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. 2026 Jun 20;15:982. [Version 1] doi: 10.12688/f1000research.182846.1

Sex Differences in the Prevalence and Correlates of Post-Stroke Insomnia: A Population-Based Study of 7,147 Indonesian Stroke Survivors

Sri Susanty 1,2, Renny Wulan Apriliyasari 3, Hsiao-Yean Chiu 3, Rusdi Bin ABD Rashid 4, Era Catur Prasetya 5, Kanjanee Phanphairoj 1, Mokh Sujarwadi 6, Faizul Hasan 1,a
PMCID: PMC13586602  PMID: 42763448

Abstract

Objectives

Post-stroke insomnia (PSI) is a prevalent issue among those who have experienced a stroke. The impact of gender on PSI prevalence within Asian stroke groups remains ambiguous. This research seeks to examine the prevalence of PSI among stroke survivors in Indonesia.

Methods

This quantitative prevalence analysis was based on the 2018 Indonesian Basic Health Research. A total of 7,147 stroke survivors who answered the insomnia questions were included. The estimated prevalence and regression models were examined utilizing SPSS software.

Results

The total prevalence of PSI among stroke survivors in Indonesia was 28.4%. Females exhibited a greater frequency of PSI than males (31.2% versus 25.6%, respectively). When categorized by age group, both females and males exhibited a trend of rising PSI prevalence with time. Moreover, daily smoking, low educational attainment, rural residency, and insufficient physical activity were correlated with insomnia symptoms in the male cohort. In females, the presence of comorbidities such as cardiovascular disease and asthma was associated with insomnia.

Conclusions

This study’s findings revealed a significant prevalence of insomnia among stroke survivors in Indonesia. Our findings indicate a gender influence on PSI prevalence, with females exhibiting a higher prevalence than males. These findings underscore the significance of sleep assessment and treatment in clinical or community environments.

Keywords: sleep, post-stroke insomnia, stroke, insomnia, Asian.

1. Introduction

Post-stroke insomnia (PSI) is a common problem around the world. The prevalence rate ranges from 35% to 43% from the acute to the chronic phase. 1 , 2 Stroke patients with insomnia have a higher risk of developing cognitive impairment 3 and reduced health-related quality of life. 4 , 5 Researchers and clinicians are now paying high attention to managing the insomnia problem.

Previously, two studies investigating the global prevalence of PSI using a meta-analytic design have been published. 1 , 2 One meta-analysis, involving 22 studies on insomnia, found the prevalence to be 38.2%. 1 The updated meta-analysis, which included 28 studies, suggested a prevalence rate of 39.7%. 2 However, most of the included studies were derived from Western populations. Adding evidence by investigating the PSI prevalence among Eastern populations is important.

As a note, gender plays a critical role in the prevalence of insomnia. Previous meta-analyses suggest that females are more prevalent than males in terms of insomnia in the general population in China. 6 However, the effect of gender on PSI remains under research. Moreover, the available studies involved a small sample size. 1 , 2 Hence, there is a need to conduct an updated study investigating the effect of gender on PSI and using a larger sample size. This study aims to investigate the effect of gender on the prevalence of PSI among stroke survivors using multicenter nationwide data.

2. Materials and methods

2.1 Study sample

The data utilized in this study were obtained from the 2018 Basic Health Research (Riset Kesehatan Dasar, RISKESDAS) conducted by the Indonesian Ministry of Health. The RISKESDAS survey is a thorough national evaluation conducted quinquennially to collect health-related data. The National Institute of Health Research and Development (NIHRD) administers it under the Ministry of Health in Indonesia. The survey was administered by enumerators possessing formal education in health, holding at least health diplomas. The enumerators performed face-to-face interviews utilizing validated questions for accuracy and dependability. Furthermore, they performed measurements and assessments during home visits, as outlined in the supplementary document issued by the Ministry of Health in Bahasa Indonesia (Kementerian Kesehatan, 2019). Members of each household (those residing on the premises for at least six months and sharing the same food income source) were solicited to partake in the survey. Health-related data on patients diagnosed with stroke was obtained from the 2018 RISKESDAS dataset.

2.2 Inclusion and exclusion criteria

We only considered participants who satisfied the requirements listed below in order to meet the inclusion criteria: 1) having received a stroke diagnosis in the past; and 2) having submitted the necessary information for the insomnia variable. Participants whose insomnia variable had missing values were not included in the study.

2.3 Dependent variable

A question related to insomnia was examined: “In the past two weeks, have you experienced any sleep disturbances, such as difficulty initiating sleep, nocturnal awakenings, or early morning arousal?” The insomnia status was assumed if participants answered ‘yes’.

2.4 Independent variables

2.4.1 Sociodemographic variables

Sociodemographic characteristics encompassed age, gender, educational attainment, marriage status, occupation, and degree of urbanization. We classified educational attainment into three categories: ‘no formal education’ (0), ‘non-university level’ (1), and ‘university level’ (2). Marital status was classified as ‘single’ (0) or ‘married’ (1), and ‘widow or widower’ (2). Occupation status was categorized as ‘unemployed’ (0) and ‘employed’ (1), and urbanization level as ‘rural’ (0) and ‘urban’ (1).

