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. 2025 Jun 18;10:100145. doi: 10.1016/j.sleepx.2025.100145

The effect and safety of sleep interventions on suicidal thoughts and behavior – A systematic review and meta-analyses

Paula von Spreckelsen a, Daan Schouten b,c, Natasha G Waslam a, Patricia Katuin d, Henriette D Heering a,e,f,, Caroline Planting e,f, Niki Antypa g, Liia Kivelä g, Marike Lancel h,i,j, Lizanne JS Schweren a
PMCID: PMC12272457  PMID: 40688431

Abstract

Background

Sleep disturbances are a risk factor for suicidal ideation, suicide attempts and suicide. While recent findings suggest that improving sleep by psychotherapeutic sleep interventions exerts a positive effect on suicidality, there are also indications that certain sleep medications are associated with an increased risk for suicidality. Given these discrepancies, the current study systematically reviewed the effect of non-pharmacological and pharmacological sleep interventions on suicidality.

Methods

A systematic literature search of various scientific databases was conducted (March 2025). Randomized controlled trials that examined the effect of sleep interventions on suicidality were searched for.

Results

The search strategy resulted in 5037 unique articles. A total of k = 44 articles (N = 14965 participants) were included in the systematic review. The results indicate that sleep interventions, particularly psychotherapeutic sleep treatments (g = −0.17, [-0.26 to −0.08]), result in a small significant reduction of suicidal ideation. No conclusive evidence was found for the effect or safety of pharmacotherapy or light therapy targeting sleep disturbance on suicidality. The findings should be interpreted in light of the limited number of studies with often small sample sizes, methodological inconsistencies in monitoring suicidality as an adverse event, restrictions on the inclusion of people with suicidality, and reliance on suicidal ideation as an outcome measure of suicidality.

Conclusion

Health care professionals are recommended to apply psychotherapeutic sleep interventions, such as cognitive behavioral therapy for insomnia, to reduce suicidal ideation in clients with disturbed sleep. When prescribing medications for disturbed sleep, we recommend professionals to closely monitor clients for potential adverse effects on suicidality.

Keywords: Meta-analysis, Sleep intervention, Suicide, Psychotherapy, Pharmacotherapy

Highlights

  • (Psychotherapeutic) Sleep interventions can reduce suicidal ideation.

  • There is uncertainty about the effect and safety of pharmacological sleep interventions on suicidality.

  • It is recommended that clinicians apply psychotherapeutic sleep interventions to target suicidality in clients with sleep disturbances.

  • Clients receiving medication for disturbed sleep should be closely monitored for adverse effects on suicidality.

1. Introduction

Suicide constitutes a serious public health problem. Worldwide, more than 700,000 people die by suicide each year. For every completed suicide, many more people attempt it. Each loss is a tragedy that impacts families, communities, and entire countries, leaving lasting effects on those left behind [1]. We define suicidality as the range of thoughts, behaviors, and tendencies related to suicide including suicidal ideation (suicidal thoughts), suicide attempts and completed suicide. There are several risk factors for suicidality. Next to non-modifiable risk factors (such as age, gender, or a history of trauma), there are also modifiable risk factors to the experience of suicidality, including depression, substance abuse and sleep disturbances [e.g., 2]. Based on several meta-analyses, sleep disturbances have been identified as a risk factor for suicidal ideation, suicide attempts and death by suicide [e.g., 3,4]. A meta-analysis of cohort studies found that sleep disturbances are predictive of suicidality, demonstrating a 3.5-fold higher risk for suicide attempt and a 1.8-fold higher risk for completed suicide in people with sleep disturbances [2]. Another meta-analysis of longitudinal studies found that sleep disturbances were weakly predictive of suicidality, with insomnia and nightmares being the strongest predictors of suicidal ideation and suicide attempt respectively [3].

Sleep is fundamental for overall well-being as well as physical and mental health [4]. However, various factors such as stress, lifestyle changes, pain and psychiatric conditions can cause sleep problems [4]. Individuals experiencing disrupted sleep often endure various adverse effects, including daytime fatigue, mood disturbances and impaired cognitive function [[5], [6], [7], [8]]. Sleep disorders (or sleep-wake disorders) involve long-lasting problems with the quality, timing, and/or duration of sleep, which result in daytime distress and impairment in functioning [9]. While insomnia is the most common sleep disorder [10], other sleep-wake disorders include hypersomnia, parasomnias (such as nightmares), obstructive sleep apnea syndrome, narcolepsy, or restless leg syndrome. Sleep disorders are known to be a risk factor for other clinical conditions (e.g., anxiety disorders, depressive disorders [6,[11], [12], [13]]). There are several mechanisms that might underlie the relation between sleep disturbances and the increased risk for suicidality [14]. For example, there is often little social support and preventative measures available during the nighttime [15], making nocturnal wakefulness risky. Insufficient or inadequate sleep may also contribute to the downward spiral of negative thinking [16,17], unhelpful emotion regulation strategies [15], reduced executive function/problem solving [18] and can promote impulsive and aggressive behavior due to a decline of self-regulation resources [19,20].

There are various approaches to treat sleep disorders [21,22]. The most frequently used are cognitive behavioral therapy for insomnia (CBT-I) and pharmacological treatment. CBT-I is an evidence-based treatment that aims to improve sleep quality and efficiency by modifying maladaptive cognitions and behaviors contributing to chronic insomnia. It typically includes components such as sleep education, sleep hygiene, cognitive restructuring, stimulus control, relaxation techniques, sleep restriction, and sleep scheduling. Furthermore, there are treatments for specific sleep disorders other than insomnia, such as continuous positive airway pressure (CPAP) for obstructive sleep apnea or imagery rehearsal therapy (IRT) and eye movement desensitization and reprocessing (EMDR) for the treatment of nightmares. Chronobiological treatments, like light therapy, have also been used to improve sleep disturbance [22]. Generally, it is recommended to first address insomnia with cognitive behavioral therapy before considering pharmacotherapy [22,23]. The most frequently prescribed medicines for insomnia, commonly referred to as sleep medications, are benzodiazepines and melatonin, but there is a wide variety of other sleep medications, such as dual orexin receptor antagonists (DORA's [24]) or Z-drugs (benzodiazepine-like drugs with mainly hypnotic effects and less anxiolytic, anti-epileptic and muscle relaxant effects). The advantage of pharmacotherapy lies in its rapid effect and often low cost. However, there are several drawbacks associated with the pharmacological approach to insomnia [22,23,25]. Although sleep duration and sleep continuity often improve, there can be a negative impact on both deep sleep and rapid eye movement (REM) sleep. Additionally, there is a risk of side effects, such as daytime drowsiness, the development of tolerance and dependence, or driving impairments (see for example [26,27]). It is not recommended to use sleep medications for the long-term management of insomnia, but instead to limit treatment duration to a short term (a maximum of 3–4 weeks). On the other side of the pharmacological spectrum, wake-promoting agents like armodafinil or solriamfetol can be used in the management of sleep disorders such as narcolepsy. Side effects of stimulant medications may include increased feelings of anxiety and risk of addiction [28,29].

Knowing that disturbed sleep can increase the risk for suicidality and that there are effective interventions for sleep disorders, one would expect that treatment of sleep disturbances reduces the risk for suicidality. However, so far it is not completely clear to what extent the treatment of sleep problems influences suicidality. There are indications that CBT-I may contribute to a reduction in suicidality. In one of the first trials examining suicidal ideation as an outcome, Manber and colleagues [30] reported data from 301 adults who participated in seven 90-min group CBT-I sessions, finding that 23 % of patients endorsed suicidal ideation before treatment, with this rate decreasing to 10 % post-treatment. A large-scale evaluation found that CBT-I was associated with reduced suicidal ideation among veterans, even after accounting for changes in depression severity, suggesting a direct link between improved insomnia and reduced suicide risk [31]. On the other hand, a large-scale analysis of U.S. survey data (2015–2018) revealed that prescription of multiple sleep medications, including Z-drugs, trazodone, and sedative benzodiazepines, are significantly associated with increased risks of suicidal ideation, planning, and attempts, even after adjusting for demographic and mental health factors [32]. These findings highlight the need for a systematic examination of the effect of both pharmacological and non-pharmacological sleep interventions on suicidality. To the best of our knowledge, no systematic review has yet been conducted on randomized controlled trials (RCTs) investigating the effects of treatments for various sleep disorders.

In the current project, we conducted a systematic review to provide insight into the extent to which the treatment of sleep disorders can affect suicidality. With this systematic investigation we aim to provide answers to the following research questions: (1) What is the overall effect of treating disturbed sleep on suicidality? and (2) What is the effect and safety of different types of sleep interventions on suicidality? Conducting a systematic review on the effect of treating disturbed sleep on suicidal thoughts and behavior is crucial for several reasons. While existing studies have evaluated specific sleep treatments for suicidality, such as the previously mentioned CBT-I or pharmacological interventions, there is a need for a comprehensive overview. Healthcare providers often face the challenge of integrating diverse findings from different studies when making treatment decisions. A systematic review and meta-analysis that synthesizes the evidence across various sleep disturbances and treatment options would provide a useful resource, offering an overview of the overall impact of sleep disorder treatment on suicidal thoughts and behavior which may guide more effective and informed clinical practices. Additionally, by examining both various sleep disorders and different treatment approaches together, we may gain deeper insights into the mechanisms underlying the relationship between sleep and suicidality.

2. Method

The current project was conducted in accordance with the PRISMA guidelines [36].

2.1. Literature search and study inclusion

The literature search was conducted on the June 4, 2023 and included all articles published before this date, using the following terms: suicide (and related terms), sleep (and related terms), randomized controlled trial (and related terms). The literature search was repeated with the same search terms on March 21, 2025. The following databases were searched for eligible articles: PubMed, Embase (including preprint archives biorxiv and medrxiv), APA PsycInfo, Web of Science, Cochrane Library - CENTRAL, and Scopus. See appendix A for the search strings used per database that were created by the medical information specialist. After removal of duplicates, articles were screened in the program Rayyan [34]. As a first step, the titles and abstracts of articles were screened by three evaluators, with each article being screened by at least two different evaluators. As a second step, the full texts of the remaining articles were screened by two evaluators. Disagreements between the evaluators were discussed among the evaluators. In cases of remaining uncertainty, the respective article(s) were discussed with the other co-authors. Further potential articles were searched from reference lists of relevant articles (including previously conducted systematic reviews/meta-analyses) and by searching the grey literature (Google Scholar search; searching for articles that cited key articles; searching other preprint databases such as psyarxiv).

2.1.1. Eligibility criteria

We included peer-reviewed articles with RCT designs, which examined the difference between an intervention that targets sleep (i.e., sleep needed to be described as the mechanism of action and needed to be measured as an outcome) compared to any control condition on the outcome of suicidality. Suicidality included suicidal ideation/thoughts/plans, suicide attempts or suicide as a primary/secondary/adverse outcome using any assessment tool. Articles written in English, Dutch, German, French or Italian were included and there were no restrictions based on sample characteristics (e.g., depressed patients, insomnia patients), study setting (e.g., online, offline) or on article publication date. Records were excluded in case the article was not accessible (after contacting authors), or did not report the relevant information. Double publications and trial protocols were excluded. Lastly, articles published in predatory journals and in which the co-authors considered reporting to be suspicious, were excluded.

2.2. Risk of bias

The risk of bias of included articles was independently assessed by three co-authors according to the Revised Cochrane risk of-bias tool for randomized trials (version March 15, 2019 [35]). In case of disagreements, consensus was reached in discussion between the co-authors.

2.3. Data extraction

Two researchers extracted the following information from all included studies: first author, publication year, number of participants (in total and per group), mean age/age range of participants, percentage of females, setting, recruitment strategy, diagnostic status of participants, inclusion criteria, exclusion criteria, type of sleep intervention, type of control condition, type of outcome (score for suicidal ideation and/or number of suicide attempts and/or death by suicide; score for sleep disturbance), effect size and any other clinical information deemed important by the researcher.

2.4. Data analysis

Studies were categorized as ‘efficacy studies’ when they examined the change from pre-intervention to post-intervention suicidality scores in the experimental vs. the control group. Studies that reported suicidality as an adverse outcome, meaning that they monitored and/or reported cases with emerging suicidality during the study in experimental and control group(s), were categorized as ‘safety studies’. For efficacy studies with the outcome suicidal ideation, SMDs (standard mean differences) were calculated based on reported means and standard deviations. In case raw means and standard deviations were not reported, reported information (e.g., regression coefficients) were converted according to the guidelines provided by Harrer and colleagues [36] to a pre-calculated SMD. If reported information was not suitable to be converted, the authors of the respective studies were contacted with a request for providing the raw means and standard deviations.

Meta-analyses were performed in case there was a sufficient number (at least 4) of studies per type of outcome measure (suicidal ideation vs. attempts vs. suicides) and, in the context of the second research question, per type of intervention (psychotherapeutic interventions; medication types; other interventions). Studies that could not be included in meta-analyses (e.g., due to incompatible outcome type/data format such as reporting suicidal ideation in dichotomous format), were described narratively in the section corresponding to the type of intervention they utilized (section 3.2.2). All meta-analyses were performed in R (R version 4.3.2 [37]) using the following packages: meta (version 7.0–0 [38]), metafor (version 4.4.0 [39]), metapsyTools (version 1.0.11 [40]), esc (version 0.5.1 [41]), metaSEM (version 1.3.1), robvis (version 0.3.0.900 [42]), following guidelines provided by Harrer and colleagues [36]. When studies provided more than one effect size (e.g. due to several study arms or outcome assessments), a clustering vector was specified to identify which effect sizes came from the same study, resulting in a three-level meta-analysis model.

For the first research question, the effects of all efficacy studies on the outcome measures suicidality and sleep disturbance were examined using separate three-level random-effects meta-analyses. As a second step, a multivariate meta-analysis was planned to estimate the association between the suicidality and sleep disturbance effect sizes of the included efficacy studies. For the second research question, the effects of efficacy studies per sleep intervention type on the outcome measure suicidality were examined via three-level random-effects meta-analyses. Binary outcomes of cases of suicidality in the safety studies were examined via three-level random effects meta-analyses using the Mantel-Haenszel method [43,44] to calculate the pooled effect estimate. When the number of studies was insufficient to conduct a meta-analysis, findings of included studies were summarized narratively.

