Survey of Women's Choice of Delivery Before Consulting With Her Obstetrician
2017年5月24日 更新者：University of California, Davis
Understanding a Woman's Choice of Mode of Delivery Before Initial Consult With Her Obstetrician After Having One Prior Cesarean Section
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.
研究概览
详细说明
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).
研究类型
观察性的
注册 (实际的)
8
联系人和位置
本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。
学习地点
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California
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Sacramento、California、美国、95817
- University of California, Davis Department of Obstetrics and Gynecology
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参与标准
研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 及以上 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
女性
取样方法
非概率样本
研究人群
Participants will be selected from the new obstetrics patients in the University of California, Davis Department of Obstetrics and Gynecology department clinics.
描述
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
学习计划
本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。
研究是如何设计的？
设计细节
- 观测模型：仅案例
- 时间观点：横截面
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
|
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
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民意调查
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研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Participant Opinions of mode of delivery as compared to actual mode of delivery
大体时间：Mode of delivery will be assessed after delivery, average 40 weeks gestational age (7-9 months after enrollment)
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Mode of delivery
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Mode of delivery will be assessed after delivery, average 40 weeks gestational age (7-9 months after enrollment)
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Factors that influence participant's opinion of mode of delivery
大体时间：Collected at time of study enrollment, typically 4-12 weeks into the subject's pregnancy.
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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).
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Collected at time of study enrollment, typically 4-12 weeks into the subject's pregnancy.
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Trust of information they receive
大体时间：Collected at study enrollment, typically 4-12 weeks into the subject's pregnancy.
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Participants will be asked if they trust the information that they receive from influencing factors, such as significant others, clinicians, family, friends, or other.
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Collected at study enrollment, typically 4-12 weeks into the subject's pregnancy.
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员：Maricela Rangel-Garcia、University of California, Davis
- 研究主任：Mitchell Creinin, MD、University of California, Davis
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2013年9月1日
初级完成 (实际的)
2015年4月1日
研究完成 (实际的)
2015年7月1日
研究注册日期
首次提交
2013年9月27日
首先提交符合 QC 标准的
2013年12月9日
首次发布 (估计)
2013年12月13日
研究记录更新
最后更新发布 (实际的)
2017年5月30日
上次提交的符合 QC 标准的更新
2017年5月24日
最后验证
2017年5月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.