Bystander Fatigue and CPR Quality Using Continuous Compressions Versus 30:2 Compressions to Ventilation
Comparison of Bystander Fatigue and CPR Quality When Using the 2010 Continuous Chest Compression Versus the 2005 30:2 Chest Compression to Ventilation Resuscitation Guidelines for Laymen: A Randomized Crossover Trial
1 other identifier
interventional
63
1 country
1
Brief Summary
STUDY OBJECTIVES The overall goal of this study is to compare bystander fatigue and CPR quality after 5 minutes of continuous chest compressions versus the 2005 30:2 chest compression to ventilation Resuscitation Guidelines, in a population aged 55 or greater. More specifically, the investigators will compare each CPR ratio with regard to:
- 1.The achieved frequency and depth of chest compressions, and
- 2.Participant rating of their perceived level of exertion.
- 3.less frequent and shallower chest compressions over the 5-minute study period; and
- 4.higher rating of perceived level of exertion when compared to the 2005 30:2 CPR ratio.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jul 2011
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 13, 2011
CompletedStudy Start
First participant enrolled
July 1, 2011
CompletedFirst Posted
Study publicly available on registry
July 19, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2011
CompletedResults Posted
Study results publicly available
November 15, 2018
CompletedNovember 15, 2018
June 1, 2017
1 month
June 13, 2011
January 20, 2017
April 13, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
CPR Quality
Count of compressions at a depth over 2 inches
5 minutes
Secondary Outcomes (3)
Heart Rate
Assessed immediately before and after 5 minutes of CPR
Blood Pressure
Assessed immediately before and after 5 minutes of CPR
Borg Rating of Perceived Exertion Scale
Assessed immediately before and after 5 minutes of CPR
Study Arms (2)
CPR 30:2
ACTIVE COMPARATOR30 chest compressions to 2 ventilations followed by cross-over to CPR with Continuous Compressions
CPR with Continuous Compressions
ACTIVE COMPARATORContinuous Chest Compressions without ventilation followed by CPR 30:2 (30 chest compressions to 2 ventilations)
Interventions
Participants will begin performing CPR using a ratio of 30 compressions to 2 ventilations. Participants will then cross over to the other intervention and use continuous compressions.
Participants will begin performing CPR using continuous chest compressions. Participants will then cross-over to the other intervention arm and perform CPR using a ratio of 30 compressions to 2 ventilations.
Eligibility Criteria
You may qualify if:
- Male or female person aged 55 or older
- Must score 3 or less on the validated Clinical Frailty Scale
- Able to follow instructions in English or French
- Able to understand and give informed consent
You may not qualify if:
- Musculoskeletal condition precluding the ability to kneel down and perform CPR (e.g. severe arthritis, cast, wrist sprain, recent joint surgery)
- Cardiovascular condition precluding the ability to perform a moderate effort (e.g. myocardial infarction or cardiovascular procedure in the last 3 months, recurrent angina, chest pain under investigation)
- Pulmonary condition precluding the ability to perform a moderate effort (e.g. emphysema, severe asthma, pneumonia)
- Active communicable disease (e.g. tuberculosis, meningitis, gastro enteritis, hepatitis A or B, herpes simplex)
- Inability to perform chest compressions at appropriate rate and depth despite positive feedback during one to two-minute practice session
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Ottawa Hospital, Civic Campus
Ottawa, Ontario, K1Y4E9, Canada
Related Publications (2)
Vaillancourt C, Midzic I, Taljaard M, Chisamore B. Performer fatigue and CPR quality comparing 30:2 to 15:2 compression to ventilation ratios in older bystanders: A randomized crossover trial. Resuscitation. 2011 Jan;82(1):51-6. doi: 10.1016/j.resuscitation.2010.09.003. Epub 2010 Oct 14.
PMID: 20947241BACKGROUNDLiu S, Vaillancourt C, Kasaboski A, Taljaard M. Bystander fatigue and CPR quality by older bystanders: a randomized crossover trial comparing continuous chest compressions and 30:2 compressions to ventilations. CJEM. 2016 Nov;18(6):461-468. doi: 10.1017/cem.2016.373. Epub 2016 Sep 21.
PMID: 27650514RESULT
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Results Point of Contact
- Title
- Dr. Christian Vaillancourt
- Organization
- Ottawa Hospital Research Institute
Study Officials
- PRINCIPAL INVESTIGATOR
Christian Vaillancourt, MD, MSc
Ottawa Hospital Research Institute
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 13, 2011
First Posted
July 19, 2011
Study Start
July 1, 2011
Primary Completion
August 1, 2011
Study Completion
September 1, 2011
Last Updated
November 15, 2018
Results First Posted
November 15, 2018
Record last verified: 2017-06