Everything Was Disrupted: Chronotype and Mental Health Among Indonesian University Students Before and During the COVID-19 Pandemic

Article information

Sleep Med Res. 2026;17(1):83-89
Publication date (electronic) : 2026 March 31
doi : https://doi.org/10.17241/smr.2025.03237
1Department of Public Health, Universitas Negeri Manado, Tondano, Indonesia
2Department of Sport Science, Universitas Negeri Manado, Tondano, Indonesia
3Sam Ratulangi General Hospital, Tondano, Indonesia
Corresponding Author Alva Supit, MD, PhD Department of Public Health, Universitas Negeri Manado, Jl. Kampus Unima No. 1, Tondano 95618, Indonesia Tel +62-85175300139 E-mail alva.supit@unima.ac.id
Received 2025 October 25; Revised 2025 November 25; Accepted 2026 January 26.

Abstract

Background and Objective

Circadian rhythms play a crucial role in human health, with disruptions linked to various mental health issues. The COVID-19 pandemic has amplified these concerns, particularly among university students who faced significant changes in their daily routines due to lockdowns and remote learning. This study aims to investigate the impact of the pandemic on chronotype and mental health among Indonesian university students.

Methods

A comparative analysis was conducted involving two student populations: those affected by COVID-19 (n=257) from 2021 and a pre-pandemic comparison group (n=325) from 2019. Participants completed the Indonesian version of the Munich Chronotype Questionnaire and the Depression, Anxiety, and Stress Scale. Statistical analyses were performed using SPSS version 20.0, employing chi-square tests, Mann-Whitney U-tests, and Spearman’s rank correlation tests.

Results

We observed significant increases in depression, anxiety, and stress levels during the pandemic compared to pre-pandemic conditions for both sexes (all p<0.01). Average sleep duration increased significantly during the pandemic for both males (6:40 to 7:13 hours) and females (6:46 to 7:13 hours), while mid-sleep times shifted later across all groups. Interestingly, traditional measures of chronotype using mid-sleep time on free days corrected for sleep debt did not reflect significant changes during this period.

Conclusions

This current study highlights profound impacts on mental health and sleep patterns among university students due to COVID-19-related disruptions. Under extreme conditions such as a pandemic, it is necessary to adapt assessment tools like questionnaires to accurately capture shifts in chronotype and associated mental health outcomes.

INTRODUCTION

The importance of circadian rhythm in terrestrial biology, including human health, has been well recognized and appreciated [1]. Numerous diseases have been associated with the disruption of circadian rhythm in various populations across different races and age groups. These include metabolic [2], psychoneurological [3], and neoplastic pathologies [4]. Among these, mental health is in particular directly affected by the disrupted sleep-wake cycle, which may form positive feedback leading to the vicious cycle of depression, anxiety, stress, and reciprocal sleep disturbances [5]. In modern society, artificial light from electronic devices has desynchronized the human circadian rhythm from the sunlight as a natural cue of the day-night cycle. Global society had just begun to be more aware of the threat of circadian-related diseases when the COVID-19 pandemic struck the planet, where poor sleep behaviour is associated with the severity of COVID-19 [6,7]. In addition to its consequential pathogenic-related morbidity and mortality, the COVID-19 pandemic has also brought significant collateral impact on mental health worldwide. The implementation of total or partial lockdown and work/study from home, in particular, has affected the well-being of workers and students worldwide [8]. Consequently, numerous studies have stated the high incidence of COVID-19-related mental health disturbances such as depression, anxiety, and stress among working communities and students [9-12].

Previously, before the pandemic, we [13] and others have shown that chronotype is associated with depression across different populations and latitudes [14-17]. During normal conditions, those who have a later chronotype tend to show higher depression symptoms. However, in pathological sleep conditions, such as during the COVID-19 restriction, it is unclear whether the correlation between chronotype and depression persisted. In this current research, we aim to compare the sleep patterns and mental health profile of students who experienced online studying due to the COVID-19 lockdown with their predecessor student group, who did not experience COVID-19 but were enrolled in the same program. Specifically, we measured their chronotype using the Munich Chronotype Questionnaire (MCTQ) and their emotional negative state by using the Depression, Anxiety, and Stress Scale (DASS) questionnaires. The comparison group was retrieved from our 2019 archival data, which measured the identical parameters in the students enrolled in the same program before the COVID-19 pandemic. We hypothesized that students affected by COVID-19 would have higher mental health negative symptoms accompanied by a shift toward the later chronotype compared to the unaffected previous batch. Furthermore, we anticipated that the depression-chronotype correlation pattern observed pre-pandemic could be disrupted during the pandemic.

