NCT01397656

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. 1.The achieved frequency and depth of chest compressions, and
  2. 2.Participant rating of their perceived level of exertion.
  3. 3.less frequent and shallower chest compressions over the 5-minute study period; and
  4. 4.higher rating of perceived level of exertion when compared to the 2005 30:2 CPR ratio.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
63

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jul 2011

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 13, 2011

Completed
18 days until next milestone

Study Start

First participant enrolled

July 1, 2011

Completed
18 days until next milestone

First Posted

Study publicly available on registry

July 19, 2011

Completed
13 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2011

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2011

Completed
7.2 years until next milestone

Results Posted

Study results publicly available

November 15, 2018

Completed
Last Updated

November 15, 2018

Status Verified

June 1, 2017

Enrollment Period

1 month

First QC Date

June 13, 2011

Results QC Date

January 20, 2017

Last Update Submit

April 13, 2018

Conditions

Keywords

cardiac arrestCPRresuscitationfatiguequality

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 COMPARATOR

30 chest compressions to 2 ventilations followed by cross-over to CPR with Continuous Compressions

Procedure: CPR using 30:2 ratio

CPR with Continuous Compressions

ACTIVE COMPARATOR

Continuous Chest Compressions without ventilation followed by CPR 30:2 (30 chest compressions to 2 ventilations)

Procedure: CPR using continuous compressions

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.

Also known as: cardiopulmonary resuscitation
CPR 30:2

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.

Also known as: cardiopulmonary resuscitation
CPR with Continuous Compressions

Eligibility Criteria

Age55 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

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: 20947241BACKGROUND
  • Liu 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.

MeSH Terms

Conditions

Heart ArrestFatigue

Interventions

Cardiopulmonary Resuscitation

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

ResuscitationEmergency TreatmentTherapeutics

Results Point of Contact

Title
Dr. Christian Vaillancourt
Organization
Ottawa Hospital Research Institute

Study Officials

  • Christian Vaillancourt, MD, MSc

    Ottawa Hospital Research Institute

    PRINCIPAL INVESTIGATOR

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

Locations