional, convenience samplingPCL-58
29Tang2020/05ChinaEstimating the prevalence of PTSD and depression.2485 home-quarantined college students. Age: 19.81 ± 1.55 Male: 975 (39.2%)Cross-sectional, convenience samplingPCL-C t PHQ-97
30Tu2020/05ChinaExamine sleep disorders in China amid pandemic COVID-19.100 frontline workers. Female nurses. Age: 34.44 ± 5.85 years Male: NA (0%)Cross-sectional, Convenience samplingPSQIPHQ-9 GAD-77
31Vitale2020/05ItalyObjectively and subjectively assess the consequence of severe symptoms of Covid-19 infection on sleep quality through wrist actigraphy.4 COVID-19 patients. Age: 54 ± 221 Male: 3(75)%Case-seriesPSQI Wrist actigraphy6
32Voitsidis2020/05GreeceExamining sleep disturbance during the COVID-19 pandemic.2, 427 young adults. Age: 18-30 years Male: 578 (23.8%)Cross-sectional, convenience samplingAIS IUS JGLS PHQ-28
33Wang2020/05ChinaInvestigating the influence of the COVID-19 outbreak on sleep quality of healthcare workers.123 healthcare workers. Age: 33.75 ± 8.41 years Male: 12 (10%)Cross-sectional, convenience samplingPSQI SAS SDS8
34Wu2020/06 PreprintCanadaDeterminants of self-reported symptoms for COVID-19.4,240 adult general population. Age: 47.3% were aged 18-45 years Males: 2031 (47.9%)Representative, stratified randomizedResearcher developed7
35Wu2020/05ChinaDescribing the differences in psychological factors and sleep status of medical staff in the fight against COVID-19 and giving exercises evidence that plays a role in relieving the stress and improve sleep quality.120 medical staff Group 1: 60 medical staff worked at the designated hospital (frontline workers), (26.7%) were males Group 2: 60 medical staff worked at the nondesignated hospital (nonfrontline workers) and (25%) were males Age: 33.5 ± 12.4 years, the age range was 25–59 yearsCross-sectional, convenience samplingSCL-90 SAS SDS PCL-C PSQI8
36Xiao2020/03ChinaExamining the effects of social capital on the sleep quality of individuals self-isolated at home for 14 days.170 general population Age: 37.78 ± 4.12 Male: 101 (59.4%)Cross-sectional, convenience samplingPSCI-16 SAS SASR PSQI8
37Xiao2020/03ChinaIdentifying the social support influence on sleep quality and function of medical staff who treated patients with COVID-19 using SEM.180 medical staff who treated patients with COVID-19 infection 28.3% were malesCross-sectional, convenience samplingSAS GSES SASR PSQI SSRS8
38Yifan2020/04ChinaAssessing the symptoms and causes of SSD among ICU nurses treating COVID-19 pneumonia.140 nurses working at COVID-19 pneumonia ICU in Wuhan Age: 29.35 ± 4.92 Male: 22 (15.7%)Cross-sectional, convenience samplingSSD6
39Yin2020/05ChinaAssessing posttraumatic stress symptoms (PTSS) and their sleep quality after one-month of stress.371 healthcare workers. Age: 35.30 ± 9.48 years Male: 143 (38.5%)Cross-sectional, snowball samplingPCL-5 PSQI7
40Zhang2020/05ChinaAssessing the adverse impact of the COVID-19 outbreak on the mental health of college students.66 college students (general population). Age: 20.70 ± 2.11 years Male: 25 (37.8%).Cross-sectional, snowball sampling. Follow-up (longitudinal element of subsample)IPAQ-S PSQI DASS-21 BPAQ6
41Zhang2020/03ChinaAssessing sleep Disturbances and posttraumatic stress symptoms (PTSS) after the massive outbreak of COVID-19.2027participants 230 participants exposed in Wuhan 1997 participants non exposed in Wuhan. Age: 35.47 ± 11.32 Male: 788 (38.8%)Cross-sectional, convenience samplingPSQI PCL-58
42Zhao2020/05ChinaExamining the impact of perceived stress on the sleep quality of the nondiseased general public during COVID-19.1,630 general population. Age: 29.17 ± 10.58 yearsCross-sectional, convenience samplingPSS PSQI SRAS RSE8
43Zheng2020/05ChinaInvestigating physical activity (PA) levels, sedentary behavior (SB) and sleep among young adults during the COVID-19 epidemic, and the change in these behaviors before and during the pandemic.Cross-sectional 631 young adults living in Hong Kong. Age: 18-35 years. Male: 245 (38.8%) Longitudinal: 70 young adults.Cross-sectional, convenience sampling. The subsample was followed in a longitudinal designSBQ PSQI8
44Zhou2020/06ChinaAssess the prevalence of poor sleep quality and its association with demographic among frontline health professionals.1, 931 frontline health professionals Age:35.08 ± 8.04 Male: 88 males (4.6%)Cross-sectional, Convenience snowball samplingPSQI8