METHODS

Participants and Survey

This is a descriptive-analytic, comparative research between two student populations in our department during and before COVID-19 pandemic. Pandemic samples (students affected by COVID-19) were drawn from the enrolled students in 2021 (n=257). The pre-pandemic subject entries were retrieved from the 2019 archival data to serve as a comparison group (n=325) [13]. This study was conducted at the Department of Public Health, Manado State University, Indonesia. All subjects have provided their written or digital consent to participate in the study. Ethical clearance was provided by the Faculty Ethical Committee (Surat Ijin Nomor 04/IKM/21). The 2021 participants were recruited via departmental announcements and provided written or digital informed consent. The target population comprised all students enrolled in the Public Health program. Sample size was determined by availability of archival data and pandemic cohort participation.

Parameter Calculation

To measure the chronotype, we employed the Indonesian version of MCTQ previously developed in our center and used in our initial studies [13]. Mental health symptoms were assessed by the 42-item DASS. The main parameters of MCTQ are the mid-sleep time on free days corrected for sleep debt (MSFsc) and average sleep duration per week (SDave), which combined the weekdays and weekends parameters. For assessing the depression, anxiety, and stress level, an Indonesian version of DASS was used. DASS was preferred because it is reliable and easy to administer, especially in conjunction with other long questionnaires to avoid survey fatigue. In both groups, the questionnaires were circulated after the end-of-semester examination to increase the participation rate. Due to the face-to-face class restrictions, the pandemic group filled out the online questionnaires using Google Form, while the pre-pandemic group filled out the paper-based questionnaire.

MSFsc was calculated as a linear scale by subtracting the midsleep time during free days with the sleep debt accumulated in a week. SDave is the average sleep duration of every night of the week. During the data analysis, we found that MSFsc was not sufficient to reflect the chronotype shift during the pandemic. We therefore calculated the midsleep time and sleep duration separately in both groups to capture the true difference between pre- and during the pandemic. DASS were calculated as ordinal data as described previously [13].

Statistical Analysis

MCTQ parameters, DASS scores, and demographic characteristics were entered into a Microsoft Excel master table. After removing incomplete entries, the statistical analyses were performed using SPSS version 20.0 (IBM Corp.). Chi-square, Mann-Whitney U-test, or Spearman’s rank correlation tests were employed to calculate the statistical significance, where p<0.05 is considered significant. Graphs were rendered using GraphPad Prism ver 9.0 (GraphPad Software).

RESULTS

From the pandemic (Pand) group, 257 subjects filled the questionnaire and were included in the study. As a comparison, we retrieved 325 valid entries from our archival data collected in 2019 (pre-pandemic, PreP). Since females and males exhibit different characteristics in terms of chronotype and sleep duration, we analyzed the data separately for each sex to faithfully capture the true phenomenon. In both PreP and Pand groups, females predominated (69.84% and 84.82% in PreP and Pand, respectively). This is due to the demographic nature of our student population. Variations between male and female subjects during PreP to Pand are presented in Table 1. When combined, only grade point average (GPA) and smoking habit differed pre-and during pandemic, while coffee/alcohol consumption, BMI, and cumulative GPA did not differ significantly. Males in the pandemic group were significantly older than pre-pandemic (p=0.008), but this is caused by the nature of the batches. The GPA, but not the cumulative GPA significantly increased during the pandemic, perhaps due to the changes and compromises during the online learning period. Daily coffee consumption significantly increased in males (p<0.001), while smoking behaviour interestingly declined during the pandemic. Other variables, including BMI and alcohol consumption, showed no significant differences. These indicate potential behavioral and academic shifts during the pandemic, particularly regarding GPA, caffeine intake, and smoking.

