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Completed Not applicable Interventional

Randomized Evaluation of Default Access to Palliative Services

ClinicalTrials.gov ID: NCT02505035

Public ClinicalTrials.gov record NCT02505035. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 6:13 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Default Palliative Care Consultation for Seriously Ill Hospitalized Patients

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT02505035
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
University of Pennsylvania
Other
Enrollment
34,239 participants

Conditions and interventions

Interventions

Behavioral

Eligibility (public fields only)

Age range
65 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 29, 2016
Primary completion
Oct 31, 2018
Completion
Aug 31, 2020
Last update posted
Sep 10, 2020

2016 – 2020

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
St. Vincent's Medical Center Bridgeport Connecticut 06606
St. Vincent's Medical Center, Riverside Jacksonville Florida 32204
St. Vincent's Medical Center, Southside Jacksonville Florida 32216
Via Christi Hospital, St. Francis Wichita Kansas 67214
Via Christi Hospital, St. Joseph Wichita Kansas 67218
Borgess Medical Center Kalamazoo Michigan 49048
Our Lady of Lourdes Memorial Hospital Binghamton New York 13905
St. Thomas West Hospital Nashville Tennessee 37205
University Medical Center Brackenridge Austin Texas 78701
Columbia St. Mary's, Ozaukee Mequon Wisconsin 53097
Columbia St. Mary's, North Lake Milwaukee Wisconsin 53211

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02505035, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 10, 2020 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02505035 live on ClinicalTrials.gov.

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