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早产儿睡在 SNOO Smart Sleeper Bassinet 中

2026年9月1日 更新者:Rakesh Sahni、Columbia University

睡眠环境对早产儿睡眠-觉醒组织的影响

The goal of this clinical trial is to compare sleeping in a SNOO Smart Sleeper bassinet (SNOO) with sleeping in traditional bassinet conditions in premature infants. The main questions it aims to answer are:

  1. Do preterm infants who sleep in the SNOO have more quiet sleep?

  2. Do preterm infants who sleep in the SNOO have improved vital signs?

    • Participants will spend two separate three-hour periods sleeping in either a SNOO (which plays white noise and rocks from side-to-side) or in a SNOO that remains off (does not play white noise and does not move). There will be at least one week separating these sleep assessments.
    • Participants will have their sleep stage and vital signs monitored (heart rate and oxygen levels).
    • Participants will also wear two stickers on their forehead that measure brain oxygen levels (NIRS) and brain waves (EEG).

There is a chance that the infant may experience more restful sleep and improved vital signs during the 2 sleep assessments.

研究概览

详细说明

Sleep plays an important role in the brain growth and development of preterm infants. Neonatal sleep is made up of three stages of sleep: quiet sleep, active sleep, and transitional sleep. Poor sleep can be a result of premature birth itself as well as from simply being in the neonatal intensive care unit (NICU) environment. The interruptions that these infants are exposed to include frequent cares, physical exams, lights, and noises.

The investigators are interested in the potential positive effects on sleep of recreating the environment of the womb. The SNOO is a bassinet that uses the combination of a secure swaddle, white noise, and gentle rocking movements to mimic the conditions that infants were exposed to in the uterus before being born. The investigators are interested in studying how recreating this environment of "within the womb" impacts the sleep-wake cycles of premature infants. To do this, the investigators will measure the amount of time that premature infants spent asleep versus awake while in the SNOO through behavior observations, electroencephalogram (brain activity monitoring), and vital signs. The investigators hypothesize that sleeping in the SNOO will increase the amount of time that the premature infants spend in quiet sleep and will improve their vital signs.

研究类型

介入性

注册 (实际的)

20

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

    • New York
      • New York、New York、美国、10032
        • Morgan Stanley Children's Hospital Neonatal Intensive Care Unit, NewYork Presbyterian

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

1周 至 2个月 (孩子)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Inpatients at the Morgan Stanley Children's Hospital NICU.
  • Singleton gestation.
  • Gestational age 28w0d to 36w6d at birth.
  • Postmenstrual age greater than 35 weeks at the time of the intervention.
  • Weight greater than 1.8 kg and less than 11.3 kg.
  • Stable thermoregulation in an open crib.
  • Stable respiratory status on room air (no nasal cannula or CPAP).
  • Normal head ultrasound (if obtained).

Exclusion Criteria:

  • Congenital brain or spinal anomalies.
  • Intracranial hemorrhage.
  • Severe encephalopathy.
  • Known or suspected genetic syndromes that could result in cerebral dysfunction.
  • Airway anomalies that could result in sleep-disordered breathing.
  • Bleeding diatheses.
  • Status post surgery or minor surgical procedures (i.e. inguinal hernia repair, circumcision).
  • Fetal opioid exposure.
  • Administration of sedating agents over the past 24 hours.
  • Ability to independently roll to hands and knees.

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:支持治疗
  • 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
实验性的:SNOO group

The SNOO Smart Sleeper will be used in accordance with the manufacturer's programming and instructions.

Infants will be secured in the SNOO Sleep Sack. They will be placed in the center of the SNOO Smart Sleeper. The SNOO will be powered on and will start playing white noise and rocking from side-to-side. The SNOO's movement and sound settings will automatically ramp up and down as needed in response to the infant's sensed level of fussiness or crying per the manufacturer's programming. The "preemie mode" will be enabled, which caps motion at level 2 out of 5.

假比较器:Traditional bassinet group

The SNOO will remain powered off to mimic the conditions of sleeping in a traditional hospital bassinet.

Infants will be swaddled using a standard hospital blanket. They will be placed in the center of the SNOO Smart Sleeper, but the SNOO will be left powered-off. No white noise will be played. No side-to-side rocking motions will occur.

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
Percent of Quiet Sleep Time During 3-hour Sleep Assessment
大体时间:At baseline sleep assessment, up to 3 hours

Quiet sleep is a marker of sleep maturation and will be measured by the researcher during the 3-hour-long sleep assessments. Quiet sleep defined as eyes closed with predominantly flaccid "rag doll" appearance, body movements limited to startles, and rhythmic jaw jerks lasting 1 to 2 seconds.

At baseline sleep assessment, up to 3 hours

次要结果测量

结果测量
措施说明
大体时间
Change in Heart Rate Variability
大体时间:At baseline sleep assessment (up to 3 hours) and second sleep assessment (up to 3 hours)

Heart rate variability is the fluctuation of beat-to-beat heart rate intervals over time and is a marker of autonomic nervous system maturation.

At baseline sleep assessment (up to 3 hours) and second sleep assessment (up to 3 hours)
Change in Cerebral Oxygenation
大体时间:At baseline sleep assessment (up to 3 hours) and second sleep assessment (up to 3 hours)

Cerebral oxygenation is a measure of the oxygen content of brain and will be measured by near-infrared spectroscopy (NIRS).

At baseline sleep assessment (up to 3 hours) and second sleep assessment (up to 3 hours)
Change in Oxygen Saturation
大体时间:At baseline sleep assessment (up to 3 hours) and second sleep assessment (up to 3 hours)

Oxygen saturation is a measure of the oxygen content of the blood, as measured by pulse oximetry.

At baseline sleep assessment (up to 3 hours) and second sleep assessment (up to 3 hours)
Change in Intermittent Hypoxemic Event Frequency
大体时间:At baseline sleep assessment (up to 3 hours) and second sleep assessment (up to 3 hours)

Intermittent hypoxemic events are episodes where oxygen saturation is low for prolonged periods, as measured by pulse oximetry.

At baseline sleep assessment (up to 3 hours) and second sleep assessment (up to 3 hours)

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:Rakesh Sahni, MD、Columbia University

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

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 (实际的)

2023年3月16日

初级完成 (实际的)

2024年5月31日

研究完成 (实际的)

2025年6月2日

研究注册日期

首次提交

2023年1月25日

首先提交符合 QC 标准的

2023年1月25日

首次发布 (实际的)

2023年2月3日

研究记录更新

最后更新发布 (实际的)

2026年9月25日

上次提交的符合 QC 标准的更新

2026年9月1日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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

是的

在美国制造并从美国出口的产品

不

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