Psychiatry Investig Search

CLOSE


Psychiatry Investig > Volume 21(12); 2024 > Article
Yeom, Park, and Lee: Managing Circadian Rhythms: A Key to Enhancing Mental Health in College Students

Abstract

Objective

To investigate the impact of circadian rhythm disruptions on mental health among college students and explore effective interventions for maintaining stable circadian rhythms.

Methods

A comprehensive review of literature was conducted, focusing on sleep patterns, circadian rhythms, and their effects on mental health. Studies were analyzed to identify common factors contributing to circadian misalignment in college students and effective treatments. Data from large-scale studies and specific clinical trials were utilized to understand the relationship between circadian rhythms and psychiatric disorders.

Results

Disruptions in circadian rhythms were linked to increased prevalence of psychiatric disorders such as depression, anxiety, and bipolar disorder. Biological changes during adolescence, academic pressures, and extensive use of electronic devices were major contributing factors. Effective interventions included light therapy, chronotherapy, melatonin supplementation, and cognitive behavioral therapy for insomnia.

Conclusion

Stable circadian rhythms are crucial for mental health, particularly in college students who are vulnerable to disruptions due to lifestyle factors. Implementing interventions such as regular sleep schedules, light exposure management, and behavioral therapies can significantly improve mental health outcomes. Further research and targeted mental health programs are essential to address circadian misalignment and its associated psychiatric disorders in this population.

INTRODUCTION

Sleep is a crucial factor in maintaining both physical health and mental stability. Sleep issues are widespread among college students as well [1,2]. According to a recent large-scale study of over 7,000 American college students, the average sleep duration for American college students is 6.85 hours, and only one-third sleep more than 7 hours each night, which falls short of the recommended 7-9 hours of sleep [1,3,4]. The average sleep duration of Korean college students is even less, reported to be 6.43 hours [5]. Sleep deprivation has detrimental effects on physical [6-8] and mental health [9,10], and daytime sleepiness and fatigue can lower students’ academic performance [11-13].
Circadian rhythms refer to the physical, mental, and behavioral changes that occur on a 24-hour cycle. This natural process is primarily influenced by the presence of light and darkness in the environment [14,15]. Although often equated with sleep patterns, circadian rhythms are not synonymous with them. Circadian rhythms result from the long-term accumulation of consistent sleep patterns and light exposure over a period of more than 2 weeks. Both sleep patterns and circadian rhythms can be associated with the exacerbation of mood disorders [16-18]. However, recent research has shown that circadian rhythms, rather than sleep patterns themselves, have a more significant impact on current mood symptoms [19].
Recent studies indicate a significant increase in the incidence of psychiatric disorders such as depression among college students. A study found that during the COVID-19 pandemic, the prevalence of post-traumatic stress disorder (PTSD), depression, and anxiety significantly increased among college students. In a study involving 6,898 college students, 32.2% experienced depression, 32.1% experienced anxiety, and 15.5% experienced PTSD. The study attributed the exacerbation of these mental health issues to pandemic-induced stress and rumination [20].
According to recent research, 40.16% of 2,318 college students reported major depressive disorder (MDD) after 1.5 years of pandemic-related social restrictions, and 72.52% showed low well-being indices. Nine months after the restrictions ended, depression decreased to 28.50%, and the low well-being index improved to 53.96%. However, the prevalence of depression and issues with quality of life remain severe [21].
Attributing the increase in depression during the COVID-19 pandemic solely to stress and social restrictions may be insufficient. The social isolation imposed during the pandemic limited individuals’ outdoor activities and disrupted daily routines, potentially causing disturbances in circadian rhythms that may also be linked to the rise in depression [22].
Understanding the connection between circadian rhythms and mental health has become increasingly important as disruptions in these rhythms have been linked to various psychiatric disorders. Undergraduate students face unique challenges that make them particularly vulnerable to these disruptions, including academic pressures, lifestyle choices, and extensive use of electronic devices. Addressing these disruptions is essential for improving mental health outcomes in this population.
Understanding the connection between circadian rhythms and mental health has become increasingly important as disruptions in these rhythms have been linked to various psychiatric disorders. Undergraduate students face unique challenges that make them particularly vulnerable to these disruptions, including academic pressures, lifestyle choices, and extensive use of electronic devices. Addressing these disruptions is essential for improving mental health outcomes in this population.

