Skip to content

Sleep Quality in Pregnancy and Its Impact on Pregnancy Outcomes

Sleep Quality in Pregnancy and Its Impact on Pregnancy Outcomes

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02016638
Enrollment
200
Registered
2013-12-20
Start date
2013-03-31
Completion date
2014-05-31
Last updated
2013-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High-Risk Pregnancy, Infant, Very Low Birth Weight, Obstructive Sleep Apnea, Pregnancy Induced Hypertension, Restless Leg Syndrome

Keywords

Obstructive Sleep Apnea in pregnancy, Pregnancy induced hypertension, Restless leg syndrome, Sleep

Brief summary

Hypothesis:Sleep Disorders are very common during pregnancy but the their exact role in causation of pregnancy related disorders is yet to be determined. OSA can complicate pregnancy given the risk factors of weight gain, upper displacement of the diaphragm, and hormonal-induced hyperaemia of the nasopharyngeal passages. SDB confers the risk of hypertensive disorders of pregnancy and is associated with adverse maternal and foetal outcomes. The study would involve pregnant females which would be prospectively followed in pregnancy and post partum to know the prevalence of sleep disorders in pregnancy. Diagnosis of sleep disorders would be confirmed by overnight polysomnography and ambulatory blood pressure monitoring. Pregnancy outcomes, both maternal and fetal would be recorded and its relation with sleep disorders in pregnancy would be analysed.

Detailed description

Objectives 1. To assess sleep quality during pregnancy 2. To know prevalence of various sleep disorders during pregnancy including restless leg syndrome, symptomatic obstructive sleep apnea etc. 3. To study the effect of sleep disorders on maternal and fetal outcome 4. To study the relation of obstructive sleep apnea with pregnancy induced hypertension. Material & Methods Study Design: Longitudinal prospective case-control study * Consecutive patients undergoing antenatal check up at the Antenatal Clinic at AIIMS hospital during will be evaluated using questionnaires for sleep quality. Preliminary screening question for sleep disturbance in pregnancy to all patients * Questionnaires used: Pittsburgh Sleep Quality Index (covers insomnia, RLS, snoring and sleep related breathing disorders); Epworth Sleepiness Score (for Excessive daytime sleepiness); Modified Wisconsin Score; Modified Berlin Questionnaires * To now association between Obstructive sleep apnea and pregnancy induced hypertension patients who develop symptomatic OSA will be offered polysomnographic evaluation during the second/third trimester. * An offer of similar services will be made to pregnant females who do not develop pregnancy induced hypertension at a similar gestational age. Case: patient with OSA Control: patients without OSA * We proposed to determine that what proportion of the cases were exposed to sleep disorders and what proportion are not. * We also planned to determine what proportion of controls is exposed and what proportion is not. Cases and controls would be matched for age ,parity, BMI,previous h/o pre-eclampsia in first trimester. Outcome parameters 1. Prevalence of various sleep disorders in pregnancy 2. Maternal outcome: Development of pregnancy induced hypertension (PIH), gestational diabetes mellitus, complicated pregnancy requiring admission, preterm delivery, ante-partum hemorrhage, delivery requiring intervention (Caesarian section, forceps/ventouse application) 3. Fetal outcome: APGAR scores at 1 and 5 min, IUGR, IUD, low birth weight Sample Size: A sample of convenience of 200 patients (who respond to questionnaire) and satisfy inclusion and exclusion criteria will be followed up prospectively to assess the effect of sleep disorders on pregnancy outcome.As per estimates from literature sample size for case control part would be 20 for cases and 40 controls. Investigation specifically related to projects: 1. Using Somnomedic systems, GmbH polysomnography machine by trained staff nurses and technicians at: * Obstetrics ward, AIIMS hospital * Home based portable PSG in non admitted 2. Ambulatory blood pressure by the Oscar 2™ system from SunTech Medical, USA. The Oscar 2 is clinically validated to all three internationally recognized standards. * British Hypertension Society1 (A/A) * European Society of Hypertension International Protocol2 * AAMI SP103 Patient comfort The Oscar 2 and the Orbit™ BP cuff make patient comfort a priority. * The SunTech Medical, Inc. patented Orbit cuff uses an innovative stretch-sleeve design to maintain cuff placement and promote patient comfort. * The Oscar 2 is a light, compact monitor that uses motion tolerant algorithms to reduce re-inflates and failed readings. The auto-intelligent inflation pressure also reduces measurement time, promoting patient comfort by controlling cuff inflation. 3. Screening Polysomnography using Apnea linkTM PLUS * A quick and easy sleep-screening tool designed to help identify more patients at risk for obstructive sleep apnea (OSA). * A premium, compact device that can be used at home Additional Investigation Required * Routine clinical antenatal examination * Blood pressure measurement * Blood parameters (done routinely in ANC) * Fasting blood sugar * Renal and hepatic function tests * Hemoglobin levels/s ferritin * Serum TSH levels * Urine examination * Routine and spot sample for protein. * Sonography: To rule out twin pregnancy and molar gestation/IUGR/Anomalies. * These investigations are routinely done in ante natal clinic at AIIMS. Data Analysis * Data will be collected on a pre-designed proforma. * Statistical analysis will be performed using STATA 11 for Windows software (intercooled version, Stata Corporation, Houston, TX, USA). * After assessing for approximate normal distribution, all continuous variables will be summarized as mean ± SD or median (interquartile range). * Categorical variables will be expressed as n (%). * The cases and controls will be compared using unpaired t-test if the data was normally distributed and the Mann-Whitney U test if not. * A p values of \<0.05 will be considered statistically significant. * Confounding factors influencing pregnancy outcomes will be subject to multivariate analysis to determine significance.

Interventions

OTHERPolysomnography and ambulatory blood pressure recording

Sponsors

All India Institute of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 20-45 years * Singleton pregnancy

Exclusion criteria

* Known hypertensives i.e SBP\>140/DBP\>90/on anti-hypertensive medications prior to pregnancy * Known diabetics (FBS\>100, 75 g OGTT positive/on medications) * Hypothyroidism * Chronic renal failure * Chronic liver disease * Twin pregnancy * Known systemic inflammatory condition e.g APLA Syndrome,SLE * Molar gestation * Patients on nephrotoxic medications e.g.NSAIDS *

Design outcomes

Primary

MeasureTime frame
Sleep quality in pregnancy and its association with pregnancy outcomesfrom recruitment during pregnancy to 6 weeks post partum

Secondary

MeasureTime frame
Number of patients who develop PIH and gestational diabetesfrom recruitment to 6 weeks post partum

Other

MeasureTime frame
to know the prevalence of sleep disorders in pregnancy and post partumfrom recruitment in pregnancy to 6 week post partum

Countries

India

Contacts

Primary ContactAbhimanyu Nehra, MBBS
abhimanyunehra@yahoo.com9868057741
Backup ContactSurendra K Sharma, MD, Ph.D.
sksharma@aiims.ac.in26593303

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026