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Effect of Cognitive Aid on Adherence to Perioperative Guidelines

NCT ID: NCT02010658

Last Updated: 2023-12-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

111 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-04-30

Study Completion Date

2013-07-31

Brief Summary

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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.

Detailed Description

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Conditions

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Perioperative Decision Making

Study Design

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Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Study Groups

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Memory

Group Type NO_INTERVENTION

No interventions assigned to this group

Cognitive Aid

Group Type EXPERIMENTAL

Cognitive Aid

Intervention Type OTHER

Interventions

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Cognitive Aid

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Any active resident or faculty member will be allowed to volunteer.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of North Carolina, Chapel Hill

OTHER

Sponsor Role collaborator

Brigham and Women's Hospital

OTHER

Sponsor Role collaborator

University of Kentucky

OTHER

Sponsor Role collaborator

Vanderbilt University

OTHER

Sponsor Role collaborator

Medical University of South Carolina

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Scott T Reeves, MD

Role: STUDY_CHAIR

Medical University of South Carolina

Other Identifiers

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Pro00018749

Identifier Type: -

Identifier Source: org_study_id