THE BIOLOGICAL MECHANISMS OF CIRCADIAN RHYTHMS

Circadian rhythms are intrinsic time-keeping mechanisms that align physiological processes with the external environment’s 24-hour light-dark cycle. These rhythms are present in almost all living organisms, from cyanobacteria to humans, and are essential for maintaining homeostasis. The central circadian clock resides in the suprachiasmatic nucleus (SCN) of the hypothalamus, which coordinates peripheral clocks located in various tissues. The SCN, a small group of neurons located in the anterior hypothalamus, is the principal pacemaker of circadian rhythms in mammals. It receives direct input from the retina through the retinohypothalamic tract, allowing it to synchronize with the external light-dark cycle [23]. The SCN orchestrates daily rhythms in behavior and physiology by sending timing signals to various brain regions and peripheral organs.
The SCN communicates timing information through neural and hormonal pathways. Neural projections from the SCN innervate other hypothalamic nuclei, influencing sleep-wake cycles, feeding behavior, and thermoregulation. Additionally, the SCN regulates the release of hormones such as melatonin from the pineal gland, which signals nighttime and promotes sleep [24].
At the heart of the circadian system are core clock genes and their protein products, which form transcriptional-translational feedback loops. The primary components of this loop include Clock, Bmal1, Period (Per), and Cryptochrome (Cry) genes [25]. During the day, CLOCK and BMAL1 proteins dimerize and bind to E-box elements in the promoters of Per and Cry genes, activating their transcription. As PER and CRY proteins accumulate, they form complexes that translocate into the nucleus and inhibit their own transcription by interfering with the CLOCK-BMAL1 complex, thus completing the feedback loop.
Post-translational modifications of clock proteins, such as phosphorylation, ubiquitination, and acetylation, play crucial roles in regulating the stability, localization, and activity of these proteins. For example, the phosphorylation of PER proteins by casein kinase 1ε/δ targets them for degradation, influencing the timing of the feedback loop [26]. Similarly, acetylation of BMAL1 by CLOCK regulates its transcriptional activity and stability [27].
Peripheral clocks exist in nearly all tissues and organs, including the liver, heart, lungs, and adipose tissue. These clocks maintain local circadian rhythms and are regulated by the central clock in the SCN but can also respond to local cues such as feeding, physical activities, and temperature [28]. Peripheral clocks are essential for the temporal coordination of tissuespecific functions, such as metabolic processes in the liver and insulin secretion in the pancreas.
The synchronization between the SCN and peripheral clocks is achieved through various signaling mechanisms, including hormonal signals (e.g., glucocorticoids), body temperature cycles, and feeding schedules [29]. Disruption in the coordination between the SCN and peripheral clocks can lead to circadian misalignment, contributing to metabolic disorders, cardiovascular diseases, and other health issues [30].
Environmental factors, known as zeitgebers (time-givers), play a crucial role in entraining circadian rhythms. The primary zeitgeber is the light-dark cycle, which resets the SCN daily. Other zeitgebers include feeding times, social interactions, and temperature [31]. Disruption of these environmental cues, such as exposure to artificial light at night or irregular eating schedules, can lead to circadian rhythm disturbances.

THE IMPORTANCE OF CIRCADIAN RHYTHMS IN MENTAL HEALTH

Circadian rhythms, the natural 24-hour cycles governing physiological and behavioral processes, are crucial for maintaining mental health. Disruptions to these rhythms have been linked to a range of psychiatric disorders, underscoring their importance in regulating mental stability. Research indicates that a misalignment between an individual’s internal clock and external environmental cues can precipitate mood disorders such as depression and anxiety [32]. For instance, irregular sleepwake cycles and insufficient sleep are commonly associated with heightened levels of stress and increased depressive symptoms [33]. This is particularly concerning given the high prevalence of these irregular sleep patterns in modern society.
Chronic stress and an irregular lifestyle can exacerbate mental health issues, including insomnia, depression, and anxiety. When the circadian rhythm is disrupted due to irregular sleep patterns or excessive stress, it can lead to prolonged psychiatric symptoms (Figure 1). The body’s inability to synchronize the sleep-wake cycle with environmental cues results in cognitive impairment and increased susceptibility to mental health disorders [32].
We demonstrated that individuals with a predisposition to circadian rhythm disruptions exhibited a significantly higher likelihood of experiencing mood disorders. This study emphasized that the stability of circadian rhythms is not merely a background factor but a critical component in the maintenance of mental health [34]. We conducted a comprehensive study involving 31 mood episodes in 26 patients with bipolar disorder (BD) and 18 controls. We evaluated the circadian rhythms of these individuals at admission, at 2-week intervals during hospitalization, and at discharge. The study revealed distinct circadian phase shifts during acute mood episodes compared to recovered states. In 23 acute manic episodes, circadian phases were advanced by approximately 7 hours. After treatment, phases in 21 of these cases returned to normal with a delay of around 7 hours, indicating a recovery of the normal circadian phase [34].
Moreover, the study found that during mixed manic episodes, circadian rhythms were delayed by approximately 6-7 hours, while depressive episodes exhibited delays of around 4-5 hours [34]. These findings highlight the critical role of circadian misalignment in the pathophysiology of BD.
Delayed circadian rhythms, characterized by later sleep and wake times, are particularly prevalent among college students. This demographic often exhibits a preference for evening activities and late-night studying, resulting in sleep phase delays. Such patterns are not merely lifestyle choices but are influenced by biological changes during adolescence and early adulthood. Crowley et al. [35] note that delayed sleep phase syndrome (DSPS) is common in this age group, affecting up to 7%-16% of young adults. This delay can lead to chronic sleep deprivation due to misalignment with academic and social schedules, further exacerbating mental health issues [36]. The cumulative effect of insufficient and irregular sleep contributes to impaired cognitive function, reduced academic performance, and increased susceptibility to psychiatric disorders. Disruptions in circadian rhythms have been associated with mood disorders, particularly depression and BD [16].
Circadian rhythms play a vital role in the mental health of college students, with disruptions linked to various psychiatric problems. The prevalence of delayed circadian rhythms in this age group, compounded by the pervasive use of smartphones, underscores the urgency of addressing sleep hygiene and circadian alignment to mitigate mental health risks. Future research and mental health interventions should focus on promoting regular sleep patterns and reducing nighttime exposure to electronic devices to improve overall well-being in college students.