2.4.2 Health and lifestyle behavior variables

In this research, we incorporated health conditions and lifestyle behaviors, including regular follow-up, comorbidities (such as cancer, asthma, cardiovascular disease, and chronic renal illness), vigorous and moderate physical activity, smoking status, and alcohol consumption.

The evaluation of regular follow-up for stroke was conducted using the subsequent inquiry: Has your stroke state been consistently monitored by a physician at the healthcare facility? the potential responses of “yes,” ‘sometimes,’ and ‘no.’

Comorbidities were identified based on the response (‘yes’ = 0 or ‘no’ = 1) to the question: ‘Have you received a diagnosis of (….) from a physician?’

Smoking status was assessed by the inquiries: ‘Are you a smoker?’ and ‘Have you smoked in the past month?’ Smoking status was classified as ‘non-smoker’ (code = 0), ‘occasional smoker’ (code = 1), and ‘daily smoker’ (code = 2).

Alcohol intake was evaluated by the inquiry: ‘Have you ingested alcohol in the past month?’ with response options of ‘yes’ and ‘no.’

Physical activity was evaluated utilizing the modified Global Physical Activity Questionnaire (GPAQ) from the World Health Organization for surveillance purposes. The GPAQ gathers data on physical activity in three areas: occupational or domestic activities, transportation, and leisure pursuits. All activities must have been conducted uninterrupted for a minimum of 10 minutes per week. Participants were requested to enumerate activities they typically engaged in daily, categorizing them as ‘yes’ for activities performed and ‘no’ for those not performed, for both vigorous and moderate physical activity. The assessment of GPAQ in Indonesia demonstrated satisfactory inter-rater reliability for categorical variables, with kappa values between 0.44 and 0.78, and test-retest reliability for continuous variables, with Spearman’s rho ranging from 0.45 to 0.80. 7

2.5 Ethical consideration and informed consent statement

Ethical approval for the original RISKESDAS 2018 data collection was granted by the Ethical Committee of Health Research, NIHRD, Ministry of Health, Republic of Indonesia (No. LB.02.01/2/KE.267/2017). Secondary analysis for the present study was approved by the Health Research Ethics Committee of the Faculty of Medicine, Universitas Halu Oleo (No. 62/UN29.20.2/ETIK/2025). Written informed consent was obtained from all participants in the original survey. As this study uses only de-identified secondary data, no additional consent was required.

2.6 Statistical analysis

Statistical analysis was conducted utilizing SPSS (Version 29, SPSS Inc., Chicago, IL, USA). Descriptive statistics were analyzed for demographic features and aggregated responses, encompassing the mean and standard deviation for continuous variables and percentages for categorical data. Subsequently, we performed analyses utilizing χ2 (Chi-square) for categorical variables and the Mann-Whitney U-test (given the data’s deviation from a normal distribution) for continuous variables to investigate the presence of gender disparities in sociodemographic characteristics, health conditions, and lifestyle behaviors.

Subsequently, forward and stepwise logistic regression analyses were conducted to examine the impact of sociodemographic variables, health problems, and lifestyle behaviors on stroke populations with and without insomnia, accounting for gender differences. Hosmer–Lemeshow goodness-of-fit tests were performed to evaluate the models’ alignment with the observed outcome. The alpha criterion for hypothesis testing was established at p < 0.05.

3. Results

3.1 Study characteristic

At the beginning, 713,783 individuals were screened for eligibility. Among them, 705,741 participants were excluded because they did not have a stroke diagnosis. Furthermore, 895 participants were excluded because they had missing values on the insomnia variable. The final analysis comprised 7,147 stroke participants ( Figure 1).

Figure 1. Participant flow chart.


Figure 1.

n = number of participants.

Table 1 presents a comparison of participants’ characteristics between males and females. The insomnia cohort exhibited a greater mean age than the non-insomnia cohort across both genders. Among males, educational attainment, work position, urbanization, consistent follow-up, and the presence of comorbidities such as cancer, heart disease, asthma, and participation in regular physical exercise exhibited significant differences between the insomnia and non-insomnia groups (all P < 0.05). Among females, educational attainment, marital status, and the occurrence of comorbidities such as cardiovascular disease and asthma exhibited significant differences between the insomnia and non-insomnia cohorts (all P < 0.05). Additional demographic information is available in Table 1 and Table 2.

Table 1. Demographic characteristic of participants.

Male (n = 3574) p-value Female (n = 3573) p-value
Total Insomnia Non-insomnia Insomnia Non-insomnia
Variables n (%) n (%) n (%) n (%) n (%)
7147 (100) 932 (26.1) 2642 (73.9) 1230 (34.4) 2343 (65.6)
Age, mean (SD) 58.7 (12.5) 60.3 (12.2) 59.1 (11.9) 0.01 57.37 (11.93) 55.87 (12.24) 0.01
Smoking status, n (%) 0.48 0.86
Non-smoker 4611 (64.5) 294 (31.5) 949 (35.9) 1161 (94.4) 2207 (94.2)
Yes (not every day) 760 (10.6) 179 (19.2) 475 (18) 34 (2.8) 72 (3.1)
Yes (everyday) 1776 (24.8) 459 (49.2) 1218 (46.1) 35 (2.8) 64 (2.7)
Education, n (%) <0.001 0.02
No formal education 732 (10.2) 79 (8.5) 168 (6.4) 181 (14.7) 304 (13)
Non-university level 5810 (81.3) 72 (7.7) 2145 (81.2) 995 (80.9) 1889 (80.6)
University level 605 (8.5) 781 (83.8) 329 (12.5) 54 (4.4) 150 (6.4)
Marital status, n (%) 0.47 0.02
Single 227 (3.2) 39 (4.2) 104 (3.9) 24 (2) 60 (2.6)
Married 5322 (74.5) 780 (83.7) 2254 (85.3) 756 (61.5) 1532 (65.4)
Widow/widower 1598 (22.4) 113 (12.1) 284 (10.7) 450 (36.6) 751 (32.1)
Employment, n (%) <0.001 0.12
Unemployed 3725 (52.1) 395 (42.4) 945 (35.8) 842 (68.5) 1543 (65.9)
Employed 3422 (47.9) 537 (57.6) 1697 (64.2) 388 (31.5) 800 (34.1)
Urbanization, n (%) <0.001 0.40
Urban 3798 (53.1) 457 (49) 1485 (56.2) 627 (51) 1229 (52.5)
Rural 3349 (46.9) 475 (51) 1157 (43.8) 603 (49) 1114 (47.5)

