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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02998307
Enrollment
244
Registered
2016-12-20
Start date
2016-04-30
Completion date
2018-01-08
Last updated
2018-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Simulation Training

Brief summary

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.

Interventions

PROCEDURECPR Training

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

Sponsors

Royal College of Physicians and Surgeons of Canada
CollaboratorOTHER
University of Calgary
CollaboratorOTHER
Health Sciences North
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Proportion of nurses in each group able to perform excellent CPR after completing CPR training programs of various frequencies12 monthsExcellent 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

MeasureTime frameDescription
Predictors of inability to perform high-quality CPR12 monthsComparison 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.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026