Understanding Perspectives of Frequently-Admitted Hospital Patients (CHAMP)

October 1, 2021 updated by: Bruce Lowell Henschen, Northwestern University
This study evaluates the clinical outcomes of a novel program designed to target patients who are high-utilizers of hospital services. Patients who are frequently admitted to medical services - "high-utilizers" - present a unique set of challenges to providers and the health care system that require a different way of approaching chronic illness. The Complex High Admission Management Program (CHAMP) is an innovative model of care consisting of a small team of providers who establish continuity relationships with high-utilizer patients. CHAMP strives to provide effective, high value care via a longitudinal relationship-based care model through provider continuity, intensive case management, and personalized care plans. To better understand the potential outcomes of CHAMP, this study is a longitudinal, prospective, randomized, controlled trial of medical high-utilizers enrolled in CHAMP compared to a group of high-utilizer patients receiving usual care.

Study Overview

Detailed Description

Frequent users of hospital services, otherwise known as hospital "high-utilizers," comprise a diverse patient population that pose unique challenges to the current US health care delivery model. The Complex High Admission Management Program (CHAMP), implemented at Northwestern Memorial Hospital in Chicago, IL, seeks to improve care for high-utilizer patients through provider continuity, intensive case management, and developing personalized care plans that span inpatient, outpatient, and emergency care environments.

Preliminary evaluation of CHAMP has shown a 38% decrease in 30-day unplanned hospital readmissions and an 18% decrease in ED encounters over a 6-month time period, when compared to an equal time period pre-CHAMP.

Patients are eligible for the program if they are readmitted to the hospital three times within a twelve-month period. Due to the time and resource limitations of the CHAMP team, not all patients meeting these criteria can be enrolled at once. Patients will thus be randomly selected to be enrolled in CHAMP or will receive usual care. This study plans to evaluate the difference in outcomes between patients enrolled in CHAMP and those receiving usual care by answering the following questions:

To what extent do high-utilizer patients enrolled in CHAMP differ in their level of trust in providers, self-assessed coping skills, daily symptom burden, perceived functionality, and attitudes about the healthcare system when compared to a control group of high utilizer patients receiving usual care? We will assess patient responses to a series of surveys assessing trust, feelings of discrimination, activation, satisfaction with care, and level of social functioning.

What are the healthcare utilization rates of high-utilizer patients enrolled in CHAMP compared to a control group of high-utilizer patients receiving usual care? We will compare rates of (a) hospital admission and (b) utilization (including length of stay) among high-utilizer patients enrolled in CHAMP as compared to high-utilizer patients not enrolled in the program.

Study Type

Interventional

Enrollment (Actual)

151

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Illinois
      • Chicago, Illinois, United States, 60611
        • Northwestern Memorial Hospital

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.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion criteria:

  • Adults (18 yrs of age or older) who are admitted to Northwestern Memorial Hospital (NMH) and identified by EDW search as having two unplanned 30-day inpatient readmissions to NMH within the prior 12 months with one of two additional criteria:at least 1 readmission in the last 6 months, or a referral from one of that patient's medical providers.
  • Admission to NMH during the study period (October 1, 2016 to September 30, 2018) and meeting criteria described above for CHAMP
  • Ability to consent for this study (including ability to read materials printed in English, understanding and communicating in English, and able to understand the risks and benefits of participating in the study).

Exclusion Criteria:

  • Patients who are admitted to the Intensive Care Unit, patients admitted to Oncology services (as we have found that this latter group has a multidisciplinary care team already in place), or patients actively followed by the Heart Failure Bridge and Transition (BAT) Team, a different quality improvement intervention designed to reduce readmissions among patients admitted for acute decompensated heart failure.
  • Participants will be excluded if they are disoriented to person, place, or time, or are unable to consent for any other reason.
  • Minors, pregnant women, and prisoners will also be excluded.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: HEALTH_SERVICES_RESEARCH
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: CHAMP
Participants enrolled in CHAMP are followed by a team of a social worker and physician across the care continuum. CHAMP team members visit patients in the ED and on inpatient floors. Along with the patient's input, the team develops an Individualized Care Plan outlining the patient's medical and social history and providing recommendations to other providers on specific aspects of their care. Care plans are reviewed with patients on an individual basis and reviewed periodically by the CHAMP providers. CHAMP-enrolled participants are scheduled for physician and social worker follow-up appointments at the CHAMP clinic; this time is used to provide intensive case management, medical care, and psychosocial support.
CHAMP team members visit patients in the ED and on inpatient floors. Along with the patient's input, the team develops an Individualized Care Plan outlining the patient's medical and social history and providing recommendations to other providers on specific aspects of their care. Care plans are reviewed with patients on an individual basis and reviewed periodically by the CHAMP providers. CHAMP-enrolled participants are scheduled for physician and social worker follow-up appointments at the CHAMP clinic; this time is used to provide intensive case management, medical care, and psychosocial support.
NO_INTERVENTION: Standard Care
Individuals in the standard care arm will receive care as they do normally when hospitalized, including medical and inpatient social work services, as well as outpatient care from their providers.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Readmission Rate
Time Frame: 180-days from indexed hospital discharge
180-day Inpatient Readmission Rate (as defined by Medicare) to Northwestern Memorial Hospital
180-days from indexed hospital discharge

