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. 2025 May 4;15:15613. doi: 10.1038/s41598-025-00288-9

Pregnant women’s sleep quality and its associated factors among antenatal care attendants in Bahir Dar City, Northwest Ethiopia

Samuel Awlachew 1, Assefa Desalew 2,3, Usmael Jibro 2,, Abera Kenay Tura 2,4
PMCID: PMC12050329  PMID: 40320398

Abstract

Good sleep quality is crucial for health and body equilibrium, particularly during pregnancy, where changes in sleep are influenced by mechanical and hormonal factors. Poor sleep can hinder daily activities and lead to adverse pregnancy outcomes. Data on sleep quality are scarce in low and middle-income countries such as Ethiopia. Hence, this study aimed to determine the magnitude of sleep quality and its associated factors among pregnant mothers in Bahir Dar City, northwest Ethiopia. A facility-based cross-sectional study was conducted with 367 randomly selected pregnant women. All pregnant women who attended public health facilities in Bahir Dar City from November 1st to December 30, 2022 were included except who were critically ill and aged less than 18 years. The data were collected through face-to-face interviews. Sleep quality was assessed by using the Pittsburgh Sleep Quality Index (PSQI). Stata v14 was used for data analysis. A binary logistic regression model was used to identify factors associated with poor sleep quality. Statistical significance was set at p < 0.05. The prevalence of poor sleep quality was 55.04%. In the multivariable analysis, older maternal age (AOR = 3.62), third trimester (AOR = 2.83), multigravidas (AOR = 2.55), low hemoglobin (AOR = 1.92), and coffee consumption (AOR = 2.19) were associated with poor sleep quality. More than half of pregnant women had poor sleep quality. Women aged ≥ 30 years, 3rd trimester, multigravidas, anemic women, and coffee consumption during pregnancy were factors associated with poor sleep quality. The concerned body should pay attention to improving Hgb level and iron/folate supplementation and reduce coffee intake in pregnant women to improve maternal sleep quality during pregnancy.

Keywords: Sleep quality, Pregnant women, Bahir Dar, Ethiopia

Subject terms: Public health, Quality of life, Risk factors

Introduction

Sleep quality is essential for normal growth and development of both the mind and body1. During pregnancy, adequate sleep is required for normal fetal growth and development2. Obtaining appropriate sleep provides the mother with the energy required for delivery. Poor sleep quality is associated with adverse outcomes during and after pregnancy and fetal well-being3. It also reduces quality of life and results in premature death48.

Sleep is a basic requirement comprising the psychological, physiological, and social dimensions; thus, it affects health and health-related quality of life9. Pregnant mothers are at greater risk of developing sleep disturbance than the general population because pregnancy creates significant anatomical, physiological, biochemical, and hormonal changes in a woman’s life10,11;1214;15;4,16. There is also a marked increase in estrogen and progesterone levels during pregnancy16;17. In contrast, progesterone increases non-REM sleep and enhances the sensitivity of the respiratory center to carbon dioxide, which may protect against upper airway occlusion18. Oxytocin, the hormone responsible for uterine contractions, peaks at night, possibly causing sleep fragmentation during late pregnancy19.

Previous studies indicated that more than two-thirds of women experience changes in sleep during pregnancy20. Global prevalence of poor sleep quality in pregnant women ranges from 15 to 96%21,22;16;23;24;25. Evidence suggests that sleep disorders may be associated with complications of pregnancy, such as gestational diabetes, gestational hypertension, preeclampsia, fetal growth disorders, preterm birth, and stillbirth8,26. Poor sleep quality during early pregnancy increases the risk of premature rupture of membranes by 12%27.

Improving sleep quality is essential, and it requires attention from pregnant women, healthcare providers, and their support systems2729. Strategies that can help enhance sleep quality include maintaining good sleep hygiene, practicing relaxation techniques before bedtime, creating a comfortable sleep environment, and seeking medical advice for any sleep disturbances3032. These measures can mitigate the negative effects of poor sleep during pregnancy.

