跳至主要内容
临床试验/NCT06530433
NCT06530433招募中不适用

Evaluation of an Enhanced Community First Responder Support System to Improve Bystander Cardiopulmonary Resuscitation Quality for Patients Experiencing Out-of-hospital Cardiac Arrest

Singapore General Hospital1 个研究点 分布在 1 个国家目标入组 165 人开始时间: 2024年8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
招募中
入组人数
165
试验地点
1
主要终点
Good Chest Compression Depth (4-6cm)

研究概览

简要总结

The rise in out-of-hospital cardiac arrest (OHCA) cases in Singapore highlights the need for effective bystander cardiopulmonary resuscitation (BCPR). Despite many lay responders performing CPR, survival rates with good neurological outcomes have not significantly improved, prompting research into the quality of CPR as a critical factor. The study by Gallagher EJ et al. showed a significant survival improvement with high-quality CPR.

To address this, the Unit of Pre-hospital and Emergency Research (UPEC) trained thousands of community first responders (CFRs) in simplified CPR techniques using hands-only and DA-CPR methods. A significant innovation is the CPRcard®, developed by Laerdal in Norway, which offers real-time feedback on the quality of chest compressions. However, only 36% of CFRs using the CPRcard® achieved the desired compression standards, indicating room for improvement.

The study proposes enhancing CFR support with information communication technology (ICT), enabling two-way audio and one-way video communication between CFRs and dispatchers. This aims to reduce stress among responders, increase their willingness to engage with OHCA alerts, and improve CPR quality.

The clinical trial in Singapore will compare the current system against the enhanced CFR support system (eCSS), focusing on the real-time relay of CPR performance data, communication ease, and implementation factors. The high-quality CFR and OHCA registries in Singapore provide a robust setting for this research, aiming to enhance CPR delivery and improve OHCA outcomes through technology and real-time support.

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

Not possible to mask participants and care provider. Outcome is assessed by a device. Analyst will be masked.

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •18 years old and above
  • •SCDF registered CFRs
  • •Trial dispatchers with an active account of myResponder® app on their mobile phones

排除标准

  • •The CFRs who are pregnant
  • •Experiencing any serious physical Conditions
  • •Mental Health Conditions

研究组 & 干预措施

SoC

Active Comparator

Standard of Care

干预措施: CPRCard Only (Device)

eCSS

Experimental

enhanced CFR support system (eCSS)

干预措施: CPRCard + TCPR Link App and Web (Device)

结局指标

主要结局

Good Chest Compression Depth (4-6cm)

时间窗: Throughout chest compression before handing over to EMS (up to 24 hours)

OHCA events achieving great proportions of adequate compressions (achieving depth within the target range of 4-6 cm)

次要结局

  • Survivor discharging rate(Throughout Hospital Admission (up to 1 year))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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