Results of cutoffs included in the analyses are the recommended by each scale (eg, PSQI = 5, ISI = 15). *Quality score measured using the Newcastle-Ottawa Scale customized for cross-sectional analysis. Further details about the domains, items, and score interpretation are available in Supplemental Table S1. AIS = Athens Insomnia Scale, ASDS = Acute Stress, BPAQ = Buss-Perry Aggressive Questionnaire, CES-D = The Center of Epidemiological Studies Depression Scale, DASS-21 = Depression Anxiety Stress Scale, With 21 Self-Reported Items, FMW = Frontline Medical Workers, GAD = General Anxiety Disorder, GAD-7 = Generalized Anxiety Disorder Scale, GAD-7 = Generalized Anxiety Disorder-7, HADS = Hospital Anxiety and Depression Scale, HAMA = Hamilton Anxiety Rating Scale, HAMD = Hamilton Depression Rating Scale, HCWS = Healthcare Workers, IAT = Internet Addiction Test, ICU = Intensive Care Unit, IPAQ-S = Short Version of International Physical Activity Questionnaire, ISI = Insomnia Severity Index, ISI = Insomnia Severity Index, IUS = Intolerance to Uncertainty Scale, JGLS = De Jong Gierveld Loneliness Scale, NSI = Nurse Stress Index, PANSS = Positive and Negative Syndrome Scale, PCL-5 = Posttraumatic Stress Disorder Checklist For DSM-5, PGWB = General Well-Being Questionnaire, PHQ-2 = Patient Health Questionnaire 2 items, PHQ-4 = The Patient Health Questionnaire 4 items, PHQ-9 = The Patient Health Questionnaire 9 items, PSCI-16 = Personal Social, PSQI = Pittsburgh Sleep Quality Index, PSS = Perceived Stress Scale, PTSD = Post-Traumatic Stress Disorder, RASS = Richmond Agitation Sedation Scale, RSE = Rosenberg Self-Esteem Scale, SAS = Self-Rating Anxiety Scale, SASR = Stanford Acute Stress Reaction, SBQ = Sedentary Behavior Questionnaire, SCL-90 = Symptom Checklist 90, SDS = Self-Rating Depression Scale, SDST = Sleep Disturbance and Suicidal Thoughts, SEM = Structural Equation Modeling, sNS = Subjective Neurological Symptoms, SSD = Somatic Symptom Disorder, SSRS = Social Support Rate Scale, STAI = State-Trait Anxiety Inventory, UCLA = Loneliness Scale, VAS = Visual Analog Scale, WHO-5 = World Health Organization–Wellbeing Index.

Forty studies (91%)6,1530,3235,3747,51,5357 reported a prevalence rate defined as the proportion of individuals with sleep problems divided by the total number of people in the sample. Four (9%)36,49,50,52 studies only reported a mean score and standard deviation of a sleep scale.

All the studies were published after March 2020. Twenty-seven studies (61%)16,17,19,2124,2732,34,35,38,4042,45,47,49,5356,58 focused on the general population; thirteen studies (30%).6,15,18,20,37,39,43,46,48,5052,57 Only a few studies, 4 (9%),25,33,36,44 investigated the sleep problems of patients infected with COVID-19. The median number of participants per study was 566 participants. The mean quality score, according to the Newcastle–Ottawa Scale, is 7.5 ± 0.7, ranging from 6 to 8 points (Table 1).

