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Evaluation of Inpatient Sleep and Activity Following Childbirth

Evaluation of Inpatient Sleep and Activity Following Childbirth

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05065203
Enrollment
78
Registered
2021-10-01
Start date
2021-10-21
Completion date
2023-01-31
Last updated
2023-06-06

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

Conditions

Sleep

Keywords

Postpartum sleep

Brief summary

Sleep is critical to mental and physical health following childbirth. However, patients who are hospitalized for labor and delivery may be admitted for days with significant impacts on sleep levels. Little is known about sleep and activity levels in inpatients during nighttime and daytime following childbirth and how this may affect their mental and physical health and wellbeing. If abnormalities are identified, targeted interventions may be possible to optimize recovery following delivery.

Interventions

PROCEDUREplanned or unplanned Cesarean, operative, or non operative delivery

All types of delivery

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* over 18 years old * live pregnancy * Single or multiple gestation * all gestational ages

Exclusion criteria

* Weekend delivery * admitted to critical care * unable to speak or understand English * known sleeping disorder * opioid requirement prior to admission * long term steroids use * significant autoimmune or neurological disease * significant psychiatric or neurodevelopment disorder

Design outcomes

Primary

MeasureTime frameDescription
Assessment of inpatient postpartum sleep using actigraphyDuring inpatient stay (up to 7 days)Participants will wear an acitgraphy watch during their inpatient stay to measure sleep.

Secondary

MeasureTime frameDescription
Association between inpatient actigraphy data and patient demographic, medical, obstetric, psychiatric, neonatal and anesthetic factorsDuring inpatient stay and outpatient follow up (up to 7 days)Participants will wear an acitgraphy watch during their inpatient stay to measure physical activity and sleep.
Association between outpatient sleep data with patient demographic, medical, obstetric, psychiatric, neonatal and anesthetic factors6 and 12 weeksParticipants will be interviewed at 6 and 12 weeks with PROM questions and sleep diaries to assess for association with demographic, medical obstetric, psychiatric neonatal and anaesthetic factors.
Association between actigraphy data with inpatient and outpatient postpartum Patient Reported Outcome Measures (PROMs)Day 1-7, 6 and 12 weeksMeasurement of postpartum actigraphy data to associate with patient reported outcome measures (PROM) (ObsQoR-10, Edinburgh Postpartum Depression Score, WHO-QOL-BREF and Bergen Insomnia Scale Score) given by face to face then remote interview
Determine population norms of objective and subjective sleep measures in the postpartum population.Day 1-7, 6 and 12 weeksParticipants will wear an acitgraphy watch during their inpatient stay to measure physical activity and sleep. PROM survey data during inpatient day 1-7 and outpatient 6 and 12 week interview.
Association between inpatient sleep and physical activity, PROMs and peripartum course with longer term outpatient sleep measuresDay 1-7, 6 and 12 weeksParticipants will wear an acitgraphy watch during their inpatient stay to measure physical activity and sleep. PROM survey data during inpatient day 1-7 and outpatient 6 and 12 week interview.
Association between objective (artigraphy) and subjective sleep assessment using diaries and PROMsDay 1-7, 6 and 12 weeksParticipants will wear an acitgraphy watch during their inpatient stay to measure physical activity and sleep. PROM survey data during inpatient day 1-7 and outpatient 6- 12 week interview.

Countries

United States

Outcome results

None listed

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