Respondent characteristics

Since males and females displayed different chronotype and mental health symptoms, we also assessed the MCTQ and DASS separately between these two sexes. Table 2 displays the significant increase in depression, anxiety, and stress levels among students before and during the pandemic, categorized by sex and combined altogether. In all DASS, there were notable increases in severe cases for both males and females (all p<0.01), reflecting the overall negative impact of the pandemic on mental health. This increase persisted when both sexes were pooled together and the raw scores of DASS were used for numerical analyses (Fig. 1). Between sexes, females in the pre-pandemic group showed a higher stress level compared to males, but with similar depression and anxiety levels. During the pandemic, there is no sex difference in all depression, anxiety, and stress levels (Supplementary Table 1 in the online-only Data Supplement).

Depression, anxiety, and stress score based on sex and pandemic status

Fig. 1.

Comparison of depression, anxiety, and stress raw score pre-pandemic (n=325) and during pandemic (n=257, showing a greater level of all three parameters during the pandemic (***p<0.005; ****p<0.001 by two-tailed t-tests).

Changes in chronotype parameters based on sex and pandemic status are presented in Table 3, comparing pre-pandemic and pandemic periods. SDave increased significantly during the pandemic for both males (6:40 to 7:13, p=0.029) and females (6:46 to 7:13, p=0.001), with the combined data showing a highly significant rise (p<0.001). Sleep duration on weekends (SDweekends) also increased notably, particularly for females (7:25 to 9:15, p<0.001) and the combined group (7:34 to 9:14, p<0.001). Mid-sleep times on weekdays (MSweekdays) and weekends (MSweekends) shifted later during the pandemic, with significant changes observed for females and the combined group (p<0.001), indicating a delay in sleep patterns. Interestingly, we observed that the MSFsc—although has been considered as the main reading of MCTQ—did not show any significant change during the pandemic (p>0.1) regardless of whether the data were analyzed in combination or separately between sexes (Table 3 and Supplementary Fig. 1 [in the online-only Data Supplement]), suggesting that during pathological community-wide chronotype shift, MSFsc may not be the most suitable parameter for reporting the chronotype, at least in our current samples.

Chronotype parameters based on sex and pandemic status

Previously, we and others reported a correlation between chronotype and depression symptoms. We then asked if this correlation persisted during the pandemic. Since the MSFsc alone could not reflect the chronotype change, we also calculated the correlation between depression (D), anxiety (A), and stress (S) scores with other chronotype parameters, comparing pre-pandemic and pandemic periods. Pre-pandemic, significant negative correlations were observed between D and SDave (R=-0.149, p=0.007) and sleep duration on weekdays (SDweekdays, R=-0.167, p=0.003). Additionally, significant positive correlations were found between D and MSFsc (R=0.177, p=0.001), MSweekdays (R=0.157, p=0.005), MSweekends (R=0.187, p=0.001), all confirming previous observations in non-pandemic situations. During the pandemic, these significant correlations between D and chronotype parameters largely disappeared, with no significant correlations observed for sleep duration or mid-sleep times. Instead, A showed new small but significant positive correlations with MSweekdays (R=0.140, p=0.025) and MSweekends (R=0.132, p=0.035), indicating that later sleep timings were associated with higher A levels during the pandemic. This suggests a shift in the relationship between mental health and sleep patterns during the pandemic, where anxiety became more related to chronotype. However, the observed correlations between A and midsleep times were statistically significant but weak (R≈0.13–0.14), thus limiting clinical relevance (Table 4).

Correlation matrix between Depression, Anxiety, and Stress Scale and chronotype pre- and during pandemic

DISCUSSION

Our results showed that during the pandemic lockdown, students experienced significantly higher depression, anxiety, and stress symptoms compared to the control batch of students before the pandemic. Moreover, students undergoing the pandemic lockdown also had a significantly longer sleep duration per week and later mid-sleep time compared to before the pandemic. Interestingly, the subject’s sleeping schedule had been altered so much that the conventional analysis of MCTQ (calculating the MSFsc) could not yield a reliable result. Instead, the middle sleep time and sleep duration should be calculated separately for working and free days to fully reflect the sleep pattern change. Finally, we also found that the previously recognized correlation between depression and chronotype diminished during COVID-19 restrictions, while a new anxiety-chronotype correlation emerged.

