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Default Palliative Care Consultation for Seriously Ill Hospitalized Patients
This is a large pragmatic, randomized controlled trial to test the real-world effectiveness of inpatient palliative care consultative services in improving a number of patient- and family-centered processes and outcomes of care among seriously ill hospitalized patients. The investigators hypothesize that improved patient-centered outcomes can be achieved without higher costs by simply changing the default option for inpatient palliative care consultation for eligible patients from an opt-in to an opt-out system. To test this hypothesis the investigators will conduct a clinical trial at 11 hospitals using the same electronic health record within Ascension Health, the largest non-profit health system in the U.S.
The REDAPS trial aims to generate large-scale, experimental evidence regarding the real-world effectiveness of inpatient palliative consultative services (IPCS) and to test the incremental effectiveness and costs of a simple, scalable method to increase IPCS utilization among properly selected patients. The REDAPS trial will also compare the effectiveness of different palliative care team structures and services and identify patient subgroups most likely to benefit from IPCS. To achieve these goals, the investigators will conduct a clinical trial at 11 Ascension Health hospitals using the same electronic health record. Participating hospitals first contribute a minimum of 4 months of data under the control paradigm (opt-in model), where physicians must identify patients who may benefit from palliative care consultation and actively order such services. Then, using a stepped-wedge design, the hospitals are randomly assigned to begin the intervention in intervals spaced approximately 2.7 months apart. During the intervention, patients meeting consensus criteria for eligibility for palliative care consultation are identified by the electronic health record, a consultation is ordered by default, physicians may cancel the order after being alerted to it, and patients or family members may decline such services. By the end of the trial, all hospitals will have utilized the intervention paradigm of palliative care consultation for at least 4 months. The REDAPS trial will compare outcomes (clinical, economic, and process measures) before and after implementation within hospitals, as well as comparisons among hospitals at given time points.
Age
65 - No limit years
Sex
ALL
Healthy Volunteers
No
St. Vincent's Medical Center
Bridgeport, Connecticut, United States
St. Vincent's Medical Center, Riverside
Jacksonville, Florida, United States
St. Vincent's Medical Center, Southside
Jacksonville, Florida, United States
Via Christi Hospital, St. Francis
Wichita, Kansas, United States
Via Christi Hospital, St. Joseph
Wichita, Kansas, United States
Borgess Medical Center
Kalamazoo, Michigan, United States
Our Lady of Lourdes Memorial Hospital
Binghamton, New York, United States
St. Thomas West Hospital
Nashville, Tennessee, United States
University Medical Center Brackenridge
Austin, Texas, United States
Columbia St. Mary's, Ozaukee
Mequon, Wisconsin, United States
Start Date
March 1, 2016
Primary Completion Date
November 1, 2018
Completion Date
September 1, 2020
Last Updated
September 11, 2020
34,239
ACTUAL participants
Default ordering of palliative consult
BEHAVIORAL
Lead Sponsor
University of Pennsylvania
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05508789