FACTORS CONTRIBUTING TO DELAYED CIRCADIAN RHYTHMS IN COLLEGE STUDENTS

Circadian rhythms relate to multiple aspects of health and well-being, including physical activity patterns. Susceptibility to circadian regulation predisposes individuals to circadian misalignment, poor sleep, sleep deprivation, increased sleepiness, and consequently, sedentary behavior.
Biological changes during adolescence and young adulthood contribute significantly to delayed circadian rhythms, marked by a preference for later sleep and wake times. Sleep pressure decreases during adolescence, resulting in delayed sleep schedules [37,38]. Weekday and weekend sleep patterns vary, with more catch-up sleep on weekends [39]. Adolescents’ circadian regulation is particularly vulnerable, which may lead to sedentary behavior [40].
The two-process model of sleep regulation, involving homeostatic sleep pressure and the circadian pacemaker, is disrupted during adolescence [41]. Sex-specific differences emerge, with adolescent girls experiencing longer sleep onset latencies and more insomnia symptoms, while boys exhibit less regular sleep patterns and later bedtimes [42].
Delayed sleep phase disorder (DSPD) is common in adolescence, characterized by a delayed sleep schedule and daytime impairment [43]. DSPD desynchronizes patients from societal schedules, leading to sleep loss and daytime sleepiness [41]. Prevalence estimates range from 3.3% to 16%, with higher rates in girls [43,44]. Delayed sleep phase is linked to mental health issues like depression and anxiety [45,46].
The demanding academic and social schedules of college students also contribute to delayed circadian rhythms. Balancing classes, homework, jobs, and social activities leads to irregular sleep patterns. Late-night studying or socializing delays sleep onset and disrupts circadian rhythms [36]. Academic pressure increases stress, exacerbating sleep disturbances and circadian misalignment [47].
Late-night social media use also mediates the association between diurnal type and sleep quality. Watching movies or listening to music late at night was the strongest mediator of the association between diurnal type and sleep and tiredness. The most prominent finding shows that of all different media forms, watching movies or listening to music late at night were associated with increased daytime tiredness, whereas late social media use was associated with poor sleep quality [48]. The proliferation of smartphones has exacerbated the disruption of circadian rhythms among college students. Exposure to blue light emitted by screens can suppress melatonin production, a hormone crucial for sleep regulation, thus delaying sleep onset [49]. The widespread use of smartphones for social media, gaming, and studying late into the night has made it increasingly difficult for students to maintain regular sleep patterns. A study by Lemola et al. [50] found a strong correlation between high smartphone usage at night and increased levels of sleep disturbances and depressive symptoms. This digital interference in natural sleep cycles is a significant contributor to the growing mental health crisis in college populations, highlighting the need for interventions aimed at reducing screen time before bed.
Lifestyle choices, including diet, exercise, and substance use, also influence circadian rhythms. Irregular eating patterns, lack of physical activity, and caffeine consumption disrupt the sleep-wake cycle. Caffeine use for late-night studying interferes with regular sleep [51]. Irregular meal times and lack of natural light exposure during the day, especially in the morning, further disrupt circadian rhythms [14].

HEALTHY LIFESTYLE HABITS TO MAINTAIN A CIRCADIAN RHYTHM

Maintaining a healthy circadian rhythm is crucial for college students as it significantly influences their overall health, academic performance, and well-being. Here are key aspects to consider (Table 1).

Consistent sleep schedule

Regular sleep and wake times

Encourage students to maintain a consistent sleep schedule by going to bed and waking up at the same time every day, including weekends. This consistency helps regulate the body’s internal clock and enhances sleep quality [35,37]. Consistent sleep schedules are linked to better academic performance and improved mental health [36,52].

Adequate sleep duration

College students should aim for 7-8 hours of sleep per night to ensure they are well-rested and can function optimally during the day [3]. Adequate sleep duration is essential for cognitive functions, mood regulation, and overall health [53,54].

Appropriate light exposure

Morning light exposure

Exposure to natural light, especially in the morning, is vital for resetting the circadian clock and promoting wakefulness. Students should spend time outdoors or in well-lit environments during the first part of the day [14,55]. Morning light exposure has been shown to improve mood and alertness [56].

Limit light at night

Minimizing exposure to artificial light, particularly blue light from screens, in the evening can help signal to the body that it is time to wind down for sleep. Using blue light filters on devices and dimming lights in the evening can be beneficial [49]. Reducing light exposure before bed can enhance melatonin production and improve sleep quality [57,58].

Meal timing

Regular meal times

Eating meals at consistent times each day supports the alignment of peripheral clocks in the body. Irregular meal times can disrupt metabolic processes and circadian rhythms [52,57]. Regular meal times are associated with better metabolic health and weight management [59].

Avoid late-night eating

Consuming large meals late at night can interfere with sleep and metabolism. Encourage students to have their last meal at least 2-3 hours before bedtime. Late-night eating has been linked to increased body fat and impaired glucose metabolism [60-62].

Physical activity

Regular exercise

Daily physical activity, especially in the morning or early afternoon, can help regulate sleep patterns and improve overall circadian rhythm stability. However, vigorous exercise close to bedtime should be avoided as it can be stimulating and interfere with sleep [40,53,63]. Regular exercise is also beneficial for reducing stress and enhancing mood [64].

Limiting stimulants

Reduce caffeine and alcohol intake

Caffeine and alcohol can interfere with sleep quality and circadian rhythms. Encourage students to limit their consumption of these substances, especially in the hours leading up to bedtime. Caffeine, even when consumed six hours before bedtime, can significantly disrupt sleep [57,65]. Alcohol consumption before bed can reduce sleep quality and alter sleep stages [66].

Sleep-friendly environment

Optimize the sleep environment

A cool, quiet, and dark room can enhance sleep quality. Us-ing blackout curtains, earplugs, and maintaining a comfortable room temperature can create an ideal sleeping environment. Optimizing the sleep environment has been shown to improve sleep quality and reduce sleep disturbances [52,67].

Smartphone use in bed

Limit screen time before bed

The blue light emitted by phones, tablets, and computers can delay sleep onset by suppressing melatonin production. Encouraging students to turn off screens at least an hour before bed can improve sleep quality [14,68]] Limiting screen time can also reduce nighttime awakenings and improve sleep duration [69].