n = number of participants; SD = standard deviation.

Continuous variable was performed by using Mann Whitney U test,

Categorical variables were performed by using chi-square test.

Table 2. Health, lifestyle behavior and insomnia.

Male p-value Female p-value
Total Insomnia Non-insomnia Insomnia Non-insomnia
Variables n (%) n (%) n (%) n (%) n (%)
5366 (100) 653 (24.6) 2002 (75.4) 895 (33) 1816 (67)
Regular follow-up, n (%) 0.02 0.47
No 2821 (39.5) 228 (24.5) 534 (20.2) 268 (21.8) 470 (20.1)
Sometime 2826 (39.5) 348 (37.3) 1037 (39.3) 487 (39.6) 954 (40.7)
Yes 2821 (39.5) 356 (38.2) 1071 (40.5) 475 (38.6) 919 (39.2)
Cancer, n (%) 0.04 0.61
No 7099 (99.3) 924 (99.1) 2633 (99.7) 1218 (99) 2324 (99.2)
Yes 48 (0.7) 8 (0.9) 9 (0.3) 12 (1) 19 (0.8)
Heart disease, n (%) 0.04 <0.001
No 6447 (90.2) 827 (88.7) 2403 (91) 1070 (87) 2147 (91.6)
Yes 700 (9.8) 105 (11.3) 239 (9) 160 (13) 196 (8.4)
Asthma, n (%) 0.03 <0.001
No 6776 (94.8) 871 (93.5) 2517 (95.3) 1143 (92.9) 2245 (95.8)
Yes 371 (5.2) 61 (6.5) 125 (4.7) 87 (7.1) 98 (4.2)
CKD, n (%) 0.19 0.43
No 7010 (98.1) 909 (97.5) 2595 (98.2) 1210 (98.4) 2296 (98)
Yes 137 (1.9) 23 (2.5) 47 (1.8) 20 (1.6) 47 (2)
Vigorous PA, n (%) <0.01 0.95
No 6295 (88.1) 805 (86.4) 2177 (82.4) 1140 (92.7) 2173 (92.7)
Yes 852 (11.9) 127 (13.6) 465 (17.6) 90 (7.3) 170 (7.3)
Moderate PA, n (%) <0.001 0.13
No 3516 (49.2) 587 (63) 1384 (52.4) 553 (45) 992 (42.3)
Yes 3631 (50.8) 345 (37) 1258 (47.6) 677 (55) 1351 (57.7)
Alcohol consumption, n (%) 0.47 0.76 †
No 7014 (98.1) 897 (96.2) 2556 (96.7) 1227 (99.8) 2334 (99.6)
Yes 133 (1.9) 35 (3.8) 86 (3.3) 3 (0.2) 9 (0.4)

n = number of participants; SD = standard deviation.

Continuous variable was performed by using Mann Whitney U test,

Categorical variables were performed by using chi-square test or

†

Fisher’s exact test.

3.2 Prevalence of post-stroke insomnia

The overall prevalence of PSI among stroke survivors in Indonesia was 28.4%. Figure 2 depicts the comparative prevalence of PSI among males and females across different age groups. Our findings demonstrate that the incidence of insomnia increases with age. We grouped the age into 13 age groups, ranging from 15–19 years old to more than 75 years old. There is a trend of increasing prevalence in the male insomnia group, ranging from 25% to 32%. Similarly, we also find an increasing trend in insomnia prevalence for the female age group (26% to 37%). Overall, we found that females have a higher trend in PSI prevalence compared to males (25.6% vs 31.2%, respectively).

Figure 2. Post-stroke insomnia prevalence by gender and age group.


Figure 2.

3.3 Analysis of regression

The univariate regression analyses are displayed in Table 3 and Table 4. Multivariate regression analyses are displayed in Table 5 and Table 6. Active smoking elevates the probability of insomnia development in comparison to non-smokers among subjects. Individuals with a greater educational attainment (university level) are less prone to developing insomnia. Individuals residing in urban environments are less prone to sleeplessness than those inhabiting rural regions. Individuals who partake in physical activity are less prone to developing insomnia. Female participants with comorbidities, including heart disease and asthma, exhibited a higher propensity for developing insomnia.

Table 3. Associations between demographic characteristics and insomnia symptom using univariate logistic regression.

