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Effects of Sleep, Fatigue, and Timing of Post-dates Inductions Among Nulliparas

Effects of Sleep, Fatigue, and Timing of Post-dates Inductions Among Nulliparas

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01542151
Enrollment
72
Registered
2012-03-02
Start date
2011-10-31
Completion date
2014-11-30
Last updated
2015-03-26

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

Conditions

Pregnancy, Prolonged

Keywords

Labor, induced, Sleep, Fatigue, Patient satisfaction, Circadian rhythm

Brief summary

This randomized clinical trial will examine if there are any differences between post-dates inductions (inductions after 40 weeks of pregnancy) begun in the morning compared to the evening for first-time mothers. Sleep and fatigue measures will be measured to see if they differ by time of induction. Other measures will include the rate of births within 24 hours of admission, length of labor, use of labor analgesics, and method of delivery.

Detailed description

Randomized clinical trial of first-time pregnant women requiring post-dates induction (induction after 40 weeks gestation). Women will be randomized to a labor induction time in the morning or the evening. On hospital admission once women have signed the study consent, they will complete sleep questionnaires and a fatigue assessment. Fatigue and sleep time assessments will subsequently done by the study subject every 4 hours until women enter active labor. At the onset of active labor, assessments will stop. Labor outcomes and patient satisfaction will be obtained once women deliver.

Interventions

OTHERTime of labor induction

Assigned time of labor induction - morning or evening

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
14 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pregnant at 40 weeks gestation or more * Nulliparous * 14 years old or older * English or Spanish speaking * Healthy maternal status * Labor induction able to be scheduled

Exclusion criteria

* Less than 40 weeks gestation * Multiparous * Younger than 14 years old * Not able to speak or write in English or Spanish * Fetal or maternal status requires immediate induction

Design outcomes

Primary

MeasureTime frameDescription
Birth within 24 hours of inductionDay 1Calculate proportion of women delivering within 24 hours of the start of labor induction between the two groups

Secondary

MeasureTime frameDescription
Change in fatigue scoresDay 1Differences in Fatigue Visual Analog Scales from admission to active labor between the two groups.
Change in hand grip strengthDay 1Differences in change in hand grip strength from admission to active labor between the two groups.
St. Mary's Sleep scalePrebaseline: Baseline - 12-24 hoursDifferences in St. Mary's Sleep scores on admission between the two groups.
Labor and birth satisfactionDay 2Differences in Labor and Birth Satisfaction between the two groups.
Cesarean rateDay 1Compare cesarean rates between the two groups
Sleep QualityPrebaseline: Baseline - 30 daysCorrelation between sleep quality in the one month prior to admission measured with the Pittsburgh Sleep Quality Index and birth within 24 hours of start of induction.
Length of time to labor interventionDay 1Measure differences between groups between length of time from admission to different labor interventions e.g., rupture of membranes, analgesia - IV or epidural
Neonatal outcomesDay 1Differences between groups on neonatal outcomes such as 5 minute Apgar scores and admission to neonatal intensive care unit.
Morning-evening chronotypeDay 1Correlation between Horne-Osteberg Morning-Eveningness chronotype and birth within 24 hours of start of induction.

Countries

United States

Outcome results

None listed

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