Education and awareness

Health education programs

Colleges can offer programs and workshops that educate students on the importance of sleep and strategies to maintain healthy circadian rhythms. Educational interventions can increase awareness and promote healthy sleep behaviors [36]. Providing access to counseling and mental health services can help students manage stress and other issues that may affect their sleep patterns. Mental health support is crucial for addressing underlying issues that contribute to sleep disturbances [70].
By considering these aspects, college students can maintain healthy circadian rhythms, leading to better academic performance, improved health, and overall well-being. Implementing these strategies can foster a supportive environment that promotes optimal sleep and circadian health for college students.

COMMON PSYCHIATRIC DISORDERS IN COLLEGE STUDENTS AND ADJUNCTIVE TREATMENTS FOR CIRCADIAN MISALIGNMENT

Early adulthood is a critical period often associated with the onset of various psychiatric disorders. MDD is one of the most common mental health disorders. In the general population, the lifetime prevalence of MDD is about 15%-20% [71,72]. However, among individuals aged 18-25, the prevalence is notably higher, with approximately 18.6% experiencing a major depressive episode [72]. This increased incidence is likely due to the significant life changes and stressors characteristic of early adulthood. Anxiety disorders are also prevalent during early adulthood. The lifetime prevalence of anxiety disorders in the general population is around 25%-30% [71]. In the 18-29 age group, the prevalence ranges from 20%-30%.
BD has a general population prevalence of about 1%-3% over a lifetime [73]. However, the first episode of BD typically occurs between the ages of 18 and 25, making early adulthood a high-risk period for the onset of this condition. Schizophrenia is another severe psychiatric disorder that often emerges in early adulthood. Its lifetime prevalence in the general population is about 0.5%-1% [74]. The typical age of onset is in the early to mid-20s for men and late 20s for women, placing early adulthood as the critical period for the first presentation of symptoms.
Eating disorders, including anorexia nervosa and bulimia nervosa, show a higher prevalence among young women aged 18-25. In the general population, the lifetime prevalence of anorexia nervosa is approximately 0.5%-1%, and bulimia nervosa is about 1%-3% [75]. In early adulthood, the prevalence can increase to around 1%-4%, particularly among females, due to heightened concerns about body image and societal pressures. Substance use disorders are also more common during early adulthood. The lifetime prevalence of alcohol use disorder is approximately 12%-17%, and drug use disorders are about 8%-10% in the general population [76]. For individuals aged 18-25, the prevalence of substance use disorders can be as high as 20%-25%.
Early adulthood mental illness treatment often involves a combination of psychotherapy, medication, and lifestyle modifications to effectively manage symptoms and improve overall well-being. However, as previously mentioned, this age period is characterized by disruptions in the circadian rhythm, and it is common for delays or disturbances in circadian rhythm to occur at this age. Therefore, it is crucial to additionally apply therapeutic approaches that help correct the circadian rhythm.

Light therapy

Bright light exposure

One of the most effective treatments for DSPS is bright light therapy. The principle behind this method is to expose the individual to bright light at specific times of the day to shift the circadian rhythm earlier. Typically, exposure to bright light in the morning (shortly after waking) can advance the sleep phase. Light boxes that emit 10,000 lux are commonly used for this purpose. The individual should sit in front of the light box for 30 minutes to an hour every morning. Studies have shown that morning light exposure is critical in advancing the circadian rhythm for individuals with DSPS [77,78].

Avoidance of evening light

In addition to morning light exposure, it is crucial to reduce exposure to bright lights in the evening, as this can further delay the circadian rhythm. This includes minimizing the use of electronic devices that emit blue light, such as smartphones, tablets, and computers. Blue light-blocking glasses or screen filters can also be helpful in reducing evening light exposure. Evidence suggests that reducing evening light exposure can significantly improve sleep onset and duration [79].

Chronotherapy

Chronotherapy is a behavioral technique that involves gradually adjusting sleep and wake times to an earlier schedule. This method requires strict adherence to a schedule where the individual goes to bed and wakes up 15 minutes earlier each day (or every few days) until the desired sleep-wake times are achieved. This gradual adjustment helps the body’s internal clock to reset in a controlled manner. Chronotherapy has been shown to be effective in managing DSPS by realigning the circadian rhythm with societal norms [80].

Melatonin supplementation

Melatonin, a hormone that regulates sleep-wake cycles, can be used to shift the circadian rhythm. Taking melatonin supplements in the early evening (typically 1-2 hours before the desired bedtime) can help advance the sleep phase. The appropriate timing and dosage of melatonin should be determined in consultation with a healthcare professional, as incorrect usage can worsen circadian misalignment. Research has demonstrated the efficacy of melatonin in advancing the circadian phase in individuals with DSPS [81,82].

Cognitive Behavioral Therapy for Insomnia (CBT-I)

CBT-I is a structured program that helps individuals change thoughts and behaviors that interfere with sleep. For those with DSPS, CBT-I can address maladaptive sleep habits and promote healthier sleep patterns. Techniques include sleep restriction therapy, stimulus control, relaxation training, and cognitive restructuring. By improving overall sleep hygiene and reducing anxiety around sleep, CBT-I can support the resetting of the circadian rhythm. Studies have shown that CBT-I can be effective in improving sleep outcomes in individuals with DSPS [83,84].