Multiple studies have confirmed the rise of mental health symptoms during the COVID-19 pandemic, with a meta-analysis reporting a seven-fold increase in depression [18]. This can be attributed to the disease itself, or the lockdown implemented by the local governments to prevent COVID-19 spread. Interestingly, while females exhibited higher stress levels in non-pandemic situations compared to males (as shown in our results [13] and others [19-21]), no significant differences were observed during the pandemic across all mental health scales. This suggests that both sexes experienced similar adverse effects on their mental well-being due to shared challenges caused by COVID-19 pandemic and restrictions. Thus, this current study conforms with previous studies while adding to the existing body of evidence the cohort sample from a group of Indonesian college students [22].

MCTQ has been previously favoured for assessing chronotype across latitudes of the planet, in addition to its easy administration. Classically, MCTQ reports the MSFsc as its main parameter [23]. In this current research, interestingly, although the sleep pattern is robustly skewed towards a later chronotype and longer duration, the MSFsc seems to be insensitive in highlighting this phenomenon. Reporting the mid-sleep time during nonphysiological conditions, such as during insomnia, may be unfavourable, as insomnia disorder is characterized by time gaps during the night due to difficulty maintaining sleep; there may be limitations in using mid-sleep time as an accurate indicator of chronotype in insomnia patients [24]. Moreover, during the pandemic, the blurring of boundaries between workdays and free days, along with highly irregular schedules, made MSFsc less sensitive under socially disrupted conditions such as pandemic lockdowns. MSFsc relies on predictable contrasts between weekdays and weekends and assumes that sleep debt correction accurately reflects accumulated restriction during workdays. These assumptions hold under stable social schedules but break down when external time cues and obligations are disrupted, as during the pandemic. Lockdowns blurred the distinction between workdays and free days, reducing the compensatory oversleep typically observed on weekends. Consequently, MSFsc loses sensitivity because its core premise (correcting mid-sleep on free days by subtracting sleep debt) becomes less sensitive when sleep debt itself is inconsistent or negligible. In contrast, raw mid-sleep times for weekdays and weekends, along with derived metrics such as social jetlag and sleep regularity indices, provide direct behavioral markers of circadian timing without relying on assumptions about debt correction (Supplementary Fig. 1 [in the online-only Data Supplement] vs. Table 3). These complementary indicators capture real delays and irregularity in sleep patterns, offering a more nuanced and robust representation of chronotype under socially disrupted conditions. Future research should prioritize these granular measures when evaluating chronotype shifts during periods of widespread schedule instability.

During the pandemic, the previously established correlation between chronotype and depression [13] diminished; instead, a new anxiety-chronotype correlation emerged. The new correlation between later mid-sleep times and increased anxiety during the pandemic may reflect a shift in the relationship between sleep patterns and mental health. As students experienced more flexible schedules and reduced external activities, many of them might have adopted later sleep timings, resulting in the disruption of their circadian rhythms and increased feelings of anxiety. The uncertainty and stress associated with the pandemic likely contributed to this shift, as heightened anxiety can lead to difficulty falling asleep and later bedtimes [15]. Additionally, as discussed above, increased screen time and reduced exposure to natural light during lockdowns may have further delayed sleep onset, creating a feedback loop that worsened anxiety, though this remains speculative [25]. Although statistically significant, the correlations between anxiety and mid-sleep times were weak (R≈0.13–0.14), explaining less than 2% of the variance in anxiety scores. This magnitude is far below thresholds typically considered clinically meaningful and suggests that the association is can be more of a statistical artifact than a robust behavioral link. The significance likely reflects the large sample size rather than a substantive effect. Therefore, these findings should be interpreted as exploratory and hypothesis-generating rather than confirmatory. Future research should prioritize effect size and practical relevance over p-values, and consider longitudinal or experimental designs to clarify whether these small associations persist under different conditions or represent transient patterns specific to pandemic-related disruptions. Therefore, it is interesting to assess whether this trend persists after the pandemic, or would it go back to the original correlation between depression and chronotype, which is currently being studied by our group.