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Readmission Rate
Time Frame: 30 days from indexed hospital discharge
Inpatient Readmission Rate
30 days from indexed hospital discharge
Readmission Rate
Time Frame: 90 days from indexed hospital discharge
Inpatient Readmission Rate
90 days from indexed hospital discharge
Inpatient Admissions
Time Frame: 30 days from indexed hospital discharge
Inpatient Admission Rate to Northwestern Memorial Hospital
30 days from indexed hospital discharge
Inpatient Admissions
Time Frame: 90 days from indexed hospital discharge
Inpatient Admission Rate to Northwestern Memorial Hospital
90 days from indexed hospital discharge
Inpatient Admissions
Time Frame: 180 days from indexed hospital discharge
Inpatient Admission Rate to Northwestern Memorial Hospital
180 days from indexed hospital discharge
Inpatient Admissions-total
Time Frame: 30 days from indexed hospital discharge
Inpatient Admissions to all hospitals, as reported by patient
30 days from indexed hospital discharge
Inpatient Admissions-total
Time Frame: 90 days from indexed hospital discharge
Inpatient Admissions to all hospitals, as reported by patient
90 days from indexed hospital discharge
Inpatient Admissions-total
Time Frame: 180 days from indexed hospital discharge
Inpatient Admissions to all hospitals, as reported by patient
180 days from indexed hospital discharge
ER Admissions
Time Frame: 180 days from indexed hospital discharge
ER Visits to Northwestern Memoria
180 days from indexed hospital discharge
ER Admissions
Time Frame: 30 days from indexed hospital discharge
ER Visits to Northwestern Memoria
30 days from indexed hospital discharge
ER Admissions
Time Frame: 90 days from indexed hospital discharge
ER Visits to Northwestern Memoria
90 days from indexed hospital discharge
ER Admissions-total
Time Frame: 30 days from indexed hospital discharge
ER Visits to all hospitals, as reported by patient
30 days from indexed hospital discharge
ER Admissions-total
Time Frame: 90 days from indexed hospital discharge
ER Visits to all hospitals, as reported by patient
90 days from indexed hospital discharge
ER Admissions-total
Time Frame: 180 days from indexed hospital discharge
ER Visits to all hospitals, as reported by patient
180 days from indexed hospital discharge
Hospital Length of Stay
Time Frame: 180 days from indexed hospital discharge
Average Length of Stay at NMH during time period
180 days from indexed hospital discharge
Hospital Length of Stay
Time Frame: 30 days from indexed hospital discharge
Average Length of Stay at NMH during time period
30 days from indexed hospital discharge
Hospital Length of Stay
Time Frame: 90 days from indexed hospital discharge
Average Length of Stay at NMH during time period
90 days from indexed hospital discharge
Clinic Visits
Time Frame: 180 days from indexed hospital discharge
Number of total clinic visits
180 days from indexed hospital discharge
Patient-Centered Outcomes
Time Frame: 30 days from indexed hospital discharge
Responses to PROMIS Profile Scales, Trust in Physicians, Patient Activation, and Feelings of Discrimination
30 days from indexed hospital discharge
Patient-Centered Outcomes
Time Frame: 90 days from indexed hospital discharge
Responses to PROMIS Profile Scales, Trust in Physicians, Patient Activation, and Feelings of Discrimination
90 days from indexed hospital discharge
Patient-Centered Outcomes
Time Frame: 180 days from indexed hospital discharge
Responses to PROMIS Profile Scales, Trust in Physicians, Patient Activation, and Feelings of Discrimination
180 days from indexed hospital discharge
Average costs
Time Frame: 180 days from indexed hospital discharge
Estimated cost from billing code data for hospitalizations during time period
180 days from indexed hospital discharge

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Bruce L Henschen, MD/MPH, Northwestern University Feinberg School of Medicine

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 Major Dates

Study Start (ACTUAL)

November 1, 2016

Primary Completion (ACTUAL)

July 1, 2020

Study Completion (ACTUAL)

October 1, 2021

Study Registration Dates

First Submitted

March 27, 2017

First Submitted That Met QC Criteria

March 27, 2017

First Posted (ACTUAL)

March 31, 2017

Study Record Updates

Last Update Posted (ACTUAL)

October 4, 2021

Last Update Submitted That Met QC Criteria

October 1, 2021

Last Verified

October 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • STU00203847

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Continuity of Patient Care

Clinical Trials on CHAMP

3
Subscribe