3. Results

3.1. Included studies

A total of 18 efficacy studies (n = 2422) and 26 safety (n = 12543) studies were included in the systematic review. The flow diagram of study inclusion is depicted in Fig. 1. Table 1 displays an overview of all included efficacy and safety studies. Of the 18 efficacy studies, 13 employed psychotherapeutic interventions [CBT; 2 of the CBT-interventions included a light intervention component], 3 studied pharmacological therapies (2 studies with insomnia/sleep medication [Med-I], 1 with an off-label medication [Med-O]), and 2 studies examined the effects of light interventions [Light]. Of the 26 safety studies, 24 used pharmacotherapy (10 studies with insomnia/sleep medication [Med-I], 10 with medications against narcolepsy [Med-N], 4 with an off-label medication [Med-O]), and 2 studies examined light interventions [Light].

Fig. 1.

Fig. 1

Flow diagram of the Study Inclusion.

Table 1.

Overview of studies included in the systematic review.

Author Intervention category Experimental Condition Control Condition Sample Size
% Women Mean Age Study Country Disorder Inclusion Suicidality Exclusion Intervention duration
Suicidality Outcome Measure of Suicidality
N1 N2 Nr. Sessions Nr. Weeks
Efficacy Studies
Batterham, 2017 [44] CBT digital intervention based on CBT-I digital control program 574 575 73.5 % 43 au insomnia; depression yes (severe) 6 6 ideation PSF
Chan, 2022 [46] CBT CBT-I group therapy 45 45 67.4 % 20 aes insomnia yes (severe) 8 9 ideation DSI-SS
digital self-help 45
Cromer, 2024 [47] CBT CBT for nightmares in children waitlist 23 23 50 % 12.1 us nightmares yes (severe) 5 5 ideation & behavior (dichot.) 8 questions assessing suicidal thoughts and behavior
Crosby, 2025 [48] CBT Digital intervention based on CBT-I digital control program 31 30 80 % 19.8 us insomnia no 1 1 ideation DSI-SS
Ioannou, 2021 [49] Light sleep deprivation & daylight sleep hygiene consultation + CAU 16 17 78.8 % 30.1 eu depression no 7 1 ideation MADRS-S suicide item
Kalmbach, 2022 [50] CBT digital CBT-I sleep education 60 66 71.4 % 41.37 us insomnia; suicidality no 6 6 ideation QIDS-SR16 suicide item
Krystal, 2007 [51] Med-I 3 mg eszopiclone + fluoxetine placebo pill + fluoxetine 187 185 67.7 % 41.9 us insomnia; depression no 56 10 ideation HAM-D
McCall, 2019 [52] Med-I 6.25–12.5 mg zolpidem-CR + SSRI placebo pill + SSRI 51 52 62 % 40.5 us insomnia; depression yes (severe) 56 8 ideation BSSI
C-SSRS
McCall, 2018 [53] Med-O prazosin + mood disorder meds placebo pill + mood disorder medication 3 3 85 % 39.8 us PTSD yes (severe) 56 8 ideation BSSI
C-SSRS
Nazem, 2024 [54] CBT digital intervention based on CBT-I sleep education 23 27 30 % 39.0 us insomnia, suicidality no 9 9 ideation ASIQ
Pigeon, 2019 [55] CBT brief CBT-I CAU for MDD and/or PTSD 24 26 20 % nr us insomnia; depression, PTSD yes (severe) 4 6 ideation C-SSRS
Pigeon, 2017 [56] CBT brief CBT-I sleep hygiene 13 14 11 % 58.5 us insomnia; depression, yes (severe) 4 5 ideation (dichot.) C-SSRS
Pruiksma, 2020 [57] CBT exposure, relaxation, and rescripting therapy minimal contact control 20 20 15 % 33.03 us nightmare; trauma yes (severe) 5 6 ideation DSI-SS
Smagula, 2024 [58] CBT (+Light) transdiagnostic intervention for sleep and circadian dysfunction CAU 40 57 53 % 46.5 us mixed yes (severe) 8 12 ideation (dichot.) QIDS-SR16 suicide item
Sheaves, 2019 [59] CBT imagery-focused CBT for nightmares + CAU CAU 12 12 42 % nr uk nightmare; psychosis no 4 4 ideation BSSI
Volf, 2020 [60] Light dynamic lighting + CAU static lighting + CAU 4 4 66.7 % nr eu depression yes (severe) 28 4 ideation SIDAS
Waite, 2023 [61] CBT (+Light) pychological therapy for sleep problems + CAU CAU 21 19 48 % 16.9 uk Psychosis, insomnia no 8 12 ideation C-SSRS
Wu, 2023 [62] CBT mindfulness waiting list 30 30 76.6 % 19.75 eas suicidality yes (severe) 8 8 ideation BSSI
Safety Studies
Ancoli-Israel, 2010 [63] Med-I 2 mg eszopiclone placebo pill 194 194 62.6 72 us insomnia no 84 12.0 suicide nr
Bogan, 2022 [64] Med-N 6 g ON-SXB 2 × 3 g SXB 28 28 54 % 39.6 us None yes (history) 2 1.0 ideation & behavior nr
Brooks, 2019 [65] Med-I seltorexant (10/20/30/40 mg) placebo pill 18 18 60 % 43 eu depression; insomnia yes (active) 4 4.0 ideation & behavior C-SSRS
Czeisler, 2009 [66] Med-N 150 mg armodafinil placebo pill 123 122 46.7 % 39.6 oth shift work disorder no 42.4 12.0 ideation nr
Dauvilliers, 2023 [67] Med-N 30 mg danavorexton placebo pill 17 17 58 % 31 oth narcolepsy yes 112 8 ideation & behavior C-SSRS/spontaneous report
90 mg danavorexton 20
180 mg danavorexton 19
Dunlop, 2007 [68] Med-N 200 mg modafinil + SSRI placebo pill + SSRI 36 36 56 % 43.9 us depression yes (severe) 42 6.0 ideation HAM-D & MADRS suicide item
During, 2023 [69] Med-N 4.5 mg–9 mg SXB Placebo pill 12 12 25 % 65.8 us isolated/Parkinson's REM sleep behavior disorder no 28 4 ideation nr
Herring, 2020 [70] Med-I 10 mg suvorexant placebo pill 142 143 65 % 69.3 oth insomnia; dementia yes (severe) 28 7.0 ideation & behavior C-SSRS
Herring, 2016 [71] Med-I suvorexant 15–20 mg placebo pill 493 767 65 % 56 oth insomnia no 420 13.0 ideation & behavior C-SSRS
suvorexant 30–40 mg 770
Kim, 2014 [72] Med-O 300 mg quetiapine XR 600 mg lithium 12 17 55 % 36.1 eas depression no 56 8.0 behavior nr
Krystal, 2022 [73] Med-N 37.5–300 mg solriamfetol placebo pill 355 119 52 % 45.6 us OSA yes (active) 84 12.0 ideation & behavior C-SSRS
Med-N 75–300 mg solriamfetol placebo pill 177 59 67 % 36.3 narcolepsy
Krystal, 2010 [74] Med-N 200 mg armodafinil placebo pill 124 124 53.8 % 49.5 us OSA; depression yes 84 12.0 ideation QIDS-SR-16 item 12
Kunz, 2023 [75] Med-I 10 mg daridorexant placebo pill 142 128 71 % 58 oth insomnia yes 280 44.3 ideation & behavior nr
25 mg daridorexant 268
50 mg daridorexant 137
Ex-placebo 25 mg daridorexant 126
Kushida, 2022 [76] Med-N 9 g ON-SXB placebo pill 107 105 67.2 % 31.2 oth narcolepsy yes 91 17.0 ideation C-SSRS
Lieverse, 2011 [77] Light 7,500lux bright pale blue light 50lux dim red light 42 47 65 % 69 eu depression no 21 6.0 suicide nr
Lipschitz, 2023 [78] Med-N 100/200 mg modafinil + SSRI placebo pill + SSRI 6 4 70 % 48.4 us bipolar disorder, sleep problems and/or cognitive impairment yes (severe) 56 8 ideation & behavior C-SSRS & BSSI
Locklear, 2013 [79] Med-O 50–300 mg quetiapine XR placebo pill 166 172 71.1 % 71.2 oth depression yes 63 11.0 behavior nr
Loving, 2005 [80] Light 1200 lux bright green light 10 lux dim red light 17 16 84.8 % 67.7 us depression no 28 21.0 behavior nr
Mellman, 2022 [81] Med-I 20 mg suvorexant placebo pill 18 19 62.2 % 35.4 us insomnia; trauma no 42 7.0 ideation C-SSRS
Mignot, 2022 [81] Med-I 10 mg daridorexant placebo pill 306 615 68 % 56 oth insomnia yes 91 40.0 ideation C-SSRS
25 mg daridorexant 616
50 mg daridorexant 308
Nirogi, 2024 [83] Med-N 2 mg samelisant placebo pill 54 57 70.7 % 32.3 us narcolepsy no 14 2 ideation & behavior C-SSRS
4 mg samelisant 53
Parmenter, 2024 [84] Med-O 5.6 mg cyclobenzaprine placebo pill 175 176 11.3 % 35.7 us PTSD yes (severe) 84 12 ideation & behavior C-SSRS
Raskind, 2018 [85] Med-O 12–20 mg prazosin placebo pill 152 152 2.3 % 52 us PTSD yes (severe) 182 26.0 ideation nr
Recourt, 2019 [86] Med-I 20 mg seltorexant placebo pill 22 12 34 % 40.6 eu depression no 19 8.5 ideation; suicide C-SSRS
Med-O 25 mg diphenhydramine 13
Sangal, 2014 [87] Med-I 1 or 2 mg eszopiclone (low) placebo pill 163 160 36.2 % 11.4 us insomnia; ADHD no 84 12.0 ideation & behavior C-SSRS
2 or 3 mg eszopiclone (high) 159
Uchimura, 2024 [88] Med-I 50 mg daridorexant 25 mg daridorexant 102 52 55 % 54.4 eas insomnia yes (severe) 364 52 ideation & behavior C-SSRS

Note. CBT = psychotherapeutic sleep intervention; Light = Light intervention; Med-I = medications against insomnia; Med-N = medications against narcolepsy; Med-O = off-label medication; CBT-I = cognitive behavioral therapy for insomnia; CAU = care as usual; PSF = Psychiatric Symptom Frequency Scale [88]; us = United States of America; eu = Europe; uk = United Kingdom; eas = East Asia; au = Australia & New Zealand; oth = other country & mix of countries; DSI-SS = Depressive Symptom Inventory Suicidality Subscale [90]; MADRS-S = Montgomery–Åsberg Depression Rating Scale (Self assessment) [91]; QIDS-SR16 = 16-Item Quick Inventory of Depressive Symptomatology [92]; ASIQ = Adult Suicidal Ideation Questionnaire [93] HAM-D = Hamilton Rating Scale for Depression [94]; BSSI = Beck's Scale for Suicide Ideation [95]; C-SSRS = Columbia-Suicide Severity Rating Scale [96]; SIDAS = suicidal ideation attributes scale [97].

3.2. Meta-analyses and descriptive results

3.2.1. Research question 1: the effect of treating disordered sleep on suicidality

All efficacy studies assessed suicidal ideation as an outcome measure. Of the 18 efficacy studies, 9 reported the means and standard errors/deviations of suicidal ideation at pre- and posttreatment for both the control and intervention groups. Pre-calculated SMDs could be computed from the information provided in 5 studies (see guidelines by Harrer et al. [36]). Of the 4 studies which did not provide data that could be recalculated into SMDs (e.g., due to dichotomous data formats), authors were contacted and one responded with providing requested means and standard deviations. Therefore, the remaining 3 studies could not be included in the meta-analysis due to incompatible data format. This resulted in a total of 15 studies with 18 effect sizes to be included in the analyses. The majority of studies used the insomnia severity index (ISI [98]; 9 studies) and the remaining studies used the Pittsburgh Sleep Quality Index (PSQI [99]; 3 studies) to assess sleep disturbance.

When examining the efficacy-studies on the outcome sleep, we found that the included sleep interventions significantly decreased sleep disturbance in the experimental vs. control conditions (Hedge's g = −0.76, 95 % CI: 1.03 to −0.48; medium effect size; see B2 in Appendix B for more information). Examining the effect of all efficacy-studies on suicidality revealed that sleep interventions resulted in a small, but significant, decrease in suicidal ideation compared to control conditions (Hedge's g = −0.16, 95 % CI: 0.24 to −0.08). For more information, see the forest plot in Fig. 2. The funnel plot and publication bias correction models did not indicate presence of publication bias and the pooled effect remained statistically significant when excluding influential studies (see B1 in Appendix B). Due to model specification errors likely related to the differences in heterogeneity estimates between the suicidality outcome (I2 = 0 %) and the sleep outcome (I2 = 82 %), we were not able to conduct the multivariate meta-analysis to estimate the association between the suicidality effect sizes and sleep disturbance effect sizes.

Fig. 2.

Fig. 2

Forest Plot of all Efficacy Studies on Suicidal Ideation

Note. CBT = psychotherapeutic sleep intervention; Light = light intervention; Med-I = medications against insomnia; Med-O = off-label medication.

3.2.2. Research question 2: the effect and safety of different types of sleep interventions on suicidality

3.2.2.1. Psychotherapeutic sleep interventions

A total of 10 efficacy studies with 11 effect sizes were included in the meta-analysis to examine the effect of psychotherapeutic sleep interventions on suicidal ideation. The results indicated that psychotherapeutic sleep interventions had a small significant effect on decreasing suicidal ideation compared to control conditions (Hedge's g = −0.17, 95 % CI: 0.26 to −0.08; see forest plot in Fig. 3). The pooled effect did not remain statistically significant when excluding influential studies (see B3 in Appendix B). There were three efficacy studies that could not be included in the meta-analysis. One study examined the percentage of remission from suicidal ideation in the experimental and control groups ([56]) and reported 40 % remission in the experimental group (CBT-I) vs. 70 % remission in the control group. Another study reported cases with suicidal ideation before (experimental group: 12; control group: 21) and after (experimental group: 5; control group: 17) a transdiagnostic sleep intervention for sleep and circadian dysfunction [58]. Lastly, another study on CBT for nightmares in children reported remission of suicidal thoughts and behavior in 4 out of 5 participants in the experimental group, and 3 out of 5 in the control group, as well as the emergence of suicidal thoughts and behavior in 2 participants in the control group [47]. There were no safety studies employing psychotherapeutic sleep interventions.

