ICU Delirium Clinical Trial
— ABCDEOfficial title:
Awakening-Breathing Coordination, Delirium Monitoring/Management & Early Mobility (ABCDE) Protocol
NCT number | NCT01413009 |
Other study ID # | 0590-10-FB |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | December 29, 2010 |
Est. completion date | June 1, 2013 |
Verified date | September 2023 |
Source | University of Nebraska |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Fully two-thirds of ICU patients develop delirium, which is associated with longer stays, billions of dollars in costs globally, and 3-fold excess mortality at 6 months. Over one-half of ICU survivors suffer a functionally debilitating dementia-like illness, which appears related to delirium duration. This study will focus on applying Awakening-Breathing Coordination, Delirium Monitoring/Management & Early Mobility (ABCDE), a program of delirium screening, prevention, and treatment developed at Vanderbilt University. Specifically, the study will implement the ABCDE program in a medical center that does not currently perform routine ICU delirium screenings and identify facilitators and barriers to program adoption; test the impact of the ABCDE program on patient outcomes, nursing quality outcomes, and system outcomes; and assess the extent to which ABCDE implementation is effective, sustainable, and conducive to dissemination into other settings.
Status | Completed |
Enrollment | 200 |
Est. completion date | June 1, 2013 |
Est. primary completion date | April 1, 2012 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years and older |
Eligibility | Inclusion Criteria: - Greater than or equal to 19 years of age - Patients at the University of Nebraska Medical Center and the Nebraska Medical Center - Admitted to either the academic medical or trauma critical care service Exclusion Criteria: - Legally authorized representative not available to provide consent to participate within 48 hours of ICU admission |
Country | Name | City | State |
---|---|---|---|
United States | University of Nebraska Medical Center | Omaha | Nebraska |
Lead Sponsor | Collaborator |
---|---|
University of Nebraska | Robert Wood Johnson Foundation |
United States,
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* Note: There are 70 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Ventilator free days (VFDs) | The primary outcome will be a comparison between the 3 month baseline period of ventilator free days and the 9 month period following the intervention. Two interim analyses will be conducted. | Change in ventlator free days at baseline to 9 months |
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