Variables Male Female
OR C (95% CI) P-value OR C (95% CI) P-value
Age 0.008 (1.002 to 1.015) <0.01 0.009 (1.003 to 1.014) <0.01
Smoking status
Non-smoker Ref. Ref.
Yes (not every day) 1.216 (0.98 to 1.51) 0.08 0.898 (0.593 to 1.358) 0.61
Yes (everyday) 1.216 (1.027 to 1.441) 0.02 1.040 (0.684 to 1.579) 0.86
Education
Non-university level Ref. Ref.
No formal education 1.291 (0.976 to 1.708) 0.07 1.13 (0.926 to 1.38) 0.23
University level 0.601 (0.456 to 0.848) <0.001 0.683 (0.496 to 0.942) 0.02
Marital status
Widow/widower Ref. Ref.
Single 0.942 (0.614 to 1.446) 0.79 0.668 (0.41 to 1.087) 0.07
Married 0.87 (0.689 to 1.098) 0.24 0.824 (0.712 to 0.953) <0.01
Employment
Employed Ref. Ref.
Unemployed 1.321 (1.134 to 1.538) <0.001 1.125 (0.971 to 1.304) 0.12
Urbanization
Rural Ref. Ref.
Urban 0.75 (0.645 to 0.871) <0.001 0.943 (0.821 to 1.082) 0.4

OR C = crude odds ratio of univariate model; Ref = reference.

Table 4. Association between health, lifestyle behavior and insomnia symptom using univariate logistic regression.

Variables Male Female
OR C (95% CI) P-value OR C (95% CI) P-value
Regular follow-up
No Ref. Ref.
Sometime 0.786 (0.645 to 0.957) 0.02 0.895 (0.744 to 1.078) 0.24
Yes 0.779 (0.64 to 0.947) 0.01 0.906 (0.752 to 1.092) 0.3
Cancer
No Ref. Ref.
Yes 2.533 (0.974 to 6.584) 0.06 1.205 (0.583 to 2.491) 0.62
Heart disease
No Ref. Ref.
Yes 1.277 (1.001 to 1.627) 0.04 1.638 (1.313 to 2.044) <0.001
Asthma
No Ref. Ref.
Yes 1.41 (1.028 to 1.934) 0.03 1.744 (1.295 to 2.348) <0.001
CKD
No Ref. Ref.
Yes 1.397 (0.844 to 2.314) 0.19 0.807 (0.476 to 1.369) 0.43
Vigorous PA
No Ref. Ref.
Yes 0.739 (0.597 to 0.913) <0.01 1.009 (0.774 to 1.316) 0.95
Moderate PA
No Ref. Ref.
Yes 0.647 (0.555 to 0.754) <0.001 0.899 (0.782 to 1.033) 0.13
Alcohol consumption
No Ref. Ref.
Yes 1.16 (0.777 to 1.73) 0.47 0.634 (0.171 to 2.346) 0.49

OR C = crude odds ratio of univariate model; Ref = reference.

Table 5. Associations between demographic characteristics and insomnia symptom using logistic regression.

Variables Male Female
OR A (95% CI) P-value OR A (95% CI) P-value
Age 0.002 (0.995 to 1.01) 0.55 0.006 (1 to 1.013) 0.07
Smoking status
Non-smoker Ref. Ref.
Yes (not every day) 1.231 (0.989 to 1.533) 0.06 0.981 (0.642 to 1.499) 0.93
Yes (everyday) 1.259 (0.057 to 1.5) 0.01 0.841 (0.553 to 1.279) 0.42
Education
Non-university level Ref. Ref.
No formal education 1.125 (0.843 to 1.503) 0.42 1.027 (0.833 to 1.266) 0.8
University level 0.649 (0.493 to 8.54) <0.01 0.72 (0.519 to 1) 0.05
Marital status
Widow/widower Ref. Ref.
Single 1.127 (0.706 to 1.800) 0.62 0.826 (0.495 to 1.377) 0.46
Married 0.984 (0.772 to 1.254) 0.89 0.912 (0.773 to 1.074) 0.27
Employment
Employed Ref. Ref.
Unemployed 1.094 (0.919 to 1.302) 0.31 1.037 (0.885 to 1.214) 0.65
Urbanization
Rural Ref. Ref.
Urban 0.767 (0.656 to 0.896) <0.01 0.934 (0.810 to 1.077) 0.34

OR A = adjusted odds ratio of multivariate model; Adjusted model is based on all variables in the univariate model in supplementary Table 1 and 2; Ref = reference.

Table 6. Association between health, lifestyle behavior and insomnia symptom using multivariable logistic regression.

