跳至主要内容
临床试验/NCT06087224
NCT06087224招募中不适用

The TELENEO Trial: A Multicenter Trial of Telemedicine for Advanced Neonatal Resuscitations in Community Hospitals

Mayo Clinic64 个研究点 分布在 2 个国家目标入组 947 人开始时间: 2024年3月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
Mayo Clinic
入组人数
947
试验地点
64
主要终点
7-day mortality rate

研究概览

简要总结

The purpose of this study is to evaluate the impact of real-time audio-video telemedicine consults with a neonatologist (termed teleneonatology) on the early health outcomes of at-risk neonates delivered in community hospitals.

详细描述

This prospective, multicenter trial will use a stepped wedge cluster randomized study design to evaluate the impact of real-time audio-video telemedicine consults with a neonatologist (termed "teleneonatology") on the risk of early mortality, early morbidity, and delivery room care for at-risk neonates delivered in community hospitals.

研究设计

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

入排标准

年龄范围
0 Days 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •GROUP 1: Community hospital clinicians
  • •To be eligible to participate in this study, an individual must meet all of the following criteria:
  • •A clinician who attends newborn resuscitations at a participating community hospital spoke site.
  • •Provision of informed oral consent prior to any mandatory study specific procedures and analyses.
  • •GROUP 2: At-risk outborn neonates To be eligible for this study, a neonate born in a participating community hospital spoke site must meet *at least one* of the following inclusion criteria
  • •Preterm birth at less than 32 weeks' gestation at delivery; OR
  • •Need for advanced resuscitation defined as:
  • •positive pressure ventilation (PPV) initiated soon after birth and continued for at least 10 minutes; OR
  • •placement of an alternative airway (endotracheal tube or laryngeal mask) to provide PPV; OR
  • •chest compressions.

排除标准

  • •GROUP 1: Community hospital clinicians None
  • •GROUP 2: At-risk outborn neonates
  • •A neonate born in a participating community hospital spoke site who meets any of the following criteria will be excluded from the study:
  • •Birth outside of the hospital birthing center.
  • •Neonatal transport team present at time of birth and providing resuscitative care.
  • •Severe congenital anomaly necessitating intensive care or surgery in the first two weeks of life.
  • •Plan for comfort care (non-resuscitation) following delivery.
  • •In-person neonatology-trained physician present for the resuscitation.

研究组 & 干预措施

Teleneonatology group

Experimental

Study eligible neonates cared for by the community hospital team with telemedicine consultation by a neonatologist from the regional neonatal intensive care unit (NICU).

干预措施: Teleneonatology (Other)

Control group

No Intervention

Study eligible neonates cared for by the community hospital team per the site's usual practice of care.

结局指标

主要结局

7-day mortality rate

时间窗: 7 days

Percentage of neonates classified as dying within 7 days, defined as death on or before 23:59 on the seventh completed day of life.

次要结局

  • Early neonatal morbidity within the first 7 days(7 days)
  • Highest level of resuscitation received in the delivery room(First hour of life)
  • Composite outcome of early mortality and morbidity(7 days)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jennifer L. Fang

Principal Investigator

Mayo Clinic

研究点 (64)

Loading locations...

相似试验