Improving Maternal and Neonatal Care-seeking Through a Video-informed Training Session During the Third Trimester of Pregnancy (Taabo T3)
2026年9月14日 更新者：Swiss Tropical & Public Health Institute
Improving Maternal and Neonatal Care-Seeking Through a Video-Informed Training Session During the Third Trimester of Pregnancy
This study is a randomized controlled trial evaluating the impact of a video-informed training session on maternal and newborn health care seeking in rural Côte d'Ivoire.
研究概览
详细说明
In Taabo, Côte d'Ivoire, many women do not receive recommended care during the third trimester of pregnancy or the early postpartum period, contributing to adverse maternal and neonatal health outcomes.
In this individual-level open-label randomized controlled trial, we will evaluate the impact of an information and planning intervention on timely care-seeking during the third trimester of pregnancy and the early postpartum period.
The study will enroll 800 women who are currently in the third trimester of pregnancy and randomize them to one of two groups: (1) control, or (2) information video and planning session for the pregnant women and her partner.
A baseline survey will be performed at the time of enrollment, and outcomes will be evaluated using an endline survey 6-8 weeks after the end of pregnancy.
The main outcome of the study is the number of health care contacts that women have between enrollment in the study and 6 weeks postpartum.
研究类型
介入性
注册 (估计的)
800
阶段
- 不适用
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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Taabo、科特迪瓦
- Centre Suisse de Recherches Scientifiques en Cote d'Ivoire
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接触：
- Siaka Koné, PhD
- 电话号码：+2250749069627
- 邮箱：Siaka.kone@csrs.ci
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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
- 孩子
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria for Pregnant Women:
- Currently pregnant
- Aged 15 years or older
- Live in the area served by the Taabo Health & Demographic Surveillance System
- Estimated gestational age between 6 completed months of pregnancy and 8 completed months of pregnancy
Inclusion Criteria for Male Partners:
- Aged 15 or older
- Married to or currently the main romantic partner of a woman who is enrolled in the study
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
- 主要用途：卫生服务研究
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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无干预：Control group
This group will not receive any intervention.
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实验性的：Information Video and Planning Session group
This group will receive the study intervention, including an information video and planning session for the pregnant woman and her partner.
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The study intervention is a video-informed information and planning session for health care during the third trimester, childbirth, and the first six weeks postpartum.
In this intervention, a member of the study team will show information videos to pregnant women and her partner, summarizing key recommendations for health and health care seeking during the third trimester of pregnancy and the first six weeks following childbirth.
After showing the videos, the study team member will guide the pregnant woman and her partner in a short discussion about planning for care-seeking during the third trimester and early postpartum period.
This discussion will include quizzing on the content of the information videos and discussions of care-seeking plans together with the couple.
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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 |
|---|---|---|
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Number of health care contacts as reported by women during endline survey
大体时间：From enrollment to 6 weeks postpartum (measured 6-8 weeks after the end of pregnancy)
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Number of health care contacts that women have between enrollment in the study and 6 weeks postpartum, including antenatal care visits, childbirth, and postpartum care visits
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From enrollment to 6 weeks postpartum (measured 6-8 weeks after the end of pregnancy)
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Number of antenatal care visits as reported by women during endline survey
大体时间：Between enrollment and the end of pregnancy (measured 6-8 weeks after the end of pregnancy)
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Number of antenatal care visits
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Between enrollment and the end of pregnancy (measured 6-8 weeks after the end of pregnancy)
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Facility-based childbirth as reported by women during endline survey
大体时间：Measured 6-8 weeks after the end of pregnancy
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Proportion of women who gave birth in a health facility
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Measured 6-8 weeks after the end of pregnancy
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Number of postpartum visits as reported by women during endline survey
大体时间：From the end of pregnancy to 6 weeks postpartum (measured 6-8 weeks after the end of pregnancy)
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Number of postpartum care visits between the end of pregnancy and 6 weeks postpartum
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From the end of pregnancy to 6 weeks postpartum (measured 6-8 weeks after the end of pregnancy)
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Fetal movement counting as reported by women during endline surveys
大体时间：Measured 6-8 weeks after the end of pregnancy
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The proportion of pregnant women who report counting fetal movements at least once during the final month of their pregnancy
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Measured 6-8 weeks after the end of pregnancy
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Perinatal mortality as reported by women during endline surveys
大体时间：Measured 6-8 weeks after end of pregnancy
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The proportion of women who experience a stillbirth or neonatal death in the first seven days of life (perinatal mortality)
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Measured 6-8 weeks after end of pregnancy
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Neonatal mortality as reported by women during endline surveys
大体时间：Measured 6-8 weeks after end of pregnancy
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The proportion of women whose child dies in the first 28 days of life
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Measured 6-8 weeks after end of pregnancy
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Average care-seeking knowledge scores among pregnant women and their partners
大体时间：Measured 6-8 weeks after the end of pregnancy
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Average scores (among pregnant women and their partners) on assessments of knowledge of care-seeking recommendations during the third trimester and the early postpartum period, as measured using five questions during endline surveys with pregnant women and their partners. We create a Care-Seeking Knowledge Scale as follows: Participants receive 1 point if they respond with 3 or more when asked how many postpartum visits women should have during the first 6 weeks after childbirth; 1 point if they correctly name at least 3 danger signs for women during pregnancy; 1 point if they correctly name at least 3 danger signs for women during the first six weeks after childbirth; and 1 point if they correctly name at least 3 danger signs for newborns. Scores range from 0 to 4 with higher scores representing greater knowledge. |
Measured 6-8 weeks after the end of 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。
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 (估计的)
2026年9月1日
初级完成 (估计的)
2027年5月1日
研究完成 (估计的)
2027年5月1日
研究注册日期
首次提交
2026年9月8日
首先提交符合 QC 标准的
2026年9月8日
首次发布 (实际的)
2026年9月14日
研究记录更新
最后更新发布 (实际的)
2026年9月17日
上次提交的符合 QC 标准的更新
2026年9月14日
最后验证
2026年9月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 2026-19
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)？
是的
IPD 计划说明
De-identified data files and analytic code will be posted on public repositories at the time of publication of results.
IPD 共享时间框架
We plan to share IPD and supporting information at the time of publication.
IPD 共享访问标准
IPD and supporting information will be made available on public repositories.
IPD 共享支持信息类型
- 研究方案
- 树液
- 国际碳纤维联合会
- 分析代码
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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.