Despite the significant burden and complications of poor sleep quality among pregnant women, it remains unrecognized and undermined by healthcare workers in Ethiopia. Understanding the factors contributing to poor sleep quality, such as stress, depression, and sleep hygiene, helps healthcare providers in screening and early detection, allowing them to create personalized care plans. Data on poor sleep quality and its associated factors among pregnant women in low and middle-income countries, including Ethiopia, are scarce. Therefore, this study aimed to determine the magnitude of poor sleep quality and its associated factors among pregnant mothers in Bahir Dar, northwest Ethiopia.

Methods and materials

Study setting and population

A facility-based cross-sectional study was conducted in public health facilities in Bahir Dar City, northwest Ethiopia. Bahir Dar city is the capital of the Amhara National Regional State and is one of the metropolitan cities in the region with an estimated 406,434 total population (DHS, 2010). It is located 565 km northwest of Addis Ababa, Ethiopia. The city has three public hospitals (Tibebe Ghion Comprehensive Specialized Hospital (TGCSH), Felege Hiwot Comprehensive Specialized Hospital (FHCSH), and Addis Alem Primary Hospital) and ten health centers. These facilities serve an estimated eight million people. The study was conducted from November 1st to December 30, 2022. All pregnant women who attended public health facilities in Bahir Dar City during the study period were included. Pregnant women who were critically ill and aged less than 18 years were excluded from the study.

Sample size and sampling technique

The sample was calculated using a single population proportion formula with the following assumptions: the proportion of poor sleep quality was 68.4% in a study in Northern Ethiopia33, a 95% confidence level, and a margin of error of 5%. Finally, we added a 10% non-response rate, and the final sample size was 367.

Of a total of thirteen public health facilities in Bahir Dar city (three hospitals and ten health centers), two hospitals, namely TGCSH and Addis Alem Primary Hospital, and four health centers, namely Bahir Dar, Han, Abay, and Shimbet health center were selected using a simple random sampling technique. The required sample size (n = 367) was allocated based on the previous month’s flow rate of pregnant women for ANC utilization in health institutions. Additionally, a simple random sampling technique was employed to select study participants.

Data collection methods

A structured interview-administered questionnaire was administered. The Questionnaire contained socio-demographic characteristics, the Pittsburgh sleeping quality index (PSQI) to assess sleep quality34, obstetrical and medical, and psychosocial factors. The PSQI is a 19-item self-report measure of sleep quality. The PSQI has seven subscale scores that measure subjective quality, latency, duration, habitual sleep efficiency (HSE), disturbance, medication use, and daytime dysfunction as they relate to sleep. These subscales were added to determine the global sleep quality score (GSQ). The GSQ score ranges from 0 to 21, with higher scores (PSQI >5) indicating poor sleep quality34. Substance use information of pregnant women, such as history of alcohol consumption, chat chewing, and cigarette smoking was collected one month before the study. Data were collected by three trained BSc midwives through interviews with women in a private room at discharge after receiving their health care. Additional obstetric and medical-related data were retrieved from the patients’ medical records.

Measurements

Good sleep quality: is a state of having a PSQI score ≤516. Poor sleep quality: is defined as a PSQI score > 534. Substance use: Intentional ingestion of one or more psycho-stimulant drugs (alcohol, khat, or cigarette smoking)35.

Data quality control

A validated structured questionnaire was used to measure the sleep quality. Training for data collectors was given for two days. The entire questionnaire, including the PSQI, was translated and adapted to the Amharic language. It was then retranslated back into English to ensure consistency and accuracy of the translation. The questionnaire was pre-tested on 5% of the sample at Felege Hiwot Comprehensive Specialized Hospital (FHCSH), with adjustments made based on the results. Its validity and reliability were then examined, with a Cronbach’s alpha of 0.82 indicating good internal consistency. The supervisors checked the data daily for accuracy, consistency, and completeness.

