Optimizing Timing of Cesarean Delivery Consent on Labor and Delivery
This study is looking at the best time to get your consent for a possible cesarean delivery (C-section) if you're planning a vaginal birth but might need a C-section. Currently, practices vary widely. Researchers want to see if getting consent earlier, when you arrive at the hospital for labor induction, improves your experience compared to getting consent only if a C-section becomes medically necessary. They are studying this because about a third of pregnant patients have a C-section, and they want to make sure the consent process is as good as possible for those who have an unplanned C-section. You can join if you are 18 or older, receiving prenatal care at Duke Perinatal Durham or Duke Women's Health Associates, and are between 34 and 41 weeks pregnant with a scheduled or intended labor induction.
- Study design
- This is a randomized-controlled trial with 200 participants. You would be randomly assigned to one of two groups: either giving consent for a possible C-section when you arrive for labor induction, or giving consent only if a C-section is medically indicated.
- What's involved
- You would be approached to join the study between 34-41 weeks of pregnancy. Your perception of the informed consent process will be measured from day 1 postpartum to 6 weeks postpartum.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your experience will be followed from the day after delivery up to 6 weeks postpartum.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Optimizing Timing of Cesarean Delivery Consent on Labor and Delivery
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Rebecca Beal · STUDY_DIRECTOR · Duke University Department of Obstetrics and Gynecology
- Kristin Weaver · STUDY_DIRECTOR · Duke University
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Patient Perception of Informed Consent ProcessFrom day 1 postpartum to 6 weeks postpartum
As measured by survey.