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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02998307
Other study ID # 16-010
Secondary ID
Status Completed
Phase N/A
First received December 13, 2016
Last updated March 13, 2018
Start date April 2016
Est. completion date January 8, 2018

Study information

Verified date March 2018
Source Health Sciences North
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Canada Health Sciences North Sudbury Ontario

Sponsors (3)

Lead Sponsor Collaborator
Health Sciences North Royal College of Physicians and Surgeons of Canada, University of Calgary

Country where clinical trial is conducted

Canada, 

Outcome

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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