Fig. 3.

Fig. 3

Forest Plot of Efficacy Studies with Psychotherapeutic Sleep Interventions on Suicidal Ideation

Note. CBT-I = cognitive behavioral therapy for insomnia; CBT-N: cognitive behavioral therapy for nightmares; ERRT = exposure, relaxation, and rescripting therapy; Mind = mindfulness intervention; CBT + Light = psychotherapeutic sleep intervention with light component.

3.2.2.2. Pharmacological sleep interventions
3.2.2.2.1. Medications for insomnia (sleep medication)

Two efficacy studies examined the effect of sleep medications on changes in suicidal ideation. The examined medications were eszopiclone (g = −0.07; 95 % CI: 0.27 - 0.13 [51]) and zolpidem (g = −0.14; 95 % CI: 0.53 - 0.25 [suicidal ideation assessed with the BSSI], g = −0.42; 95 % CI: 0.80 to −0.03 [suicidal ideation assessed with the C-SSRS] [58]). The number of efficacy studies was not sufficient to conduct a meta-analysis. There were 7 safety studies with 14 effect sizes that reported monitoring cases of suicidal ideation in studies comparing sleep medications with placebo. The meta-analyses results did not indicate that the number of cases with suicidal ideation were significantly different between the control and experimental conditions (OR = 0.98, 95 % CI: 0.34–2.79; see forest plot in Fig. 4). Five of the 7 safety studies included in the analysis on suicidal ideation also monitored suicidal behavior but reported no cases of suicidal behavior [65,70,71,75,87]. One study comparing different dosages of daridoxant (50 mg vs. 25 mg), reported no cases of suicidal ideation or behavior in either group [88]. One study testing eszoplicone reported one suicide in the experimental group (n = 194) and no suicides in the control group (n = 194 [63]). Another study reported no suicides in either the seltorexant nor the placebo control group [86].

Fig. 4.

Fig. 4

Forest Plot of Safety Studies with Medications Treating Insomnia on Suicidal Ideation

Note. SXB(ON) = sodium oxybate (once-nightly).

3.2.2.2.2. Medications for narcolepsy

We did not find any efficacy studies examining the effect of narcolepsy medications on changes in suicidality. There were 9 safety studies with 13 effect sizes that reported monitoring cases of suicidal ideation in studies testing narcolepsy medications (in any target group; see Table 1 for details) against placebo. The meta-analysis results do not indicate that cases of suicidal ideation were significantly different between the control and experimental conditions (pooled OR = 1.67, 95 % CI: 0.52–5.50; see forest plot in Fig. 5). Four of the 9 safety studies included in the analysis on suicidal ideation also monitored suicidal behavior but reported no cases of suicidal behavior [67,73,78,83]. One study comparing ON-SXB (Once-nightly sodium oxybate; n = 28) with SXB (sodium oxybate; n = 28) reported zero cases of suicidal ideation or behavior in both medication groups [64].

Fig. 5.

Fig. 5

Forest plot of safety studies with medications treating narcolepsy on suicidal ideation.

3.2.2.2.3. Off-label medications

In total, 6 studies examined different off-label medications. One efficacy study examined the effect of prazosin as a medication against nightmares on changes in suicidal ideation (g = 0.14; 95 % CI: 1.47- 1.77 [suicidal ideation assessed with the BSSI], g = 0.50; 95 % CI: 1.12 – 2.12 [suicidal ideation assessed with the C-SSRS] [53]). Prazosin was also examined in one safety study [85], which found 15 cases of suicidal ideation in the experimental group (n = 152) and 23 cases of suicidal ideation in the control group (n = 152). One study in veterans with PTSD reported no cases of suicidal ideation or behavior occurring in the control group (n = 176) or experimental group (n = 175) receiving cyclobenzaprine [84]. Quetiapine was examined as a pharmacological intervention to improve sleep quality in two studies: Kim and colleagues [72] reported one suicide attempt in the experimental group (n = 12) vs. zero suicide attempts in the control group (n = 17) and Locklear and colleagues [79] reported one suicide attempt in the experimental group (n = 166) and one suicide attempt in the control group (n = 166). One study using diphenhydramine as a negative control (because this study also tested a sleep medication it is counted as MED-I in the description of included studies in section 3.1) reported one suicide in the diphenhydramine group (n = 13) vs. zero suicides in the placebo control group (n = 12 [86]).

3.2.2.3. Sleep interventions using light exposure

In total, 4 studies examined sleep interventions using light exposure in relation to suicidality. Two efficacy studies examined the effect of light interventions on changes in suicidal ideation (g = 0.00; 95 % CI: 0.68 - 0.69 [49]; g = −0.72; 95 % CI: 2.16 - 0.72 [60]). Two additional efficacy studies examined a psychotherapeutic intervention that included a light component [58,61]. The results of these studies are described in the section on psychotherapeutic interventions (textual description & Fig. 3). No cases of suicide attempts [80] and no cases of suicides [77] were reported in two safety studies.

3.3. Risk of bias

Of the 18 included efficacy studies, 12 studies were rated to have a moderate risk of bias, 5 were rated to have a high risk of bias, and 1 was rated to have a low risk of bias. Of the 26 included safety studies, 4 were rated to have a low risk of bias, 19 as moderate risk of bias, and 3 as high risk of bias. See B3 in Appendix B for the risk of bias plots of the efficacy and safety studies.

4. Discussion

Sleep disturbances appear to be a risk factor for suicidal ideation, suicide attempts and death by suicide. In the current study, we conducted a systematic literature review and meta-analyses to examine the effect of pharmacological and non-pharmacological sleep interventions on suicidal thoughts and behavior. Screening through an initial number of 5037 retrieved unique articles resulted in a final sample of 44 articles (k = 18 efficacy studies; k = 26 safety studies) with in total N = 14965 participants. We found that sleep interventions, particularly psychotherapeutic sleep interventions, had a small positive effect on reducing suicidal ideation. No conclusive evidence was found for the effectiveness or safety of pharmaceutical sleep interventions or of interventions using light exposure.

4.1. The effect of improving disturbed sleep on suicidality

Examining all efficacy studies revealed that the included sleep treatments markedly reduced sleep disturbance. The sleep therapies also appeared to slightly, but significantly reduce suicidal ideation. Due to model specification errors, we could not test whether reductions in sleep disturbances were associated with reductions in suicidality. This may have been due to the deflated heterogeneity estimate of the suicidality outcome which likely resulted from the large error margins of the included studies and the high weight of one study relative to the weight of the other studies. Nonetheless, the findings do show that suicidal ideation can be effectively reduced when sleep is targeted. As such, the current review contributes to the existing literature on sleep disturbance acting as a contributing factor to the experience of suicidality [e.g., 3–6]. Sleep interventions therefore seem to be an appropriate treatment choice to target suicidality in patients with co-morbid sleep disturbances.

Although statistically significant, the treatment effect of sleep interventions on suicidality was relatively small. A recent systematic review of 8 articles examined the effect of sleep interventions on suicidal ideation and similarly reported a small, albeit not statistically significant, pooled effect size [100]. The small effect of the current analysis could be explained by the majority of the efficacy studies not specifically including people with (high levels of) suicidality, which might have restricted the observable treatment effects on suicidality. It could also reflect that sleep interventions may not be sufficient to markedly reduce suicidality, for example, when sleep disturbances are secondary to another mental health issue (e.g., depression, PTSD). In these contexts, targeting these underlying issues or suicidality directly may have additional benefits [e.g., 78,79]. Given the detrimental effects of disturbed sleep on mental and physical functioning [4], it nonetheless remains imperative to target sleep disturbances alongside other treatments to promote recovery and relapse prevention [e.g., 80–82].

4.2. The effect and safety of different types of sleep interventions on suicidality

4.2.1. Psychotherapeutic sleep interventions

Concerning the effect of different sleep interventions, we found that psychotherapeutic sleep interventions had a small positive effect on reducing suicidal ideation. As the pooled effect size was no longer significant when the study with the highest weight was excluded from the analysis, the findings should be interpreted with caution. Of all included psychotherapeutic sleep intervention studies, the majority utilized CBT-I (6 studies), with the other studies utilizing a mix of other psychotherapeutic interventions (CBT for nightmares; Exposure, Relaxation, and Rescripting Therapy for nightmares; Mindfulness intervention to promote sleep quality). As such, CBT-I may be a promising psychotherapeutic intervention to reduce suicidal ideation alongside to improving sleep. Next to alleviating insomnia, CBT-I appears to effectively improve comorbid mental health conditions, such as depression, anxiety, PTSD and substance abuse disorders [101,102]. There is evidence suggesting that these ‘secondary’ treatment effects are mediated by improvements in insomnia as a result of CBT-I [103,103]. In line with that, one of the articles included in this review [50] found that insomnia remission due to CBT-I mediated reductions in suicidal ideation.

So far, the exact mechanisms of action of psychotherapeutic sleep interventions, such as CBT-I, on reducing suicidality remain unclear. CBT-I has been found to improve quality of life [104] and to be associated with increased energy levels, self-esteem, and functioning [30,105]. These effects of CBT-I on well-being may also contribute to improvements in suicidal ideation. In addition, by decreasing sleeplessness, CBT-I may also reduce the chance of escalation into suicidal behavior. For example, people would be less likely to get into a suicidal crisis at night, when there is little opportunity for support [15] and executive functions are reduced [18], or be less likely to engage in impulsive behavior that is associated with poor sleep [e.g., 22,23]. Unfortunately, none of the included studies utilizing psychotherapeutic sleep interventions examined suicidal behavior as an outcome. More research is needed to understand how psychotherapeutic sleep interventions reduce suicidality, and particularly how they affect suicidal behavior.

4.2.2. Pharmacological sleep interventions

We also examined the effect and safety of different pharmacological sleep therapies on suicidality: medications targeting insomnia (eszopiclone, zolpidem, daridoxerant, seltorexant, suvorexant), medications targeting narcolepsy symptoms (armodafinil, modafinil, ON-SXB, solriamfetol) and off-label medications targeting nightmares or insomnia (prazosin, quetiapine, diphenhydramine). We could not test the effect of these medications on suicidality due to an insufficient number of efficacy studies. With regard to safety, neither medications treating insomnia nor medications for narcolepsy were found to be associated with an increased or decreased likelihood for the occurrence of suicidal ideation as an adverse event compared to placebo pills. Due to the rarity of events within these studies, the individual and pooled odds ratios had very large error margins, thus resulting in a low certainty of evidence. Too few safety medication studies reported on the occurrence of suicide attempts and suicides to allow drawing conclusions on the basis of these observations. We can thus conclude that little is known about the effect and safety of pharmacological sleep interventions on suicidality. Importantly, none of the pharmacological studies specifically included participants with suicidality, and around half (57.6 %) of the medication safety studies explicitly excluded participants with suicidality. In order to properly examine the effect/safety of (pharmacological) treatments on inherently rare events, particularly suicidal behavior, it is crucial that individuals with suicidality are not excluded from intervention trials. This means that there is substantial uncertainty about the possibility of suicidal adverse effects of pharmacological sleep interventions in people with (high levels of) suicidality.

There were striking differences in the monitoring and reporting of suicidality between the included medication safety studies. While some studies simply described participants self-reporting suicidal adverse effects, other studies monitored suicidality at each study visit. Within the latter group, not all studies described the monitoring instrument that was used and even fewer reported on pre-specified cut-off scores used for determining whether a suicidal adverse effect had occurred. Research indicates that inconsistencies in monitoring methods and underreporting of suicidality is a common problem in clinical trials [106,107]. This is particularly problematic in light of research finding associations between sleep medication use and increased risk of suicide [e.g., 30,91]. Pharmacological sleep interventions have several side effects, including reduced sleep quality, rebound insomnia, cognitive impairments, fatigue, somnolence, and the development of dependence [22,25,108]. Residual effects of pharmacotherapy for disturbed sleep further appear to be associated with impaired functioning (e.g., work impairment, difficulties in relationships) and decreased quality of life [109]. Such decreased life quality and impairments may contribute to increases in suicidality [110,111]. As such, occurrences of suicide attempts and suicides in medication groups should be seen as potentially concerning signals to be investigated further.

4.2.3. Other sleep interventions and sleep interventions not included in the review

The current review only included interventions which were described as specifically targeting sleep. Some of the interventions included (e.g., mindfulness intervention, seltorexant, prazosin) can also, or even primarily, be used to target other (mental) health symptoms such as anxiety, depression, or high blood pressure. Studies examining such interventions to target (mental) health conditions other than disturbed sleep were not included in the current review. As such, the current findings should not be interpreted as reflecting the effect or safety of an intervention outside the context of sleep. It is notable that no studies on some common pharmacological sleep interventions such as benzodiazepines were identified in the current review, despite their association with suicidal behavior [e.g., 91]. Similarly, a number of non-pharmacological sleep interventions [22,112], such as behavior change methods (e.g., parents setting up scheduled bedtimes for children), physical exercise interventions (e.g., aerobic exercises) or listening to music, were not identified by the current review. It is possible that RCTs of such interventions did not assess suicidality and/or were examined outside the context of sleep (e.g., benzodiazepines being examined in the context of anxiety disorders). In addition, studies that did monitor suicidality but did not report on it (e.g., because no suicidal events occurred or because the study was terminated when suicidal events occurred), would be missed by systematic literature searches such as the current one. The reliance on active reporting of suicidal adverse events thus constitutes a selection bias of the current review. With regard to environmental/chronotherapeutic sleep interventions, we included four studies (2 efficacy studies, 2 safety studies) that used light exposure in the current review. Due to the low number of studies, no firm conclusions could be drawn about the effect or safety of light interventions on suicidality.