Variables Male Female
OR A (95% CI) P-value OR A (95% CI) P-value
Regular follow-up
No Ref. Ref.
Sometime 0.816 (0.667 to 0.997) 0.04 0.906 (0.751 to 1.092) 0.29
Yes 0.833 (0.68 to 1.021) 0.07 0.916 (0.758 to 1.107) 0.36
Cancer
No Ref. Ref.
Yes 2.483 (0.935 to 6.589) 0.07 1.104 (0.53 to 2.301) 0.79
Heart disease
No Ref. Ref.
Yes 1.282 (0.997 to 1.648) 0.05 1.615 (1.287 to 2.025) <0.001
Asthma
No Ref. Ref.
Yes 1.297 (0.937 to 1.795) 0.12 1.658 (1.226 to 2.243) <0.01
CKD
No Ref. Ref.
Yes 1.375 (0.819 to 2.309) 0.23 0.724 (0.422 to 1.241) 0.24
Vigorous PA
No Ref. Ref.
Yes 0.736 (0.583 to 0.929) 0.01 1.076 (0.817 to 1.418) 0.6
Moderate PA
No Ref. Ref.
Yes 0.679 (0.577 to 0.8) <0.001 0.987 (0.847 to 1.150) 0.87
Alcohol consumption
No Ref. Ref.
Yes 1.334 (0.876 to 2.032) 0.18 0.61 (0.162 to 2.288) 0.46

OR A = adjusted odds ratio of multivariate model; Adjusted model is based on significant variables in the univariate model in Supplementary Table 1 and 2; Ref = reference.

4. Discussion

This study is the first to investigate the impact of gender on the prevalence of post-stroke irrationality (PSI) among stroke survivors in Indonesia, to the best of our knowledge. Our findings indicate that the overall prevalence of PSI remains high among the Indonesian population. It is worth noting that females have a higher prevalence of PSI than males. Our research should be considered credible due to the utilization of a substantial sample size and stringent methodology.

It is important to observe that the prevalence of insomnia following a stroke has increased over time. Females were found to have a higher increase in prevalence than males. Consistent with a previous study, increasing age was associated with the presence of insomnia. 8 Moreover, females exhibited a greater prevalence of sleep disturbances than males among American adults. 9 This indicates the necessity of improving sleep instruction uniformly across various genders.

The study reveals a prevalence of insomnia at 28.4%. This contrasts with previous meta-analyses that suggested the prevalence of PSI was between 35% and 43%. 1 , 2 The disparity in insomnia prevalence arises from the variability in assessment methodologies; research employing standardized diagnoses reveal lower prevalence rates than those utilizing self-reported instruments. 2 , 10 However, this present study has a higher estimation compared to previous work that used hospital-based data and found the PSI incidence to be 8.2% in Taiwan (using ICD codes). 3 Early detection of insomnia using precise measurement scales is critical.

Although the mechanics underlying PSI remain undetermined, the putative mechanisms can be explained in part. The stroke’s site, including the right hemisphere, thalamus, or brainstem, is associated with PSI. 11 Moreover, a confluence of environmental factors (e.g., hospitalization) 12 and biological factors (e.g., heightened sympathetic activation, intermittent hypoxemia, oxidative stress, inflammatory processes leading to frequent arousals, and disrupted sleep-wake regulation) may exacerbate post-stroke insomnia. 13

Interestingly, male participants engage in physical activity associated with fewer insomnia symptoms. A previous meta-analysis found that exercise may increase sleep quality. 14 The results are also consistent with previous research indicating that exercise improves sleep quality across all age groups. 15 , 16 Hence, we recommend regular exercise to improve sleep quality.

This study identifies a number of limitations. This dataset’s absence of objective data, such as polysomnographic information, may result in other sleep disorders being undiscovered or misinterpreted as insomnia. The failure to acquire pertinent confounders, including dietary details, environmental influences, and possible hypnotic usage, may compromise internal validity. This study possesses several strengths. The study population was selected from volunteers across Indonesia, assuring national representation. Secondly, each interviewer received training to comprehend the structure and methodology of the questionnaire.

5. Conclusions

In conclusion, the prevalence of PSI remains high over time among stroke survivors in Indonesia. Females have a higher prevalence of PSI compared to males. These preliminary findings provide crucial insights for healthcare providers and policymakers. Implementing early insomnia screening with accurate metrics is strongly advised.

Ethics statement

Ethical approval for the original RISKESDAS 2018 data collection was granted by the Ethical Committee of Health Research, NIHRD, Ministry of Health, Republic of Indonesia (No. LB.02.01/2/KE.267/2017). Secondary analysis for the present study was approved by the Health Research Ethics Committee of the Faculty of Medicine, Universitas Halu Oleo (No. 62/UN29.20.2/ETIK/2025).

Informed consent statement

Written informed consent was obtained from all participants (or their legal guardians for minors or cognitively impaired individuals) during the original RISKESDAS 2018 data collection. As the present study involves only secondary analysis of de-identified, publicly available data, no additional informed consent was required.

Funding Statement

This research was supported by the the Exchange Faculty Travel Grant Ratchadaphiseksomphot Endowment Fund for Fiscal Year 2025 (B.E. 2568) no. TG169004.

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

[version 1; peer review: 1 approved with reservations

Data availability statement

All datasets supporting this article are accessible via the following link: https://doi.org/10.5281/zenodo.20229933. 17

Data are available under the terms of the Creative Commons Attribution 4.0 International.

Extended data

Zenodo: Supplementary data: https://doi.org/10.5281/zenodo.20229933. 17

This project contains the following extended data:

  • •

    Tripod Checklist.docx.

Data are available under the terms of the Creative Commons Attribution 4.0 International.

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F1000Res. 2026 Jul 20. doi: 10.5256/f1000research.201829.r498291

Reviewer response for version 1

Citra Windani Mambang Sari 1

This study addresses an important and under-researched topic using a large national Indonesian dataset. The analysis has potential value for understanding self-reported sleep disturbance among people with a history of stroke. The large sample, inclusion of sociodemographic and health-related variables, and public availability of the underlying dataset are notable strengths.

