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Survey of Women's Choice of Delivery Before Consulting With Her Obstetrician

Understanding a Woman's Choice of Mode of Delivery Before Initial Consult With Her Obstetrician After Having One Prior Cesarean Section

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02010671
Enrollment
8
Registered
2013-12-13
Start date
2013-09-30
Completion date
2015-07-31
Last updated
2017-05-30

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

Conditions

Pregnancy, Previous Cesarean Section

Keywords

Pregnancy, Cesarean Section, Survey, Delivery

Brief summary

We are surveying women who have had a previous cesarean section at the time of entry into prenatal care for their next pregnancy about their thoughts related to a trial of labor after cesarean (TOLAC) or repeat c-section.

Detailed description

This is a survey for women who have had a previous cesarean section, also known as a c-section, with their last pregnancy. The study is looking at what factors and people may influence the decisions women make about their birthing plan after they have had a previous c-section. If they qualify, women will be asked to complete a brief survey at their initial Ob/Gyn appointment before they see their Ob doctor. In order to qualify, women must: * Be pregnant * Have not seen an obstetrician for this pregnancy * Be at least 18 years old * Be able to read English * Have had a prior pregnancy delivered by c-section * Only had one prior c-section * The c-section must have been the last pregnancy before this one Questions that will be asked include: * Demographic information (examples: age, race/ethnicity) * Pregnancy information * Delivery questions * Factors that may influence her birthing plan Participants will also be asked if the study staff can follow up after her delivery to see what kind of delivery she had (vaginal or c-section).

Interventions

OTHERSurvey

Survey

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* Pregnant Women * 18 years old or older * Prior pregnancy with cesarean delivery * No prior obstetric physician care during current pregnancy

Exclusion criteria

* More than one prior cesarean * Women who cannot read English

Design outcomes

Primary

MeasureTime frameDescription
Participant Opinions of mode of delivery as compared to actual mode of deliveryMode of delivery will be assessed after delivery, average 40 weeks gestational age (7-9 months after enrollment)Mode of delivery

Secondary

MeasureTime frameDescription
Factors that influence participant's opinion of mode of deliveryCollected at time of study enrollment, typically 4-12 weeks into the subject's pregnancy.Participants will be asked what influences their opinions of mode of delivery, such as significant other, clinicians, family, friends, or others. They will also be asked how much these factors may influence their decisions (high influence, some influence, no influence).

Other

MeasureTime frameDescription
Trust of information they receiveCollected at study enrollment, typically 4-12 weeks into the subject's pregnancy.Participants will be asked if they trust the information that they receive from influencing factors, such as significant others, clinicians, family, friends, or other.

Countries

United States

Outcome results

None listed

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