All 44 studies used observational, cross-sectional research design. A range of research measures were used. Thirty-five (80%) of the studies used sleep-specific measures. Altogether, 27 (61%) of the studies used a well-established validated scale: 2 (5%) used the Athens Insomnia Scale15,45; 3 (7%) used the Insomnia Severity Index (ISI)30,31,34; and 22 (50%) used the Pittsburgh Sleep Quality Index (PSQI).6,18,21,22,27,3537,39,43,44,46,4850,5256,58 Eight (19%)17,19,20,24,25,38,40,47 used researcher-developed measures designed specifically to measure sleep problems. The remaining 9 (20%)16,23,28,29,33,41,42,51,59 used a subsection or cluster of questions to report sleep problems using an established psychologic measure.

Meta-analysis of sleep problems

Meta-analysis of the prevalence of sleep problems in all populations using all available studies (K = 40, n = 53,489) yielded an estimated pooled prevalence rate of 35.7% (95% CI, 29.4–42.4%) with heterogeneity (Q = 7477[39], τ2 = 0.8, I2 = 99.5%, P < .001). The raw prevalence estimates for sleep problems reported among all populations using any measure ranged from 8% to 91%. Figure 2 illustrates the forest plot of the meta-analysis of sleep problems in all populations using all measures. Sensitivity analysis revealed that no study affected the prevalence estimate by more than 1%. Results of the sensitivity analysis suggest that the overall pooled prevalence is robust and powered by the methodologic quality of each research study included. Visual inspection to funnel plot (Supplemental Figure S1) indicated no observed publication bias. Kendall’s τ without continuity correction was −0.04 (P = .70), and Egger’s regression was P = .72.

Figure 2: Meta-analysis of the prevalence of sleep problems (all populations, all measures). Cases refer to persons with positive sleep problem.

Subgroup analysis by country of research origin found that reports from China (K = 18, n = 28,000) yielded an estimated pooled prevalence of sleep problems of 26.5% (95% CI, 26–27.1%) with heterogeneity (Q = 3217, τ2 = 0.8, I2 = 99.5%, P < .001). Italy and France had higher pooled prevalence rates of 55% (95% CI, 53.6–56.5%) and 50.8% (95% CI, 49–52.6%), respectively. Finally, Germany had a similar prevalence rate to that found overall (38.8%; 95% CI, 37–40.3%).

Subgroup analysis of sleep problems by population showed that most of the studies were conducted on the general population, followed by health care providers, and last on patients infected with SARS-COV-2 and those with symptoms of COVID-19. Meta-analysis of the prevalence of sleep problem in the general population (K = 26, n = 46,751) yielded an estimated pooled prevalence rate of 32.3% (95% CI, 25.3–40.2%) with heterogeneity (Q = 6137[25], τ2 = 0.8, I2 = 99.5%, P < .001). Health care workers (K = 11, n = 4854) had a slightly higher prevalence of sleep problems (36.0%; 95% CI, 21.1–54.2%) with heterogeneity (Q = 1048[10], τ2 = 1.6, I2 = 99%, P < .001). Patients infected with COVID-19 (K = 3, n = 1884) appeared to be the most affected group with a prevalence of sleep problems of 74.8% (95% CI, 28.7–95.6%) with heterogeneity (Q = 50[2], τ2 = 2.7, I2 = 96%, P < .001). Detailed results are presented in a subgroup analysis forest plot in Supplemental Figure S2.

Moderator analysis revealed that higher age (β = 0.13, P = .001) and male sex (β = 3.6, P = .001) are associated with higher prevalence of sleep problems in the subgroup of patients with COVID-19.

