Compression Only CardioPulmonary Resuscitation in telephone-assisted bystanders (COCPR III)
Not Applicable
Completed
- Conditions
- Cardiopulmonary resuscitationCirculatory System
- Registration Number
- ISRCTN82728488
- Lead Sponsor
- Medical University of Vienna (Austria)
- Brief Summary
1. 2015 results in https://www.ncbi.nlm.nih.gov/pubmed/29094836 (added 21/01/2019)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 36
Inclusion Criteria
1. Voluntary participants
2. Informed consent
3. Age over 18 years
4. Blood pressure less than 160 mmHg (systolic) before starting CPR simulation
Exclusion Criteria
1. Healthcare professionals
2. Basic Life Support course performed within the last 6 months
3. Pregnancy
4. Blood pressure over 150 mm Hg (systolic) before starting CPR simulation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Chest compression depth, measured continously via the pc skillmeter software of the Resusci® Anne skillmeter
- Secondary Outcome Measures
Name Time Method <br> 1. Quality of ECC defined as number of percent of adequately achieved compression depth, continously assesed via skillmeter pc<br> 2. Time to measurable decay in chest compression depth, continously assesed via skillmeter pc<br> 3. Frequency of chest compression, continously assesed via skillmeter pc<br> 4. Correct recoiling of the manikin's chest, continously assesed via skillmeter pc<br> 5. Heart rate/systolic blood pressure ratio reflecting physical strain, measured before and immediately after chest compression<br> 6. BORG rate of perceived exertion measured at 2nd, 4th, 6th and 10th minute of chest compressions<br> 7. Systolic and diastolic blood pressure, measured before and immediately after chest compression<br> 8. Nine Hole Peg Test, measured before and immediately after chest compression<br>