CONCLUSION

Maintaining stable circadian rhythms is essential for mental health, particularly among undergraduate students. Modern lifestyle factors, including the pervasive use of electronic devices and the implications of social distancing measures, significantly challenge circadian rhythm stability. However, with appropriate interventions, such as lifestyle modifications and the utilization of technological tools, it is feasible to mitigate these effects and enhance mental health outcomes. Continued research and the implementation of circadian rhythm-focused strategies in mental health care are imperative. Resetting an already delayed circadian rhythm necessitates a multifaceted approach that combines light therapy, chronotherapy, melatonin supplementation, cognitive-behavioral strategies, and lifestyle adjustments. It is crucial for individuals to collaborate closely with healthcare providers to develop a personalized treatment plan tailored to their specific needs and circumstances. With consistency and adherence to these methods, it is possible to realign the circadian rhythm and improve overall sleep quality and daily functioning.

Notes

Availability of Data and Material

Data sharing not applicable to this article as no datasets were generated or analyzed during the study.

Conflicts of Interest

Heon-Jeong Lee, a contributing editor of the Psychiatry Investigation, were not involved in the editorial evaluation or decision to publish this article. All remaining authors have declared no conflicts of interest.

Author Contributions

Conceptualization: Heon-Jeong Lee. Data curation: Ji Won Yeom, Soohyun Park. Formal analysis: Ji Won Yeom. Funding acquisition: Heon-Jeong Lee. Investigation: Ji Won Yeom, Soohyun Park. Methodology: Heon-Jeong Lee. Project administration: Heon-Jeong Lee. Writing—original draft: all authors. Writing—review & editing: al authors.

Funding Statement

This study was supported by grant number HI22C147200 from the Ministry of Health & Welfare.

ACKNOWLEDGEMENTS

None

Figure 1.
The importance of circadian rhythm in the development of mental disorders. Exposure to stress can commonly lead to temporary symptoms of depression, anxiety, and insomnia. However, maintaining a regular daily routine generally allows these psychiatric symptoms to resolve on their own. On the other hand, if an individual has a habit of irregular living or continues irregular routines after experiencing stress, this can lead to a delay in the circadian rhythm in susceptible individuals, resulting in mood disorders such as depression and bipolar disorder.
pi-2024-0250f1.jpg
Table 1.
Summary of the key aspects of maintaining a healthy circadian rhythm for college students
Aspect Recommendation Details
Consistent sleep schedule Regular sleep and wake times Maintain a consistent sleep schedule by going to bed and waking up at the same time every day, including weekends
Adequate sleep duration Aim for 7-8 hours of sleep per night to ensure optimal functioning during the day
Appropriate light exposure Morning light exposure Exposure to natural light in the morning is vital for resetting the circadian clock and promoting wakefulness
Limit light at night Minimize exposure to artificial light, especially blue light from screens, in the evening to help signal to the body that it is time to wind down for sleep
Meal timing Regular meal times Eating meals at consistent times each day supports the alignment of peripheral clocks in the body and is associated with better metabolic health and weight management
Avoid late-night eating Avoid consuming large meals late at night as it can interfere with sleep and metabolism
Physical activity Regular exercise Engage in daily physical activity, especially in the morning or early afternoon, to help regulate sleep patterns and improve overall circadian rhythm stability. Avoid vigorous exercise close to bedtime
Limiting stimulants Reduce caffeine and alcohol Limit the consumption of caffeine and alcohol, especially in the hours leading up to bedtime, as they can interfere with sleep quality and circadian rhythms
Sleep-friendly environment Optimize the sleep environment Enhance sleep quality by optimizing the sleep environment
Smartphone use in bed Limit screen time before bed Turn off screens at least an hour before bed to avoid delaying sleep onset by suppressing melatonin production
Education and awareness Health education programs Colleges can offer programs and workshops to educate students on the importance of sleep and strategies to maintain healthy circadian rhythms

REFERENCES

1. Becker SP, Jarrett MA, Luebbe AM, Garner AA, Burns GL, Kofler MJ. Sleep in a large, multi-university sample of college students: sleep problem prevalence, sex differences, and mental health correlates. Sleep Health 2018;4:174-181.
crossref pmid pmc
2. Lund HG, Reider BD, Whiting AB, Prichard JR. Sleep patterns and predictors of disturbed sleep in a large population of college students. J Adolesc Health 2010;46:124-132.
crossref pmid
3. Hirshkowitz M, Whiton K, Albert SM, Alessi C, Bruni O, DonCarlos L, et al. National Sleep Foundation’s updated sleep duration recommendations: final report. Sleep Health 2015;1:233-243.
crossref pmid
4. Zhong J, Katigbak C, Gregas M, Ye L. Patterns of sleep habits and their impact on nighttime sleep quality in college students. Sleep 2023;46(Suppl 1):A77-A78.

5. Han HH. [The relationship among smartphone addiction, lack of sleep and sleeping hours of university students]. J Converg Inf Technol 2019;9:213-219. Korean.

