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

Pregnancy Clinical Trial

Official title:

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

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02010671
• Other study ID #: 477211
• Status: Terminated
• Phase: N/A
• First received: September 27, 2013
• Last updated: May 24, 2017
• Start date: September 2013
• Est. completion date: July 2015

Study information

• Verified date: May 2017
• Source: University of California, Davis
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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).

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 8
• Est. completion date: July 2015
• Est. primary completion date: April 2015
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Pregnancy
• Previous Cesarean Section

Intervention

Other:
• Survey
Survey

Locations

Country	Name	City	State
United States	University of California, Davis Department of Obstetrics and Gynecology	Sacramento	California

Sponsors (1)

Lead Sponsor	Collaborator
University of California, Davis

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Trust of information they receive	Participants will be asked if they trust the information that they receive from influencing factors, such as significant others, clinicians, family, friends, or other.	Collected at study enrollment, typically 4-12 weeks into the subject's pregnancy.
Primary	Participant Opinions of mode of delivery as compared to actual mode of delivery	Mode of delivery	Mode of delivery will be assessed after delivery, average 40 weeks gestational age (7-9 months after enrollment)
Secondary	Factors that influence participant's opinion of mode of delivery	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).	Collected at time of study enrollment, typically 4-12 weeks into the subject's pregnancy.