This study has several limitations that should be acknowledged. First, the reliance on self-reported data for sleep patterns and mental health symptoms may introduce biases, such as recall or social desirability bias. To address this, future studies could incorporate objective measures like actigraphy to validate sleep data. Second, the cross-sectional design limits the ability to establish causality between changes in sleep patterns and mental health outcomes. The cross-sectional design comparing two different cohorts may introduce confounding factors. It is noteworthy that the observed differences may partly reflect cohort-specific characteristics such as age and academic stage rather than pandemic effects alone. These confounders limit causal inference and highlight the need for longitudinal designs in future research to provide more robust insights into these relationships. Third, the study focused on a specific student population from the same department but in different batches, which may limit the generalizability of the findings. Expanding the sample to include diverse demographic groups and educational contexts would enhance the applicability of the results. Additionally, the pre-pandemic group filled out a paper-based questionnaire, while the pandemic group completed an online survey, which could introduce methodological inconsistencies. Differences in survey mode (paper vs. online) may have influenced response patterns and variance. Survey mode effects have been previously documented: online surveys often yield higher disclosure of sensitive information but may introduce measurement error and lower completion rates compared to paper surveys [26]. This methodological inconsistency could partly explain observed differences. Future studies should standardize data collection methods. Lastly, the pandemic group may have been more prone to survey or Zoom fatigue, potentially affecting the accuracy and reliability of their responses. Mitigating this issue could involve shorter, more engaging surveys and ensuring participants are well-rested before completing the questionnaire. Including these considerations in future analyses would provide a more comprehensive understanding of the phenomenon.

In conclusion, COVID-19 pandemic increased depression, anxiety, and stress in Indonesian university students, while also altering the chronotype towards a later one. During pandemic-level pathological sleeping conditions, it is essential to adapt the questionnaires rather than relying solely on standard formats to accurately capture the true phenomenon.

Supplementary Materials

The online-only Data Supplement is available with this article at https://doi.org/10.17241/smr.2025.03237.

Supplementary Table 1.

Sex difference of depression, anxiety, and stress score pre- and during pandemic

smr-2025-03237-Supplementary-Table-1.pdf

Supplementary Fig. 1.

Non-significant (NS) difference of midsleep time on free days corrected for sleep debt (MSFsc) pre- and during pandemic.

smr-2025-03237-Supplementary-Fig-1.pdf

Notes

Availability of Data and Material

Raw data can be shared by the corresponding author upon reasonable request.

Author Contributions

Conceptualization: Richard Palilingan, Alva Supit. Data curation: Richard Palilingan. Formal analysis: Richard Palilingan, Alva Supit. Investigation: Richard Palilingan, Christian Pajung, Ellen Lomboan. Methodology: Ellen Lomboan, Alva Supit. Project administration: Melky Pangemanan. Resources: Melky Pangemanan. Software: Alva Supit. Supervision: Alva Supit, Ellen Lomboan. Validation: Alva Supit. Visualization: Richard Palilingan, Alva Supit. Writing—original draft: Richard Palilingan. Writing—review & editing: Alva Supit.

Conflicts of Interest

The authors have no potential conflicts of interest to disclose.

Funding Statement

None

Acknowledgements

Microsoft Copilot was used to assist with grammatical corrections and improving the flow of the manuscript. The authors take full responsibility for the content.