Data processing and analysis

The collected data were checked for completeness, coded, entered into EpiData 4.6, and exported to STATA v14 for analysis. Factors associated with sleep quality were identified using a binary logistic regression analysis. All variables with p < 0.25 in the binary analysis were entered into the multiple logistic regression after checking for multicollinearity. Association was described using an adjusted odds ratio (AOR) along with its 95% Confidence Interval (CI). Finally, a p-value < 0.05 was used to declare a significant association.

Results

Socio-demographic characteristics

A total of 347 pregnant women were included in this study, with a response rate of 94.6%. The mean (± SD) age of pregnant women was 25.8 ± (3.93) years, with age ranges from 18 to 42 years. Regarding marital status and religion of participants, the majority were married and Orthodox, 330 (95.10%) and 271 (78.10%) respectively. Two hundred forty (69.16%) pregnant women attended high school education. One hundred forty-five (41.79%) of the participants’ husbands were government employees, and 219 (63.11%) of them had a diploma and higher educational status. Regarding the place of residence, 88.76% of pregnant mothers lived in rural areas (Table 1).

Table 1.

Socio-demographic characteristics of pregnant women attending antenatal care services in Bahir Dar City (n = 347).

Variables Frequency Percent (%)
Age (in years)
 18–24 112 32.28
 25–29 159 45.82
 Inline graphic 30 76 21.90
Religion
 Orthodox 271 78.10
 Muslim 56 16.14
 Protestant 18 5.19
 Catholic 2 0.58
Marital status
 Single 8 2.31
 Married 330 95.10
 Divorced 5 1.44
 Widowed 4 1.15
Educational status (women)
 Unable to read and write 33 9.51
 Primary 74 21.33
 High school 99 28.53
 Diploma and above 141 40.63
Educational status (Partner)
 Unable to read and write 13 3.75
 Primary 34 9.80
 High school 81 23.34
 Diploma and above 219 63.11
Occupational status (women)
 Gov’t employee 85 24.50
 Private 57 16.43
 Merchant 23 6.63
 Farmer 13 3.75
 Housewife 161 46.40
 Others 8 2.31
Occupational status (partner)
 Gov’t employee 145 41.79
 Private 64 18.44
 Merchant 78 22.48
 Farmer 25 7.20
 Daily laborer 22 6.34
 Others 13 3.75
Mean monthly income (ETB)*
 < 3,073 81 23.34
 Inline graphic 3,073 266 76.66
Residency
 Urban 308 88.76
 Rural 39 11.24

*1USD ~ 54.90ETB

Pregnancy and comorbidities related characteristics

One hundred sixty-two (46.69%) pregnant mothers were in their 2nd trimester of pregnancy. More than three-quarters were multigravidas (77.81%) and (76.08%) were multiparas. Three hundred six (88.18%) pregnancies were planned. Fifty-seven (16.43%) of pregnant women had a history of pregnancy-related complications of any other type, and almost half (49.12%) of them had preeclampsia/eclampsia. Thirty (8.65%), 13 (3.75%), and 12 (3.46%) pregnant women had comorbidities such as hypertension, diabetes mellitus, and HIV/AIDS, respectively. Seventy-eight 22.48% of pregnant women were anemic. More than half (58.2%) of the participants did not initiate pre-conception folate supplementation. Regarding pre-pregnancy Body Mass Index, two hundred ninety (83.57%) pregnant women were in the normal BMI category (Table 2).

Table 2.

Pregnancy-related characteristics of women attending antenatal care services in Bahir Dar City (n = 347).

