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临床试验/NCT07042061
NCT07042061尚未招募不适用

Out-of-Hospital Cardiac Arrest Care Through Empowered and Equipped Community First Responders: Mobile External Defibrillation Investigation for Cardiac Arrest in Singapore (MEDICS).

Singapore General Hospital0 个研究点目标入组 1,000 人开始时间: 2026年5月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
1,000
主要终点
Feasibility of a full scale trial

研究概览

简要总结

The goal of this clinical trial is to learn the feasibility of equipping the volunteer community responders (VCR) with the mobile external automated defibrillators (mAEDs) for the management of adults experiencing out-of-hospital cardiac arrest (OHCA) patients. It will also provide early signals if this enhanced system can help increase the frequency of defibrillation and doing it earlier. The main questions it aims to answer are:

  • Can equipped VCRs apply mAEDs more frequently and earlier to potentially get more patients successfully resuscitated?
  • Is this system enhancement is feasible in the long run.

Participants, the VCRs, will:

  • Carry a 450 gm mAED with them all the time for up to an year and use it on an OHCA patient if and when alerted to help.
  • They will hand over this single-use battery-operated device to the EMS crew for data retrieval and potential replacement
  • They will be interviewed for their experience of being equipped and use of the mAED.

研究设计

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

入排标准

年龄范围
21 Years 至 74 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Inclusion Criteria
  • Study participants must meet all the inclusion criteria to participate in this study:
  • Must be proficient in English. Able to read and understand English fluently.
  • Be aged 21-74 years of age at point of recruitment.
  • Willing and able to move rapidly to a scene that can be 400 meters away from their location.
  • Be a registered CFR with SCDF.
  • Must be active myResponder® mobile phone app user so they can receive alerts about nearby OHCA cases.

排除标准

  • All subjects meeting any of the following exclusion criteria will be excluded from participation in this study.
  • Not proficient in English. Cannot read and understand English.
  • Aged less than 21 and over 74 years of age.
  • Not willing to be a myResponder app user.
  • Not able to move rapidly to a scene that can be 400 meters away from their location.
  • Given the short duration of the trial, those who are pregnant will be ineligible.
  • Those experiencing any serious physical injury or handicap and those with obvious mental handicap.

研究组 & 干预措施

AED arm

Experimental

干预措施: Mobile external automated defibrillator (Device)

结局指标

主要结局

Feasibility of a full scale trial

时间窗: Through study completion, an average of 1 year

A validated AIM/FIM tool will be used to collect perceptions of the users and managers using a likert scale measurement reporting on feasibility and acceptability of the intervention

次要结局

  • Qualitative experiences of CFR elicited through semi-structured interviews(1 year)

研究者

申办方类型
Other
责任方
Sponsor

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