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Improvement in night sleep duration and the effect on diabetes in pregnancy

Not Applicable
Completed
Conditions
Glucose tolerance in pregnancy
Pregnancy and Childbirth
Registration Number
ISRCTN17526076
Lead Sponsor
niversity Malaya Medical Centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
240
Inclusion Criteria

1. Self-reported sleep less than 7 hours
2. Gestation less than 34 weeks
3. Singleton pregnancy
4. Aged 18 to 40 years old

Exclusion Criteria

1. Inability to use eye mask and earplugs
2. Inability to use ActiGraph wGT3X-BT device
3. Pre-existing sleep disorders: chronic insomnia, sleep apnea
4. Pre-existing psychiatric disorders: depression, schizophrenia etc
5. Pre-existing medical disorders: diabetic mellitus, systemic lupus erythematosus, thyroid disorders, epilepsy, heart diseases etc
6. Active smoker
7. Current alcohol consumption
8. Multipara with co-sleeping child/children
9. Night shift workers
10. Night care-taker of other family members
11. Gross fetal anomalies
12. Intrauterine fatal death
13. Body mass index (BMI) =35 kg/m²

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Night sleep duration measured using the Actigraph wGT3X-BT device at the end of week 1<br>2. Fasting blood sugar and 2-hour post glucose tolerance test measured using oral glucose tolerance test performed at the end of week 1
Secondary Outcome Measures
NameTimeMethod
1. Actigraphy-derived Wake After Sleep Onset (WASO) and actigraphy-derived sleep efficiency measured using the Actigraph wGT3X-BT device at the end of week 1 <br>2. Sleep satisfaction measured using the Pittsburgh Sleep Quality Index (PSQI) during recruitment, and the modified Pittsburgh Sleep Quality Index at the end of week 1
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