Variables Frequency Percent (%)
Pregnancy term
 1st trimester 41 11.82
 2nd trimester 162 46.69
 3rd trimester 144 41.50
Gravidity
 Primigravida 77 22.19
 Multigravida 270 77.81
Parity
 Nullipara 83 23.92
 Multipara 264 76.08
Current pregnancy status
 Planned 306 88.18
 Unplanned 41 11.82
Previous history of complicated pregnancy
 Yes 57 16.43
 No 290 83.57
Previous pregnancy complication type
 Antepartum/postpartum hemorrhage 12 21.05
 Preeclampsia/eclampsia 28 49.12
 Premature membrane rupture 10 17.54
 Obstructed labor 7 12.28
Hypertension history
 Yes 30 8.65
 No 317 91.35
Presence of HIV/AIDS
 Yes 12 3.46
 No 335 96.54
Diabetes history
 Yes 13 3.75
 No 334 96.25
Hemoglobin level
 < 12 mg/dl 76 21.90
 Inline graphic 12 mg/dl 271 78.10
Pre-pregnancy BMI (kg/m2)
 < 18.5 14 4.03
 18.5–24.9 290 83.57
 25-29.9 28 8.07
 > 30 15 4.32
Iron and folate supplementation
 Yes 202 58.21
 No 145 41.79

Substance use-related factors

The majority of pregnant women did not ever khat use, 339 (97.69%). Ninety-seven (27.95%) of pregnant women had a history of alcohol use; of which, 15 (15.46%) of them stated alcohol use in the past month. Regarding coffee consumption, from a total of 190 (54.76%) pregnant women who drank coffee, 153 (80.53%) of them had a once-daily coffee intake (Table 3).

Table 3.

Substance use and related characteristics of women attending antenatal care services in Bahir Dar City (n = 347).

Variables Frequency Percent (%)
Khat use Ever khat use
Yes 7 2.02
No 340 97.98
How long have you chewed khat? (year)
< 1 2 28.57
1–5 4 57.14
6–10 1 14.29
How often do you chew khat?
Daily 2 28.57
Weekly 5 71.43
The amount you chew khat per day (gram)
25–50 5 71.43
51–100 2 28.57
Alcohol use Ever alcohol use
Yes 97 27.95
No 250 72.05
Type of alcohol you drink
Local drinks* 55 56.70
Beer 42 43.30
How long have you been drinking?
< 6 months 13 13.40
6–11 months 19 19.59
1–2 years 24 24.74
> 2 years 41 42.27
Current alcohol use (in the last 30 days)
Yes 15 15.46
No 82 84.54
How many liters did you drink per week?
Inline graphic 1 lt. 20 20.62
> 1 - <5 lt. 36 37.11
Inline graphic 5 lt. 41 42.27
Tobacco use Ever smoking history
Yes 0 0.00
No 347 100.00
Does your partner smoke?
Yes 14 4.03
No 333 95.97
Did you/your partner smoke in the last 30 days?
Yes 0 0.00
No 14 100.00
Caffeine use Do you drink coffee currently?
Yes 191 54.04
No 156 44.96
How frequently did you drink per day?
Once daily 153 80.53
Twice daily 30 15.79
Thrice a day 7 3.68

*Tella, Tej, and local areke.

The magnitude of poor sleep quality

The overall magnitude of poor sleep quality among pregnant women was 55.04% (95% CI 49.78–60.30%). Among the total respondents, 83 (23.92%) rated their overall sleep quality as very poor. More than two-thirds (69.16%) of the pregnant women had a minimum of 6 h of sleep duration per night. Almost all 337 (97.12%) pregnant women had never used sleeping medication for their sleep disturbance, and approximately a quarter (25.65%%) of pregnant women had more than 85% sleep efficiency (Table 4).

Table 4.

Sleep quality and its seven components score characteristics of women attending antenatal care services in Bahir Dar City (n = 347).