However, several issues should be addressed in a revised version. Most importantly, the single survey question used in this study identifies self-reported sleep disturbance rather than clinically defined insomnia. The terminology in the title, abstract, Methods, Results, and Discussion should therefore be revised accordingly. The term “post-stroke” should also be interpreted cautiously because the dataset does not establish whether the sleep disturbance began after the stroke.

The authors should additionally clarify whether survey weights, clustering, and stratification were incorporated into the analyses. The inconsistencies in prevalence estimates between the Abstract and Table 1, the unexplained difference between the overall sample and the denominator in Table 2, and apparent errors in several odds ratios and confidence intervals should be resolved. The multivariable modelling strategy, variable-selection criteria, collinearity assessment, missing-data handling, and rationale for sex-stratified models should also be described more clearly.

The study has academic merit, but the conclusions should be moderated until these methodological and reporting concerns are addressed.

1. Outcome misclassification: The dependent variable is based on one question asking about “any sleep disturbances” during the previous two weeks (Page 3, Section 2.3). This does not satisfy diagnostic criteria for insomnia because duration, frequency, daytime impairment, adequate sleep opportunity, and differential diagnoses were not assessed. “Sleep disturbance” should replace “insomnia” throughout.

2. Unsupported use of “post-stroke”: Participants only reported a previous stroke and recent sleep symptoms. The dataset does not establish whether symptoms began after stroke or provide stroke date, phase, recurrence, severity, lesion location, or pre-stroke sleep status. The title, objective, and conclusions therefore imply temporality that the cross-sectional data cannot demonstrate.

3.  Survey design is not addressed: RISKESDAS is a national survey, yet Section 2.6 reports standard chi-square tests, Mann–Whitney tests, and logistic regression without survey weights, clusters, or strata. Consequently, the prevalence cannot be considered nationally representative unless design-based analyses are conducted.

4. Inconsistent prevalence estimates: The Abstract reports 31.2% in females and 25.6% in males, whereas Table 1 on Page 5 reports 34.4% and 26.1%. The overall prevalence of 28.4% is also not accompanied by a confidence interval. These discrepancies must be resolved.

5. Unexplained sample-size changes: Figure 1 reports 7,147 participants, while Table 2 begins with 5,366. Variable-specific missingness and the analytic denominator for each regression model are not reported. Complete-case selection may introduce bias.

6. Regression results contain apparent numerical errors: Tables 3 and 5 report age odds ratios of 0.008 and 0.002 despite confidence intervals around 1.00. Table 5 also reports implausible confidence intervals, including 1.259 with 0.057–1.500 and 0.649 with 0.493–8.54. These values are uninterpretable and require verification against the statistical output.

7. Model-building strategy is unclear: The manuscript does not explain stepwise entry/removal criteria, collinearity assessment, missing-data handling, interaction testing, or why demographic and health variables were analysed in separate adjusted models. Separate male and female models do not prove that associations differ by sex; formal interaction terms are required.

8. Age-trend interpretation is unsupported: Figure 2 shows unstable age-specific percentages, especially in younger groups, but provides no denominators, confidence intervals, survey-weighted estimates, or statistical trend test. Claims that prevalence increased with age should not be made from this figure alone.

Is the work clearly and accurately presented and does it cite the current literature?

Partly

If applicable, is the statistical analysis and its interpretation appropriate?

Partly

Are all the source data underlying the results available to ensure full reproducibility?

Partly

Is the study design appropriate and is the work technically sound?

Partly

Are the conclusions drawn adequately supported by the results?

Yes

Are sufficient details of methods and analysis provided to allow replication by others?

Partly

Reviewer Expertise:

community health nursing, family nursing and gerontological nursing

I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard, however I have significant reservations, as outlined above.

F1000Res. 2026 Jul 31.
faizul hasan 1

Dr Citra Windani Mambang Sari, Department of Community Health Nursing, Faculty of Nursing, Universitas Padjadjaran, Bandung, West Java, Indonesia

This study addresses an important and under-researched topic using a large national Indonesian dataset. The analysis has potential value for understanding self-reported sleep disturbance among people with a history of stroke. The large sample, inclusion of sociodemographic and health-related variables, and public availability of the underlying dataset are notable strengths. However, several issues should be addressed in a revised version. Most importantly, the single survey question used in this study identifies self-reported sleep disturbance rather than clinically defined insomnia. The terminology in the title, abstract, Methods, Results, and Discussion should therefore be revised accordingly. The term “post-stroke” should also be interpreted cautiously because the dataset does not establish whether the sleep disturbance began after the stroke. The authors should additionally clarify whether survey weights, clustering, and stratification were incorporated into the analyses. The inconsistencies in prevalence estimates between the Abstract and Table 1, the unexplained difference between the overall sample and the denominator in Table 2, and apparent errors in several odds ratios and confidence intervals should be resolved. The multivariable modelling strategy, variable-selection criteria, collinearity assessment, missing-data handling, and rationale for sex-stratified models should also be described more clearly.

Response: Thank you for your acknowledgement. An exhaustively categorized response to each comment is outlined below. Any revisions have been indicated in red in the manuscript for convenient reference. We believe that these revisions effectively address your concerns as well as to improve the manuscript's overall quality. Thank you again for your valuable comments and consideration.

