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Multifaceted Intervention for Increasing Performance of CPR by Laypersons in Out-of-hospital Cardiac Arrest

Not Applicable
Completed
Conditions
Cardiac Arrest
Interventions
Other: Multifaceted intervention including 3 components
Registration Number
NCT03633370
Lead Sponsor
University Hospital, Grenoble
Brief Summary

Cardiac arrest (CA) early recognition is essential in order to rapidly activate emergency services and for bystanders to begin cardiopulmonary resuscitation (CPR).

As soon as a call is received, EMS dispatchers should try to identify CA. This may be difficult, in a context of stress and distress of the person calling. Yet, it is vital for bystanders to initiate CPR. Survival can be multiplied by 2 to 4 if the bystanders initiate a CPR before the arrival of the emergency medical services.

This work aim to assess a multifaceted intervention combining 3 elements to improve the initial phone recognition of CA and raise the number of patients benefiting from CPR before EMS arrival on scene.

The first element is a dispatcher training to the early phone recognition of CA. This training will be based on the concept of active teaching, favouring the interactive work of learners in particular by listening to real dispatch recordings. It will be completed by continuing education with a distance teaching platform including the systematic listening of recorded CA calls.

The second element is based on the deployment of a software aiming to notify CA thanks to mobile phones. This system interfaced to a control software enables to request the participation of CPR-trained volunteers automatically. The volunteers have to be located in the patient's surroundings. The deployment of this mobile application will rely on first-aid volunteers, health personal and any trained volunteers willing to participate. A randomized control study in one city area proved the efficiency of a similar software to improve the proportion of CPR by bystanders.

The third element consists in a motivational feedback. A weekly overview of the management and the outcomes of patients who suffered CA will be broadcast to all the responders and volunteers in the mobile application.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
2481
Inclusion Criteria
  • All adults with nontraumatic, out-of-hospital cardiac arrest diagnosed during the emergency medical service call
  • Cardiac arrest located in urban area
Exclusion Criteria
  • Pregnant or breastfeeding women
  • Patients under the law
  • Patients deprived of liberty by court ruling or administrative ruling
  • Traumatic cardiac arrest
  • CA occurring under the eyes of a professional emergency services patrol on duty
  • Cardiac arrest for which resuscitation seem unjustified (inevitable death, terminally ill irreversible condition, too long duration of cardiac arrest, non-resuscitation personal directive...)

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
Test GroupMultifaceted intervention including 3 componentsMultifaceted intervention 1. Training using distance learning for medical regulation assistants to recognise cardiac arrest on phone 2. Activation of the location-software application to send bystanders on cardiac arrest location before the arrival of emergency medical services (EMS) 3. Motivation feed-back Volunteers will received feed-back regarding CPR initiated before EMS arrival and survival
Primary Outcome Measures
NameTimeMethod
CPR initiated by bystanders before the arrival of first professionals rescuersDay 0

Proportion of patients who's received CPR initiated by bystander before EMS arrival.

Secondary Outcome Measures
NameTimeMethod
Survival at 72h after out-of-hospital cardiac arrest72 hours

survival at 72h

Return of Spontaneous CirculationDay 0

Proportion of patients who's recovered a spontaneous circulation after CPR

Survival to hospital admissionDay 0

Vital status at hospital admission

Survival to hospital dischargeup to 30 days

Vital status at hospital discharge

Survival at 30 days30 days

Vital status at 30 days

Neurological functional status CPCup to 30 days

As measured by Cerebral Performance Category (CPC) at hospital discharge and at 30 days Score less or equal to 2 will be considered as favorable neurological outcome

Neurological functional status mRS30 days

As measured by modified Rankin Scale (mRS) at hospital discharge and at 30 days:

modified Rankin Scale (mRS): 0 - No symptoms.

1. - No significant disability. Able to carry out all usual activities, despite some symptoms.

2. - Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities.

3. - Moderate disability. Requires some help, but able to walk unassisted.

4. - Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted.

5. - Severe disability. Requires constant nursing care and attention, bedridden, incontinent.

6. - Dead Score less or equal to 3 will be considered as favorable neurological outcome

First recorded rhythm30 min

First recorded cardiac rhythm by EMS

Trial Locations

Locations (15)

SAMU 33 - CHU HΓ΄pital Pellegrin

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Bordeaux, France

SAMU 74 - CH Annecy Genevois

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Annecy, France

SAMU 29 - CHRU La Cavale Blanche

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Brest, France

SAMU 54 - CHU Nancy

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Nancy, France

SAMU 44 - HΓ΄tel Dieu

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Nantes, France

SAMU 80 - CHU Amiens Picardie

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Amiens, France

SAMU 21 - CHU Dijon

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Dijon, France

SAMU 31 - CHU Toulouse

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Toulouse, France

SAMU 01 - CH Fleyriat

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Bourg en bresse, France

SAMU 38 - CHU Grenoble Alpes

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Grenoble, France

SAMU 06 - CHU de Nice

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Nice, France

SAMU 73 - Centre Hospitalier MΓ©tropΓ΄le Savoie

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ChambΓ©ry, France

Samu 85 - Chd Les Oudairies

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La Roche-sur-Yon, France

SAMU 26 - CH de Valence

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Valence, France

SAMU 42 -CHU Saint-Etienne

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Saint-Γ‰tienne, France

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