跳至主要内容
临床试验/NCT05910320
NCT05910320终止不适用

Evaluation of an Investigational Wearable Vital Signs Monitoring Device in Healthy Infants

Johns Hopkins University2 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2023年5月23日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
3
试验地点
2
主要终点
Signal morphology of wearable monitoring device

研究概览

简要总结

The primary objective of this study is to evaluate the feasibility of the use of an investigational wearable vital sign monitoring device in infants.

详细描述

Vital sign monitoring of infants outside of a traditional healthcare setting has already been shown to significantly decrease mortality for children with single ventricle congenital heart disease (1V CHD), a fragile group of patients with congenital heart disease (CHD). Therefore, there is a critical need to develop an accurate, at-home vital sign monitoring system for infants to expand the benefits of remote monitoring to further patient populations. The investigators believe that allowing for continuous monitoring at a clinical standard with interpretations and alerts built into the technology will result in an even greater decline in mortality for infants with 1V CHD, improved clinical outcomes for all infants with CHD, and increased well-being for healthy infants.

To achieve this goal, the investigators are developing a health monitoring system that collects numerical data and physiological waveforms describing heart rate (HR), respiratory rate (RR), pulse oximetry (SpO2), regional oxygen saturation, temperature, and infant motion.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
1 Day 至 1 Year(Child)
性别
All
接受健康志愿者

入选标准

  • Patient admitted to either the newborn nursery, pediatric cardiac intensive care unit (PCICU), or pediatric care unit (PCU)
  • Parent provided written informed consent

排除标准

  • Foster or ward of the state

结局指标

主要结局

Signal morphology of wearable monitoring device

时间窗: From device placement to removal, up to 1 hour

Feasibility of a wearable monitoring device as determined by signal morphology of wearable monitoring device

Signal-to-noise ratio of wearable monitoring device

时间窗: From device placement to removal, up to 1 hour

Feasibility of a wearable monitoring device as determined by signal-to-noise ratio

Signal-to-noise ratio of reusable electrodes

时间窗: From electrode placement to removal, up to 15 minutes

Feasibility of reusable electrodes as determined by the signal-to-noise ratio

Percent error of wearable monitoring device compared to clinical bedside monitors

时间窗: From device placement to removal, up to 1 hour

Feasibility of a wearable monitoring device as determined by percent error compared to clinical bedside monitors

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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