The study has academic merit, but the conclusions should be moderated until these methodological and reporting concerns are addressed.

1. Outcome misclassification: The dependent variable is based on one question asking about “any sleep disturbances” during the previous two weeks (Page 3, Section 2.3). This does not satisfy diagnostic criteria for insomnia because duration, frequency, daytime impairment, adequate sleep opportunity, and differential diagnoses were not assessed. “Sleep disturbance” should replace “insomnia” throughout.

Response: We thank the reviewer for raising this crucial methodological point. We fully concur that a single-item question on sleep disturbance does not meet the diagnostic criteria for insomnia as defined by the DSM-5 or ICSD-3. The limitations of our outcome measurement are a key weakness of the study, and we have now made this clearer in the manuscript. In accordance with the reviewer's suggestion, we have revised the terminology throughout the manuscript. The terms "post-stroke insomnia" (PSI) and "insomnia" have been replaced with "sleep disturbance among stroke survivors" and "sleep disturbance(s)" where appropriate, and the title has been amended to reflect this. We have also expanded on this limitation in the Discussion section, clearly stating that our findings are based on self-reported sleep disturbance rather than a clinical insomnia diagnosis.

2. Unsupported use of “post-stroke”: Participants only reported a previous stroke and recent sleep symptoms. The dataset does not establish whether symptoms began after stroke or provide stroke date, phase, recurrence, severity, lesion location, or pre-stroke sleep status. The title, objective, and conclusions therefore imply temporality that the cross-sectional data cannot demonstrate.

Response: The reviewer has identified a significant issue with the causal inference in our study. We agree that the cross-sectional nature of the RISKESDAS data does not allow us to confirm that the sleep disturbance occurred after the stroke. We have revised the manuscript to soften this terminology. We have changed references to "post-stroke" to "sleep disturbance among stroke survivors" to reflect the data more accurately. The title has been adjusted accordingly. Furthermore, we have added a more explicit statement in the Discussion regarding the cross-sectional design and its limitations in establishing temporality and causality.

3. Survey design is not addressed: RISKESDAS is a national survey, yet Section 2.6 reports standard chi-square tests, Mann–Whitney tests, and logistic regression without survey weights, clusters, or strata. Consequently, the prevalence cannot be considered nationally representative unless design-based analyses are conducted.

Response: This is a critical point. While our study aimed to use a large population-based dataset, we acknowledge that our analysis did not incorporate the complex survey design features of the RISKESDAS, such as clustering, stratification, and sampling weights. In our initial submission, we treated the data as a simple random sample for convenience, which is a limitation. We have now revised the manuscript to explicitly acknowledge this methodological shortcoming. We have added a statement in the Statistical Analysis section clarifying that, due to technical constraints, we did not apply survey weights, and we have moved the claim of "national representativeness" to a caveated statement, noting it would require design-based analyses. This is a key limitation we now prominently discuss, and we recommend this as an important area for future research.

4. Inconsistent prevalence estimates: The Abstract reports 31.2% in females and 25.6% in males, whereas Table 1 on Page 5 reports 34.4% and 26.1%. The overall prevalence of 28.4% is also not accompanied by a confidence interval. These discrepancies must be resolved.

Response: We thank the reviewer for identifying this error. The discrepancy arose from a mistake in abstracting the data during the final manuscript preparation. Based on the SPSS output, the correct sex-specific prevalence rates are: 34.4% for females and 26.1% for males. The Abstract incorrectly reported 25.6% and 31.2%, which have now been corrected to 26.1% and 34.4%, respectively, matching Table 1. Furthermore, we have now calculated and included the 95% confidence interval for the overall prevalence of 28.4% (95% CI: 27.4%–29.4%) in both the abstract and the results section (Section 3.2).

5. Unexplained sample-size changes: Figure 1 reports 7,147 participants, while Table 2 begins with 5,366. Variable-specific missingness and the analytic denominator for each regression model are not reported. Complete-case selection may introduce bias.

Response: We appreciate the reviewer highlighting this discrepancy. We have now corrected Table 2 to reflect the full sample of 7,147 participants based on the SPSS output.

6. Regression results contain apparent numerical errors: Tables 3 and 5 report age odds ratios of 0.008 and 0.002 despite confidence intervals around 1.00. Table 5 also reports implausible confidence intervals, including 1.259 with 0.057–1.500 and 0.649 with 0.493–8.54. These values are uninterpretable and require verification against the statistical output.

Response: The reviewer is entirely correct. These values are typographical errors and are not interpretable. The age odds ratios in Tables 3 and 5 should have been presented as 1.008 and 1.006, respectively. The CI for the age variable in Table 5 should read 1.000 to 1.013. We have also corrected the other errors: the CI for Education (University level) in Table 5 should be (0.493 to 0.854), not (0.493 to 8.54). We have meticulously verified all other odds ratios and confidence intervals in Tables 3-6 against the original SPSS output and have corrected all errors in the revised manuscript.

7. Model-building strategy is unclear: The manuscript does not explain stepwise entry/removal criteria, collinearity assessment, missing-data handling, interaction testing, or why demographic and health variables were analysed in separate adjusted models. Separate male and female models do not prove that associations differ by sex; formal interaction terms are required.

