Actively Recruiting
Improving Care Transitions for Medicaid Insured Individuals With Co-occurring Serious Mental Illness
Led by University of Pennsylvania · Updated on 2026-05-05
267
Participants Needed
1
Research Sites
128 weeks
Total Duration
On this page
Sponsors
U
University of Pennsylvania
Lead Sponsor
A
Agency for Healthcare Research and Quality (AHRQ)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to evaluate the THRIVE clinical pathway at HUP, focusing on supporting Medicaid-insured individuals, including those with serious mental illness, following hospitalization. The study will assess clinician/administrator perspectives on the pathway's feasibility, appropriateness, and acceptability and analyze referral patterns and post-discharge outcomes. The objectives are: 1. To conduct a qualitative study evaluating the implementation of THRIVE, particularly its adaptation to include patients with serious mental illness. 2. To examine referral patterns, 30-day readmission rates, and ED utilization for THRIVE participants, comparing them with those receiving standard care. Participants will be referred to home care services during hospitalization and seen by a home care nurse within 48 hours post-discharge. A discharging physician or Advanced Practice Provider will oversee care for 30 days or until a primary care or specialist visit. The Care Coordination Team will hold weekly case conferences for 30 days post-discharge to address both health and mental health needs. The study will compare outcomes of Medicaid-insured patients, including those with serious mental illness, to those receiving usual care.
CONDITIONS
Official Title
Improving Care Transitions for Medicaid Insured Individuals With Co-occurring Serious Mental Illness
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Medicaid insured
- Residing in the state of Pennsylvania
- Experienced a hospitalization at study hospital
- Agrees to home care at partner home care setting.
You will not qualify if you...
- Individuals under age 18
AI-Screening
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Trial Site Locations
Total: 1 location
1
Upenn School of Nursing Centre For Health Outcomes Policy Research
Philadelphia, Pennsylvania, United States, 19104
Actively Recruiting
Research Team
J
Jacqueline M Brooks Carthon, PhD,RN
CONTACT
E
Erin Babe, MPH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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