Variables Frequency Percent (%)
Subjective sleep quality
 Very good 124 35.73
 Fairly good 140 40.35
 Fairly bad 59 17.00
 Very bad 24 6.92
Sleep latency
 0 72 20.75
 1–2 145 41.79
 3–4 87 25.07
 5–6 43 12.39
Sleep duration in hours
 > 7 118 34.01
 6–7 122 35.16
 5–6 71 20.46
 < 5 36 10.37
Habitual sleep efficiency
 ≥ 85% 89 25.65
 75–84% 159 45.82
 65–74% 69 19.88
 < 65% 30 8.65
Sleep disturbance
 0 40 11.53
 1–9 237 68.30
 10–18 49 14.12
 19–27 21 6.05
Use of sleep medication
 Never 337 97.12
 < Once a week 8 2.31
 Once/twice a week 2 0.58
 ≥ 3 times a week 0 0.00
Daytime dysfunction over the last month
 0 113 32.56
 1–2 179 51.59
 3–4 42 12.10
 5–6 13 3.75
Overall Sleep Quality
 Good sleep quality 156 44.96
 Poor sleep quality 191 55.04

Factors associated with poor sleep quality

In the multivariable analysis, older maternal age (≥ 30 years), being in 3rd trimester of pregnancy, multigravidas, low hemoglobin, and coffee consumption during pregnancy were statistically associated with poor sleep quality.

The odds of having poor sleep quality among older pregnant women aged (≥ 30 years) were 3.62 times (AOR = 3.62, 95% CI (1.83–7.18) higher as compared with their counterparts. As the gestational age progressed, the odds of having poor sleep quality increased, as being in 3rd trimester of pregnancy was 2.83 times (AOR = 2.83, 95% CI 1.31–6.16) more likely to have poor sleep quality as compared to those in 1st trimester of pregnancy.

Moreover, the odds of having poor sleep quality among multigravida pregnant women were 2.55 times (AOR = 2.55, 95% CI 1.44–4.53) higher as compared with primigravida pregnant women. Pregnant women who had low Hgb levels (< 12 mg/dl) were 1.92 times (AOR = 1.92, 95% CI 1.07–3.44) more likely to suffer from poor sleep quality compared with those with normal Hgb levels. Furthermore, pregnant women who drank coffee were two times (AOR = 2.19, 95% CI 1.37–3.50) more likely to have poor sleep quality as compared to the non-coffee consumers (Table 5).

Table 5.

Factors associated with poor sleep quality among pregnant women attending antenatal care services in Bahir Dar City (n = 347).

Variables Category Sleep Quality COR, (95% CI) AOR, (95% CI)
Good Poor
Age 18–24 year 63 49 1 1
25–29 year 74 85 1.47 (0.91, 2.40) 1.51 (0.89, 2.57)
≥ 30 years 19 57 3.88 (2.03, 7.31) 3.62 (1.83, 7.18) *
Gestational age 1st trimester 24 17 1 1
2nd trimester 81 81 1.41 (0.70, 2.82) 1.61 (0.76, 3.44)
3rd trimester 51 93 2.57 (1.27, 5.23) 2.83 (1.31, 6.16) *
Gravidity Primigravida 50 27 1 1
Multigravida 106 164 2.87 (1.69, 4.86) 2.55 (1.44, 4.53) *
Hemoglobin level < 12 mg/dl 24 52 2.06 (1.20, 3.53) 1.92 (1.07, 3.44) *
≥ 12 mg/dl 132 139 1 1
Coffee use Yes 67 124 2.46 (1.59, 3.80) 2.19 (1.37, 3.50) *
No 89 67 1 1

*p < 0.05, Hosmer-lemshow test = 0.8197.

Discussion

Sleep is essential for fetal growth and development and is vital for ensuring a positive pregnancy experience36. Poor sleep quality during pregnancy can have various negative effects on both the mother and the fetus. It can increase the risk of complications such as gestational diabetes, preeclampsia, preterm birth, low birth weight, and a higher likelihood of requiring a cesarean delivery28,37,38. This study aimed to assess the magnitude of poor sleep quality and its associated factors among pregnant women in Bahir Dar, northwest Ethiopia. The present study found the magnitude of poor sleep quality was 55.04% (95% CI 49.78–60.30) among pregnant women. We found that older maternal age (≥ 30 years), being in 3rd trimester of pregnancy, multigravidas, low hemoglobin levels, and coffee consumption during pregnancy were statistically associated with poor sleep quality. The present findings on the magnitude of poor sleep quality are similar to studies in different countries such as China (51.9%)39, Pakistan (53.3%)23, Peru (52%)40, Ethiopia, Nekemte (59.1%)41, and Mettu (57.0%)42.

