Behavioral Economic & Staffing Strategies for Critical Illness
(BEST-ICU Trial)
Trial Summary
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications.
What data supports the effectiveness of the treatment Realtime audit and feedback, Real-time audit and feedback, Audit and feedback strategy, RN Implementation Facilitator, Registered Nurse Implementation Facilitator, RN Implementation Facilitator?
Is the audit and feedback strategy safe for humans?
How does the treatment in the 'Behavioral Economic & Staffing Strategies for Critical Illness' trial differ from other treatments for critical illness?
This treatment is unique because it focuses on using audit and feedback strategies to improve healthcare practices in the ICU, rather than relying on traditional medical interventions. It aims to enhance the quality of care by providing healthcare professionals with performance feedback and suggested actions to bridge the gap between intention and behavior.13111213
What is the purpose of this trial?
The overarching goal of this study is to support the "real world" assessment of strategies used to foster adoption of several highly efficacious evidence-based practices in healthcare systems that provide care to critically ill adults with known health disparities. Investigators will specifically evaluate two discrete strategies grounded in behavioral economic and implementation science theory (i.e., real-time audit and feedback and registered nurse implementation facilitation) to increase adoption of the ABCDEF bundle in critically ill adults.
Research Team
Michele C Balas, PhD, RN
Principal Investigator
University of Nebraska
Eligibility Criteria
This trial is for adults over 19 who are admitted to the ICU, have been on a ventilator there, and stayed at least 24 hours. It's not for patients already on long-term ventilation from home or care facilities, nor prisoners.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Implementation Phase
ICUs receive either real-time audit and feedback or a Registered Nurse implementation facilitator to increase adoption of the ABCDEF bundle
Follow-up
Implementation and clinical outcomes are collected for an additional 3 months to evaluate the effects of removing the implementation strategies
Treatment Details
Interventions
- Realtime audit and feedback
- RN Implementation Facilitator
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Nebraska
Lead Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Collaborator
Ohio State University
Collaborator
University of Wisconsin, Madison
Collaborator
University of Iowa
Collaborator