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临床试验/NCT03527771
NCT03527771已完成不适用

Video-assisted Telephone CPR With the EmergencyEye-Software - a Pilot Study

University of Cologne1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2018年8月8日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
150
试验地点
1
主要终点
CPR Compression Frequency

研究概览

简要总结

Technical advance as broad-bandwidth wireless internet coverage and the ubiquity utilization of smartphones has opened up new possibilities which surpass the normal audio-only telephony. High quality and real-time video-telephony is now feasible. However until now this technology hasn't been deployed in the emergency respond service.

In the hope of helping the detection of the cardiac arrest, offer the possibility to evaluate and correct via a video-instructed CPR (V-CPR) and to facilitate a fast localization of the emergency site, a new software (EmergencyEye®/RAMSES®) was developed which enables the dispatcher a video-telephony with the callers mobile terminal (smartphone) if suitable.

This technology hasn't been tested in a randomized controlled trail yet and no data exists that shows if V-CPR in comparison to T-CPR and non-instructed CPR leads to a better bystander CPR-performance.

详细描述

Technical advance as broad-bandwidth wireless internet coverage and the ubiquity utilization of smartphones has opened up new possibilities which surpass the normal audio-only telephony. High quality and real-time video-telephony is now feasible. However until now this technology hasn't been deployed in the emergency respond service.

In the hope of helping the detection of the cardiac arrest, offer the possibility to evaluate and correct via a video-instructed CPR (V-CPR) and to facilitate a fast localization of the emergency site, a new software (EmergencyEye®/RAMSES®) was developed which enables the dispatcher a video-telephony with the callers mobile terminal (smartphone) if suitable.

This technology hasn't been tested in a randomized controlled trail yet and no data exists that shows if V-CPR in comparison to T-CPR and non-instructed CPR leads to a better bystander CPR-performance.

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
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • healthy volunteer

排除标准

  • healthcare providers (medical practitioners, nurses, paramedics etc.)
  • pregnant women
  • people with cardio-pulmonary and musculoskeletal diseases or any other impairment that would risk harm for the volunteer while performing CPR for 8 minutes

研究组 & 干预措施

T-CPR

Active Comparator

telephone assisted CPR according to ERC Guidelines 2015

干预措施: telephone-assisted CPR (Drug)

V-CPR

Experimental

video-assisted CPR according to ERC Guidelines 2015

干预措施: Video-assisted CPR (Device)

结局指标

主要结局

CPR Compression Frequency

时间窗: 8 minutes

CPR Compression Frequency

次要结局

  • Cumulative No-Flow Time(Up to 8 minutes)
  • Compression Depth(8 minutes)
  • Time to diagnosis(Up to 8 minutes)
  • Time to beginning of chest compressions(Up to 8 minutes)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

PD Dr. med. Wolfgang A. Wetsch

Principal Investigator

University of Cologne

研究点 (1)

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