Evaluation of Inpatient Sleep and Activity Following Childbirth
NCT ID: NCT05065203
Last Updated: 2023-06-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
78 participants
OBSERVATIONAL
2021-10-21
2023-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Sleep Improvement Intervention for Hospitalized Antepartum Patients
NCT04485728
A Cohort Study on Sleep Disorders During Pregnancy
NCT05765149
The Effects of Acute Total Sleep Deprivation Versus Normal Sleep on Metabolism
NCT01800253
Dietary Impact on Sleep, Rhythms and Related Physiology
NCT07138313
Phenotypic and Genotypic Markers of Performance Vulnerability to Sleep Loss
NCT02130791
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Postpartum patients
Women booked and have delivery of their child(ren) at Lucile Packard Children's Hospital
planned or unplanned Cesarean, operative, or non operative delivery
All types of delivery
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
planned or unplanned Cesarean, operative, or non operative delivery
All types of delivery
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* live pregnancy
* Single or multiple gestation
* all gestational ages
Exclusion Criteria
* 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
18 Years
60 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Stanford University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
PSultan
Associate Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Pervez Sultan, MD
Role: PRINCIPAL_INVESTIGATOR
Stanford University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Lucile Packard Children's Hospital
Stanford, California, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
60762
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.