4.3. Treatment implications and directions for future research

In sum, the current review indicates that sleep interventions, particularly psychotherapeutic sleep interventions, not only improve sleep but can additionally reduce suicidal ideation. Most of the included study samples contained individuals with (sub)clinical levels of insomnia and/or depression. Next to that, other samples included participants with various other sleep disturbances (nightmares, shift work disorder, obstructive sleep apnea, narcolepsy) and/or other mental health conditions (PTSD/trauma, psychotic disorder, ADHD). As such, the findings primarily have implications for people with insomnia and/or depression but may also apply to individuals with other sleep disturbances or psychological conditions. As discussed earlier, CBT-I may be a potentially promising psychotherapeutic intervention to effectively reduce suicidality with comorbid insomnia. CBT-I is the first-line treatment for insomnia [113] and some initial findings suggest that it could potentially affect other sleep issues such as nightmares [114,115] and fear of sleep [116]. There are several training programs for CBT-I available to health care professionals [117]. CBT-I programs with direct contact between the health care professional and patient (in individual, group, or digital formats) are more effective in improving insomnia than self-help CBT-I programs [118]. Clinicians are recommended to discuss CBT-I format preferences with their patients [119] and closely monitor treatment adherence when digital CBT-I formats are utilized [45,117,120]. In people with mental health comorbidities (e.g., depression, PTSD), CBT-I should not be used as replacement of but rather as an add-on to disorder-specific treatment [102].

Even though we did not find that medications for sleep disorders increase the risk for suicidality, the possibility of suicidal adverse effects cannot be excluded due to the high uncertainty of evidence. As a result, medications targeting sleep disorders should be prescribed with caution, particularly in people with high levels of suicidality. Research indicates that the prescription and use of multiple medications, a phenomenon termed ‘polypharmacy’ [121], is common in people with suicidality/depression [122,123]. Polypharmacy is associated with detrimental outcomes, including overdose and suicidal behavior [124,125]. As such, it is critical to pay close attention to concurrent medication use, particularly in people with multiple comorbidities. In case pharmacotherapy is deemed necessary (e.g., to target severe sleeplessness in the context of a crisis situation), health care professionals are recommended to prescribe these medications only for short periods of time and to closely monitor suicidal ideation and behavior.

In order to draw more definitive conclusions and refine treatment implications, more research is needed to tackle the limitations of the existing literature. Overall, there is currently a limited number of high quality RCTs on the effect and safety of different types of sleep interventions on suicidality. As such, the reliance on small studies with large error margins decreased the certainty in the observed overall effect and, due to deflated heterogeneity estimates, prevented examining the association between suicidality and sleep effect sizes. Moreover, we observed large inconsistencies in practices of monitoring and reporting suicidality as adverse effects, and suicidality being used as an exclusion criterion for study participation, particularly in the safety studies. Most efficacy studies relied on suicidal ideation as a measure of suicidality, and only a few examined suicidality at follow-up assessments [e.g., 43,46]. Some studies used unvalidated and/or single-item assessments of suicidality. Consequently, more large and high quality RCTs are needed to investigate the (long-term) effect and safety of different types of sleep interventions on suicidal thoughts and behavior (assessed with validated instruments), particularly in people with elevated levels of suicidality. More high quality RCTs across various sleep disturbances and/or psychological conditions would allow for more targeted reviews and/or analyses (e.g., meta-regressions; moderator analyses) and thus for drawing more refined treatment recommendations in specific patient populations. Importantly, we strongly recommend adherence to guidelines for monitoring and reporting adverse effects [126]. During the literature search of the current review, we came across several promising study protocols, such as the TAILOR study protocol (ClinicalTrials.gov ID: NCT05390918) and a protocol of a sleep study in veterans (ClinicalTrials.gov ID: NCT03603717). This suggests that it may soon be possible to draw firmer conclusions on the effect and safety of different types of sleep interventions on suicidality.

4.4. Conclusion

Taken together, this review provides support for the positive effects of sleep interventions on reducing suicidal ideation, primarily in people with insomnia and/or depression. Based on the results, we recommend health care professionals to utilize psychotherapeutic sleep interventions such as CBT-I, to reduce suicidal ideation in the context of disturbed sleep. Due to the uncertainty of evidence surrounding the effect and safety of pharmacological sleep interventions on suicidality, health care professionals are recommended to closely monitor suicidality when prescribing medications targeting sleep disturbance.

Funding

This work was supported by the Ministry of Health, Welfare and Sport. The funders of the study had no role in study design, data collection, data analysis, data interpretation, or writing of the report.

CRediT authorship contribution statement

Paula von Spreckelsen: Writing – review & editing, Writing – original draft, Visualization, Software, Methodology, Formal analysis, Data curation, Conceptualization. Daan Schouten: Writing – review & editing, Writing – original draft, Methodology, Formal analysis, Data curation, Conceptualization. Natasha G. Waslam: Writing – review & editing, Data curation. Patricia Katuin: Writing – review & editing, Conceptualization. Henriette D. Heering: Writing – review & editing, Supervision. Caroline Planting: Writing – review & editing, Data curation. Niki Antypa: Writing – review & editing, Validation. Liia Kivelä: Writing – review & editing, Validation. Marike Lancel: Writing – review & editing, Supervision, Conceptualization. Lizanne J.S. Schweren: Writing – review & editing, Supervision, Resources, Project administration, Methodology, Conceptualization.

Declaration of competing interest

None of the authors declare competing interests.

Acknowledgments

We would like to thank Farhat Wafa who participated in the abstract screening.

Appendix A. Search Strings and Number of Articles retrieved per Database

Database searched Platform Years of coverage Records Records after duplicates removed
PubMed PubMed 1946 – Present 644 644
Embase Embase.com 1971 - Present 3.680 3.232
APA PsycInfo EBSCO 1968 - Present 409 121
Web of Science Clarivate 1900 - Present 662 175
Cochrane CENTRAL Wiley 1992 - Present 525 540
Scopus Elsevier 1970 - Present 2.556 325
Total 8.476 5.037
Search
PubMed
Results
Query
#4 Search: #1 AND #2 AND #3 Sort by: Most Recent 644
#3 Search: “Randomized Controlled Trial" [pt] OR “Controlled Clinical Trial" [pt] OR “Randomized Controlled Trials as Topic" [Mesh] OR “Random allocation" [Mesh] OR “Double-blind method" [Mesh] OR “Single-blind method" [Mesh] OR “control groups" [Mesh] OR “Clinical Trials as Topic" [Mesh] OR “Placebos" [Mesh] OR random [tw] OR randomly [tw] OR randomised [tw] OR randomized [tw] OR randomizing [tw] OR randomizing [tw] OR placebo [tiab] OR ((singl∗[tw] OR doubl∗[tw] OR trebl∗[tw] OR tripl∗[tw]) AND (mask∗[tw] OR blind∗[tw] OR dumm∗[tw])) OR RCT [tiab] OR RCTs [tiab] OR “clinical trial∗" [tiab] OR “controlled trial∗" [tiab] OR crossover∗[tiab] OR “cross-over∗" [tiab] Sort by: Most Recent 2,513,327
#2 Search: “Sleep" [Mesh] OR “Sleep Wake Disorders" [Mesh] OR sleep∗[tiab] OR “sleep disorder∗" [tiab] OR “sleep wake disorder∗" [tiab] OR “sleep initiation" [tiab] OR “sleep onset" [tiab] OR “sleep latency" [tiab] OR “sleep deprivation" [tiab] OR “sleep quality" [tiab] OR “sleep hygiene" [tiab] OR “sleep disturbance∗" [tiab] OR “sleep problem∗" [tiab] OR “sleep maintenance" [tiab] OR “sleep fragmentation∗" [tiab] OR “sleep duration∗" [tiab] OR insomni∗[tiab] OR “insomnia disorder∗" [tiab] OR hypersomnolen∗[tiab] OR “hypersomnolence disorder∗" [tiab] OR narcolep∗[tiab] OR apnea∗[tiab] OR “obstructive sleep apnea∗" [tiab] OR “central sleep apnea∗" [tiab] OR “sleep-related hypoventilation" [tiab] OR “circadian rhythm∗" [tiab] OR “circadian rhythm sleep-wake disorder∗" [tiab] OR parasomni∗[tiab] OR “non-Rapid Eye Movement∗" [tiab] OR “non-REM∗" [tiab] OR “nonRapid Eye Movement∗" [tiab] OR nonREM∗[tiab] OR “non-Rapid Eye Movement sleep arousal disorder∗" [tiab] OR nightmare∗[tiab] OR “nightmare disorder∗" [tiab] OR “Rapid Eye Movement∗" [tiab] OR REM [tiab] OR “Rapid Eye Movement Sleep behavior disorder∗" [tiab] OR dream∗[tiab] OR nap [tiab] OR naps [tiab] OR bedtime∗[tiab] OR “bed time∗" [tiab] OR “night rest∗" [tiab] OR “time in bed" [tiab] OR “sleep time∗" [tiab] OR “night waking" [tiab] OR drowsiness [tiab] OR somnolen∗[tiab] OR hypersomni∗[tiab] OR “early awakening∗" [tiab] OR sleepwalking∗[tiab] OR “restless legs syndrome∗" [tiab] OR “restless leg syndrome∗" [tiab] OR “periodic limb movement disorder∗" [tiab] Sort by: Most Recent 382,875
#1 Search: “Suicide" [Mesh] OR suicid∗[tiab] OR “self-kill∗" [tiab] OR “self-poison∗" [tiab] OR “self-stabb∗" [tiab] OR parasuicid∗[tiab] Sort by: Most Recent 126,062

Key: [Mesh] = medical subject heading, [tiab] = title, abstract, author supplied keywords.

No. Embase (Embase.com)
Results
Query
#5 #4 AND ('article'/it OR ‘article in press'/it OR ‘chapter'/it OR ‘preprint'/it) 3680
#4 #1 AND #2 AND #3 6409
#3 ‘controlled clinical trial'/de OR ‘randomized controlled trial'/exp OR ‘randomized controlled trial topic'/de OR ‘controlled clinical trial'/exp OR ‘controlled study'/exp OR ‘clinical trial topic'/de OR ‘clinical trial'/de OR ‘randomization'/exp OR ‘double blind procedure'/exp OR ‘single blind procedure'/de OR ‘placebo'/exp OR ‘crossover procedure'/exp OR ‘crossover procedure':ab,ti,kw OR ‘double blind procedure':ab,ti,kw OR ‘randomized controlled trial':ab,ti,kw OR ‘single blind procedure':ab,ti,kw OR ‘placebo':ab,ti,kw OR ‘clinical trial':ab,ti,kw OR random:ab,ti,kw OR randomly:ab,ti,kw OR randomised:ab,ti,kw OR randomized:ab,ti,kw OR randomizing:ab,ti,kw OR randomizing:ab,ti,kw OR factorial∗:ab,ti,kw OR crossover∗:ab,ti,kw OR ‘cross-over∗':ab,ti,kw OR placebo∗:ab,ti,kw OR rct:ab,ti,kw OR rcts:ab,ti,kw OR ((singl∗:ab,ti,kw OR doubl∗:ab,ti,kw OR trebl∗:ab,ti,kw OR tripl∗:ab,ti,kw) AND (mask∗:ab,ti,kw OR blind∗:ab,ti,kw OR dumm∗:ab,ti,kw)) OR ‘clinical trial∗':ab,ti,kw OR ‘controlled trial∗':ab,ti,kw 13,271,273
#2 ‘sleep'/exp OR ‘sleep disorder'/exp OR sleep∗:ab,ti,kw OR ‘sleep disorder∗':ab,ti,kw OR ‘sleep wake disorder∗':ab,ti,kw OR ‘sleep initiation':ab,ti,kw OR ‘sleep onset':ab,ti,kw OR ‘sleep latency':ab,ti,kw OR ‘sleep deprivation':ab,ti,kw OR ‘sleep quality':ab,ti,kw OR ‘sleep hygiene':ab,ti,kw OR ‘sleep disturbance∗':ab,ti,kw OR ‘sleep problem∗':ab,ti,kw OR ‘sleep maintenance':ab,ti,kw OR ‘sleep fragmentation∗':ab,ti,kw OR ‘sleep duration∗':ab,ti,kw OR insomni∗:ab,ti,kw OR ‘insomnia disorder∗':ab,ti,kw OR hypersomnolen∗:ab,ti,kw OR ‘hypersomnolence disorder∗':ab,ti,kw OR narcolep∗:ab,ti,kw OR apnea∗:ab,ti,kw OR ‘obstructive sleep apnea∗':ab,ti,kw OR ‘central sleep apnea∗':ab,ti,kw OR ‘sleep-related hypoventilation':ab,ti,kw OR ‘circadian rhythm∗':ab,ti,kw OR ‘circadian rhythm sleep-wake disorder∗':ab,ti,kw OR parasomni∗:ab,ti,kw OR ‘non-rapid eye movement∗':ab,ti,kw OR ‘non-rem∗':ab,ti,kw OR ‘nonrapid eye movement∗':ab,ti,kw OR nonrem∗:ab,ti,kw OR ‘non-rapid eye movement sleep arousal disorder∗':ab,ti,kw OR nightmare∗:ab,ti,kw OR ‘nightmare disorder∗':ab,ti,kw OR ‘rapid eye movement∗':ab,ti,kw OR rem:ab,ti,kw OR ‘rapid eye movement sleep behavior disorder∗':ab,ti,kw OR dream∗:ab,ti,kw OR nap:ab,ti,kw OR naps:ab,ti,kw OR bedtime∗:ab,ti,kw OR ‘bed time∗':ab,ti,kw OR ‘night rest∗':ab,ti,kw OR ‘time in bed':ab,ti,kw OR ‘sleep time∗':ab,ti,kw OR drowsiness:ab,ti,kw OR somnolen∗:ab,ti,kw OR hypersomni∗:ab,ti,kw OR ‘early awakening∗':ab,ti,kw OR ‘night waking∗':ab,ti,kw OR sleepwalking∗:ab,ti,kw OR ‘restless leg∗ syndrome∗':ab,ti,kw OR ‘periodic limb movement disorder∗':ab,ti,kw 694,782
#1 ‘suicide'/exp OR ‘suicidal behavior'/exp OR ‘suicidal behavior':ab,ti,kw OR suicid∗:ab,ti,kw OR ‘self-kill∗':ab,ti,kw OR ‘self-poison∗':ab,ti,kw OR ‘self-stab∗':ab,ti,kw 180,823

Key: Ab, ti, kw searches in abstract, title and author supplied keywords,/exp searches Emtree preferred indexing term, it = publication type