References

1. Burki T. Nobel Prize awarded for discoveries in circadian rhythm. Lancet 2017;390:e25.
2. Maury E. Off the clock: from circadian disruption to metabolic disease. Int J Mol Sci 2019;20:1597.
3. Karatsoreos In. Links between circadian rhythms and psychiatric disease. Front Behav Neurosci 2014;8:162.
4. Fekry B, Eckel-Mahan K. The circadian clock and cancer: links between circadian disruption and disease Pathology. J Biochem 2022;171:477–86.
5. Walker WH 2nd, Walton JC, DeVries AC, Nelson RJ. Circadian rhythm disruption and mental health. Transl Psychiatry 2020;10:28.
6. Li P, Zheng X, Ulsa MC, Yang HW, Scheer FAJL, Rutter MK, et al. Poor sleep behavior burden and risk of COVID-19 mortality and hospitalization. Sleep 2021;44:zsab138.
7. Liu Z, Luo Y, Su Y, Wei Z, Li R, He L, et al. Associations of sleep and circadian phenotypes with COVID-19 susceptibility and hospitalization: an observational cohort study based on the UK Biobank and a two-sample Mendelian randomization study. Sleep 2022;45:zsac003.
8. Panchal U, Salazar de Pablo G, Franco M, Moreno C, Parellada M, Arango C, et al. The impact of COVID-19 lockdown on child and adolescent mental health: systematic review. Eur Child Adolesc Psychiatry 2023;32:1151–77.
9. Elmer T, Mepham K, Stadtfeld C. Students under lockdown: comparisons of students’ social networks and mental health before and during the COVID-19 crisis in Switzerland. PLoS One 2020;15:e0236337.
10. Evans S, Alkan E, Bhangoo JK, Tenenbaum H, Ng-Knight T. Effects of the COVID-19 lockdown on mental health, wellbeing, sleep, and alcohol use in a UK student sample. Psychiatry Res 2021;298:113819.
11. Meda N, Pardini S, Slongo I, Bodini L, Zordan MA, Rigobello P, et al. Students’ mental health problems before, during, and after COVID-19 lockdown in Italy. J Psychiatr Res 2021;134:69–77.
12. Patsali ME, Mousa DV, Papadopoulou EVK, Papadopoulou KKK, Kaparounaki CK, Diakogiannis I, et al. University students’ changes in mental health status and determinants of behavior during the COVID-19 lockdown in Greece. Psychiatry Res 2020;292:113298.
13. Supit A, Gosal M, Mamuaja P, Kumaat S, Paturusi A. Later chronotype correlates with severe depression in Indonesian college students. Sleep Med Res 2021;12:133–9.
14. Antypa N, Vogelzangs N, Meesters Y, Schoevers R, Penninx BWJH. Chronotype associations with depression and anxiety disorders in a large cohort study. Depress Anxiety 2016;33:75–83.
15. Antypa N, Verkuil B, Molendijk M, Schoevers R, Penninx BWJH, Van Der Does W. Associations between chronotypes and psychological vulnerability factors of depression. Chronobiol Int 2017;34:1125–35.
16. Au J, Reece J. The relationship between chronotype and depressive symptoms: a meta-analysis. J Affect Disord 2017;218:93–104.
17. Haraden DA, Mullin BC, Hankin BL. The relationship between depression and chronotype: a longitudinal assessment during childhood and adolescence. Depress Anxiety 2017;34:967–76.
18. Bueno-Notivol J, Gracia-García P, Olaya B, Lasheras I, López-Antón R, Santabárbara J. Prevalence of depression during the COVID-19 outbreak: a meta-analysis of community-based studies. Int J Clin Health Psychol 2021;21:100196.
19. Klein EM, Brähler E, Dreier M, Reinecke L, Müller KW, Schmutzer G, et al. The German version of the Perceived Stress Scale - psychometric characteristics in a representative German community sample. BMC Psychiatry 2016;16:159.
20. Iqbal S, Gupta S, Venkatarao E. Stress, anxiety and depression among medical undergraduate students and their socio-demographic correlates. Indian J Med Res 2015;141:354–7.
21. Yalçın T, Ayyıldız F, Yılmaz MV, Asil E. Relationship of perceived depression, stress, anxiety levels and hedonic hunger. Int J Obes (Lond) 2023;47:717–23.
22. Sarfika R, Malini H, Putri DE, Buanasari A, Abdullah KL, Freska W. Factors influencing depression among Indonesians during the COVID-19 outbreak. Nurse Media Journal of Nursing 2021;11:380–8.
23. Zavada A, Gordijn MC, Beersma DG, Daan S, Roenneberg T. Comparison of the Munich Chronotype Questionnaire with the Horne-Ostberg’s Morningness-Eveningness Score. Chronobiol Int 2005;22:267–78.
24. Suh S, Ryu H, Kim S, Choi S, Joo EY. Using mid-sleep time to determine chronotype in young adults with insomnia-related symptoms. Sleep Med Res 2017;8:107–11.
25. Zhong C, Masters M, Donzella SM, Diver WR, Patel AV. Electronic screen use and sleep duration and timing in adults. JAMA Netw Open 2025;8:e252493.
26. Dillman DA, Smyth JD, Christian LM. Internet, phone, mail, and mixed mode surveys: The tailored design method, 4th ed Hoboken: John Wiley & Sons, Inc.; 2014.

Article information Continued

Fig. 1.

Comparison of depression, anxiety, and stress raw score pre-pandemic (n=325) and during pandemic (n=257, showing a greater level of all three parameters during the pandemic (***p<0.005; ****p<0.001 by two-tailed t-tests).

