RECRUITING

Behavioral Economic & Staffing Strategies in the ICU

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Behavioral Economic and Staffing Strategies To Increase Adoption of an Evidence Based Bundle in the Intensive Care Unit (BEST ICU): A Stepped Wedge Cluster Randomized Controlled Trial

Quick Facts

Study Start:2024-07-01
Study Completion:2028-04
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06184945

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:19 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age \>19 years at time of ICU admission
  2. * Received invasive mechanical ventilation while in the ICU
  3. * Admitted to participating cluster ICU
  4. * ICU length of stay of at least 24 hours
  1. * Patient who is admitted to the hospital who is already receiving chronic long-term mechanical ventilation from the home, assisted living, or long-term care setting
  2. * Prisoners

Contacts and Locations

Study Contact

Michele C Balas, PhD, RN
CONTACT
(614) 949-5555
mibalas@unmc.edu
Eduard Vasilevskis, MD
CONTACT
(608) 261-1571
vasilevskis@wisc.edu

Principal Investigator

Michele C Balas, PhD, RN
PRINCIPAL_INVESTIGATOR
University of Nebraska

Study Locations (Sites)

University of Iowa Hospitals and Clinics
Iowa City, Iowa, 52242
United States
University of Nebraska Medical Center
Omaha, Nebraska, 68198
United States
Ohio State University
Columbus, Ohio, 43201
United States

Collaborators and Investigators

Sponsor: University of Nebraska

  • Michele C Balas, PhD, RN, PRINCIPAL_INVESTIGATOR, University of Nebraska

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-07-01
Study Completion Date2028-04

Study Record Updates

Study Start Date2024-07-01
Study Completion Date2028-04

Terms related to this study

Additional Relevant MeSH Terms

  • Implementation Science
  • Delirium
  • Critical Illness
  • Mechanical Ventilation Complication
  • ICU Acquired Weakness
  • Pain