# APA PsycInfo (EBSCO)
Results
Query
S5 S1 AND S2 AND S3 – Limiters Academic journals 409
S4 S1 AND S2 AND S3 436
S3 DE “Treatment Effectiveness Evaluation” OR DE “Mental Health Program Evaluation” OR DE “Placebo” OR DE “Clinical Trials” OR DE “Randomized Clinical Trials” OR DE “Experimental Design” OR DE “Randomized Controlled Trials” OR DE “Experiment Controls” OR DE “Random Sampling” OR TI (placebo∗ OR random OR randomly OR randomised OR randomized OR randomizing OR randomizing OR factorial∗ OR ((singl∗ OR doubl∗ OR trebl∗ OR tripl∗) N3 (blind∗ OR mask∗ OR dummy)) OR (control∗ N3 trial∗) OR allocat∗ OR assign∗ OR crossover∗ OR “cross over∗" OR RCT OR RCTs OR “clinical trial∗” OR “controlled trial∗“) OR AB (placebo∗ OR random OR randomly OR randomised OR randomized OR randomizing OR randomizing OR factorial∗ OR ((singl∗ OR doubl∗ OR trebl∗ OR tripl∗) N3 (blind∗ OR mask∗ OR dummy)) OR (control∗ N3 trial∗) OR allocat∗ OR assign∗ OR crossover∗ OR “cross over∗" OR RCT OR RCTs OR “clinical trial∗” OR “controlled trial∗“) OR KW((placebo∗ OR random OR randomly OR randomised OR randomized OR randomizing OR randomizing OR factorial∗ OR ((singl∗ OR doubl∗ OR trebl∗ OR tripl∗) N3 (blind∗ OR mask∗ OR dummy)) OR (control∗ N3 trial∗) OR allocat∗ OR assign∗ OR crossover∗ OR “cross over∗" OR RCT OR RCTs OR “clinical trial∗” OR “controlled trial∗“) OR MR (“clinical trial”) 477,452
S2 DE “Dreaming” OR DE “Napping” OR DE “NREM Sleep” OR DE “REM Sleep” OR DE “Sleepiness” OR DE “Sleepwalking” OR DE “Sleep” OR DE “REM Sleep” OR DE “Sleep Onset” OR DE “Sleep Quality” OR DE “Sleep Apnea” OR DE “Sleep-Related Hypoventilation” OR DE “Sleep Arousal Disorders” OR DE “Sleep Terrors” OR DE “Sleep Deprivation” OR DE “Sleep Wake Cycle” OR DE “Sleep Wake Disorders” OR DE “Hypersomnia” OR DE “Insomnia” OR DE “Narcolepsy” OR DE “Parasomnias” OR DE “Sleep Apnea” OR DE “Nightmares” OR DE “REM Sleep Behavior Disorder” OR DE “REM Dream Deprivation” OR DE “REM Sleep” DE “Restless Leg Syndrome” OR TI (sleep∗ OR “sleep disorder∗” OR “sleep wake disorder∗” OR “sleep initiation” OR “sleep onset” OR “sleep latency” OR “sleep deprivation” OR “sleep quality” OR “sleep hygiene” OR “sleep disturbance∗” OR “sleep problem∗” OR “sleep maintenance” OR “sleep fragmentation∗” OR “sleep duration∗” OR insomni∗ OR “insomnia disorder∗” OR hypersomnolen∗ OR “hypersomnolence disorder∗” OR narcolep∗ OR apnea∗ OR “obstructive sleep apnea∗” OR “central sleep apnea∗” OR “sleep-related hypoventilation” OR “circadian rhythm∗” OR “circadian rhythm sleep-wake disorder∗” OR parasomni∗ OR “non-Rapid Eye Movement∗” OR “non-REM∗” OR “nonRapid Eye Movement∗” OR nonREM∗ OR “non-Rapid Eye Movement sleep arousal disorder∗” OR nightmare∗ OR “nightmare disorder∗” OR “Rapid Eye Movement∗” OR REM OR “Rapid Eye Movement Sleep behavior disorder∗” OR dream∗ OR nap OR naps OR bedtime∗ OR “bed time∗” OR “night rest∗” OR “time in bed” OR “sleep time∗” OR drowsiness∗ OR somnolen∗ OR hypersomni∗ OR “early awakening∗” OR “night waking” OR sleepwalking OR “Restless Leg∗ Syndrome∗" OR “periodic limb movement disorder∗“) OR AB (sleep∗ OR “sleep disorder∗” OR “sleep wake disorder∗” OR “sleep initiation” OR “sleep onset” OR “sleep latency” OR “sleep deprivation” OR “sleep quality” OR “sleep hygiene” OR “sleep disturbance∗” OR “sleep problem∗” OR “sleep maintenance” OR “sleep fragmentation∗” OR “sleep duration∗” OR insomni∗ OR “insomnia disorder∗” OR hypersomnolen∗ OR “hypersomnolence disorder∗” OR narcolep∗ OR apnea∗ OR “obstructive sleep apnea∗” OR “central sleep apnea∗” OR “sleep-related hypoventilation” OR “circadian rhythm∗” OR “circadian rhythm sleep-wake disorder∗” OR parasomni∗ OR “non-Rapid Eye Movement∗” OR “non-REM∗” OR “nonRapid Eye Movement∗” OR nonREM∗ OR “non-Rapid Eye Movement sleep arousal disorder∗” OR nightmare∗ OR “nightmare disorder∗” OR “Rapid Eye Movement∗” OR REM OR “Rapid Eye Movement Sleep behavior disorder∗” OR dream∗ OR nap OR naps OR bedtime∗ OR “bed time∗” OR “night rest∗” OR “time in bed” OR “sleep time∗” OR drowsiness OR somnolen∗ OR hypersomni∗ OR “early awakening∗” OR “night waking” OR sleepwalking OR “Restless Leg∗ Syndrome∗" OR “periodic limb movement disorder∗“) OR KW(sleep∗ OR “sleep disorder∗” OR “sleep wake disorder∗” OR “sleep-wake disorder∗” OR “sleep initiation” OR “sleep onset” OR “sleep latency” OR “sleep deprivation” OR “sleep quality” OR “sleep hygiene” OR “sleep disturbance∗” OR “sleep problem∗” OR “sleep maintenance” OR “sleep fragmentation∗” OR “sleep duration∗” OR insomni∗ OR “insomnia disorder∗” OR hypersomnolen∗ OR “hypersomnolence disorder” OR narcolep∗ OR apnea∗ OR “obstructive sleep apnea∗” OR “central sleep apnea∗” OR “sleep-related hypoventilation” OR “circadian rhythm∗” OR “circadian rhythm sleep-wake disorder∗” OR parasomni∗ OR “non-Rapid Eye Movement∗” OR “non-REM∗” OR “nonRapid Eye Movement∗” OR nonREM∗ OR “non-Rapid Eye Movement sleep arousal disorder∗” OR nightmare∗ OR “nightmare disorder∗” OR “Rapid Eye Movement∗” OR REM OR “Rapid Eye Movement Sleep behavior disorder∗” OR dream∗ OR nap OR naps OR bedtime∗ OR “bed time∗” OR “night rest∗” OR “time in bed” OR “sleep time∗” OR drowsiness OR somnolen∗ OR hypersomni∗ OR “early awakening∗” OR “night waking” OR sleepwalking OR “Restless Leg∗ Syndrome∗" OR “periodic limb movement disorder∗“) 148,200
S1 DE “Suicide” OR DE “Attempted Suicide” OR DE “Suicidality” OR DE “Suicidal Ideation” OR DE “Suicide Prevention” OR DE “Suicidology” OR DE “Self-Poisoning” OR DE “Military Suicide” OR DE “Youth Suicide” OR TI (suicid∗ OR “self-kill∗” OR “self-poison∗” OR “self-stabb∗” OR parasuicid∗) OR AB (suicid∗ OR “self-kill∗” OR “self-poison∗” OR “self-stabb∗” OR parasuicid∗) OR KW(suicid∗ OR “self-kill∗” OR “self-poison∗” OR “self-stabb∗” OR parasuicid∗) 86,285

Key: DE = Descriptors,TI = title, AB = abstract and KW= Searches for keywords in the uncontrolled content description of the document

Web of Science (Core collection) – Clarivate
  • -

    WOS.SCI: 1900 to 2025

  • -

    WOS.AHCI: 1975 to 2025

  • -

    WOS.ESCI: 2005 to 2025

  • -

    WOS.SSCI: 1956 to 2025

Nr. Query Results
#5 Search: #3 AND #2 AND #1 and Article or Early Access or Book Chapters (Document Types) 662
#4 Search: #3 AND #2 AND #1 864
#3 Search: TS=(placebo∗ OR random OR randomly OR randomised OR randomized OR randomizing OR randomizing OR factorial∗ OR ((singl∗ OR doubl∗ OR trebl∗ OR tripl∗) N3 (blind∗ OR mask∗ OR dummy)) OR (control∗ N3 trial∗) OR allocat∗ OR assign∗ OR crossover∗ OR “cross over∗" OR RCT OR RCTs OR “clinical trial∗” OR “controlled trial∗” OR “double-blind”) 4,154,060
#2 Search: TS=(sleep∗ OR “sleep disorder∗” OR “sleep wake disorder∗” OR “sleep initiation” OR “sleep onset” OR “sleep latency” OR “sleep deprivation” OR “sleep quality” OR “sleep hygiene” OR “sleep disturbance∗” OR “sleep problem∗” OR “sleep maintenance” OR “sleep fragmentation∗” OR “sleep duration∗” OR insomni∗ OR “insomnia disorder∗” OR hypersomnolen∗ OR “hypersomnolence disorder∗” OR narcolep∗ OR apnea∗ OR “obstructive sleep apnea∗” OR “central sleep apnea∗” OR “sleep-related hypoventilation” OR “circadian rhythm∗” OR “circadian rhythm sleep-wake disorder∗” OR parasomni∗ OR “non-Rapid Eye Movement∗” OR “non-REM∗” OR “nonRapid Eye Movement∗” OR nonREM∗ OR “non-Rapid Eye Movement sleep arousal disorder∗” OR nightmare∗ OR “nightmare disorder∗” OR “Rapid Eye Movement∗” OR REM OR “Rapid Eye Movement Sleep behavior disorder∗” OR dream∗ OR nap OR naps OR bedtime∗ OR “bed time∗” OR “night rest∗” OR “time in bed” OR “sleep time∗” OR drowsiness OR somnolen∗ OR hypersomni∗ OR “early awakening∗” OR “night waking” OR sleepwalking OR “Restless Leg∗ Syndrome∗" OR “periodic limb movement disorder∗“) 543,127
#1 Search: TS=(suicid∗ OR “self-kill∗” OR “self-poison∗” OR “self-stabb∗“) 147,335

Key: TS = topic, which includes title, abstract, author keywords and Web of Science Keywords Plus./TI = title, AK = author keywords

ID Cochrane CENTRAL (Wiley)
Hits
Search
#1 (suicid∗ OR self-killing∗ OR self-poisoning∗ OR self-stabbing∗):ab,ti,kw 9300
#2 (sleep∗ OR “sleep disorder” OR “sleep disorders” OR “sleep wake disorder” OR “sleep wake disorders” OR “sleep initiation” OR “sleep onset” OR “sleep latency” OR “sleep deprivation” OR “sleep quality” OR “sleep hygiene” OR “sleep disturbance” OR “sleep disturbances” OR “sleep problem” OR “sleep problems” OR “sleep maintenance” OR “sleep fragmentation” OR “sleep fragmentations” OR “sleep duration” OR “sleep durations” OR insomni∗ OR “insomnia disorder” OR “insomnia disorders” OR hypersomnolen∗ OR “hypersomnolence disorder” OR “hypersomnolence disorders” OR narcolep∗ OR apnea∗ OR “obstructive sleep apnea” OR “obstructive sleep apneas” OR “central sleep apnea” OR “central sleep apneas” OR “sleep related hypoventilation” OR “circadian rhythm” OR “circadian rhythm sleep wake disorder” OR “circadian rhythm sleep wake disorders” OR parasomni∗ OR “non Rapid Eye Movement” OR “non Rapid Eye Movement sleep arousal disorder” OR “non Rapid Eye Movement sleep arousal disorders” OR “non REM” OR “non REM sleep arousal disorder” OR “non REM sleep arousal disorders” OR “nonRapid Eye Movement” OR “nonRapid Eye Movement sleep arousal disorder” OR “nonRapid Eye Movement sleep arousal disorders” OR nonREM OR “nonREM sleep arousal disorder” OR “nonREM sleep arousal disorders” OR nightmare OR nightmares OR “nightmare disorder” OR “nightmare disorders” OR “Rapid Eye Movement” OR “Rapid Eye Movements” OR REM OR “Rapid Eye Movement Sleep behavior disorder” OR “Rapid Eye Movement Sleep behavior disorders” OR dream∗ OR nap OR naps OR bedtime∗ OR “bed time” OR “bed times” OR “night rest” OR “night rests” OR “time in bed” OR “sleep time” OR “sleep times” OR “night waking” OR “night wakings” OR drowsiness OR somnolen∗ OR hypersomni∗ OR “early awakening” OR “early awakenings” OR “night waking” OR sleepwalking OR “restless leg syndrome” OR “restless legs syndrome” OR “periodic limb movement disorder” OR “periodic limb movement disorders”):ab,ti,kw 86,085
#3 #1 AND #2 1489
#4 #3 AND CENTRAL 1468
#5 #4 AND (CT-gov OR ICTRP) 525

