Completed
NCT Number: NCT02010658
Effect of Cognitive Aid on Adherence to Perioperative Guidelines
The objective of this prospective randomized trial is to ascertain whether the use of a cognitive aid improves adherence to best published practices for the management of simulated patients regarding perioperative cardiac evaluation and management.
Completed
Looking for future studies?
Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Any active resident or faculty member will be allowed to volunteer.
Exclusion criteria
There are no exclusion criteria (notably we will include residents on academic probation)
Treatment and study plan
Primary outcomes
-
Adherence of ACC/AHA Guideline
Time frame: Up to 6 weeks
Adherence in terms of selection of the correct option for multiple choice question.
Sponsors and collaborators
Lead sponsor
Medical University of South Carolina
Other
Collaborators
- Brigham and Women's Hospital
- University of Kentucky
- University of North Carolina, Chapel Hill
- Vanderbilt University
Registry information
Important dates
- Study start
- 2013
- Primary completion
- 2013
- Study completion
- 2013
- First posted
- Dec 13, 2013
- Registry last updated
- Dec 12, 2023
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.