- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02529215
Improving Team Training During Mock Code Blue Simulations
February 24, 2021 updated by: Catharine Walsh, The Hospital for Sick Children
Improving the Quality of Team Training and Performance During Interprofessional in Situ Mock Code Blue Simulations: A Randomized Controlled Mixed-methods Study
Communication and teamwork failures are the leading causes of errors in healthcare settings.
In situ mock code simulations are a potential means to train team-based skills using simulation within real clinical care environments where errors occur; however, debriefing discussions often focus on gaps in learners' clinical skills as opposed to team functioning.
This study aims to determine whether learners who are pre-trained using just-in-time simulation regarding CPR quality and medication administration will exhibit improved performance with respect to these skills during in situ mock codes as well as improved team functioning.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
264
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 Locations
-
-
Ontario
-
Toronto, Ontario, Canada, M5G 1X8
- Hospital for Sick Children (Sickkids)
-
-
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
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Health professionals, including nurses, pediatric residents, physicians and/or respiratory therapists scheduled to participate in interprofessional, team-based in situ mock codes.
Exclusion Criteria:
- None
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 |
---|---|
Experimental: Just-in-time training (JITT) group
Receive a 20min just-in-time simulation-based teaching session targeting: (1) CPR quality and (2) medication administration within 3 hours of the scheduled in situ simulation.
|
The JITT training is a 20 minute simulation-based teaching session targeting: (1) CPR quality and (2) medication administration.
|
No Intervention: No additional training (control) group
Control group who receives no additional training.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Team-based non-technical skills
Time Frame: Time Frame: All data will be collected during the one hour when participants engage in the in situ mock code simulation
|
Measured using the Team Emergency Assessment Measure (TEAM) scale
|
Time Frame: All data will be collected during the one hour when participants engage in the in situ mock code simulation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
CPR quality
Time Frame: Time Frame: All data will be collected during the one hour when participants engage in the in situ mock code simulation
|
Measured using the Zoll R series defibrillator (compressions per minute (cpm), depth in millimeters (mm), and compression fraction)
|
Time Frame: All data will be collected during the one hour when participants engage in the in situ mock code simulation
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Medication errors
Time Frame: Time Frame: All data will be collected during the one hour when participants engage in the in situ mock code simulation
|
Time Frame: All data will be collected during the one hour when participants engage in the in situ mock code simulation
|
|
Focus of debriefing
Time Frame: Time Frame: All data will be collected during the one hour when participants engage in the in situ mock code simulation
|
Qualitative analysis of audio-recordings
|
Time Frame: All data will be collected during the one hour when participants engage in the in situ mock code simulation
|
Cognitive load
Time Frame: Time Frame: All data will be collected during the one hour when participants engage in the in situ mock code simulation
|
Measured using the Paas scale, Cognitive Load Component Questionnaire, and NASA-TLX cogntiive load questionnaires
|
Time Frame: All data will be collected during the one hour when participants engage in the in situ mock code simulation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Catharine M Walsh, MD, PhD, The Hospital for Sick Children
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
April 1, 2015
Primary Completion (Actual)
September 1, 2016
Study Completion (Anticipated)
December 1, 2021
Study Registration Dates
First Submitted
August 18, 2015
First Submitted That Met QC Criteria
August 19, 2015
First Posted (Estimate)
August 20, 2015
Study Record Updates
Last Update Posted (Actual)
February 25, 2021
Last Update Submitted That Met QC Criteria
February 24, 2021
Last Verified
February 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 1000048092
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.
Clinical Trials on Education, Simulation
-
Rigshospitalet, DenmarkWithdrawnEducation, Professional | Ultrasound Simulation | Simulation-based Medical Education
-
Université Paris-SudNot yet recruiting
-
Université Paris-SudActive, not recruitingSimulation | EducationFrance
-
Gregory WietNational Institute on Deafness and Other Communication Disorders (NIDCD)CompletedEducation | Computer SimulationUnited States
-
Johns Hopkins UniversityCompletedSurgical Simulation Education
-
St. Justine's HospitalCHU de Quebec-Universite Laval; Université de Sherbrooke; Jewish General Hospital and other collaboratorsCompletedIntubation | Education | Simulation TrainingCanada
-
University Hospital, AngersUnknownEducation | Simulation Training | IVfFrance
-
Rigshospitalet, DenmarkTechnical University of DenmarkCompletedSimulation Training | Education, MedicalDenmark
-
Royal College of Surgeons, IrelandHealth Service ExecutiveUnknownTraining | Education | Computer SimulationIreland
-
Odense University HospitalCompletedSimulation | Endoscopy | Education | GastroscopyDenmark
Clinical Trials on Just-in-time training (JITT)
-
St. Justine's HospitalCHU de Quebec-Universite Laval; Université de Sherbrooke; Jewish General Hospital and other collaboratorsCompletedIntubation | Education | Simulation TrainingCanada
-
Children's Hospital of PhiladelphiaAgency for Healthcare Research and Quality (AHRQ)Completed
-
Virginia MoyerAgency for Healthcare Research and Quality (AHRQ)CompletedPatient DischargeUnited States
-
Florida International UniversityNot yet recruitingAttention Deficit Hyperactivity DisorderUnited States
-
Wageningen University and ResearchZonMw: The Netherlands Organisation for Health Research and DevelopmentCompleted
-
University of Alabama, TuscaloosaUniversity of Alabama at BirminghamUnknownCancer | Aging | Comorbidities and Coexisting Conditions
-
University of MichiganNational Institute on Drug Abuse (NIDA)Recruiting
-
University of MichiganNational Institute of Nursing Research (NINR)CompletedCaregiversUnited States
-
University of MichiganNational Center for Advancing Translational Sciences (NCATS)CompletedCaregiversUnited States
-
University of MichiganNational Heart, Lung, and Blood Institute (NHLBI)RecruitingHypertension | Blood PressureUnited States