The PulsePoint Randomized Controlled Trial
Out-of-hospital Cardiac Arrest
About this trial
This is an interventional health services research trial for Out-of-hospital Cardiac Arrest focused on measuring Cardiac Arrest, cardiopulmonary resuscitation, automated external defibrillators, smartphones
Eligibility Criteria
Inclusion Criteria:
- Patients with 911 calls assigned MPDS code 09-E-01 (Suspected atraumatic cardiac arrest not breathing), and 09-E-02 (Suspected cardiac arrest, not breathing normally),
- Out-of-hospital cardiac arrest as defined within the ROC Epistry Database
Exclusion Criteria:
- Trauma (including burns) associated with cardiac arrest
- Cardiac arrests occurring in prisons, etc
- Patients not treated by paramedics because of a DNR order or signs of obvious death as per Ontario provincial paramedic medical directives (e.g. decapitation, decomposition, rigour mortis)
Sites / Locations
- Toronto Emergency Medical Services
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
PulsePoint notification
Usual Care
Conventional Emergency Dispatch PLUS The PulsePoint notification. In the event of a potential cardiac arrest identified by 911call-takers, data will be automatically pushed to PulsePoint smartphone application users within very close proximity to the emergency. This will be done in parallel with normal emergency dispatch of paramedics and fire fighters to the scene of the emergency. The activation radius around the emergency is somewhat variable, depending on phone signal strength, climate conditions and whether the phone is inside or outside, but is approximately 200-500 meters.
Patients randomized to the control arm will receive conventional emergency medical dispatching procedures but no PulsePoint notification will be sent to nearby PulsePoint users.