Table 1.

Respondent characteristics

Variable Male
Female
Male+female
Pre-pandemic (n=98) Pandemic (n=39) p-value Pre-pandemic (n=227) Pandemic (n=218) p-value Pre-pandemic (n=325) Pandemic (n=257) p-value
Age (yr) 19.76±1.51 20.55±1.54 0.008* 19.95±1.70 19.89±1.40 0.699 19.89±1.65 19.99±1.43 0.443
Cumulative GPA 3.25±0.34 3.51±0.36 0.070 3.32±0.30 3.62±0.38 <0.001** 3.38±1.46 3.42±0.38 0.691
GPA 3.23±0.34 3.36±0.34 <0.001** 3.32±0.28 3.43±0.39 0.003* 3.30±0.31 3.60±0.38 <0.001**
Body mass index (kg/m2) 22.12±3.25 23.59±7.44 0.240 21.31±3.37 21.78±8.97 0.467 21.56±3.35 22.05±8.76 0.349
 Underweight 7 (7.1) 6 (15.3) 46 (20.2) 58 (26.6) 53 (16.3) 64 (24.9)
 Normal 73 (74.4) 25 (64.1) 148 (65.1) 138 (63.3) 221 (68.0) 163 (63.4)
 Overweight 17 (17.3) 4 (10.2) 31 (13.6) 18 (8.3) 48 (14.7) 22 (8.6)
 Obese 1 (1.0) 4 (10.2) 2 (0.9) 4 (1.8) 3 (0.9) 8 (3.1)
Smoking, any qty, daily 19 (19.3) 6 (15.3) 0.584 12 (5.3) 1 (0.5) 0.003* 31 (9.5) 7 (2.7) 0.001*
Coffee, daily 30 (30.6) 33 (84.6) <0.001** 57 (25.1) 55 (25.2) 0.977 87 (26.7) 88 (34.2) 0.051
Alcohol, at least 1/week 13 (13.2) 9 (23.0) 0.158 12 (5.3) 4 (1.8) 0.051 25 (7.7) 13 (5.1) 0.202
Sleeping pil consumption 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0)

Values are presented as mean±standard deviation or n (%).

*

p<0.05;

**

p<0.001 by chi-square or t-test.

GPA, grade point average.

Table 2.

Depression, anxiety, and stress score based on sex and pandemic status

Variable Male
Female
Male+female
Pre-pandemic (n=98) Pandemic (n=39) p-value Pre-pandemic (n=227) Pandemic (n=218) p-value Pre-pandemic (n=325) Pandemic (n=257) p-value
Depression 0.010* 0.016* <0.001**
 Normal 69 (70.40) 19 (48.71) 162 (71.36) 142 (65.13) 231 (71.07) 161 (62.64)
 Mild 11 (11.22) 5 (12.82) 25 (11.01) 18 (8.26) 36 (11.07) 23 (8.95)
 Moderate 15 (15.30) 7 (17.94) 32 (14.09) 33 (15.13) 47 (14.46) 40 (15.56)
 Severe 3 (3.06) 7 (17.94) 7 (3.08) 16 (7.34) 10 (3.08) 23 (8.95)
 Extremely severe 0 (0) 1 (2.56) 1 (0.44) 9 (4.13) 1 (0.31) 10 (3.89)
Anxiety 0.009* <0.001** <0.001**
 Normal 31 (31.63) 8 (20.51) 49 (21.58) 39 (17.88) 80 (24.61) 47 (18.28)
 Mild 26 (26.53) 6 (15.38) 60 (26.43) 33 (15.13) 86 (26.46) 39 (15.17)
 Moderate 23 (23.46) 10 (25.64) 80 (35.24) 52 (23.85) 103 (31.69) 62 (24.12)
 Severe 15 (15.30) 7 (17.94) 25 (11.01) 46 (21.10) 40 (12.30) 53 (20.62)
 Extremely severe 3 (3.061) 8 (20.51) 13 (5.726) 48 (22.01) 16 (4.92) 56 (21.78)
Stress <0.001** <0.001** <0.001**
 Normal 50 (51.02) 7 (17.94) 82 (36.12) 51 (23.39) 132 (40.61) 58 (22.56)
 Mild 39 (39.79) 15 (38.46) 117 (51.54) 84 (38.53) 156 (48.00) 99 (38.52)
 Moderate 8 (8.16) 12 (30.76) 24 (10.57) 45 (20.64) 32 (9.85) 57 (22.17)
 Severe 0 (0) 4 (10.25) 4 (1.76) 27 (12.38) 4 (1.23) 31 (12.06)
 Extremely severe 1 (1.02) 1 (2.564) 0 (0) 11 (5.05) 1 (0.31) 12 (4.67)

Values are presented as n (%).