6. Itani O, Jike M, Watanabe N, Kaneita Y. Short sleep duration and health outcomes: a systematic review, meta-analysis, and meta-regression. Sleep Med 2017;32:246-256.
crossref pmid
7. Sivertsen B, Hysing M, Harvey AG, Petrie KJ. The epidemiology of insomnia and sleep duration across mental and physical health: the SHoT study. Front Psychol 2021;12:662572
crossref pmid pmc
8. Tobaldini E, Costantino G, Solbiati M, Cogliati C, Kara T, Nobili L, et al. Sleep, sleep deprivation, autonomic nervous system and cardiovascular diseases. Neurosci Biobehav Rev 2017;74(Pt B):321-329.
crossref pmid
9. Blake MJ, Trinder JA, Allen NB. Mechanisms underlying the association between insomnia, anxiety, and depression in adolescence: implications for behavioral sleep interventions. Clin Psychol Rev 2018;63:25-40.
crossref pmid
10. Danielsson NS, Harvey AG, Macdonald S, Jansson-Fröjmark M, Linton SJ. Sleep disturbance and depressive symptoms in adolescence: the role of catastrophic worry. J Youth Adolesc 2013;42:1223-1233.
crossref pmid pdf
11. Curcio G, Ferrara M, De Gennaro L. Sleep loss, learning capacity and academic performance. Sleep Med Rev 2006;10:323-337.
crossref pmid
12. Hartmann ME, Prichard JR. Calculating the contribution of sleep problems to undergraduates’ academic success. Sleep Health 2018;4:463-471.
crossref pmid
13. Okano K, Kaczmarzyk JR, Dave N, Gabrieli JDE, Grossman JC. Sleep quality, duration, and consistency are associated with better academic performance in college students. NPJ Sci Learn 2019;4:16
crossref pmid pmc pdf
14. Brown TM, Brainard GC, Cajochen C, Czeisler CA, Hanifin JP, Lockley SW, et al. Recommendations for daytime, evening, and nighttime indoor light exposure to best support physiology, sleep, and wakefulness in healthy adults. PLoS Biol 2022;20:e3001571
crossref pmid pmc
15. Walbeek TJ, Harrison EM, Gorman MR, Glickman GL. Naturalistic intensities of light at night: a review of the potent effects of very dim light on circadian responses and considerations for translational research. Front Neurol 2021;12:625334
crossref pmid pmc
16. Lee HJ. Circadian misalignment and bipolar disorder. Chronobiol Med 2019;1:132-136.
crossref pdf
17. Yeom JW, Lee HJ. Exploring the relationship between circadian rhythm shifts and postpartum depression. Chronobiol Med 2023;5:53-57.
crossref pdf
18. Lee HJ, Cho CH, Lee T, Jeong J, Yeom JW, Kim S, et al. Prediction of impending mood episode recurrence using real-time digital phenotypes in major depression and bipolar disorders in South Korea: a prospective nationwide cohort study. Psychol Med 2023;53:5636-5644.
crossref pmid
19. Song YM, Jeong J, de Los Reyes AA 5th, Lim D, Cho CH, Yeom JW, et al. Causal dynamics of sleep, circadian rhythm, and mood symptoms in patients with major depression and bipolar disorder: insights from longitudinal wearable device data. EBioMedicine 2024;103:105094
crossref pmid pmc
20. Quan L, Lu W, Zhen R, Zhou X. Post-traumatic stress disorders, anxiety, and depression in college students during the COVID-19 pandemic: a cross-sectional study. BMC Psychiatry 2023;23:228
crossref pmid pmc pdf
21. Holm-Hadulla RM, Wendler H, Baracsi G, Storck T, Möltner A, Herpertz SC. Depression and social isolation during the COVID-19 pandemic in a student population: the effects of establishing and relaxing social restrictions. Front Psychiatry 2023;14:1200643
crossref pmid pmc
22. Lee HJ. Human circadian rhythm and social distancing in the COVID-19 crisis. Chronobiol Med 2020;2:45-46.
crossref pdf
23. Reppert SM, Weaver DR. Coordination of circadian timing in mammals. Nature 2002;418:935-941.
crossref pmid pdf
24. Golombek DA, Rosenstein RE. Physiology of circadian entrainment. Physiol Rev 2010;90:1063-1102.
crossref pmid
25. Ko CH, Takahashi JS. Molecular components of the mammalian circadian clock. Hum Mol Genet 2006;15(Suppl 2):R271-R277.
crossref pmid
26. Gallego M, Virshup DM. Post-translational modifications regulate the ticking of the circadian clock. Nat Rev Mol Cell Biol 2007;8:139-148.
crossref pmid pdf
27. Hirayama J, Sahar S, Grimaldi B, Tamaru T, Takamatsu K, Nakahata Y, et al. CLOCK-mediated acetylation of BMAL1 controls circadian function. Nature 2007;450:1086-1090.
crossref pmid pdf
28. Mohawk JA, Green CB, Takahashi JS. Central and peripheral circadian clocks in mammals. Annu Rev Neurosci 2012;35:445-462.
crossref pmid pmc
29. Balsalobre A, Brown SA, Marcacci L, Tronche F, Kellendonk C, Reichardt HM, et al. Resetting of circadian time in peripheral tissues by glucocorticoid signaling. Science 2000;289:2344-2347.
crossref pmid
30. Bass J, Takahashi JS. Circadian integration of metabolism and energetics. Science 2010;330:1349-1354.
crossref pmid pmc
31. Roenneberg T, Wirz-Justice A, Merrow M. Life between clocks: daily temporal patterns of human chronotypes. J Biol Rhythms 2003;18:80-90.
crossref pmid pdf
32. Palagini L, Geoffroy PA, Miniati M, Perugi G, Biggio G, Marazziti D, et al. Insomnia, sleep loss, and circadian sleep disturbances in mood disorders: a pathway toward neurodegeneration and neuroprogression? A theoretical review. CNS Spectr 2022;27:298-308.
crossref pmid
33. Lyall LM, Wyse CA, Graham N, Ferguson A, Lyall DM, Cullen B, et al. Association of disrupted circadian rhythmicity with mood disorders, subjective wellbeing, and cognitive function: a cross-sectional study of 91 105 participants from the UK Biobank. Lancet Psychiatry 2018;5:507-514.
crossref pmid
34. Moon JH, Cho CH, Son GH, Geum D, Chung S, Kim H, et al. Advanced circadian phase in mania and delayed circadian phase in mixed mania and depression returned to normal after treatment of bipolar disorder. EBioMedicine 2016;11:285-295.
crossref pmid pmc
35. Crowley SJ, Wolfson AR, Tarokh L, Carskadon MA. An update on adolescent sleep: new evidence informing the perfect storm model. J Adolesc 2018;67:55-65.
crossref pmid pmc pdf
36. Hershner SD, Chervin RD. Causes and consequences of sleepiness among college students. Nat Sci Sleep 2014;6:73-84.
crossref pmid pmc
37. Taylor DJ, Jenni OG, Acebo C, Carskadon MA. Sleep tendency during extended wakefulness: insights into adolescent sleep regulation and behavior. J Sleep Res 2005;14:239-244.
crossref pmid
38. Kuula L, Pesonen AK, Merikanto I, Gradisar M, Lahti J, Heinonen K, et al. Development of late circadian preference: sleep timing from childhood to late adolescence. J Pediatr 2018;194:182-189.e1.
crossref pmid
