- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01646372
Does Instruction on Cognitive Aid Use Improve Performance and Retention of Skills?
April 26, 2017 updated by: Ottawa Hospital Research Institute
Does Instruction on Cognitive Aid Use Improve Performance and Retention of Skills? A Simulation Based Randomized Controlled Trial
The purpose of this study is to investigate whether formal instruction on the use of cognitive aids in managing a crisis will result in better longterm retention of knowledge and skills.
In particular, this study examines the impact of cognitive aid teaching on the Advanced Cardiac Life Support course.
Study Overview
Status
Completed
Study Type
Interventional
Enrollment (Actual)
55
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
-
Ottawa, Ontario, Canada, K1Y 4E9
- The Ottawa Hospital
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Post-graduate Medical trainee in departments of Anesthesia, Emergency Medicine, Critical Care, Family Medicine, Internal Medicine
- Has taken ACLS Course at least once
Exclusion Criteria:
- Never taken ACLS Course
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: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Control Group
This group gets a simulation based ACLS refresher as treatment, but no access to cognitive aids for any of the tests.
|
45min-1 hour time.
15 minutes didactic review of 2010 ACLS guidelines followed by practice simulated megacodes
|
Active Comparator: 2nd Control Group
This group receives a standard Simulation based ACLS refresher as the intervention, like the control group.
No mention is made of Cognitive Aids in the teaching, but they are available during the post-test and retention post-test.
|
45min-1 hour time.
15 minutes didactic review of 2010 ACLS guidelines followed by practice simulated megacodes
|
Experimental: Cognitive Aid Group
This group receives Cognitive Aid based teaching as the intervention.
They also have access to cognitive aids for post-test and retention post-test
|
45min-1 hour time.
15 minutes didactic review of 2010 ACLS guidelines followed by simulated ACLS megacode practice focused on the use of Cognitive Aids to guide management.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
ACLS Megacode Examination Scale Score
Time Frame: 6 months
|
Simulated scenarios will be videotaped.
These will be scored according to the ACLS megacode testing checklist by trained video raters
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Anesthesia Non-Technical Skills Scale (ANTS)
Time Frame: 6 Months
|
Simulated Scenarios will be videotaped.
Videos will be scored by trained raters according to the validated Anesthesia Nontechnical Skills Scale.
|
6 Months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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
July 1, 2012
Primary Completion (Actual)
October 31, 2016
Study Completion (Actual)
January 31, 2017
Study Registration Dates
First Submitted
July 16, 2012
First Submitted That Met QC Criteria
July 19, 2012
First Posted (Estimate)
July 20, 2012
Study Record Updates
Last Update Posted (Actual)
April 28, 2017
Last Update Submitted That Met QC Criteria
April 26, 2017
Last Verified
April 1, 2017
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- OHRI-20120006
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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