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OpenTrials
Completed

NCT Number: NCT02998307

Optimal Training Frequency for Attainment and Maintenance of High-quality CPR on a High-fidelity Manikin

Objectives: The primary objective is to determine the least frequent CPR training interval associated with continued performance of guideline-compliant CPR. The secondary objective is to determine whether certain physical characteristics, such as age, gender, exercise tolerance, height, and weight may be able to identify HCPs at high risk of being unable to perform high-quality CPR.

Design: Randomized trial to compare the effect of different training frequencies on long-term CPR performance.

Participants and setting: Nurses in all adult departments at Health Sciences North. Subjects will be randomly assigned to a group that undertakes short CPR assessment and training sessions either 1) every month, 2) every 3 months, 3) every 6 months, or 4) every 12 months (control group) over the course of a twelve-month period.

Analysis: The proportion of nurses in each group that is able to perform "excellent CPR" at the twelve-month time point will be determined. Excellent CPR is defined as a two-minute CPR session where 90% of compressions are performed with correct depth (50-60 mm), 90% with correct rate (100-120 /min), and 90% with full chest recoil. A subgroup analysis will also be performed where the demographic data of individuals who are unable to perform excellent CPR at the twelve-month time point regardless of intervention group are compared against those who are successful.

Conclusion: The results of our study will help determine the longest CPR training interval associated with maintenance of high-quality CPR skills to minimize training sessions required and decrease associated costs. The results will also generate hypotheses for future study about optimizing role assignments and team performance in resuscitation.

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Key information

Conditions

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Health Sciences North

Greater Sudbury, Ontario, P3E 5J1, Canada

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Practicing nurses from multiple clinical environments (operating room, intensive care unit, emergency room, medical and surgical wards) at Health Sciences North.

Exclusion criteria

  • Refusal to participate

Treatment and study plan

CPR Training

Procedure

Brief CPR assessment and training done during working hours with real-time performance feedback

Primary outcomes

  1. Proportion of nurses in each group able to perform "excellent CPR" after completing CPR training programs of various frequencies

    Time frame: 12 months

    "Excellent CPR" is a dichotomous variable achieved if 90% of compressions are performed with correct depth (50-60 mm), 90% with correct rate (100-120 /min), and 90% with full chest recoil.

    The proportion of nurses in each group able to perform "excellent CPR" after completing CPR training programs of various frequencies.

Secondary outcomes

  1. Predictors of inability to perform high-quality CPR

    Time frame: 12 months

    Comparison of the following factors in participants able to perform "excellent CPR" and those who are not at the twelve-month time point: percentage of participants who are female or have self-declared shortness of breath when climbing two flights of stairs, and average age, height and weight.

Sponsors and collaborators

Lead sponsor

Health Sciences North

Other

Collaborators

  • Royal College of Physicians and Surgeons of Canada
  • University of Calgary

Registry information

Official study title

Optimal Serial Training Frequency for Attainment and Maintenance of High Quality CPR Using Real-Time Automated Performance Feedback Combined With Verbal Feedback From a CPR Instructor

Important dates

Study start
2016
Primary completion
2017
Study completion
2018
First posted
Dec 20, 2016
Registry last updated
Mar 15, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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