The PSQI was used in a total of 18 studies (n = 20,570) to estimate sleep problems. Nine of these studies focused on the general population (n = 16,516), 8 studies focused on health care workers (n = 4854), and 1 study focused on patients (n = 4). The overall pooled prevalence of sleep problems for all populations using the PSQI was 39.6% (95% CI, 29.6–50.6%) with heterogeneity (Q = 2933[17], τ2 = 0.8, I2 = 99.5%, P < .001). Figure 3 illustrates the forest plot of meta-analysis of sleep problems in all populations using the PSQI. Sensitivity analysis revealed that no study affected the prevalence estimate by more than 1%. The sensitivity analysis results suggest that the overall pooled prevalence is robust and powered by the methodologic quality of each research study. Visual inspection of the funnel plot (Supplemental Figure S3) indicated no observed publication bias. Kendall’s τ without continuity correction = −0.04 (P = .80), and Egger’s regression was P = .42. One possible explanation for the large heterogeneity is that different sleep measures assess symptoms across somewhat different time frames (eg, PSQI and Athens Insomnia Scale = past month, ISI = past 2 weeks). Thus, given the rapidly evolving nature of the COVID-19 pandemic, this makes it harder to generalize across studies.

Figure 3: Meta-analysis of the prevalence of sleep problems (all populations, PSQI only). Cases refer to persons with positive sleep problem. PSQI = Pittsburgh Sleep Quality Index.

Subgroup analysis of sleep problems using the PSQI indicated that the general population and health care workers had comparable sleep problems, with rates of 37.9% (95% CI, 25.2–52.4%) and 39.7% (95% CI, 21.2–61.6%), respectively. Details of the analyses are presented in Table 2 and illustrated in Supplemental Figure S4.

Table 2 Meta-analysis of sleep problems during COVID-19: by population and by research measure.

ComponentKNRandom-Effects Meta-AnalysisHeterogeneityModeratorsPublication Bias
Pooled Results [95% CI]I2τ2QAgeSex (%Male)
Sleep problems (all populations, all measures*)4053,48935.7% [29.4%–42.4%]99.5%0.87477 (39)NSNSKendall’s P = .70, Egger’s P = .72
Sleep problems (general population, all measures)2646,75132.3% [25.3%–40.2%]99.5%0.86137 (25)NSNSKendall’s P = .80; Egger’s P = .90
Sleep problems (health care workers, all measures)11485436.0% [21.1%–54.2%]99%1.61048 (10)NSNSKendall’s P = .70; Egger’s P = .80
Sleep problems (COVID-19 patients, all measures)393274.8% [28.7%–95.6%]96%2.750 (2)P = .001P = .001Kendall’s P = .60; Egger’s P = .80
Sleep problems (all populations, PSQI only)1820,57039.6% [29.6%–50.6%]99.5%0.82933 (17)NSNSKendall’s P = .80; Egger’s P = .42
Sleep problems (general population, PSQI only)916,51637.9% [25.2%–52.4%]99.6%0.82018 (8)P = .001NSKendall’s P = .80; Egger’s P = .42
Sleep problems (health care workers, PSQI only)8485439.7% [21.2%–61.6%]99%1.6853 (7)NSNSKendall’s P = 1.0; Egger’s P = .96
Sleep problems (general population, SD)6853825.2% [9.3%–52.6%]99.7%2.21774 (5)NSNSKendall’s P = .85; Egger’s P = .96
Sleep problems (general population, ISI)3722029.7% [11.9%–56.9%]99.6%1.1531 (2)NSNSKendall’s P = .60; Egger’s P = .71
Mean sleep quality (all populations, PSQI)1592307.1 [6.3–8.0]99.1%2.41716 (14)NSNSKendall’s P = .08; Egger’s P = .045
Mean sleep quality (general population, PSQI)447226.0 [5.3–6.8]98%0.6182 (3)NSP = .04Kendall’s P = 1.0; Egger’s P = .47
Mean sleep quality (health care workers, PSQI)944837.7 [6.1–9.2]99%5.41358 (9)NSNSKendall’s P = .14; Egger’s P = .13
Mean (C1) self-reported sleep quality (health care workers, PSQI)628971.3 [0.3–2.3]99.8%1.51219 (5)NSNSKendall’s P = .34; Egger’s P = .02
Mean (C2) sleep latency (health care workers, PSQI)1.5 [0.9–2.2]99.8%0.72662 (5)NSNSKendall’s P = .57; Egger’s P = .38
Mean (C3) sleep duration (health care workers, PSQI)0.9 [−0.2 to 2.0]99.9%2.017713 (5)NSNSKendall’s P = .34; Egger’s P = .34
Mean (C4) habitual sleep efficiency (health care workers, PSQI)0.9 [−0.1 to 1.9]99.9%1.513197 (5)NSNSKendall’s P = .85; Egger’s P = .40
Mean (C5) sleep disturbances (health care workers, PSQI)1.4 [0.4–1.9]99.9%1.09829 (5)NSNSKendall’s P = .60; Egger’s P = .20
Mean (C6) use of sleep-promoting medications (health care workers, PSQI)0.7 [−0.1 to 1.6]99.9%1.214010 (5)NSNSKendall’s P = .85; Egger’s P = .15
Mean (C7) daytime dysfunction (health care workers, PSQI)1.0 [−0.1 to 2.0]99.9%2.017641 (5)NSNSKendall’s P = .85; Egger’s P = .72