This finding is lower than studies conducted in the USA (88%)43, India (72.9%)44, Turkey (88%)45, and Debre Birhan Ethiopia (62.8%)46. The discrepancy might be related to the variation in the population for example in the Indian findings conducted among 3rd trimester pregnant women. In Turkey’s study, the timing was during the COVID-19 pandemic, and data were collected through a self-administered online form, which could have influenced the outcome. This might also be explained by the significant number of older (≥ 46 years) pregnant women in Debre Birhan’s study.

However, the present findings were higher than those reported in Northwest Ethiopia (39.4%)47, 42.2%48 Iran (14.6%)49. USA 39.0%50, Peru (17%)51, Bangladesh, 38.9%52, and Vietnam, 4.02%53. A possible explanation for this finding may be the variation in the use of different sleep quality assessment tools. Moreover, a study conducted in the USA focused solely on women in early pregnancy (6–20 weeks), while a study from Bangladesh exclusively included healthy pregnant women.

According to this study, older pregnant women are almost four times more susceptible to poor sleep quality during pregnancy than are younger women. This finding is supported by other studies carried out in different countries such as Ethiopia33,35,46, Iran54, Turkey55, China56, and the USA50.

The above correlation could be explained by the fact that as people get older, problems associated with sleep quality are likely to become more severe57, and women who are advanced in age typically have more responsibilities when it comes to household chores and taking care of others, which may cause them to feel physical discomfort26. This may also be due to pre-existing health conditions that may be more common among older pregnant women, and a correlation between sleep patterns and the usual transformations that occur in adolescence and old age58.

The study finding revealed that there is a significant association between gestational age and sleep quality. This means that as pregnancy progresses, sleep quality tends to worsen. Therefore, women in the third trimester of pregnancy have a higher chance of experiencing poor sleep quality, which is nearly three times higher than women in the first trimester. This is in line with studies conducted in China39, Ethiopia33,46, and Turkey6,9. This is because as pregnancy progresses, women might find it more challenging to sleep due to physical discomfort, hormonal fluctuations, and anxiety about the upcoming birth. In addition, conditions such as restless leg syndrome and sleep apnea are more common in the later stages of pregnancy and can also contribute to poor sleep quality10. In addition, there is an increase in the proportion of changes seen in sleep patterns, ranging from 13 to 80% during the first trimester to 66–97% in the third trimester59.

Moreover, the present study found a strong relationship between the number of times a woman became pregnant and sleep quality. This implies that women who have experienced pregnancies were 2.55 times more prone to have poor sleep quality than their counterparts. This is supported by studies conducted in Ethiopia35,46 and South Korea60. A potential reason could be that women who expect a second child are relatively advanced in age and confront various kinds of stress from their familial, professional, or even societal relations. As a result, they are more prone to experiencing unwanted psychological feelings such as pessimism, unease, and gloominess and subsequently encounter sleep disturbances40,61,62.

Furthermore, low hemoglobin level was identified as a factor associated with poor sleep quality. The study found that poor sleep quality was 1.92 times more common in pregnant women with low hemoglobin levels than in women with normal hemoglobin levels. This is consistent with research conducted in India44 and Turkey, which revealed that there is a statistically significant increase in the number of people who suffered from iron deficiency anemia and reported poor sleep quality63. Iron deficiency can lead to alterations in the metabolism of neurotransmitters, which may have negative effects on psychological well-being and disrupt sleep by triggering restless legs syndrome (RLS)64. Evidence supports the multifaceted impact of iron on dopamine function in the brain. Dopamine-mediated modulation of the nervous system plays a significant role in regulating sleep patterns, including the quality, amount, and timing of rapid eye movement (REM) sleep6567.

