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临床试验/NCT06863597
NCT06863597尚未招募不适用

A Multi-Center Randomized, Parallel-Group Study to Compare Knowledge Translation Between Different Media in Pregnant and Lactating Women

Semmelweis University0 个研究点目标入组 380 人开始时间: 2025年8月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
380
主要终点
Knowledge translation

研究概览

简要总结

Pharmacotherapy for lactating women in Hungary presents a unique challenge. While certain medications may pose risks to the infant or reduce breast milk production, the unnecessary avoidance of treatment can also be harmful. Despite this, no dedicated Hungarian website currently provides guidance on the safe use of over-the-counter (OTC) medications for breastfeeding mothers.

To address this gap, the aim is to develop a website that not only meets clinical standards but also presents essential information in a clear, accessible format that helps mothers understand and retain key details by choosing the best medium.

Our main question is: What is the most effective way to educate lactating women about OTC medication use through an online platform?

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

盲法说明

Blinding is not feasible.

入排标准

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

入选标准

  • Target population is adult (>18 years), 3rd trimester pregnant women; and breastfeeding women after childbirth (max. 7 days postpartum; 24:00), who intend to breastfeed.
  • Participants have to have internet access with no regard to the type of internet connection.

排除标准

  • A mother will not breastfeed, either because they cannot or do not want it.
  • Anyone who do not want to participate in the study.

结局指标

主要结局

Knowledge translation

时间窗: From enrollment in the first week, followed by an assessment after 6 months.

Knowledge translation will be measured by the difference in test scores before and after the intervention. The tests will be developed through common consensus. Since topic-specific tests will be created individually for each topic, only their utility will be assessed in a pilot study, and validation is not planned.

次要结局

  • User-satisfaction(From enrollment in the first week, followed by an assessment after 6 months.)

研究者

申办方类型
Other
责任方
Sponsor

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