- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02998307
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
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.
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ontario
-
Sudbury, Ontario, Canada, P3E 5J1
- Health Sciences North
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Monthly
Receive bedside CPR training monthly
|
Brief CPR assessment and training done during working hours with real-time performance feedback
|
EXPERIMENTAL: 3 months
Receive bedside CPR training every 3 months
|
Brief CPR assessment and training done during working hours with real-time performance feedback
|
EXPERIMENTAL: 6 months
Receive bedside CPR training every 6 months
|
Brief CPR assessment and training done during working hours with real-time performance feedback
|
NO_INTERVENTION: Control
No additional training and only performance evaluation after 1 year
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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. |
12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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.
|
12 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 16-010
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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