Response: We appreciate the reviewer's request for more detail on our methodological procedures. We have substantially expanded the Statistical Analysis section to provide a clear, step-by-step description of our modeling strategy. This now includes:

  • Criteria for variable entry and removal (we used a forward stepwise method with entry and removal p-values set at 0.05 and 0.10, respectively).

  • A statement that we assessed collinearity using variance inflation factors (VIFs).

  • Clarification that our primary interest was to identify correlates of sleep disturbance separately in males and females due to known biological and social differences, which is why we ran sex-stratified models. We have also added an interaction analysis (sex * independent variable) and reported the results, which provides a formal test for sex differences.

  • An explanation that demographic and health/lifestyle variables were kept in separate adjusted models (Tables 5 & 6) for the sake of parsimony and to avoid over-adjustment and multi-collinearity, as much health/lifestyle variables are strongly correlated with demographics.

8. Age-trend interpretation is unsupported: Figure 2 shows unstable age-specific percentages, especially in younger groups, but provides no denominators, confidence intervals, survey-weighted estimates, or statistical trend test. Claims that prevalence increased with age should not be made from this figure alone.

Response: The reviewer's point is well-taken. The age-specific percentages in Figure 2, especially for groups with a small number of participants, can be unstable. We have revised the Results section to temper our claims about an age-related trend. We now state that there "appears to be a general pattern of increasing prevalence with age," but we also note that this is not a statistically confirmed trend based on this figure alone. We have now performed a formal Cochran-Armitage test for trend, which showed a significant trend (p<0.01), and this has been added to the Results section. We have also included the denominators and 95% CIs for each age group in the figure caption and a supplementary table to provide more context and transparency.

Is the work clearly and accurately presented, and does it cite the current literature?

Partly

Is the study design appropriate and is the work technically sound?

Partly

Are sufficient details of methods and analysis provided to allow replication by others?

Partly

If applicable, is the statistical analysis and its interpretation appropriate?

Partly

Are all the source data underlying the results available to ensure full reproducibility?

Partly

Are the conclusions drawn adequately supported by the results?

Yes

Response: Thank you for your acknowledgment. We are confident that these revisions have significantly strengthened the manuscript by addressing the key methodological and reporting concerns raised. We are grateful for the reviewer's expert guidance.

F1000Res. 2026 Jul 14. doi: 10.5256/f1000research.201829.r496002

Reviewer response for version 1

Melanie Fleming 1

This study sought to examine post-stroke insomnia in a large existing sample of data from Indonesia. This is an interesting use of the dataset and a worthwhile question. However, in its current form the paper is very brief and could do with some clarity regarding the assessment of insomnia, the analyses and the description of the findings.

Main comments

 

  • The introduction is very brief and could do with more depth of what is known and the possible reasons why you might anticipate findings from Western populations to be different, thus making clearer the impact that this paper brings. Similarly, there could do with more explanation as to the rationale for the interest in effects of gender/sex - given there are lots of factors influencing insomnia it is not currently clear why this factor is of particular interest

  • My main concern is the use of the term ‘insomnia’ throughout. The presence of “any sleep disturbance” does not feel sufficient to give someone the status of having insomnia. I suggest reframing the paper to instead be aiming to understand self-reported sleep disturbance, rather than insomnia

  • The regression analyses could do with more clarity in my opinion. There are results presented in tables which don’t seem to be described in the methods section (e.g. the purpose of the univariate regression and whether/how this informed the subsequent stepwise model). Similarly, it is not clear where the analyses of different age groups presented in the results has come from, was this planned or was it a way of exploring a finding from the regression? For the stepwise model what were the criteria for retaining or excluding a variable, did you check for collinearity, how did you “account for gender differences” (e.g. did you run one analysis for males and another for females, or did you check whether gender/sex improved the model fit). From tables 5 and 6 it seems you kept demographic variables separate from health/lifestyle variables, but it's not clear why.

  • The presentation of results is quite hard to follow in my opinion. There is a lot of reliance on tables, and minimal explanation of the findings in the text. The results text also seems to be missing statistics, so it is not clear to me whether you are discussing statistically significant effects or not (e.g. the “higher trend in PSI prevalence for females – is this based on a statistical comparison?). 

  • I was able to follow the link to the source data but there didn’t seem to be a README file that I could find easily, and so I’m not sure what the columns are referring to.

Is the work clearly and accurately presented and does it cite the current literature?

No

If applicable, is the statistical analysis and its interpretation appropriate?

No

Are all the source data underlying the results available to ensure full reproducibility?

Partly

Is the study design appropriate and is the work technically sound?

Partly

Are the conclusions drawn adequately supported by the results?

No

Are sufficient details of methods and analysis provided to allow replication by others?

No

Reviewer Expertise:

Sleep, Stroke Recovery

I confirm that I have read this submission and believe that I have an appropriate level of expertise to state that I do not consider it to be of an acceptable scientific standard, for reasons outlined above.

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Data Availability Statement

    All datasets supporting this article are accessible via the following link: https://doi.org/10.5281/zenodo.20229933. 17

    Data are available under the terms of the Creative Commons Attribution 4.0 International.

    Extended data

    Zenodo: Supplementary data: https://doi.org/10.5281/zenodo.20229933. 17

    This project contains the following extended data:

    • •

      Tripod Checklist.docx.

    Data are available under the terms of the Creative Commons Attribution 4.0 International.


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