PATient Navigator to rEduce Readmissions

NCT02114515 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1029

Last updated 2019-02-15

Study results available
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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.

Conditions

Interventions

BEHAVIORAL

Hospital usual care

Written discharge instructions provided to patients prior to hospital discharge.

BEHAVIORAL

Navigator intervention

A Patient Navigator will provide social support, literacy appropriate education, and act as a conduit between the patient and the patient's medical team

BEHAVIORAL

Peer-led telephone support line

The peer-led telephone support line will provide social support, peer-to-peer coaching, and facilitate communication with the patient's medical care team.

Sponsors & Collaborators

  • Patient-Centered Outcomes Research Institute

    collaborator OTHER
  • Society of Hospital Medicine

    collaborator OTHER
  • COPD Foundation

    collaborator OTHER
  • University of Kentucky

    collaborator OTHER
  • Mended Hearts

    collaborator UNKNOWN
  • American Heart Association

    collaborator OTHER
  • Sickle Cell Disease Association of Illinois

    collaborator UNKNOWN
  • AcademyHealth

    collaborator OTHER
  • The National Association of Social Workers Foundation

    collaborator UNKNOWN
  • Respiratory Health Association

    collaborator UNKNOWN
  • University of Illinois Sickle Cell Patient Council

    collaborator UNKNOWN
  • National Jewish Health

    collaborator OTHER
  • Baystate Medical Center

    collaborator OTHER
  • University of Illinois at Chicago

    lead OTHER

Principal Investigators

  • Jerry A Krishnan, MD, PhD · University of Illinois at Chicago

  • Elizabeth Calhoun, PhD · University of Arizona

  • Mark V. Williams, MD · University of Kentucky

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2016-10-31
Completion
2016-10-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02114515 on ClinicalTrials.gov