Key: ti,ab,kw searches in title, abstract and author supplied keywords

History Count Scopus (Elsevier)
Results
Search
#5 #1 AND #2 AND #3 AND (LIMIT-TO (DOCTYPE, “ar”) OR LIMIT-TO (DOCTYPE, “ch”)) 2556
#4 #1 AND #2 AND #3 4222
#3 TITLE-ABS-KEY (placebo∗ OR random OR randomly OR randomised OR randomized OR randomizing OR randomizing OR factorial∗ OR ((singl∗ OR doubl∗ OR trebl∗ OR tripl∗) W/3 (blind∗ OR mask∗ OR dummy)) OR (control∗ W/3 trial∗) OR allocat∗ OR assign∗ OR crossover∗ OR “cross over∗" OR rct OR rcts OR “clinical trial∗" OR “controlled trial∗" OR “double-blind”) 6,369,87
#2 TITLE-ABS-KEY (sleep∗ OR “sleep disorder∗" OR “sleep wake disorder∗" OR “sleep initiation” OR “sleep onset” OR “sleep latency” OR “sleep deprivation” OR “sleep quality” OR “sleep hygiene” OR “sleep disturbance∗" OR “sleep problem∗" OR “sleep maintenance” OR “sleep fragmentation∗" OR “sleep duration∗" OR insomni∗ OR “insomnia disorder∗" OR hypersomnolen∗ OR “hypersomnolence disorder∗" OR narcolep∗ OR apnea∗ OR “obstructive sleep apnea∗" OR “central sleep apnea∗" OR “sleep-related hypoventilation” OR “circadian rhythm∗" OR “circadian rhythm sleep-wake disorder∗" OR parasomni∗ OR “non-Rapid Eye Movement∗" OR “non-REM∗" OR “nonRapid Eye Movement∗" OR nonrem∗ OR “non-Rapid Eye Movement sleep arousal disorder∗" OR nightmare∗ OR “nightmare disorder∗" OR “Rapid Eye Movement∗" OR rem OR “Rapid Eye Movement Sleep behavior disorder∗" OR dream∗ OR nap OR naps OR bedtime∗ OR “bed time∗" OR “night rest∗" OR “time in bed” OR “sleep time∗" OR drowsiness OR somnolen∗ OR hypersomni∗ OR “early awakening∗" OR “night waking” OR sleepwalking OR “Restless Leg∗ Syndrome∗" OR “periodic limb movement disorder∗") 787,533
#1 TITLE-ABS-KEY (suicid∗ OR “self-kill∗" OR “self-poison∗" OR “self-stabb∗") 199,789

Key: ABS, TITLE, AUTHKEY searches in abstract, title and author supplied keywords

Appendix B. Additional Information on the Meta-analyses Results

B1. The effect of treating sleep on suicidality (research question 1)

graphic file with name fx1.jpg

Influence analysis meta-analysis model on suicidal ideation as outcome

graphic file with name fx2.jpg

Funnel plot and publication bias correction results (outcome: suicidal ideation)

B2. The effect of treating sleep on sleep disturbance (research question 1)

graphic file with name fx3.jpg

Forest Plot of all Efficacy Studies on sleep disturbance

B3. The effect and safety of psychotherapeutic sleep interventions (research question 2)