*

p<0.05;

**

p<0.001 by chi-square test.

Table 3.

Chronotype parameters based on sex and pandemic status

Variable Male
Female
Male+female
Pre-pandemic (n=98) Pandemic (n=39) p-value Pre-pandemic (n=227) Pandemic (n=218) p-value Pre-pandemic (n=325) Pandemic (n=257) p-value
SDave (h:mm) 6:40±1:16 7:13±1:10 0.029* 6:46±1:15 7:13±1:23 0.001* 6:44±1:15 7:13±1:20 <0.001**
 SDweekdays (h:mm) 6:28±1:22 6:53±1:10 0.117 6:39±1:17 6:53±1:30 0.181 6:36±1:19 6:53±1:27 0.041*
 SDweekends (h:mm) 7:54±1:44 9:09±2:39 0.018* 7:25±1:33 9:15±2:30 <0.001** 7:34±1:37 9:14±2:31 <0.001**
MSFsc (local time) 4:21±1:32 4:03±1:24 0.304 3:41±1:18 3:46±1:24 0.469 3:52±1:24 3:48±1:24 0.642
 MSweekdays (local time) 3:22±1:04 3:40±1:05 0.164 2:50±0:47 3:20±0:56 <0.001** 2:59±0:55 3:23±0:58 <0.001**
 MSweekends (local time) 5:00±1:33 5:08±1:35 0.441 4:05±1:20 4:51±1:34 <0.001** 4:22±1:28 4:54±1:35 <0.001**

Values are presented as mean±standard deviation.

*

p<0.05;

**

p<0.001, t-test.

SDave, average sleep duration per week; SDweekdays, sleep duration on weekdays; SDweekends, sleep duration on weekends; MSFsc, mid-sleep time on free days corrected for sleep debt; MSweekdays, mid-sleep times on weekdays; MSweekends, mid-sleep times on weekends.

Table 4.

Correlation matrix between Depression, Anxiety, and Stress Scale and chronotype pre- and during pandemic

Variables Pre-pandemic
Pandemic
R p-value R p-value
D vs. SDave -0.149 0.007* -0.027 0.670
D vs. SDweekdays -0.167 0.003* -0.036 0.562
D vs. SDweekends -0.007 0.894 -0.021 0.740
D vs. MSFsc 0.177 0.001* 0.055 0.381
D vs. MSweekdays 0.157 0.005* 0.113 0.069
D vs. MSweekends 0.187 0.001* 0.088 0.161
A vs. SDave -0.073 0.189 -0.109 0.081
A vs. SDweekdays -0.073 0.190 -0.120 0.055
A vs. SDweekends -0.034 0.540 -0.065 0.301
A vs. MSFsc 0.054 0.366 0.073 0.246
A vs. MSweekdays 0.072 0.195 0.140 0.025*
A vs. MSweekends 0.025 0.654 0.132 0.035*
S vs. SDave -0.068 0.224 -0.094 0.132
S vs. SDweekdays -0.085 0.128 -0.092 0.142
S vs. SDweekends 0.041 0.460 -0.101 0.105
S vs. MSFsc 0.046 0.405 0.084 0.177
S vs. MSweekdays 0.085 0.126 0.098 0.118
S vs. MSweekends 0.056 0.312 0.092 0.143

Significant correlations were marked with stronger shades and asterisks at their p-values. Red and green shades indicate positive and negative correlation, respectively.

*

p<0.05 by Spearman’s rho.

D, depression; A, anxiety; S, stress; SDave, average sleep duration per week; SDweekdays, sleep duration on weekdays; SDweekends, sleep duration on weekends; MSFsc, mid-sleep time on free days corrected for sleep debt; MSweekdays, mid-sleep times on weekdays; MSweekends, midsleep times on weekends.