- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04572048
Longitudinal One Year vs Single Day NRP Training.
November 20, 2023 updated by: Ahmed Moussa
Longitudinal One Year vs Single Day NRP Training: A Randomized Controlled Trial.
The Neonatal Resuscitation Program (NRP) recommends providers renew their certification every 2 years.
However, many Neonatal Intensive Care Units (NICUs) in Canada face challenges of significant budget cuts in training and a large number of caregivers to train with a high turnover rate.
This situation makes it difficult for managers and nurse educators to ensure up-to-date certification and competence for all clinical staff.
In addition, considering that only 0.1% of newborns will require cardiac massage and/or epinephrine, health care professionals' exposure to critical events is low to insure maintenance of expertise.
Furthermore, it is shown that there is a significant decrease in knowledge among learners who have undergone specific training after only 3 months.
This is worrisome considering that some nurses will not renew their certification if the course is not paid for by the employer, or if they are not released from clinical duties to attend.
While keeping in mind the various required components of NRP training: book reading, online exam, performance stations, Integrated Skills Station Assessment (ISSA) and simulations, we would like to assess the educational and financial impact of a new educational strategy developed as to allow more nurses to be retrained thus ensuring maintenance of their neonatal resuscitation expertise.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
250
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ahmed Moussa, MD
- Phone Number: 3109 514-345-4931
- Email: ahmed.moussa@umontreal.ca
Study Contact Backup
- Name: Audrey Larone Juneau, M.Sc
- Phone Number: 4445 514-345-4931
- Email: audrey.larone.juneau.hsj@ssss.gouv.qc.ca
Study Locations
-
-
-
Montréal, Canada
- Recruiting
- Jewish General Hospital
-
Contact:
- Nina Nourayean
-
Québec, Canada
- Recruiting
- CHUL
-
Contact:
- Georges Caouette, MD
-
Repentigny, Canada
- Not yet recruiting
- Pierre-Legardeur
-
Contact:
- Ana Maria Preziosi
-
-
Quebec
-
Laval, Quebec, Canada
- Not yet recruiting
- Cité de la santé de Laval
-
Contact:
- Tania Giannone
-
Montreal, Quebec, Canada, H2X 3E4
- Recruiting
- University of Montreal Health Center
-
Contact:
- Wissal Ben Jmaa
- Phone Number: 514-890-8000
-
Montréal, Quebec, Canada, H3T 1C5
- Recruiting
- CHU Sainte-Justine, Dept Neonatology
-
Contact:
- Ahmed Moussa, MD
- Phone Number: 3109 514-345-4931
- Email: ahmed-moussa@hotmail.com
-
Principal Investigator:
- Ahmed Moussa, MD
-
Sherbrooke, Quebec, Canada, J1H 5N4
- Recruiting
- Université de Sherbrooke
-
Contact:
- Édith Masse, MD
- Phone Number: 74634 819-346-1110
- Email: Edith.Masse@USherbrooke.ca
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Newly recruited ( in the last 3 months) neonatal and delivery room registered nurses from level 2 and 3 perinatal centers
Exclusion Criteria:
- Registered nurses that have already completed a NRP training in the past.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Other: Single-day NRP training
This group will follow the single-day NRP training course that is currently the standard.
It usually takes 8 hours to complete this training course and the nurses are released from their clinical duty to attend the training course.
|
NRP training course completed in one single day of 8 hours
|
Experimental: Longitudinal one year NRP Training
This group will follow the longitudinal NRP training course.
The longitudinal NRP training course will consist of nine 30-minute modules that will be taught every 6-8 weeks over a period of one year.
The nurses will attend the different modules of the training course at their work place and during their work shift so they will have to be released from their clinical duty only 30 minutes at a time.
|
NRP training course completed over one year by attending nine 30-minute modules.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Knowledge
Time Frame: 1 year
|
Integrated Skills Stations Assessment Score.
The higher the score, the better the performance.
Scores range from 0 to 100 %.
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Confidence and behavior
Time Frame: 1 year
|
continuing professional development (CPD) reaction questionnaire (REACT).
The higher the score, the better the outcome.
Scores range from 12 to 82.
|
1 year
|
Cost-efficiency
Time Frame: 1 year
|
Cost of each educational intervention (each arm).
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2021
Primary Completion (Estimated)
January 1, 2025
Study Completion (Estimated)
January 31, 2025
Study Registration Dates
First Submitted
September 3, 2020
First Submitted That Met QC Criteria
September 27, 2020
First Posted (Actual)
October 1, 2020
Study Record Updates
Last Update Posted (Estimated)
November 21, 2023
Last Update Submitted That Met QC Criteria
November 20, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- MP-21-2020-2444
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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