graphic file with name fx4.jpg

Influence analysis meta-analysis model on suicidal ideation as outcome

B3. Risk of Bias Graphs

graphic file with name fx5.jpg

Risk of Bias Graph for all Efficacy Studies

graphic file with name fx6.jpg

Risk of Bias Graph for all Safety Studies

References

  • 1.World Health Organisation . 2021. Suicide. [Google Scholar]
  • 2.Dong M., Lu L., Sha S., Zhang L., Zhang Q., Ungvari G.S., et al. Sleep disturbances and the risk of incident suicidality: a systematic review and meta-analysis of cohort studies. Psychosom Med. 2021;83:739–745. doi: 10.1097/PSY.0000000000000964. [DOI] [PubMed] [Google Scholar]
  • 3.Harris L.M., Huang X., Linthicum K.P., Bryen C.P., Ribeiro J.D. Sleep disturbances as risk factors for suicidal thoughts and behaviours: a meta-analysis of longitudinal studies. Sci Rep. 2020;10 doi: 10.1038/s41598-020-70866-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Lancel M., Veen van M., Kamphuis J. Bohn Stafleu van Loghum; Houten: 2020. Slaapstoornissen in de psychiatrie: diagnose en behandeling. [Google Scholar]
  • 5.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. doi: 10.1016/j.sleep.2016.08.006. [DOI] [PubMed] [Google Scholar]
  • 6.Hertenstein E., Feige B., Gmeiner T., Kienzler C., Spiegelhalder K., Johann A., et al. Insomnia as a predictor of mental disorders: a systematic review and meta-analysis. Sleep Med Rev. 2019;43:96–105. doi: 10.1016/j.smrv.2018.10.006. [DOI] [PubMed] [Google Scholar]
  • 7.Wardle-Pinkston S., Slavish D.C., Taylor D.J. Insomnia and cognitive performance: a systematic review and meta-analysis. Sleep Med Rev. 2019;48 doi: 10.1016/j.smrv.2019.07.008. [DOI] [PubMed] [Google Scholar]
  • 8.Malik S., Kanwar A., Sim L.A., Prokop L.J., Wang Z., Benkhadra K., et al. The association between sleep disturbances and suicidal behaviors in patients with psychiatric diagnoses: a systematic review and meta-analysis. Syst Rev. 2014;3:18. doi: 10.1186/2046-4053-3-18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.American Psychiatric Association Diagnostic and statistical manual of mental disorders. 2013. [DOI]
  • 10.Morin C.M., Jarrin D.C. Epidemiology of insomnia: prevalence, course, risk factors, and public health burden. Sleep Med Clin. 2022;17:173–191. doi: 10.1016/j.jsmc.2022.03.003. [DOI] [PubMed] [Google Scholar]
  • 11.Lancel M., Marle H.J.F., Veen M.M., Schagen A.M. Disturbed sleep in PTSD: thinking beyond nightmares. Front Psychiatr. 2021;12 doi: 10.3389/fpsyt.2021.767760. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Baglioni C., Battagliese G., Feige B., Spiegelhalder K., Nissen C., Voderholzer U., et al. Insomnia as a predictor of depression: a meta-analytic evaluation of longitudinal epidemiological studies. J Affect Disord. 2016;193:10–19. doi: 10.1016/j.jad.2011.01.011. [DOI] [PubMed] [Google Scholar]
  • 13.Ritter P.S., Höfler M., Wittchen H.U., Lieb R., Bauer M., Pfennig A., et al. Disturbed sleep as risk factor for the subsequent onset of bipolar disorder–data from a 10-year prospective-longitudinal study among adolescents and young adults. J Psychiatr Res. 2015;68:76–82. doi: 10.1016/j.jpsychires.2015.06.005. [DOI] [PubMed] [Google Scholar]
  • 14.McCall W.V., Black C.G. The link between suicide and insomnia: theoretical mechanisms. Curr Psychiatry Rep. 2013;15:389. doi: 10.1007/s11920-013-0389-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Littlewood D., Kyle S.D., Pratt D., Peters S., Gooding P. Examining the role of psychological factors in the relationship between sleep problems and suicide. Clin Psychol Rev. 2017;54:1–16. doi: 10.1016/j.cpr.2017.03.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Fernandes S.N., Zuckerman E., Miranda R., Baroni A. When night falls fast: sleep and suicidal behavior among adolescents and young adults. Child Adolesc Psychiatr Clin North Am. 2021;30:269–282. doi: 10.1016/j.chc.2020.08.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Kivelä L.M.M., Does W., Antypa N. Sleep, hopelessness, and suicidal ideation: an ecological momentary assessment and actigraphy study. J Psychiatr Res. 2024;177:46–52. doi: 10.1016/j.jpsychires.2024.06.039. [DOI] [PubMed] [Google Scholar]
  • 18.Perlis M.L., Grandner M.A., Chakravorty S., Bernert R.A., Brown G.K., Thase M.E. Suicide and sleep: is it a bad thing to be awake when reason sleeps? Sleep Med Rev. 2016;29:101–107. doi: 10.1016/j.smrv.2015.10.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Anderson C., Platten C.R. Sleep deprivation lowers inhibition and enhances impulsivity to negative stimuli. Behav Brain Res. 2011;217:463–466. doi: 10.1016/j.bbr.2010.09.020. [DOI] [PubMed] [Google Scholar]
  • 20.van Veen M.M., Lancel M., Beijer E., Remmelzwaal S., Rutters F. The association of sleep quality and aggression: a systematic review and meta-analysis of observational studies. Sleep Med Rev. 2021;59 doi: 10.1016/j.smrv.2021.101500. [DOI] [PubMed] [Google Scholar]
  • 21.Abad V.C., Guilleminault C. Diagnosis and treatment of sleep disorders: a brief review for clinicians. Dialogues Clin Neurosci. 2003;5:371–388. doi: 10.31887/DCNS.2003.5.4/vabad. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Riemann D., Espie C.A., Altena E., Arnardottir E.S., Baglioni C., Bassetti C.L.A., et al. The European insomnia guideline: an update on the diagnosis and treatment of insomnia 2023. J Sleep Res. 2023;32 doi: 10.1111/jsr.14035. [DOI] [PubMed] [Google Scholar]
  • 23.N.H.G.-werkgroep. Slaapproblemen en slaapmiddelen. NHG-Richtlijnen; 2014. [Google Scholar]
  • 24.Rocha R.B., Bomtempo F.F., Nager G.B., Cenci G.I., Telles J.P.M. Dual orexin receptor antagonists for the treatment of insomnia: systematic review and network meta-analysis. Arq Neuropsiquiatr. 2023;81:475–483. doi: 10.1055/s-0043-1768667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Parrino L., Terzano M.G. Polysomnographic effects of hypnotic drugs: a review. Psychopharmacology. 1996;126:1–16. doi: 10.1007/BF02246405. [DOI] [PubMed] [Google Scholar]
  • 26.Instituut verantwoord medicijngebruik. Rij veilig met medicijnen: temazepam. n.d.
  • 27.Rapoport M.J., Lanctôt K.L., Streiner D.L., Bédard M., Vingilis E., Murray B., et al. Benzodiazepine use and driving: a meta-analysis. J Clin Psychiatry. 2009;70:663–673. doi: 10.4088/JCP.08m04325. [DOI] [PubMed] [Google Scholar]
  • 28.Mignot E.J.M. A practical guide to the therapy of narcolepsy and hypersomnia syndromes. Neurotherapeutics. 2012;9:739–752. doi: 10.1007/s13311-012-0150-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Bhattarai J., Sumerall S. Current and future treatment options for narcolepsy: a review. Sleep Sci. 2017;10:19–27. doi: 10.5935/1984-0063.20170004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Manber R., Bernert R.A., Suh S., Nowakowski S., Siebern A.T., Ong J.C. CBT for insomnia in patients with high and low depressive symptom severity: adherence and clinical outcomes. J Clin Sleep Med : JCSM : Off Public Am Acad Sleep Med. 2011;7:645–652. doi: 10.5664/jcsm.1472. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Trockel M., Karlin B.E., Taylor C.B., Brown G.K., Manber R. Effects of cognitive behavioral therapy for insomnia on suicidal ideation in veterans. Sleep. 2015;38:259–265. doi: 10.5665/sleep.4410. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Tubbs A.S., Fernandez F.X., Ghani S.B., Karp J.F., Patel S.I., Parthasarathy S., et al. Prescription medications for insomnia are associated with suicidal thoughts and behaviors in two nationally representative samples. J Clin Sleep Med : JCSM : Off Public Am Acad Sleep Med. 2021;17:1025–1030. doi: 10.5664/jcsm.9096. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Page M.J., McKenzie J.E., Bossuyt P.M., Boutron I., Hoffmann T.C., Mulrow C.D., et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021:n71. doi: 10.1136/bmj.n71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Ouzzani M., Hammady H., Fedorowicz Z., Elmagarmid A. Rayyan—A web and mobile app for systematic reviews. Syst Rev. 2016;5:210. doi: 10.1186/s13643-016-0384-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Higgins J.P., Savović J., Page M.J., Jonathan A.C.S. 2019. Revised Cochrane risk-of-bias tool for randomized trials (RoB 2) [Google Scholar]
  • 36.Harrer M., Cuijpers P., Furukawa T.A., Ebert D.D. Chapman & Hall/CRC Press; Boca Raton, FL and London: 2021. Doing meta-analysis with R: a Hands-On guide. [Google Scholar]
  • 37.R Core Team . 2023. R: a language and environment for statistical computing. [Google Scholar]
  • 38.Balduzzi S., Rücker G., Schwarzer G. Evidence-Based Mental Health; 2019. How to perform a meta-analysis with R: a practical tutorial; pp. 153–160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Viechtbauer W. Conducting meta-analyses in R with the metafor package. J Stat Software. 2010;36(3):1–48. doi: 10.18637/jss.v036.i03. [DOI] [Google Scholar]
  • 40.Harrer M., Kuper P., Sprenger A., Cuijpers P. 2022. metapsyTools: several R helper functions for the “metapsy” database. [Google Scholar]
  • 41.Lüdecke D. Esc: effect size computation for Meta analysis (version 0.5.1) 2019. [DOI]
  • 42.McGuinness L.A., Higgins J.P. Risk-of-bias VISualization (robvis): an R package and shiny web app for visualizing risk-of-bias assessments. Res Synth Methods. 2020 doi: 10.1002/jrsm.1411. [DOI] [PubMed] [Google Scholar]
  • 43.Greenland S., Robins J.M. Estimation of a common effect parameter from sparse follow-up data. Biometrics. 1985;41:55–68. [PubMed] [Google Scholar]
  • 44.Robins J., Breslow N., Greenland S. Estimators of the mantel-haenszel variance consistent in both sparse data and large-strata limiting models. Biometrics. 1986;42:311–323. [PubMed] [Google Scholar]
  • 45.Batterham P.J., Christensen H., Mackinnon A.J., Gosling J.A., Thorndike F.P., Ritterband L.M., et al. Trajectories of change and long-term outcomes in a randomised controlled trial of internet-based insomnia treatment to prevent depression. BJPsych Open. 2017;3:228–235. doi: 10.1192/bjpo.bp.117.005231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Chan N.Y., Lam S.P., Zhang J., Chan J.W.Y., Yu M.M.W., Suh S., et al. Efficacy of email-delivered versus face-to-face group cognitive behavioral therapy for insomnia in youths: a randomized controlled trial. J Adolesc Health. 2022;70:763–773. doi: 10.1016/j.jadohealth.2021.11.005. [DOI] [PubMed] [Google Scholar]
  • 47.Cromer L.D., Bell S.B., Prince L.E., Hollman N., El Sabbagh E., Buck T.R. Efficacy of a telehealth cognitive behavioral therapy for improving sleep and nightmares in children aged 6–17. Front Sleep. 2024;3 doi: 10.3389/frsle.2024.1401023. [DOI] [Google Scholar]
  • 48.Crosby E.S., Troop-Gordon W., Witte T.K. A pilot randomized-controlled trial of sleep scholar: a brief, internet-based insomnia intervention for college students. Behav Ther. 2025;56:366–380. doi: 10.1016/j.beth.2024.06.007. [DOI] [PubMed] [Google Scholar]
  • 49.Ioannou M., Szabó Z., Widmark-Jensen M., Vyrinis G., Karlsson C., Steingrimsson S. Total sleep deprivation followed by bright light therapy as rapid relief for depression: a pragmatic randomized controlled trial. Front Psychiatr. 2021;12 doi: 10.3389/fpsyt.2021.705090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Kalmbach D.A., Cheng P., Ahmedani B.K., Peterson E.L., Reffi A.N., Sagong C., et al. Cognitive-behavioral therapy for insomnia prevents and alleviates suicidal ideation: insomnia remission is a suicidolytic mechanism. Sleep. 2022;45:251. doi: 10.1093/sleep/zsac251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Krystal A., Fava M., Rubens R., Wessel T., Caron J., Wilson P., et al. Evaluation of eszopiclone discontinuation after cotherapy with fluoxetine for insomnia with coexisting depression. J Clin Sleep Med : JCSM : Off Public Am Acad Sleep Med. 2007;3:48–55. [PubMed] [Google Scholar]
  • 52.McCall W.V., Benca R.M., Rosenquist P.B., Youssef N.A., McCloud L., Newman J.C., et al. Reducing suicidal ideation through insomnia treatment (REST-IT): a randomized clinical trial. Am J Psychiatr. 2019;176:957–965. doi: 10.1176/appi.ajp.2019.19030267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.McCall W.V., Pillai A., Case D., McCloud L., Nolla T., Branch F., et al. A pilot, randomized clinical trial of bedtime doses of prazosin versus placebo in suicidal posttraumatic stress disorder patients with nightmares. J Clin Psychopharmacol. 2018;38:618–621. doi: 10.1097/JCP.0000000000000968. [DOI] [PubMed] [Google Scholar]
  • 54.Nazem S., Sun S., Barnes S.M., Monteith L.L., Hostetter T.A., Forster J.E., et al. Impact of an internet-based insomnia intervention on suicidal ideation and associated correlates in veterans at elevated suicide risk. Translat Behav Med. 2024;14:673–683. doi: 10.1093/tbm/ibae032. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Pigeon W.R., Funderburk J.S., Cross W., Bishop T.M., Crean H.F. Brief CBT for insomnia delivered in primary care to patients endorsing suicidal ideation: a proof-of-concept randomized clinical trial. Translat Behav Med. 2019;9:1169–1177. doi: 10.1093/tbm/ibz108. [DOI] [PubMed] [Google Scholar]
  • 56.Pigeon W.R., Funderburk J., Bishop T.M., Crean H.F. Brief cognitive behavioral therapy for insomnia delivered to depressed veterans receiving primary care services: a pilot study. J Affect Disord. 2017;217:105–111. doi: 10.1016/j.jad.2017.04.003. [DOI] [PubMed] [Google Scholar]
  • 57.Pruiksma K.E., Taylor D.J., Mintz J., Nicholson K.L., Rodgers M., Young-McCaughan S., et al. A pilot randomized controlled trial of cognitive behavioral treatment for trauma-related nightmares in active duty military personnel. J Clin Sleep Med : JCSM : Off Public Am Acad Sleep Med. 2020;16:29–40. doi: 10.5664/jcsm.8116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Smagula S.F., Gasperetti C.E., Buysse D.J., Irwin M.R., Krafty R.T., Lim S.E., et al. Efficacy of the transdiagnostic intervention for sleep and circadian dysfunction for depression symptoms and sleep-wake disruption in older and younger adults: secondary age-stratified analysis of a randomized controlled trial. Am J Geriatr Psychiatr. 2024;32:478–488. doi: 10.1016/j.jagp.2023.11.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Sheaves B., Holmes E.A., Rek S., Taylor K.M., Nickless A., Waite F., et al. Cognitive behavioural therapy for nightmares for patients with persecutory delusions (nites): an assessor-blind, pilot randomized controlled trial. Canad J Psychiatry Revue Canadienne de Psychiatrie. 2019;64:686–696. doi: 10.1177/0706743719847422. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Volf C., Aggestrup A.S., Svendsen S.D., Hansen T.S., Petersen P.M., Dam-Hansen C., et al. Dynamic LED light versus static LED light for depressed inpatients: results from a randomized feasibility trial. Pilot Feasib Stud. 2020;6:5. doi: 10.1186/s40814-019-0548-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Waite F., Černis E., Kabir T., Iredale E., Johns L., Maughan D., et al. A targeted psychological treatment for sleep problems in young people at ultra-high risk of psychosis in England (SleepWell): a parallel group, single-blind, randomised controlled feasibility trial. Lancet Psychiatry. 2023;10:706–718. doi: 10.1016/S2215-0366(23)00203-1. [DOI] [PubMed] [Google Scholar]
  • 62.Wu R., Zhong S.Y., Wang G.H., Wu M.Y., Xu J.F., Zhu H., et al. The effect of brief mindfulness meditation on suicidal ideation, stress and sleep quality. Arch Suicide Res : Off J Int Acad Suic Res. 2023;27:215–230. doi: 10.1080/13811118.2021.1982800. [DOI] [PubMed] [Google Scholar]
  • 63.Ancoli-Israel S., Krystal A.D., McCall W.V., Schaefer K., Wilson A., Claus R., et al. A 12-week, randomized, double-blind, placebo-controlled study evaluating the effect of eszopiclone 2 mg on sleep/wake function in older adults with primary and comorbid insomnia. Sleep. 2010;33:225–234. doi: 10.1093/sleep/33.2.225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Bogan R., Thorpy M.J., Winkelman J.W., Dubow J., Gudeman J., Seiden D. Randomized, crossover, open-label study of the relative bioavailability and safety of FT218, a once-nightly sodium oxybate formulation: phase 1 study in healthy volunteers. Sleep Med. 2022;100:442–447. doi: 10.1016/j.sleep.2022.09.011. [DOI] [PubMed] [Google Scholar]
  • 65.Brooks S., Jacobs G.E., Boer P., Kent J.M., Nueten L., Amerongen G., et al. The selective orexin-2 receptor antagonist seltorexant improves sleep: an exploratory double-blind, placebo controlled, crossover study in antidepressant-treated major depressive disorder patients with persistent insomnia. J Psychopharmacol. 2019;33:202–209. doi: 10.1177/0269881118822258. (Oxford) [DOI] [PubMed] [Google Scholar]
  • 66.Czeisler C.A., Walsh J.K., Wesnes K.A., Arora S., Roth T. Armodafinil for treatment of excessive sleepiness associated with shift work disorder: a randomized controlled study. Mayo Clin Proc. 2009;84:958–972. doi: 10.1016/S0025-6196(11)60666-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Dauvilliers Y., Mignot E., Del Río Villegas R., Du Y., Hanson E., Inoue Y., et al. Oral orexin receptor 2 agonist in narcolepsy type 1. N Engl J Med. 2023;389:309–321. doi: 10.1056/NEJMoa2301940. [DOI] [PubMed] [Google Scholar]
  • 68.Dunlop B.W., Crits-Christoph P., Evans D.L., Hirschowitz J., Solvason H.B., Rickels K., et al. Coadministration of modafinil and a selective serotonin reuptake inhibitor from the initiation of treatment of major depressive disorder with fatigue and sleepiness: a double-blind, placebo-controlled study. J Clin Psychopharmacol. 2007;27:614–619. doi: 10.1097/jcp.0b013e31815abefb. [DOI] [PubMed] [Google Scholar]
  • 69.During E.H., Hernandez B., Miglis M.G., Sum-Ping O., Hekmat A., Cahuas A., et al. Sodium oxybate in treatment-resistant rapid-eye-movement sleep behavior disorder. SLEEP. 2023;46 doi: 10.1093/sleep/zsad103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Herring W.J., Ceesay P., Snyder E., Bliwise D., Budd K., Hutzelmann J., et al. Polysomnographic assessment of suvorexant in patients with probable Alzheimer's disease dementia and insomnia: a randomized trial. Alzheimer's Dementia : J Alzh Assoc. 2020;16:541–551. doi: 10.1002/alz.12035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Herring W.J., Connor K.M., Snyder E., Snavely D.B., Zhang Y., Hutzelmann J., et al. Suvorexant in patients with insomnia: pooled analyses of three-month data from Phase-3 randomized controlled clinical trials. J Clin Sleep Med : JCSM : Off Public Am Acad Sleep Med. 2016;12:1215–1225. doi: 10.5664/jcsm.6116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Kim S.J., Lee Y.J., Lee Y.J., Cho S.J. Effect of quetiapine XR on depressive symptoms and sleep quality compared with lithium in patients with bipolar depression. J Affect Disord. 2014;157:33–40. doi: 10.1016/j.jad.2013.12.032. [DOI] [PubMed] [Google Scholar]
  • 73.Krystal A.D., Benca R.M., Rosenberg R., Schweitzer P.K., Malhotra A., Babson K., et al. Solriamfetol treatment of excessive daytime sleepiness in participants with narcolepsy or obstructive sleep apnea with a history of depression. J Psychiatr Res. 2022;155:202–210. doi: 10.1016/j.jpsychires.2022.08.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Krystal A.D., Harsh J.R., Yang R., Rippon G.A., Lankford D.A. A double-blind, placebo-controlled study of armodafinil for excessive sleepiness in patients with treated obstructive sleep apnea and comorbid depression. J Clin Psychiatry. 2010;71:32–40. doi: 10.4088/JCP.09m05536gry. [DOI] [PubMed] [Google Scholar]
  • 75.Kunz D., Dauvilliers Y., Benes H., García-Borreguero D., Plazzi G., Seboek Kinter D., et al. Long-term safety and tolerability of daridorexant in patients with insomnia disorder. CNS Drugs. 2023;37:93–106. doi: 10.1007/s40263-022-00980-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Kushida C.A., Shapiro C.M., Roth T., Thorpy M.J., Corser B.C., Ajayi A.O., et al. Once-nightly sodium oxybate (FT218) demonstrated improvement of symptoms in a phase 3 randomized clinical trial in patients with narcolepsy. Sleep. 2022;45:200. doi: 10.1093/sleep/zsab200. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Lieverse R., Someren E.J., Nielen M.M., Uitdehaag B.M., Smit J.H., Hoogendijk W.J. Bright light treatment in elderly patients with nonseasonal major depressive disorder: a randomized placebo-controlled trial. Arch Gen Psychiatry. 2011;68:61–70. doi: 10.1001/archgenpsychiatry.2010.183. [DOI] [PubMed] [Google Scholar]
  • 78.Lipschitz J.M., Perez-Rodriguez M., Majd M., Larsen E., Locascio J., Pike C.K., et al. Modafinil's effects on cognition and sleep quality in affectively-stable patients with bipolar disorder: a pilot study. Front Psychiatr. 2023;14 doi: 10.3389/fpsyt.2023.1246149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Locklear J.C., Svedsäter H., Datto C., Endicott J. Effects of once-daily extended release quetiapine fumarate (quetiapine XR) on quality of life and sleep in elderly patients with major depressive disorder. J Affect Disord. 2013;149:189–195. doi: 10.1016/j.jad.2013.01.021. [DOI] [PubMed] [Google Scholar]
  • 80.Loving R.T., Kripke D.F., Knickerbocker N.C., Grandner M.A. Bright green light treatment of depression for older adults [ISRCTN69400161. BMC Psychiatry. 2005;5:42. doi: 10.1186/1471-244X-5-42. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Mellman T.A., Birku K., Sandhu I., Lavela P., Kobayashi I. Evaluation of suvorexant for trauma-related insomnia. Sleep. 2022;45:68. doi: 10.1093/sleep/zsac068. [DOI] [PubMed] [Google Scholar]
  • 82.Mignot E., Mayleben D., Fietze I., Leger D., Zammit G., Bassetti C.L.A., et al. Safety and efficacy of daridorexant in patients with insomnia disorder: results from two multicentre, randomised, double-blind, placebo-controlled, phase 3 trials. Lancet Neurol. 2022;21:125–139. doi: 10.1016/S1474-4422(21)00436-1. [DOI] [PubMed] [Google Scholar]
  • 83.Nirogi R., Shinde A., Goyal V.K., Ravula J., Benade V., Jetta S., et al. Samelisant (SUVN-G3031), a histamine 3 receptor inverse agonist: results from the phase 2 double-blind randomized placebo-controlled study for the treatment of excessive daytime sleepiness in adult patients with narcolepsy. Sleep Med. 2024;124:618–626. doi: 10.1016/j.sleep.2024.10.037. [DOI] [PubMed] [Google Scholar]
  • 84.Parmenter M.E., Lederman S., Weathers F.W., Davis L.L., Vaughn B., Engels J., et al. A phase 3, randomized, placebo-controlled, trial to evaluate the efficacy and safety of bedtime sublingual cyclobenzaprine (TNX-102 SL) in military-related posttraumatic stress disorder. Psychiatry Res. 2024;334 doi: 10.1016/j.psychres.2024.115764. [DOI] [PubMed] [Google Scholar]
  • 85.Raskind M.A., Peskind E.R., Chow B., Harris C., Davis-Karim A., Holmes H.A., et al. Trial of prazosin for post-traumatic stress disorder in military veterans. N Engl J Med. 2018;378:507–517. doi: 10.1056/NEJMoa1507598. [DOI] [PubMed] [Google Scholar]
  • 86.Recourt K., Boer P., Zuiker R., Luthringer R., Kent J., Ark P., et al. The selective orexin-2 antagonist seltorexant (JNJ-42847922/MIN-202) shows antidepressant and sleep-promoting effects in patients with major depressive disorder. Transl Psychiatry. 2019;9:216. doi: 10.1038/s41398-019-0553-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 87.Sangal R.B., Blumer J.L., Lankford D.A., Grinnell T.A., Huang H. Eszopiclone for insomnia associated with attention-deficit/hyperactivity disorder. Pediatrics. 2014;134:1095–1103. doi: 10.1542/peds.2013-4221. [DOI] [PubMed] [Google Scholar]
  • 88.Uchimura N., Ozone M., Suzuki M., Taniguchi M., Kuriyama K., Togo O., et al. Long-term safety and efficacy of daridorexant in Japanese patients with insomnia disorder. Sleep Med. 2024;122:64–70. doi: 10.1016/j.sleep.2024.07.036. [DOI] [PubMed] [Google Scholar]
  • 89.Lindelow M., Hardy R., Rodgers B. Development of a scale to measure symptoms of anxiety and depression in the general UK population: the psychiatric symptom frequency scale. J Epidemiol Community. 1997;51:549–557. doi: 10.1136/jech.51.5.549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 90.Joiner T.E., Pfaff J.J., Acres J.G. A brief screening tool for suicidal symptoms in adolescents and young adults in general health settings: reliability and validity data from the Australian national general practice youth suicide prevention project. Behav Res Ther. 2002;40:471–481. doi: 10.1016/S0005-7967(01)00017-1. [DOI] [PubMed] [Google Scholar]
  • 91.Montgomery S.A., Åsberg M. A new depression scale designed to be sensitive to change. Br J Psychiatry. 1979;134:382–389. doi: 10.1192/bjp.134.4.382. [DOI] [PubMed] [Google Scholar]
  • 92.Rush A.J., Trivedi M.H., Ibrahim H.M., Carmody T.J., Arnow B., Klein D.N., et al. The 16-Item quick inventory of depressive symptomatology (QIDS), clinician rating (QIDS-C), and self-report (QIDS-SR): a psychometric evaluation in patients with chronic major depression. Biol Psychiatry. 2003;54:573–583. doi: 10.1016/S0006-3223(02)01866-8. [DOI] [PubMed] [Google Scholar]
  • 93.Reynolds W.M. Adult suicidal ideation questionnaire. 2011. [DOI] [PubMed]
  • 94.Hamilton M. A rating scale for depression. J Neurol Neurosurg Psychiatr. 1960;23:56–62. doi: 10.1136/jnnp.23.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 95.Beck A.T., Kovacs M., Weissman A. Assessment of suicidal intention: the scale for suicide ideation. J Consult Clin Psychol. 1979;47:343–352. doi: 10.1037/0022-006X.47.2.343. [DOI] [PubMed] [Google Scholar]
  • 96.Posner K., Brown G.K., Stanley B., Brent D.A., Yershova K.V., Oquendo M.A., et al. The columbia–suicide severity rating scale: Initial validity and internal consistency findings from three multisite studies with adolescents and adults. Aust J Pharm. 2011;168:1266–1277. doi: 10.1176/appi.ajp.2011.10111704. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97.Van Spijker B.A.J., Batterham P.J., Calear A.L., Farrer L., Christensen H., Reynolds J., et al. The suicidal ideation attributes scale (SIDAS): community-based validation study of a new scale for the measurement of suicidal ideation. Suicide Life-Threatening Behav. 2014;44:408–419. doi: 10.1111/sltb.12084. [DOI] [PubMed] [Google Scholar]
  • 98.Morin C.M. Guilford Press; 1993. Insomnia: psychological assessment and management. [Google Scholar]
  • 99.Buysse D.J., Reynolds C.F., Monk T.H., Berman S.R., Kupfer D.J. The Pittsburgh sleep quality index: a new instrument for psychiatric practice and research. Psychiatry Res. 1989;28:193–213. doi: 10.1016/0165-1781(89)90047-4. [DOI] [PubMed] [Google Scholar]
  • 100.Mournet A.M., Kleiman E.M. A systematic review and meta‐analysis on the efficacy of sleep interventions to treat suicidal ideation. J Sleep Res. 2024;33 doi: 10.1111/jsr.14133. [DOI] [PubMed] [Google Scholar]
  • 101.Taylor D.J., Pruiksma K.E. Cognitive and behavioural therapy for insomnia (CBT-I) in psychiatric populations: a systematic review. Int Rev Psychiatr. 2014;26:205–213. doi: 10.3109/09540261.2014.902808. [DOI] [PubMed] [Google Scholar]
  • 102.Hertenstein E., Trinca E., Wunderlin M., Schneider C.L., Züst M.A., Fehér K.D., et al. Cognitive behavioral therapy for insomnia in patients with mental disorders and comorbid insomnia: a systematic review and meta-analysis. Sleep Med Rev. 2022;62 doi: 10.1016/j.smrv.2022.101597. [DOI] [PubMed] [Google Scholar]
  • 103.Blanken T.F., Zweerde T., Straten A., Someren E.J.W., Borsboom D., Lancee J. Introducing network intervention analysis to investigate sequential, symptom-specific treatment effects: a demonstration in Co-Occurring insomnia and depression. Psychother Psychosom. 2019;88:52–54. doi: 10.1159/000495045. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Cunningham J.E.A., Shapiro C.M. Cognitive behavioural therapy for insomnia (CBT-I) to treat depression: a systematic review. J Psychosom Res. 2018;106:1–12. doi: 10.1016/j.jpsychores.2017.12.012. [DOI] [PubMed] [Google Scholar]
  • 104.Alimoradi Z., Jafari E., Broström A., Ohayon M.M., Lin C.Y., Griffiths M.D., et al. Effects of cognitive behavioral therapy for insomnia (CBT-I) on quality of life: a systematic review and meta-analysis. Sleep Med Rev. 2022;64 doi: 10.1016/j.smrv.2022.101646. [DOI] [PubMed] [Google Scholar]
  • 105.Kjørstad K., Sivertsen B., Vedaa Ø., Langsrud K., Vethe D., Faaland P.M., et al. The effects of digital CBT-I on work productivity and activity levels and the mediational role of insomnia symptoms: data from a randomized controlled trial with 6-month follow-up. Behav Res Ther. 2022;153 doi: 10.1016/j.brat.2022.104083. [DOI] [PubMed] [Google Scholar]
  • 106.Hughes S., Cohen D., Jaggi R. Differences in reporting serious adverse events in industry sponsored clinical trial registries and journal articles on antidepressant and antipsychotic drugs: a cross-sectional study. BMJ Open. 2014;4 doi: 10.1136/bmjopen-2014-005535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107.Miguel C., Cecconi J., Harrer M., Ballegooijen W., Bhattacharya S., Karyotaki E., et al. Assessment of suicidality in trials of psychological interventions for depression: a meta-analysis. Lancet Psychiatry. 2024;11:252–261. doi: 10.1016/S2215-0366(24)00027-0. [DOI] [PubMed] [Google Scholar]
  • 108.Sateia M.J., Buysse D.J., Krystal A.D., Neubauer D.N., Heald J.L. Clinical practice guideline for the pharmacologic treatment of chronic insomnia in adults: an American academy of sleep medicine clinical practice guideline. J Clin Sleep Med: JCSM : Off Public Am Acad Sleep Med. 2017;13:307–349. doi: 10.5664/jcsm.6470. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 109.Fitzgerald T., Vietri J. Residual effects of sleep medications are commonly reported and associated with impaired patient-reported outcomes among insomnia patients in the United States. Sleep Disorders. 2015 doi: 10.1155/2015/607148. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.Alves V.M.F.C.L., Belo F.M., de-Melo-Neto V.L., Barros V.G., et al. Evaluation of the quality of life and risk of suicide. Clinics. 2016;71:135–139. doi: 10.6061/clinics/2016(03)03. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111.Liu X., Liu Z.Z., Wang Z.Y., Yang Y., Liu B.P., Jia C.X. Daytime sleepiness predicts future suicidal behavior: a longitudinal study of adolescents. Sleep. 2019;42(10):1093–1225. doi: 10.1093/sleep/zsy225. [DOI] [PubMed] [Google Scholar]
  • 112.Albakri U., Drotos E., Meertens R. Sleep health promotion interventions and their effectiveness: an umbrella review. Int J Environ Res Publ Health. 2021;18:5533. doi: 10.3390/ijerph18115533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 113.Morgenthaler T., Kramer M., Alessi C., Friedman L., Boehlecke B., Brown T., et al. Practice parameters for the psychological and behavioral treatment of insomnia: an update. Am Acad Sleep Med Report Sleep. 2006;29:1415–1419. [PubMed] [Google Scholar]
  • 114.Talbot L.S., Maguen S., Metzler T.J., Schmitz M., McCaslin S.E., Richards A., et al. Cognitive behavioral therapy for insomnia in posttraumatic stress disorder: a randomized controlled trial. Sleep. 2014;37:327–341. doi: 10.5665/sleep.3408. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115.Walters E.M., Jenkins M.M., Nappi C.M., Clark J., Lies J., Norman S.B., et al. The impact of prolonged exposure on sleep and enhancing treatment outcomes with evidence-based sleep interventions: a pilot study. Psychological trauma : theory, research. Pract Pol. 2020;12:175–185. doi: 10.1037/tra0000478. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Kanady J.C., Talbot L.S., Maguen S., Straus L.D., Richards A., Ruoff L., et al. Cognitive behavioral therapy for insomnia reduces fear of sleep in individuals with posttraumatic stress disorder. J Clin Sleep Med : JCSM : Off Public Am Acad Sleep Med. 2018;14:1193–1203. doi: 10.5664/jcsm.7224. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 117.Walker J., Muench A., Perlis M.L., Vargas I. Cognitive behavioral therapy for insomnia (CBT-I): a primer. Clin Psychol Spec Educat. 2022;11:123–137. doi: 10.17759/cpse.2022110208. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 118.Simon L., Steinmetz L., Feige B., Benz F., Spiegelhalder K., Baumeister H. Comparative efficacy of onsite, digital, and other settings for cognitive behavioral therapy for insomnia: a systematic review and network meta-analysis. Sci Rep. 2023;13 doi: 10.1038/s41598-023-28853-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 119.Cheung J.M.Y., Bartlett D.J., Armour C.L., Laba T.L., Saini B. Patient perceptions of treatment delivery platforms for cognitive behavioral therapy for insomnia. Behav Sleep Med. 2019;17:81–97. doi: 10.1080/15402002.2017.1293539. [DOI] [PubMed] [Google Scholar]
  • 120.Zachariae R., Lyby M.S., Ritterband L.M., O'Toole M.S. Efficacy of internet-delivered cognitive-behavioral therapy for insomnia - a systematic review and meta-analysis of randomized controlled trials. Sleep Med Rev. 2016;30:1–10. doi: 10.1016/j.smrv.2015.10.004. [DOI] [PubMed] [Google Scholar]
  • 121.Geller A.I., Nopkhun W., Dows-Martinez M.N., Strasser D.C. Polypharmacy and the role of physical medicine and rehabilitation. PM & R : J Injur Funct Rehabilit. 2012;4:198–219. doi: 10.1016/j.pmrj.2012.02.012. [DOI] [PubMed] [Google Scholar]
  • 122.Kern D.M., Cepeda M.S., Wiegand F. Treatment patterns of patients diagnosed with major depressive disorder and suicidal ideation or attempt: a U.S. population-based study utilizing real-world data. BMC Psychiatry. 2021;21:608. doi: 10.1186/s12888-021-03616-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 123.Kim A.M., Salstein L., Goldberg J.F. A systematic review of complex polypharmacy in bipolar disorder: prevalence, clinical features, adherence, and preliminary recommendations for practitioners. J Clin Psychiatry. 2021;82 doi: 10.4088/JCP.20r13263. 20 13263. [DOI] [PubMed] [Google Scholar]
  • 124.Eide R.P., Stahlman S. Polypharmacy involving opioid, psychotropic, and central nervous system depressant medications, period prevalence and association with suicidal ideation, active component, U.S. armed forces, 2016. MSMR. 2018;25:2–9. [PubMed] [Google Scholar]
  • 125.Collett G.A., Song K., Jaramillo C.A., Potter J.S., Finley E.P., Pugh M.J. Prevalence of central nervous system polypharmacy and associations with overdose and suicide-related behaviors in Iraq and Afghanistan war veterans in VA care 2010-2011. Drugs - Real World Outcomes. 2016;3:45–52. doi: 10.1007/s40801-015-0055-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 126.Junqueira D.R., Zorzela L., Golder S., Loke Y., Gagnier J.J., Julious S.A., et al. CONSORT harms 2022 statement, explanation, and elaboration: updated guideline for the reporting of harms in randomised trials. 2023. [DOI] [PubMed]

