Trial of Mobile External Defibrillator for Out-of-hospital Cardiac Arrest in Singapore.

Официальное название

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

Обзор

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.

Вмешательства

• Устройство Mobile external automated defibrillator
  A single-use, hand-held, chocolate bar sized portable AED

Первичные конечные точки

• Feasibility of a full scale trial [Срок оценки: Through study completion, an average of 1 year]

Вторичные конечные точки (3)

• Qualitative experiences of CFR elicited through semi-structured interviews [Срок оценки: 1 year]
• Qualitative experiences of CFR elicited through semi-structured interviews [Срок оценки: 1 year]
• Qualitative experiences of CFR elicited through semi-structured interviews [Срок оценки: 1 year]

Критерии участия

1.1. 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.

1.2. Exclusion Criteria 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.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Организация здравоохранения

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Публикации

• Weiner BJ, Lewis CC, Stanick C, Powell BJ, Dorsey CN, Clary AS, Boynton MH, Halko H. Psychometric assessment of three newly developed implementation outcome measures. Implement Sci. 2017 Aug 29;12(1):108. doi: 10.1186/s13012-017-0635-3. PMID 28851459

Идентификаторы

NCT: NCT07042061 · ECOS 2024-3485

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