39. Sadeh A, Dahl RE, Shahar G, Rosenblat-Stein S. Sleep and the transition to adolescence: a longitudinal study. Sleep 2009;32:1602-1609.
crossref pmid pmc
40. Kuula L, Lipsanen J, Partonen T, Kauramäki J, Halonen R, Pesonen AK. Endogenous circadian temperature rhythms relate to adolescents’ daytime physical activity. Front Physiol 2022;13:947184
crossref pmid pmc
41. Crowley SJ, Acebo C, Carskadon MA. Sleep, circadian rhythms, and delayed phase in adolescence. Sleep Med 2007;8:602-612.
crossref pmid
42. Hysing M, Pallesen S, Stormark KM, Lundervold AJ, Sivertsen B. Sleep patterns and insomnia among adolescents: a population-based study. J Sleep Res 2013;22:549-556.
crossref pmid pdf
43. Feder MA, Baroni A. Just let me sleep in: identifying and treating delayed sleep phase disorder in adolescents. Child Adolesc Psychiatr Clin N Am 2021;30:159-174.
pmid
44. Sivertsen B, Pallesen S, Stormark KM, Bøe T, Lundervold AJ, Hysing M. Delayed sleep phase syndrome in adolescents: prevalence and correlates in a large population based study. BMC Public Health 2013;13:1163
crossref pmid pmc pdf
45. Sivertsen B, Harvey AG, Pallesen S, Hysing M. Mental health problems in adolescents with delayed sleep phase: results from a large populationbased study in Norway. J Sleep Res 2015;24:11-18.
pmid
46. Lee HJ, Rex KM, Nievergelt CM, Kelsoe JR, Kripke DF. Delayed sleep phase syndrome is related to seasonal affective disorder. J Affect Disord 2011;133:573-579.
crossref pmid pmc
47. Bahammam AS, Alaseem AM, Alzakri AA, Almeneessier AS, Sharif MM. The relationship between sleep and wake habits and academic performance in medical students: a cross-sectional study. BMC Med Educ 2012;12:61
crossref pmid pmc pdf
48. Kortesoja L, Vainikainen MP, Hotulainen R, Merikanto I. Late-night digital media use in relation to chronotype, sleep and tiredness on school days in adolescence. J Youth Adolesc 2023;52:419-433.
crossref pmid pmc pdf
49. Chang AM, Aeschbach D, Duffy JF, Czeisler CA. Evening use of lightemitting eReaders negatively affects sleep, circadian timing, and nextmorning alertness. Proc Natl Acad Sci U S A 2015;112:1232-1237.
crossref pmid pmc
50. Lemola S, Perkinson-Gloor N, Brand S, Dewald-Kaufmann JF, Grob A. Adolescents’ electronic media use at night, sleep disturbance, and depressive symptoms in the smartphone age. J Youth Adolesc 2015;44:405-418.
crossref pmid pdf
51. Burke TM, Markwald RR, McHill AW, Chinoy ED, Snider JA, Bessman SC, et al. Effects of caffeine on the human circadian clock in vivo and in vitro. Sci Transl Med 2015;7:305ra146
crossref pmid pmc
52. BaHammam AS, Pirzada A. Timing matters: the interplay between early mealtime, circadian rhythms, gene expression, circadian hormones, and metabolism-a narrative review. Clocks Sleep 2023;5:507-535.
crossref pmid pmc
53. Potter GD, Skene DJ, Arendt J, Cade JE, Grant PJ, Hardie LJ. Circadian rhythm and sleep disruption: causes, metabolic consequences, and countermeasures. Endocr Rev 2016;37:584-608.
crossref pmid pmc pdf
54. Watson NF, Badr MS, Belenky G, Bliwise DL, Buxton OM, Buysse D, et al. Recommended amount of sleep for a healthy adult: a joint consensus statement of the American Academy of Sleep Medicine and Sleep Research Society. Sleep 2015;38:843-844.
crossref pmid pmc
55. Roenneberg T, Merrow M. The circadian clock and human health. Curr Biol 2016;26:R432-R443.
crossref pmid
56. Czeisler CA, Kronauer RE, Allan JS, Duffy JF, Jewett ME, Brown EN, et al. Bright light induction of strong (type 0) resetting of the human circadian pacemaker. Science 1989;244:1328-1333.
crossref pmid
57. Meléndez-Fernández OH, Liu JA, Nelson RJ. Circadian rhythms disrupted by light at night and mistimed food intake alter hormonal rhythms and metabolism. Int J Mol Sci 2023;24:3392
crossref pmid pmc
58. Gooley JJ, Chamberlain K, Smith KA, Khalsa SB, Rajaratnam SM, Van Reen E, et al. Exposure to room light before bedtime suppresses melatonin onset and shortens melatonin duration in humans. J Clin Endocrinol Metab 2011;96:E463-E472.
crossref pmid pmc
59. Scheer FA, Hilton MF, Mantzoros CS, Shea SA. Adverse metabolic and cardiovascular consequences of circadian misalignment. Proc Natl Acad Sci U S A 2009;106:4453-4458.
crossref pmid pmc
60. Vujović N, Piron MJ, Qian J, Chellappa SL, Nedeltcheva A, Barr D, et al. Late isocaloric eating increases hunger, decreases energy expenditure, and modifies metabolic pathways in adults with overweight and obesity. Cell Metab 2022;34:1486-1498.e7.
crossref pmid pmc
61. Kim S, Lee HJ. Sleep and circadian rhythm disturbances in eating disorders. Chronobiol Med 2020;2:141-147.
crossref pdf
62. Lee HJ. Unraveling the significance of circadian rhythms for health. Chronobiol Med 2022;4:93-94.
crossref pdf
63. Kline CE. The bidirectional relationship between exercise and sleep: implications for exercise adherence and sleep improvement. Am J Lifestyle Med 2014;8:375-379.
pmid
64. Mikkelsen K, Stojanovska L, Polenakovic M, Bosevski M, Apostolopoulos V. Exercise and mental health. Maturitas 2017;106:48-56.
crossref pmid
65. Drake C, Roehrs T, Shambroom J, Roth T. Caffeine effects on sleep taken 0, 3, or 6 hours before going to bed. J Clin Sleep Med 2013;9:1195-1200.
crossref pmid pmc
66. Roehrs T, Roth T. Sleep, sleepiness, sleep disorders and alcohol use and abuse. Sleep Med Rev 2001;5:287-297.
crossref pmid
67. Stepanski EJ, Wyatt JK. Use of sleep hygiene in the treatment of insomnia. Sleep Med Rev 2003;7:215-225.
crossref pmid
68. Cajochen C, Frey S, Anders D, Späti J, Bues M, Pross A, et al. Evening exposure to a light-emitting diodes (LED)-backlit computer screen affects circadian physiology and cognitive performance. J Appl Physiol (1985) 2011;110:1432-1438.
crossref pmid
69. Hale L, Guan S. Screen time and sleep among school-aged children and adolescents: a systematic literature review. Sleep Med Rev 2015;21:50-58.
crossref pmid pmc
70. Hunt J, Eisenberg D. Mental health problems and help-seeking behavior among college students. J Adolesc Health 2010;46:3-10.
crossref pmid
71. Kessler RC, Berglund P, Demler O, Jin R, Merikangas KR, Walters EE. Lifetime prevalence and age-of-onset distributions of DSM-IV disorders in the national comorbidity survey replication. Arch Gen Psychiatry 2005;62:593-602.
crossref pmid
72. National Institute of Mental Health. Major depression [Internet]. Available at: https://www.nimh.nih.gov/health/statistics/major-depression. Accessed July 20, 2024.

