Actively Recruiting

Phase Not Applicable
Age: 8Years +
All Genders
ID04446585

A Cluster Randomized Clinical Trial of Strategic AED Deployment in High-risk Residential Areas Combined With Activation of Local Residents

Led by Emergency Medical Services, Capital Region, Denmark · Updated on 2023-09-15

260

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

E

Emergency Medical Services, Capital Region, Denmark

Lead Sponsor

T

TrygFonden, Denmark

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to increase the rates of bystander defibrillation during out-of-hospital cardiac arrests in densely populated residential areas with many cardiac arrest incidents. Despite the growing number of Automated External Defibrillators (AEDs), survival and defibrillation rates remain low in these areas. The study focuses on improving bystander defibrillation and 30-day survival through strategic AED placement and resident involvement as citizen responders. The study compares two approaches: standard emergency response with ambulance and physician-staffed mobile care units plus activation of citizen responders via the Heart Runner app, against an enhanced intervention. The enhanced intervention adds strategically placed AEDs within a 1.5-minute walking distance to residences, registration of AEDs with emergency dispatch, and training courses for about 120 residents per area in CPR and AED use to recruit them as citizen responders. Participants will be part of emergency calls for suspected cardiac arrest, where dispatchers provide telephone-assisted CPR instructions and guide bystanders to retrieve AEDs if available. Data from AED use will be collected. The study measures bystander defibrillation rates up to five years after intervention and 30-day survival post-cardiac arrest. Participation involves monitoring cardiac arrest cases, AED deployment, citizen responder activation, and outcomes within the study areas.

CONDITIONS

Brief Title

Cardiac Arrest in Residential Areas With Mobile First-responder Activation

Who Can Participate

Age: 8Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Witnessed cardiac arrest registered in the Danish Cardiac Arrest Registry within study sites
  • Cardiac arrest must be witnessed
  • Cardiac arrest with non-traumatic cause (excluding intoxication, drowning, or suicide)
Not Eligible

You will not qualify if you...

  • Cardiac arrest occurring in a nursing home
  • Cardiac arrest not treated by emergency medical services for ethical reasons or obvious signs of death
  • Suspected cardiac arrest not verified as true cardiac arrest
  • Cardiac arrests witnessed by emergency medical personnel

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

Duration - Up to five years

Participants in intervention areas receive strategically deployed AEDs and some residents are trained in CPR and AED use to act as citizen responders activated through an app during cardiac arrests.

Long-term Monitoring

Duration - Up to five years

Participants are observed for bystander defibrillation and 30-day survival after cardiac arrest.

Trial Site Locations

Total: 1 location

1

Emergency Medical Services Copenhagen

Ballerup Municipality, The Capital Region, Denmark, 2750

Actively Recruiting

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Research Team

A

Anne J Jørgensen, MD

F

Fredrik Folke, MD, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Community intervention to improve defibrillation before ambulance arrival in residential neighbourhoods with a high risk of out-of-hospital cardiac arrest: study protocol of a cluster-randomised trial (the CARAMBA trial).

Anne Juul Grabmayr, Carolina Malta Hansen, Nanna Bo...

https://pubmed.ncbi.nlm.nih.gov/37816557