CI = confidence interval, Cochran’s Q = calculated as the weighted sum of squared differences between individual study effects and the pooled effect across studies, with the weights being those used in the pooling method, I2= statistic describing the percentage of variation across studies due to heterogeneity rather than chance, K = number of studies, Moderators = a method of moments estimator for random effect multivariate meta-analysis, N = number of participants, NS = not significant, 𝜏-squared = the extent of variation among the effects observed in different studies (between-study variance) in a random-effects meta-analysis, Publication bias was not observed in Funnel plot. *Measures used to estimate sleep problems were as follows: AIS = Athens Insomnia Scale, GAD-7 = General Anxiety Disorder-7, HADS = Hospital Anxiety and Depression Scale, ISI = Insomnia Severity Index, PCL5 = Posttraumatic Stress Disorder Checklist For DSM-5, PHQ-9 = Patient Health Questionnaire-9, PSQ = Psychological Stress Questionnaire, PSQI = Pittsburgh Sleep Quality Index, RASS = Richmond Agitation Sedation Scale, RD = Researcher-developed, SDS = Self-Rating Depression Scale, SNS = Subjective Neurological Symptoms.

Moderator analysis revealed that age (β = 0.01, P = .001) was associated with a higher prevalence of sleep problems in the general population subgroup only. Individuals with younger age appeared to have a greater magnitude of sleep problems during the pandemic when measured using PSQI.

Researcher-developed measures and the ISI were commonly used measures among the general population. Meta-analysis of sleep problems measured using researcher-developed measures in the general population (K = 6, n = 8538) yielded an estimated pooled prevalence rate of 25.2% (95% CI, 9.3-52.6%) with heterogeneity (Q = 1774[5], τ2 = 2.2, I2 = 99.7%, P < .001). Details of the analyses are presented in Table 2 and illustrated in Supplemental Figure S5. Three studies (K = 3, n = 7220) reported prevalence of sleep problems using ISI among the general population, and results yielded a prevalence rate of 29.7% (95% CI, 11.9–56.9%) with heterogeneity (Q = 532[2], τ2 = 1.1, I2 = 99.6%, P < .001). Details of the analyses are presented in Table 2 and illustrated in Supplemental Figure S6.

The mean PSQI score was reported for 15 studies (K = 15, n = 9230). The global mean PSQI for all populations was 7.1 (95% CI, 6.3–8.0) with heterogeneity (Q = 1716[14], τ2 = 2.4, I2 = 99%, P < .001). Scores for the general population were reported in 6 studies (K = 6, n = 4722), and the mean PSQI was 6.0 (95% CI, 5.3–6.8) with heterogeneity (Q = 182[3], τ2 = 0.6, I2 = 98%, P < .001). Health care workers had higher mean score (K = 9, n = 4483), with global PSQI score of 7.7 (95% CI, 6.1–9.2) with heterogeneity (Q = 1358[9], τ2 = 5.4, I2 = 99%, P < .001). Details of the analyses are presented in Table 2 and illustrated in Figure 4. Visual inspection to funnel plot (Supplemental Figure S7) indicated no observed publication bias. Subgroup analysis by population of mean PSQI score is available in Supplemental Figure S8.

