- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03894644
Simulation-based Learning for Neurosurgical Instruments in Perioperative Nurses
Knowledge Transfer and Retention of Simulation-based Learning for Neurosurgical Instruments: a Randomized Trial of 100 Perioperative Nurses
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Simulation-based learning is designed to engage, challenge and enrich the learner's knowledge base and skill set. It presents the opportunity to experience a variety of clinical scenarios, both common and uncommon, in a safe environment allowing repeated skills training and facilitating the transfer of classroom-knowledge to real situations.Research demonstrates that simulation can improve student engagement and learning and is being increasingly used as an educational strategy for nursing students. This prospective randomized controlled study that was undertaken with the following goals:
- to investigate the effectiveness of simulation-based training in a large sample of perioperative nurses, measured as nurses' learning progress in the simulation environment;
- to determine whether the learning acquired through this training is transferable to recognizing real surgical instruments; and
- to evaluate whether simulation-based learning is retained at least one week.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Perioperative nurse
- Employed at Queen Elizabeth II Health Sciences Center
Exclusion Criteria:
-Unable to provide informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group A: simulation training before instruments
Group A performed simulation training before the recognition of real surgical instruments.
|
The intervention involves three consecutive sessions of the PeriopSim™ Instrument Trainer, followed by two consecutive sessions of the PeriopSim™ for Burr Hole Surgery (https://periopsim.com).
|
|
Active Comparator: Group B:instruments before simulation training
Group B performed the recognition of real surgical instruments without prior simulation training.
|
The intervention involves three consecutive sessions of the PeriopSim™ Instrument Trainer, followed by two consecutive sessions of the PeriopSim™ for Burr Hole Surgery (https://periopsim.com).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in time saved for simulation task
Time Frame: Day 1 and Day 7
|
Time saved is defined as the duration in seconds from the time the participant correctly submits an instrument prior to the maximum allotted time.
Change is measured over repeated sessions on Day 1 and Day 7.
|
Day 1 and Day 7
|
|
Change in number of errors for simulation task
Time Frame: Day 1 and Day 7
|
Number of errors are counted as the number of incorrectly selected instruments on the first attempt.
Change is measured over repeated sessions on Day 1 and Day 7.
|
Day 1 and Day 7
|
|
Change in total score for simulation task
Time Frame: Day 1 and Day 7
|
Total score is a gamification-based algorithm dependent upon the number of correct responses in the first attempt and time saved.
Change is measured over repeated sessions on Day 1 and Day 7.
|
Day 1 and Day 7
|
|
Difference in total score for knowledge transfer task
Time Frame: Day 7
|
Score is defined as the number of correctly identified instruments from the instrument tray during the instrument recognition task.
The difference in score is measured between arms.
|
Day 7
|
|
Difference in time for knowledge transfer task
Time Frame: Day 7
|
Time is the number of seconds (to a maximum of 45) taken to complete the real instrument task.
The difference in score is measured between arms.
|
Day 7
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: David Clarke, NSHA
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
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
- 100 Nurses
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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