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RN Implementation Facilitator for Mechanical Ventilation Complication (BEST-ICU Trial)
N/A
Waitlist Available
Led By Michele C Balas, PhD, RN
Research Sponsored by University of Nebraska
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Received invasive mechanical ventilation while in the ICU
ICU length of stay of at least 24 hours
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 27 months
Awards & highlights
BEST-ICU Trial Summary
This trial aims to evaluate different strategies that can be used to help healthcare systems adopt effective practices for treating critically ill adults with known health disparities. The two strategies being studied are real-time audit and feedback,
Who is the study for?
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.Check my eligibility
What is being tested?
The study tests two strategies in ICUs: real-time audit and feedback plus nurse-led implementation facilitation. The goal is to see if these improve the use of ABCDEF bundle practices among critically ill adults.See study design
What are the potential side effects?
Since this trial focuses on adoption of care practices rather than medication, traditional side effects aren't applicable. However, there may be indirect effects related to changes in ICU management protocols.
BEST-ICU Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I was on a breathing machine in the ICU.
Select...
I have stayed in the ICU for at least 24 hours.
Select...
I was older than 19 when I was admitted to the ICU.
BEST-ICU Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 27 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~27 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Proportional ABCDEF bundle performance
Secondary outcome measures
Complete ABCDEF bundle performance
Duration of mechanical ventilation
Other outcome measures
Days with significant pain
Discharge destination
ICU days with acute brain dysfunction
+18 moreBEST-ICU Trial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: RN Implementation FacilitatorExperimental Treatment1 Intervention
ICUs receive a extra RN who help facilitate ABCDEF bundle implementation
Group II: Audit and FeedbackExperimental Treatment1 Intervention
ICUs receive electronic dashboard that display realtime ABCDEF bundle performance data
Group III: Usual careActive Control1 Intervention
Usual ICU care
Find a Location
Who is running the clinical trial?
University of NebraskaLead Sponsor
540 Previous Clinical Trials
1,136,658 Total Patients Enrolled
Ohio State UniversityOTHER
832 Previous Clinical Trials
497,805 Total Patients Enrolled
4 Trials studying Mechanical Ventilation Complication
258 Patients Enrolled for Mechanical Ventilation Complication
University of Wisconsin, MadisonOTHER
1,190 Previous Clinical Trials
3,161,527 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are researchers currently enrolling participants for this medical study?
"According to the information provided on clinicaltrials.gov, this particular study is not currently recruiting participants. Its initial posting date was April 1st, 2024, and it was last edited on December 13th, 2023. However, it's worth noting that there are presently 704 other studies actively seeking eligible individuals for participation."
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