Figure 4: Meta-analysis of mean global PSQI (all populations). PSQI = Pittsburgh Sleep Quality Index.

Six studies reported the individual 7 components of the PSQI. Details of the analyses are presented in Table 2 The results of this analysis indicated that sleep latency, sleep disturbances, and sleep duration had the highest scores, with 1.5, 1.4, and 1.3, respectively.

DISCUSSION

These meta-analyses aimed to comprehensively describe the pooled prevalence of sleep problems in several populations using different measurement measures worldwide during the ongoing COVID-19 pandemic. First, the global pooled prevalence rate of sleep problems among all populations is 35.7% (95% CI, 29.4–42.4%). Second, patients with COVID-19 appeared to be the most affected group, with a pooled rate of 74.8% (95% CI, 28.7–95.6%). Third, health care workers and the general population had comparative rates of sleep problems with rates of 36.0% (95% CI, 21.1–54.2%) and 32.3% (95% CI, 25.3–40.2%), respectively. Similar findings on sleep problems were obtained using the PSQI, suggesting that health care providers and the general population were affected comparatively with rates of 39.7% (95% CI, 21.2–61.6%) and 37.9% (95% CI, 25.2–52.4%), respectively. Fourth, researcher-developed measures appeared to be less sensitive in detecting sleep problems, with prevalence rate of 25.2% (95% CI, 9.3–52.6%), compared with the well-established sleep self-assessment questionnaires such as the PSQI (39.6%; 95% CI, 29.6%–50.6%). Also, The PSQI captures a very broad range of sleep-related issues (eg, nightmares, snoring, sleep medication use), which may explain the higher prevalence rates compared with the Athens Insomnia Scale, ISI, or researcher-developed measures.

In the current meta-analysis, the prevalence of sleep problems among the general population of 32.3% (95% CI, 25.3–40.2%) appeared to be higher than a previous meta-analysis reporting the prevalence of sleep problems in the adult general population in China (15.0%; 95% CI, 12.1–18.5%).60 Another meta-analysis reported the prevalence of sleep problems among older adults with a pooled prevalence of 35.9% (95% CI, 30.6–41.2%).61 Interestingly, a recent meta-analysis that summarized the prevalence of stress, anxiety symptoms, and depressive symptoms in the general population during the COVID-19 pandemic reported prevalence rates of 29.6% (95% CI, 24.3–35.4%), 31.9% (95% CI, 27.5–36.7%), and 33.7% (95% CI, 27.5–40.6%],62 respectively, comparable to our findings of sleep problems. The overlapping prevalence rates between psychologic distress symptoms and our findings of sleep problems point to the potential bidirectional relationships between sleep and psychiatric comorbidities, especially when more comorbidities are present (eg, anxiety and depression), suggesting that sleep specialists should consider psychiatric comorbidities when treating sleep problems and vice versa.

It was expected that patients with COVID-19 would have the highest frequency of disturbed sleep (∼75%), because the core symptoms of the disease involve coughing, fever, and difficulty in breathing, all of which have been associated with sleep problems.63,64 The higher risk of sleep problems among patients with COVID-19 might also be attributable to physical pain and side effects of medications administered for the treatment of the virus.65 One might argue that the higher prevalence rates of sleep problems among patients with COVID-19 are a byproduct of a smaller study sample size. However, it is important to consider this finding seriously, until larger better-designed studies are available.

Prevalence of sleep problems among health care using all measures (36.0%; 95% CI, 21.1–54.2%) or PSQI only (39.7%; 95% CI, 21.2–61.6%) are similar to the pooled prevalence among Chinese health care professionals before the pandemic (39.2%; 95% CI, 36.0–42.7%).66 This suggests that reporting sleep problems has not increased among health care working during the COVID-19 pandemic.

