Quality of Cardiopulmonary Resuscitation Without and With Defibrillator Feedback
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Purpose
Quality of bystander cardiopulmonary resuscitation (CPR) affect patient survival. Quality of professional CPR on patients has not been studied in detail, but it is regularly reported that the quality when tested on manikins deteriorates dramatically within months after training. Automated direct feedback on CPR quality from manikins brings quality back within a couple of minutes. Similar feedback has been incorporated into a defibrillator which also monitors quality of CPR. We hypothesise that quality of professional clinical CPR improves with such feedback
| Condition | Intervention | Phase |
|---|---|---|
|
Cardiac Arrest |
Device: automated direct feedback on CPR from defibrillator |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Can the Quality of Cardiopulmonary Resuscitation Improve With Direct Online Feedback From the Defibrillator to the Rescuers on Their Resuscitation Efforts |
- fraction of time without CPR
- chest compression depth
- chest compression frequency
- chest compression/decompression duty cycle
- ventilation frequency
- rate of return of spontaneous circulation
| Estimated Enrollment: | 300 |
| Study Start Date: | March 2002 |
| Study Completion Date: | June 2006 |
Defibrillators which monitor quality of CPR via changes in thoracic impedance (for ventilation) and movement of the sternum employing an accelerometer (for chest compressions) will be employed in ambulances in Akershus county (Norway), Stockholm (Sweden) and London (UK). During phase 1 quality of CPR will be monitored without feedback from the defibrillator. During phase 2 the ambulance personnel will receive feedback via the defibrillator. During phase 3 the ambulance personnel will be retrained with particular attention to the quality problems that became apparent in phase 3.
Quality of CPR will be continuously recorded by the defibrillators and the data collected and sent via internet to Laerdal Medical. All other cardiac arrest data including survival will be recorded using standard datasets for cardiac arrest research as developed by a task force with members from the organisations in International Liaison Committee on resuscitation (Utstein guidelines). The data will be annotated and analyzed in detail by researchers at University of Oslo
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Cardiac arrest out-of-hospital
Exclusion Criteria:
- < 18 years old
Contacts and Locations| Norway | |
| Ulleval University Hospital | |
| Oslo, Norway, N-0407 | |
| Sweden | |
| Stockholm Ambulance Service | |
| Stockholm, Sweden | |
| United Kingdom | |
| London Ambulance Service | |
| London, United Kingdom | |
| Principal Investigator: | Petter A Steen | University of Oslo, Ulleval University Hospital |
More Information
Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| ClinicalTrials.gov Identifier: | NCT00138996 History of Changes |
| Other Study ID Numbers: | 402-01139, 2002-OSL-MDD-0009 (DNVeritas) |
| Study First Received: | August 29, 2005 |
| Last Updated: | August 24, 2007 |
| Health Authority: | Norway:National Committee for Medical and Health Research Ethics |
Keywords provided by University of Oslo:
|
cardiac arrest resuscitation quality feedback training |
Additional relevant MeSH terms:
|
Heart Arrest Heart Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on May 19, 2013