73. Merikangas KR, Akiskal HS, Angst J, Greenberg PE, Hirschfeld RM, Petukhova M, et al. Lifetime and 12-month prevalence of bipolar spectrum disorder in the national comorbidity survey replication. Arch Gen Psychiatry 2007;64:543-552.
crossref pmid pmc
74. Saha S, Chant D, Welham J, McGrath J. A systematic review of the prevalence of schizophrenia. PLoS Med 2005;2:e141
crossref pmid pmc
75. Hudson JI, Hiripi E, Pope HG Jr, Kessler RC. The prevalence and correlates of eating disorders in the national comorbidity survey replication. Biol Psychiatry 2007;61:348-358.
crossref pmid pmc
76. Grant BF, Stinson FS, Dawson DA, Chou SP, Dufour MC, Compton W, et al. Prevalence and co-occurrence of substance use disorders and independent mood and anxiety disorders: results from the national epidemiologic survey on alcohol and related conditions. Arch Gen Psychiatry 2004;61:807-816.
crossref pmid
77. Rosenthal NE, Joseph-Vanderpool JR, Levendosky AA, Johnston SH, Allen R, Kelly KA, et al. Phase-shifting effects of bright morning light as treatment for delayed sleep phase syndrome. Sleep 1990;13:354-361.
pmid
78. Khalsa SB, Jewett ME, Cajochen C, Czeisler CA. A phase response curve to single bright light pulses in human subjects. J Physiol 2003;549(Pt 3):945-952.
crossref pmid pmc pdf
79. Brown TM, Brainard GC, Cajochen C, Czeisler CA, Hanifin JP, Lockley SW, et al. Recommendations for daytime, evening, and nighttime indoor light exposure to best support physiology, sleep, and wakefulness in healthy adults. PLOS Biology 2022;20:e3001571
crossref pmid pmc
80. Bjorvatn B, Pallesen S. A practical approach to circadian rhythm sleep disorders. Sleep Med Rev 2009;13:47-60.
crossref pmid
81. Lewy AJ, Sack RL. The dim light melatonin onset as a marker for circadian phase position. Chronobiol Int 1989;6:93-102.
pmid
82. Arendt J. Melatonin and human rhythms. Chronobiol Int 2006;23:21-37.
crossref pmid
83. Edinger JD, Means MK. Cognitive-behavioral therapy for primary insomnia. Clin Psychol Rev 2005;25:539-558.
crossref pmid
84. Harvey AG. A cognitive model of insomnia. Behav Res Ther 2002;40:869-893.
crossref pmid


ABOUT
AUTHOR INFORMATION
ARTICLE CATEGORY

Browse all articles >

BROWSE ARTICLES
Editorial Office
#522, 27, Seochojungang-ro 24-gil, Seocho-gu, Seoul 06601, Korea
Tel: +82-2-717-0892    E-mail: psychiatryinvest@gmail.com                

Copyright © 2025 by Korean Neuropsychiatric Association.

Developed in M2PI

Close layer
prev next