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临床试验/NCT07819201
NCT07819201尚未招募不适用

Improving Maternal and Neonatal Care-Seeking Through a Video-Informed Training Session During the Third Trimester of Pregnancy

Swiss Tropical & Public Health Institute1 个研究点 分布在 1 个国家目标入组 800 人开始时间: 2026年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
800
试验地点
1
主要终点
Number of health care contacts as reported by women during endline survey

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
15 Years 至 —(Child, Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 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

排除标准

  • 未提供

研究组 & 干预措施

Control group

No Intervention

This group will not receive any intervention.

Information Video and Planning Session group

Experimental

This group will receive the study intervention, including an information video and planning session for the pregnant woman and her partner.

干预措施: Information video and planning session (Other)

结局指标

主要结局

Number of health care contacts as reported by women during endline survey

时间窗: From enrollment to 6 weeks postpartum (measured 6-8 weeks after the end of pregnancy)

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

次要结局

  • Number of antenatal care visits as reported by women during endline survey(Between enrollment and the end of pregnancy (measured 6-8 weeks after the end of pregnancy))
  • Facility-based childbirth as reported by women during endline survey(Measured 6-8 weeks after the end of pregnancy)
  • Number of postpartum visits as reported by women during endline survey(From the end of pregnancy to 6 weeks postpartum (measured 6-8 weeks after the end of pregnancy))
  • Fetal movement counting as reported by women during endline surveys(Measured 6-8 weeks after the end of pregnancy)
  • Perinatal mortality as reported by women during endline surveys(Measured 6-8 weeks after end of pregnancy)
  • Neonatal mortality as reported by women during endline surveys(Measured 6-8 weeks after end of pregnancy)
  • Average care-seeking knowledge scores among pregnant women and their partners(Measured 6-8 weeks after the end of pregnancy)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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