QCPR: Improving the Quality of Cardiopulmonary Resuscitation (CPR) During Pediatric Cardiac Arrest

Sponsor
Express Collaborative (Other)
Overall Status
Completed
CT.gov ID
NCT02075450
Collaborator
Canadian Institutes of Health Research (CIHR) (Other), Heart and Stroke Foundation of Canada (Other)
324
11
4
36
29.5
0.8

Study Details

Study Description

Brief Summary

Our project aims to improve the delivery and assessment of cardiopulmonary resuscitation (CPR) during pediatric cardiac arrest by introducing 2 novel approaches: 1. We will evaluate the effectiveness of a novel, credit card sized, and highly affordable "nano-card" CPR visual feedback device to improve compliance with HSFC CPR guidelines when used during simulated pediatric cardiac arrest; 2. We will also develop and study a novel, "Just-in-Time" (JIT) CPR training video, integrating proven educational methods (video-based lecture, expert modeling, practice-while-watching), and use the CPR visual feedback device to provide real-time coaching.

We hypothesize that:

H1: The use of a CPR visual feedback device will improve compliance with current HSFC CPR and resuscitation guidelines during a simulated pediatric in-hospital cardiac arrest scenario compared with standard CPR with no visual feedback.

H2: A JIT CPR Training Video, viewed by healthcare providers 2-4 weeks prior to the resuscitation event, will improve compliance with current HSFC CPR and resuscitation guidelines during simulated pediatric cardiac arrest compared with those healthcare providers with no prior exposure to the JIT CPR Training Video.

H3: That there is poor correlation between providers' perception of CPR quality and actual measured CPR quality H4: That task load varies depending on provider role and type of clinical scenario

Condition or Disease Intervention/Treatment Phase
  • Device: CPRcard
  • Other: Just in Time Video
N/A

Detailed Description

Aim 1 - To evaluate the effectiveness of a CPR visual feedback device to improve compliance with current Heart and Stork Foundation of Canada (HSFC) CPR and resuscitation guidelines during simulated pediatric cardiac arrest for a team of healthcare providers.

Aim 2 - To evaluate the effectiveness of a "Just in Time" CPR Training Video to improve compliance with current HSFC CPR and resuscitation guidelines during simulated pediatric cardiac arrest for a team of healthcare providers.

Aim 3 - To determine if there is a synergistic effect when adding Just in Time CPR Training Video with the use of the CPR visual feedback device to improve compliance with current HSFC CPR and resuscitation guidelines during a simulated pediatric cardiac arrest scenario.

Aim 4 - To determine the degree to which provider's perception of CPR quality matches actual quality of CPR

Aim 5 - To describe the task load of healthcare providers in sepsis and cardiac arrest scenarios

Participants will be recruited from ten pediatric tertiary care centers in Canada, the United States, and the United Kingdom using the methodology already piloted and studied in our existing EXPRESS investigators collaborative. Participants recruited to participate in the study will be asked to perform as members of a pediatric resuscitation team. Each team of healthcare providers will be randomized into one of four study arms. In study arm 1, resuscitation teams will participate in a simulated pediatric cardiac arrest scenario, and provide standard CPR without prior JIT training and blinded to any feedback from the CPR card during the scenario. Instead, the CPR card will be placed on the chest during compressions to collect real-time data, but the feedback lights on the card will be covered by black tape and thus, not visible to the members of the resuscitation team. In study arm 2, resuscitation teams will participate in the same scenario without prior JIT training, but provide chest compressions with the CPR card placed on the chest (and providing visual feedback) during compressions. In study arm 3, participants will be given a CPR card and asked to view the JIT training video. Following practice, they will be asked to participate in the simulated cardiac arrest scenario, and provide standard CPR without feedback from the CPR card. As in study arm 1, the CPR card will still be placed on the chest, but the feedback lights will be covered and not visible to the resuscitation team members. Finally, participants in study arm 4 will received JIT training prior to the simulated scenario, and have the CPR card in place during chest compressions to provide immediate visual feedback.

Study Design

Study Type:
Interventional
Actual Enrollment :
324 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Outcomes Assessor)
Official Title:
Assessing and Improving the Quality of Cardiopulmonary Resuscitation (CPR) Delivered During Simulated Pediatric Cardiac Arrest Using a Novel Pediatric CPR Feedback Device
Study Start Date :
Jul 1, 2012
Actual Primary Completion Date :
Jul 1, 2015
Actual Study Completion Date :
Jul 1, 2015

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Arm 1

Practice CPRcard lights not visible, Practice Just in Time Video - not provided to study participants, CPRcard lights not visible during study scenario

Experimental: Arm 2

Practice CPRcard light- not visible, Practice CPR Just in Time Video- not provided, CPRcard light visible during study scenario.

Device: CPRcard
CPR Card in place during chest compressions to provide immediate visual feedback.
Other Names:
  • CPRcard = CPR feedback device
  • Experimental: Arm 3

    Practice CPRcard light- visible, Practice Just in Time Video- watched by study participant, CPRcard light- not visible during study scenario.

