Does Instruction on Cognitive Aid Use Improve Performance and Retention of Skills?
This study is currently recruiting participants.
Verified July 2012 by Ottawa Hospital Research Institute
Sponsor:
Ottawa Hospital Research Institute
Collaborators:
The Academy for Innovation in Medical Education
The Ottawa Hospital Academic Medical Organization
Information provided by (Responsible Party):
Daniel Power, Ottawa Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT01646372
First received: July 16, 2012
Last updated: July 19, 2012
Last verified: July 2012
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Long-term Retention of Advanced Cardiac Life Support Skills |
Other: Standard Simulation Based ACLS Refresher Teaching Other: Cognitive Aid based ACLS Refresher training |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Outcomes Assessor) |
| Official Title: | Does Instruction on Cognitive Aid Use Improve Performance and Retention of Skills? A Simulation Based Randomized Controlled Trial |
Further study details as provided by Ottawa Hospital Research Institute:
Primary Outcome Measures:
- ACLS Megacode Examination Scale Score [ Time Frame: 6 months ] [ Designated as safety issue: No ]Simulated scenarios will be videotaped. These will be scored according to the ACLS megacode testing checklist by trained video raters
Secondary Outcome Measures:
- Anesthesia Non-Technical Skills Scale (ANTS) [ Time Frame: 6 Months ] [ Designated as safety issue: No ]Simulated Scenarios will be videotaped. Videos will be scored by trained raters according to the validated Anesthesia Nontechnical Skills Scale.
| Estimated Enrollment: | 66 |
| Study Start Date: | July 2012 |
| Estimated Primary Completion Date: | January 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
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.
|
Other: Standard Simulation Based ACLS Refresher Teaching
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.
|
Other: Standard Simulation Based ACLS Refresher Teaching
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
|
Other: Cognitive Aid based ACLS Refresher training
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.
|
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
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
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01646372
Contacts
| Contact: Daniel J Power, MD | 613-7980-5555 ext 15927 | dapower@toh.on.ca |
Locations
| Canada, Ontario | |
| The Ottawa Hospital | Recruiting |
| Ottawa, Ontario, Canada, K1Y 4E9 | |
| Contact: Daniel J Power, MD 613-798-5555 ext 15927 dapower@toh.on.ca | |
| Principal Investigator: Daniel J Power, MD | |
Sponsors and Collaborators
Ottawa Hospital Research Institute
The Academy for Innovation in Medical Education
The Ottawa Hospital Academic Medical Organization
More Information
No publications provided
| Responsible Party: | Daniel Power, Assistant Professor of Anesthesiology, Ottawa Hospital Research Institute |
| ClinicalTrials.gov Identifier: | NCT01646372 History of Changes |
| Other Study ID Numbers: | OHRI-20120006 |
| Study First Received: | July 16, 2012 |
| Last Updated: | July 19, 2012 |
| Health Authority: | Canada: Ethics Review Committee |
Keywords provided by Ottawa Hospital Research Institute:
|
Medical Education Cognitive Aid Crisis Resource Management Advanced Cardiac Life Support Skills Retention |
Additional relevant MeSH terms:
|
Urinary Retention Urination Disorders Urologic Diseases |
ClinicalTrials.gov processed this record on May 23, 2013