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Inadequate enrollment
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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.
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:
Questions that will be asked include:
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).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Women with a prior cesarean section | Survey of women who had a cesarean section with their last pregnancy and no other prior cesarean section deliveries |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Survey | Other | Survey |
|
| Measure | Description | Time Frame |
|---|---|---|
| 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) |
| Measure | Description | Time Frame |
|---|---|---|
| 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. |
| Measure | Description | Time Frame |
|---|---|---|
| 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. |
Inclusion Criteria:
Exclusion Criteria:
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Participants will be selected from the new obstetrics patients in the University of California, Davis Department of Obstetrics and Gynecology department clinics.
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| Name | Affiliation | Role |
|---|---|---|
| Maricela Rangel-Garcia | University of California, Davis | Principal Investigator |
| Mitchell Creinin, MD | University of California, Davis | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of California, Davis Department of Obstetrics and Gynecology | Sacramento | California | 95817 | United States |
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| ID | Term |
|---|---|
| D011795 | Surveys and Questionnaires |
| ID | Term |
|---|---|
| D003625 | Data Collection |
| D004812 | Epidemiologic Methods |
| D008919 | Investigative Techniques |
| D017531 | Health Care Evaluation Mechanisms |
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| D011787 | Quality of Health Care |
| D017530 | Health Care Quality, Access, and Evaluation |
| D011634 | Public Health |
| D004778 | Environment and Public Health |