In addition, coffee/caffeinated substances during pregnancy negatively affect sleep quality, with a two-fold higher risk of poor sleep quality than those who don’t consume coffee. Similar finding was observed in studies conducted in Gondar48, and Turkey68. This may be related to the fact that drinking coffee can impact sleep quality as it contains caffeine. Caffeine is known for its potent effect on adenosine receptors, which are responsible for regulating sleep, cognitive function, and brain arousal. Therefore, coffee consumption can reduce the overall quality and duration of sleep6971.

Evidence showed that improving pregnant women’s sleeping quality associated with decreased complications of pregnancy, such as gestational diabetes, gestational hypertension, preeclampsia, fetal growth disorders, preterm birth, and stillbirth8,26. Therefore, police maker should have to develop a guideline and protocols for healthcare providers to assess pregnant women’s sleeping quality as part of routine antenatal care. Future longitudinal studies should explore effectives of interventions to improve sleeping quality during pregnancy and its prevention of maternal and neonatal complications.

Limitations

This cross-sectional study didn’t establish a cause-and-effect relationship between sleep quality and potential risk factors. This was a subjective assessment of sleep quality, and some of the information required participants to recall, which could lead to recall bias. Another limitation of the study was that birth outcomes were not assessed, which could enable a better understanding of the effects of poor sleep quality on pregnancy.

Conclusion

In conclusion, the magnitude of poor sleep quality among pregnant women is relatively high. Women aged ≥ 30 years, 3rd-trimester pregnancy, multigravidas, low hemoglobin, and coffee consumption during pregnancy were associated with poor sleep quality among pregnant women. Prompt detection and screening of sleep problems are essential to improve maternal sleep quality and health status. Moreover, we recommend providing special concern for those pregnant women with 3rd-trimester pregnancy, higher coffee consumption to be screened for sleep problems as early as possible, and pregnant women must give attention to iron/folate supplementation and hemoglobin.

Acknowledgements

We thank Haramaya University for its nonfinancial and unreserved technical support. We would also like to extend our gratitude to hospital staff, data collectors, and supervisors for their collaboration in conducting the study.

Glossary

Abbreviations

ANC

Antenatal Care

BMI

Body Mass Index

CI

Confidence Interval

EDS

Excessive Daytime Sleepiness

GSQ

Global Sleep Quality Score

Hgb

Hemoglobin

HSE

Habitual Sleep Efficiency

NREM

Non-Rapid Eye Movement

OSA

Obstructive Sleep Apnea

PSQI

Pittsburgh Sleep Quality Index

REM

Rapid Eye Movement

RLS

Restless Legs Syndrome

SD

Standard Deviation

SPSS

Statistical Package for Social Sciences

TGCSH

Tibebe Ghion Comprehensive Specialized Hospital

Author contributions

SA, AD, and AKT designed the study. SA led the data collection and analysis under the supervision of AD and AKT. UJ and AD drafted the manuscript under the supervision of AKT. SA, AD, UJ, and AKT reviewed the manuscript for intellectual content. All authors read and approved the final version of the manuscript.

Funding

No specific funding was received for this study.

Data availability

All data of this study is available from the corresponding author upon reasonable request.

Declarations

Competing interests

The authors declare no competing interests.

Ethics approval and consent to participate

This study was conducted in accordance with the declaration of Helsinki. The study was ethically cleared and approved by the Ethical Review Committee of the Haramaya University College of Health and Medical Science (Ref. No: IHRERC/198/2022). Following approval, an official written letter of cooperation was given to the administrative health bureau and facilities. Written informed consent was obtained from each pregnant woman. Confidentiality was ensured throughout the process.

Footnotes

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Associated Data

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

Data Availability Statement

All data of this study is available from the corresponding author upon reasonable request.


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