Skip to main content
Clinical Trials/NCT02114515
NCT02114515
Completed
Not Applicable

PATient Navigator to rEduce Readmissions

University of Illinois at Chicago1 site in 1 country1,029 target enrollmentJuly 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease
Sponsor
University of Illinois at Chicago
Enrollment
1029
Locations
1
Primary Endpoint
PROMIS Emotional Distress-Anxiety (v1.0, SF4a)
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Staying out of the hospital is valued by patients and their caregivers. Their interests converge with those of hospitals now that high 30-day readmission rates for some conditions place hospitals at risk for financial penalties from the Centers for Medicare and Medicaid Services. This study focuses on developing and testing a program that combines a community health worker (lay patient advocate, acting as a "Patient Navigator") and a peer-led telephone support line to improve patient experience during hospital to home transition.

Registry
clinicaltrials.gov
Start Date
July 2014
End Date
October 2016
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jerry Krishnan

Professor of Medicine and Public Health; Associate Vice Chancellor for Population Health Sciences

University of Illinois at Chicago

Eligibility Criteria

Inclusion Criteria

  • Age 18 years or older on date of hospital admission
  • Hospitalized at the University of Illinois Hospital, Chicago
  • Admission diagnosis, per treating physician, of pneumonia, COPD, sickle cell disease, heart failure, or myocardial infarction
  • Receive medical care on an inpatient medical service

Exclusion Criteria

  • Unable to understand and speak English
  • Unable/decline to give informed consent
  • Previous participant in PArTNER
  • Planned transfer to another acute care facility
  • Planned discharge to facility other than home (e.g. long term care facility)
  • Currently on hospice or plans to discharge home to hospice
  • Current plans to leave against medical advice

Outcomes

Primary Outcomes

PROMIS Emotional Distress-Anxiety (v1.0, SF4a)

Time Frame: 30 days post discharge

Change in T-score from baseline to 30 days post discharge (30 days minus baseline). A change in t-score \<0 indicates improvement. A change equal to 0 indicates no change. A change \>0 indicates worsening.

PROMIS Informational Support (v2.0, SF4a)

Time Frame: 30 days post discharge

Change in T-score from baseline to 30 days post discharge (30 days minus baseline). A change in t-score \<0 indicates worsening. A change equal to 0 indicates no change. A change \>0 indicates improvement.

Secondary Outcomes

  • PROMIS Emotional Support (v2.0, SF4a)(60 days post discharge)
  • PROMIS Instrumental Support (v2.0, SF4a)(60 days post discharge)
  • PROMIS Global Health, Mental (v1.1, SF)(60 days post discharge)
  • Re-hospitalization or Death(60 days post discharge)
  • PROMIS Global Health, Physical (v1.1, SF)(60 days post discharge)
  • PROMIS Emotional Distress-Anxiety (v1.0, SF4a)(60 days post discharge)
  • PROMIS Informational Support (v2.0, SF4a)(60 days post discharge)
  • Death(60 days post discharge)
  • ED Visit, Re-hospitalization, or Death(60 days post discharge)
  • Outpatient Healthcare Visit(14 days post discharge)

Study Sites (1)

Loading locations...

Similar Trials