- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02010151
Dispatcher-Activated Neighborhood Access Defibrillation and Cardiopulmonary Resuscitation
March 16, 2020 updated by: Sang Do Shin, Seoul National University Hospital
Population Based Intervention Trial of Dispatcher-Activated Neighborhood Access Defibrillation and Cardiopulmonary Resuscitation
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).
Study Overview
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.
Study Type
Interventional
Enrollment (Actual)
3194
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Seoul, Korea, Republic of
- Seoul Metropolitan City
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
15 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: NAD-CPR
When dispatcher detects a patient with OHCA, the dispatcher activates trained neighborhoods by informing events nearby using short message service via cellular phone.
The neighborhood within geographically accessible area who could perform effective CPR and defibrillation would be alerted with event of OHCA and the nearest AED.
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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.
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No Intervention: Conventional dispatcher assisted CPR
When dispatcher detects OHCA, they instruct the caller with CPR instructions.
This is conventional dispatcher assisted CPR performed in Seoul.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Participants Surviving at Hospital Discharge
Time Frame: discharge time from first admission from emergency department within 2 month
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we compared the survival to discharge rate between before intervention period and intervention period. Survival to discharge checked at the discharge point of hospital. |
discharge time from first admission from emergency department within 2 month
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Participants With Pre-Hospital Return of Spontaneous Circulation (ROSC)
Time Frame: hospital arriving time from ambulance within 2 hours
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we compared the Pre-hospital return of spontaneous circulation (ROSC) rate between before intervention period and intervention period.
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hospital arriving time from ambulance within 2 hours
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Number of Participants With Good Neurological Recovery
Time Frame: discharge time from first admission from emergency department within 2 month
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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.
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discharge time from first admission from emergency department within 2 month
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Sang Do Shin, MD, PhD, Seoul National University Hospital
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2015
Primary Completion (Actual)
December 1, 2017
Study Completion (Actual)
December 1, 2017
Study Registration Dates
First Submitted
December 9, 2013
First Submitted That Met QC Criteria
December 9, 2013
First Posted (Estimate)
December 12, 2013
Study Record Updates
Last Update Posted (Actual)
March 30, 2020
Last Update Submitted That Met QC Criteria
March 16, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SNUEMS201309
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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