References

  • 1.Favril L., Yu R., Geddes J.R., Fazel S. Individual-level risk factors for suicide mortality in the general population: an umbrella review. Lancet Public Health. 2023;8:868–877. doi: 10.1016/S2468-2667(23)00207-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Bernert R.A., Kim J.S., Iwata N.G., Perlis M.L. Sleep disturbances as an evidence-based suicide risk factor. Curr Psychiatry Rep. 2015;17:554. doi: 10.1007/s11920-015-0554-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Pigeon W.R., Pinquart M., Conner K. Meta-analysis of sleep disturbance and suicidal thoughts and behaviors. J Clin Psychiatry. 2012;73:1160–1167. doi: 10.4088/JCP.11r07586. [DOI] [PubMed] [Google Scholar]
  • 4.Meerwijk E.L., Parekh A., Oquendo M.A., Allen I.E., Franck L.S., Lee K.A. Direct versus indirect psychosocial and behavioural interventions to prevent suicide and suicide attempts: a systematic review and meta-analysis. Lancet Psychiatry. 2016;3:544–554. doi: 10.1016/S2215-0366(16)00064-X. [DOI] [PubMed] [Google Scholar]
  • 5.Van Ballegooijen W., Rawee J., Palantza C., Miguel C., Harrer M., Cristea I., et al. Suicidal ideation and suicide attempts after direct or indirect psychotherapy: a systematic review and meta-analysis. JAMA Psychiatry. 2025;82:31. doi: 10.1001/jamapsychiatry.2024.2854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Belleville G., Guay S., Marchand A. Persistence of sleep disturbances following cognitive-behavior therapy for posttraumatic stress disorder. J Psychosom Res. 2011;70:318–327. doi: 10.1016/j.jpsychores.2010.09.022. [DOI] [PubMed] [Google Scholar]
  • 7.Brower K.J., Aldrich M.S., Robinson E.A., Zucker R.A., Greden J.F. Insomnia, self-medication, and relapse to alcoholism. Am J Psychiatr. 2001;158:399–404. doi: 10.1176/appi.ajp.158.3.399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.McCrae C.S., Lichstein K.L. Secondary insomnia: diagnostic challenges and intervention opportunities. Sleep Med Rev. 2001;5:47–61. doi: 10.1053/smrv.2000.0146. [DOI] [PubMed] [Google Scholar]
  • 9.Khan H., Garg A., Yasmeen A. B.N., Yadav D.K., Ashif Khan M., et al. Zolpidem use and risk of suicide: a systematic review and meta-analysis. Psychiatry Res. 2022;316 doi: 10.1016/j.psychres.2022.114777. [DOI] [PubMed] [Google Scholar]

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