Trials / Completed
CompletedNCT02992873
The Scandinavian AED and Mobile Bystander Activation Trial
The Scandinavian AED and Mobile Bystander Activation Trial - a Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 815 (actual)
- Sponsor
- Karolinska Institutet · Academic / Other
- Sex
- All
- Age
- 8 Years – 120 Years
- Healthy volunteers
- Not accepted
Summary
Sudden cardiac death is a major health problem in the western world. In Europe alone nearly 300 000 patients are affected annually. The majority of victims suffering from an Out-of-Hospital Cardiac Arrest (OHCA have an initial cardiac rhythm that can be treated by means of defibrillation. In most emergency medical systems (EMS) time to defibrillation is too long and survival averages 10 %.However, when laymen operated Automated External Defibrillators (AEDs) are used within the first minutes, 7 out of 10 may survive. The aim of "The Scandinavian AED and Mobile Bystander Activation" (SAMBA) trial is to evaluate if a Mobile Phone Positioning system and a smartphone application will increase the proportions of patients with an attached Automated External Defibrillator (AED) before arrival of the Emergence Medical System (EMS). Mobile phone technology and a smartphone application will be used identify and recruit nearby CPR-trained lay people and automated external defibrillators (AEDs) to patients suffering out-of-hospital cardiac arrest (OHCA). The system is currently running in Stockholm Sweden and in the Gothenburg region.
Detailed description
Early defibrillation in out-of-hospital cardiac arrest is associated with high survival rates. If the operator at the dispatch center suspects an out-of-hospital cardiac arrest he or she will activate the mobile positioning system (MPS) wich is integrated in the operators computer environment. After activation, the system will locate all CPR-trained volunteers nearby the suspected OHCA. By computer based 1:1 randomization lay volunteers will be alerted and dispatched in 50 % of all suspected OHCAs in where the system is triggered by the dispatchers. In the intervention group, the activation of the system is supposed to result in lay volunteers to be alerted and directed to fetch the nearest AED and commence early defibrillation. Dependent on geographical and logistical circumstances, at a minimum one lay volunteer or more will be alerted to provide bystander CPR only. In the control group the MPS will be activated and lay responders will be dispatched to suspected OHCA to perform CPR only. In both groups the ordinary EMS services are dispatched in a regular fashion.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Layperson allocated to start CPR and fetch nearest AED | Dispatching laypersons to fetch an AED and start CPR in out-of-hospital cardiac arrest |
| DEVICE | Layperson allocated to start CPR | Dispatching laypersons to start CPR out-of-hospital cardiac arrest |
Timeline
- Start date
- 2018-12-01
- Primary completion
- 2020-10-20
- Completion
- 2020-10-20
- First posted
- 2016-12-14
- Last updated
- 2020-11-24
Locations
2 sites across 1 country: Sweden
Source: ClinicalTrials.gov record NCT02992873. Inclusion in this directory is not an endorsement.