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Dispatcher-Activated Neighborhood Access Defibrillation and Cardiopulmonary Resuscitation

Population Based Intervention Trial of Dispatcher-Activated Neighborhood Access Defibrillation and Cardiopulmonary Resuscitation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02010151
Enrollment
3194
Registered
2013-12-12
Start date
2015-03-31
Completion date
2017-12-31
Last updated
2020-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Out of Hospital Cardiac Arrest

Keywords

Out of Hospital Cardiac Arrest, Cardiopulmonary Resuscitation, dispatch, emergency medicine

Brief summary

The hypothesis of this study is Dispatcher-Activated Neighborhood Access Defibrillation and Cardiopulmonary Resuscitation (NAD-CPR) would improve survival of out-of-hospital cardiac arrest (OHCA).

Detailed description

Out-of-hospital cardiac arrest (OHCA) is a major health problem, occurring in about 1 in 1,500 adults in the developed countries each year. Although layperson CPR and defibrillation are crucial components of chain of survival, layperson CPR rate and it's quality is low and public-access defibrillation (PAD) program is not cost-effective.If trained bystanders can know the information of occurrence of OHCA and nearest place for automated external defibrillator (AED) at the same time by dispatch center, these neighborhoods could run and give high quality CPR and early defibrillation. If this protocol ,Dispatcher-Activated Neighborhood Access Defibrillation and Cardiopulmonary Resuscitation(NAD-CPR), is introduced to community, it may improve survival of OHCA.

Interventions

OTHERNAD-CPR

When Dispatcher detects OHCA, short message service (SMS)about the OHCA event and information about the location of nearest AED is sent to trained laypersons within geographically accessible area.

Sponsors

Korean Center for Disease Control and Prevention
CollaboratorOTHER_GOV
Seoul Metropolitan Government Health and Welfare Office
CollaboratorUNKNOWN
Seoul Metropolitan Fire and Disaster Headquater
CollaboratorUNKNOWN
Korea Association for Safety Community
CollaboratorUNKNOWN
Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* all OHCA with presumed cardiac etiology more than 15 years old * assessed by emergency medical service (EMS) providers dispatched by dispatch center * dispatcher detected OHCA patients

Exclusion criteria

* OHCA with non-cardiac etiology * prolonged cardiac arrest with a suspected duration more than 30 minutes * cases with rigor mortis or rivor mortis, decapitated or decomposed body * Non detected cases by dispatcher

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants Surviving at Hospital Dischargedischarge time from first admission from emergency department within 2 monthwe compared the survival to discharge rate between before intervention period and intervention period. Survival to discharge checked at the discharge point of hospital.

Secondary

MeasureTime frameDescription
Number of Participants With Pre-Hospital Return of Spontaneous Circulation (ROSC)hospital arriving time from ambulance within 2 hourswe compared the Pre-hospital return of spontaneous circulation (ROSC) rate between before intervention period and intervention period.
Number of Participants With Good Neurological Recoverydischarge time from first admission from emergency department within 2 monthCerebral performance category 1 or 2 is defined as good neurological recovery. we compared the good neurological recovery rate between before intervention period and intervention period.

Countries

South Korea

Participant flow

Participants by arm

ArmCount
Conventional Dispatcher CPR
patients enrolled in period that conventional dispatcher CPR was provided to the patients.
1,498
NAD-CPR
patients enrolled in period that NAD-CPR was provided to the patients.
1,696
Total3,194

Baseline characteristics

CharacteristicConventional Dispatcher CPRTotalNAD-CPR
Age, Continuous71 years72 years72 years
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
South Korea
1498 Participants3194 Participants1696 Participants
Sex: Female, Male
Female
532 Participants1109 Participants577 Participants
Sex: Female, Male
Male
966 Participants2085 Participants1119 Participants
TM sent0 Participants598 Participants598 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
1,363 / 1,4981,480 / 1,696
other
Total, other adverse events
0 / 1,4980 / 1,696
serious
Total, serious adverse events
1,363 / 1,4981,480 / 1,696

Outcome results

Primary

Number of Participants Surviving at Hospital Discharge

we compared the survival to discharge rate between before intervention period and intervention period. Survival to discharge checked at the discharge point of hospital.

Time frame: discharge time from first admission from emergency department within 2 month

Population: Study population excluding exclusion criteria

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Conventional Dispatcher CPRNumber of Participants Surviving at Hospital Discharge135 Participants
NAD-CPRNumber of Participants Surviving at Hospital Discharge216 Participants
Secondary

Number of Participants With Good Neurological Recovery

Cerebral performance category 1 or 2 is defined as good neurological recovery. we compared the good neurological recovery rate between before intervention period and intervention period.

Time frame: discharge time from first admission from emergency department within 2 month

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Conventional Dispatcher CPRNumber of Participants With Good Neurological Recovery68 Participants
NAD-CPRNumber of Participants With Good Neurological Recovery140 Participants
Secondary

Number of Participants With Pre-Hospital Return of Spontaneous Circulation (ROSC)

we compared the Pre-hospital return of spontaneous circulation (ROSC) rate between before intervention period and intervention period.

Time frame: hospital arriving time from ambulance within 2 hours

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Conventional Dispatcher CPRNumber of Participants With Pre-Hospital Return of Spontaneous Circulation (ROSC)107 Participants
NAD-CPRNumber of Participants With Pre-Hospital Return of Spontaneous Circulation (ROSC)223 Participants

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026