Simulation Training Clinical Trial
Official title:
Optimal Serial Training Frequency for Attainment and Maintenance of High Quality CPR Using RealāTime Automated Performance Feedback Combined With Verbal Feedback From a CPR Instructor
Verified date | March 2018 |
Source | Health Sciences North |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 244 |
Est. completion date | January 8, 2018 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility |
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 |
Country | Name | City | State |
---|---|---|---|
Canada | Health Sciences North | Sudbury | Ontario |
Lead Sponsor | Collaborator |
---|---|
Health Sciences North | Royal College of Physicians and Surgeons of Canada, University of Calgary |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Proportion of nurses in each group able to perform "excellent CPR" after completing CPR training programs of various frequencies | "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. |
12 months | |
Secondary | Predictors of inability to perform high-quality CPR | 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. | 12 months |
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