    Other: Just in Time Video
    CPR Just in Time training video administered before the simulation case

    Experimental: Arm # 4

    Practice CPRcard visible and the study participants watch the Just in Time Video,CPRcard light visible during study scenario

    Device: CPRcard
    CPR Card in place during chest compressions to provide immediate visual feedback.
    Other Names:
  • CPRcard = CPR feedback device
  • Other: Just in Time Video
    CPR Just in Time training video administered before the simulation case

    Outcome Measures

    Primary Outcome Measures

    1. Chest Compression Depth [up to 6 months]

      Chest compression depth is considered shallow if <40 mm and deep if >49.99 mm. The proportion of Chest Compression with depth between 40 and 49.99 mm will be reported.

    Secondary Outcome Measures

    1. Chest Compression Rate [up to 6 months]

      Chest compression rates will be calculated for the entire episode. The proportion of time spent doing compressions between 90-110 compressions/min will be reported.

    Other Outcome Measures

    1. No Flow Fraction [up to 6 months]

      No flow time (time during cardiac arrest without chest compression delivery) will be calculated as the total scenario time minus the time with no chest compression delivery. No flow fraction (no flow fraction: proportion of cardiac arrest time without chest compression delivery) will be calculated as the no flow time divided by the total arrest time. In accordance with previous pediatric and adult CPR studies, pauses in chest compression delivery are defined as period of interruptions > 1.5 seconds.

    2. Residual Leaning Force [up to 6 months]

      Residual leaning force (grams) of delivered chest compression will be captured. The proportion of chest compression with excessive residual leaning force (>2500 grams) will be reported

    3. Frequency of Chest Compression Switches [up to 6 months]

      The number of chest compression provider switches will be recorded as the number of times there is a change in chest compression provider. A provider can be counted more than once if, in the interim, another provider has preformed chest compression of more than 1 minute before the same provider resumes compressions.

    4. Mean difference between perceived and actual quality of CPR [up to 6 months]

      As calculated by perceived performance minus actual performance, for depth and rate

    5. Accurate estimation of CPR quality [up to 6 months]

      As calculated by the absolute difference of less than 10% between perceived and actual quality of CPR, for depth and rate

    6. NASA TLX Score [up to 6 month]

      NASA TLX measures the perceived task load for healthcare providers. To be filled out by participants after each scenario

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Team Member: Pediatric healthcare providers, such as nurses, nurse practitioners, and residents (pediatric emergency medicine, anesthesia, family medicine)

    • Team Member: No prior experience with CPR feedback devices

    • Team Member: Basic Life Support, Pediatric Advanced Life Support or Advanced Cardiac Life Support certifications within the past two years

    • Team Leader: Residents (Year 2,3, or 4) in pediatrics, family medicine, anesthesia, emergency medicine training programs

    • Team Leader: fellows in pediatric emergency medicine, pediatric critical care or pediatric anesthesia sub specialty training programs, attending in-patient pediatricians.

    • Team Leader: No prior experience with CPR feedback devices

    • Team Leader: Pediatric Advanced Life Support in the past 2 years or are Pediatric Advanced Life Support instructors

    Exclusion Criteria:
    • Team Member and Leader: Previous experience using, teaching with, or learning with a CPR feedback device

    • Team Member and Leader: No Basic Life Support, Pediatric Advance Life Support or Adult Cardiac Life Support Certification

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Alabama at Birmingham Birmingham Alabama United States 35233
    2 Yale University Hospital New Haven Connecticut United States 06510
    3 Children's Memorial Hospital Chicago Chicago Illinois United States 60611
    4 John Hopkins Children's Hospital Baltimore Maryland United States 21287
    5 Columbia University Hospital New York New York United States 10032
    6 Hasbro Children's Hosptial Providence Rhode Island United States 02903
    7 Children's Medical Center of Dallas Dallas Texas United States 75235
    8 Alberta Children's Hosptial Calgary Alberta Canada T3B 6A8
    9 Jon Duff Edmonton Alberta Canada T6G 2L9
    10 Montreal Children's Hospital Montreal Quebec Canada H3H 1P3
    11 Bristol Royal Hospital for Children Bristol United Kingdom Bs2 8BJ

    Sponsors and Collaborators

    • Express Collaborative
    • Canadian Institutes of Health Research (CIHR)
    • Heart and Stroke Foundation of Canada

    Investigators

    • Study Chair: Vinay Nadkarni, MD, Children's Hospital of Philadelphia

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Express Collaborative
    ClinicalTrials.gov Identifier:
    NCT02075450
    Other Study ID Numbers:
    • E-23697
    First Posted:
    Mar 3, 2014
    Last Update Posted:
    Aug 19, 2015
    Last Verified:
    Aug 1, 2015
    Keywords provided by Express Collaborative
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 19, 2015