Two meta-analyses on nursing staff before the pandemic demonstrated that the pooled prevalence of sleep problems using the PSQI in Iran67 and China68were 64% (55–73%) and 61.0% (55.8–66.1%), respectively. In the current meta-analysis, one of the included studies focused only on female nurses and reported a prevalence rate of 60%.43 This may imply that the discrepancy is because of heterogeneous health care workers populations. This may suggest that the stress of nursing and/or being female may be the cause of increased sleep problems.

Thus, future meta-analyses may consider investigating various subgroups of health care workers (eg, nurses vs physicians, frontline vs nonfrontline). Nearly one-third of health care workers were found to have poor sleep quality with greater severity among frontline workers compared with second-line workers.69 Similarly, when sleep quality was compared among health care workers providing care to COVID-19–positive cases vs those working negative cases, it was found the sleep quality was poorer among those posted in COVID-19–positive hospitals.48 These studies suggest that poorer sleep quality was associated with exposure to COVIS-19–positive patients. Furthermore, these health care workers had higher scores on somatization, depression, anxiety, and stress scales.48 Symptoms of depression, anxiety, and stress among frontline medical workers who were treating patients with COVID-19 are related to social support and sleep quality, as reported in a similar study conducted among self-isolated patients.49,50

The prevalence of sleep problems observed dropped significantly when a subgroup analysis was performed using researcher-developed assessment measures, but this was not noted in the global analysis and when comparing the PSQI with the other validated measures. A recent meta-analysis of diagnostic accuracy of 3 screening measures (PSQI, ISI, Athens Insomnia Scale) for sleep problems indicated that summary estimates of sensitivity and specificity did not differ significantly among the 3 measures,70 but this was apparently not the case for researcher-developed assessment instruments.

Because of the rapid publication of COVID-19 research, this meta-analysis serves as a summary of the research literature for only the first 8 months of the pandemic. The major strength of this meta-analysis is the timely, large-pooled analysis stratified by target population and measurement measure. However, 2 limitations should be addressed. First, heterogeneity remained high after subgroup analyses and meta-regression, but heterogeneity cannot be eliminated in large epidemiologic meta-analyses.61,71 Second, additional investigation of other lifestyle factors such as physical activity, smoking, and substance use need to be considered when adjusting for moderators, with special emphasis on adjusting for stress-related disorders including posttraumatic stress disorder, adjustment disorders, anxiety, and depression. Future original research might also consider the role of social confounding factors (eg, change in marital status or employment) and their impact on sleep.

Cellini et al22 reported in a sample of 1310 Italians that sleep problems were greater among people with a higher level of depression, anxiety, and symptoms of stress. It has also been shown that social support improves sleep quality among people who were self-isolated at home for 14 days because of COVID-19,49 because patients with greater support had lower anxiety and stress.

Sleep problems among the general population cannot be ignored because persistent sleep problems may have serious consequences.72 A recent study demonstrated anxiety about COVID-19 correlated positively with insomnia severity and suicidal ideation.30

It is important to assess the impact of COVID-19 on sleep in different ethnicities and strata of society. It is expected that those with limited access to health care services and preventive measures for a contagious disease like COVID-19 will have higher levels of anxiety of catching the infection and hence higher levels of sleep disturbances.73

Given the results of this systematic review, there is an urgent need to improve sleep quality in both the general population and health care workers during this pandemic. Currently, available methods that may improve sleep quality include social and administrative support, relaxation techniques, and reasonable working schedules to allow for recovery.

CONCLUSIONS

The prevalence of sleep problems during the COVID-19 pandemic is high and affects approximately 40% of people from general and health care populations. Patients with active COVID-19 appeared to have higher prevalence rates of sleep problems. Further studies, particularly longitudinal studies to determine trajectories of sleep problems over time in these various COVID-19–impacted populations are warranted.

DISCLOSURE STATEMENT

All authors have seen and approved the manuscript. This article does not contain any studies with human participants performed by any of the authors. For this type of study (meta-analysis), formal consent is not required. The authors report no conflict of interest.

ABBREVIATIONS

CI

confidence interval

ISI

Insomnia Severity Index

PSQI

Pittsburg Sleep Quality Index

REFERENCES