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Clinical Trials/NCT05714605
NCT05714605Enrolling By InvitationNot Applicable

Implementation and Evaluation of THRIVE: A Health Innovation to Support Care Transitions for Medicaid-Insured Individuals Following Hospitalization

University of Pennsylvania2 sites in 1 country267 target enrollmentStarted: March 27, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
267
Locations
2
Primary Endpoint
Rates of Referrals to Homecare

Study Overview

Brief Summary

The goal of this stepped wedge pragmatic trial is to compare referral patterns and post discharge outcomes in Medicaid insured individuals discharge following a hospitalization]. The aims are to 1) evaluate the implementation of the THRIVE clinical pathway, including feasibility, appropriateness, and acceptability and 2) examine referral patterns, 30- day readmission and Emergency Department (ED) utilization patterns for participants who receive THRIVE support services. During hospitalization participants will receive a referral to home care services and will be seen by a home care nurse within 48 hours following discharge. A discharging physician or Advanced Practice Provider will maintain clinical oversight for 30 days or until the patient sees primary care provider or specialist. A Care Coordination Team conducts weekly case conferences to ensure social and health needs are being addressed for 30 days post-discharge. Researchers will compare Medicaid insured patients discharged during the study, to those receiving usual care to determine if there are differences in post-acute utilization outcomes.

Detailed Description

This is a prospective single site Type 1 hybrid effectiveness-implementation parallel mixed methods (QUANT + qual) quasi-experimental study. This study design involves simultaneous collection and analysis of quantitative and qualitative data, giving priority weight to the quantitative data to evaluate program referrals, outcomes, and program fidelity, while qualitative data will evaluate process through detailed descriptions of perspectives of barriers and facilitators faced by health care providers in implementing the THRIVE intervention. Qualitative interviews will also assess stakeholder perspectives of the value of the intervention in addressing health inequities among Medicaid insured individuals cared for in the acute and home care settings. Nesting the qualitative interview within a single-site randomized trial of a the THRIVE intervention will allow us to determine whether the intervention improved primary outcomes (referrals to homecare, 30-day readmission, ED utilization, connection to PCP) and to identify professional and organizational barriers to implementation. Combining these insights with that of effectiveness outcome date will allow consideration for meaningful contextual factors that are viewed as critical to the implementation of THRIVE and subsequent outcomes. Our stepped wedge design with include a randomized roll-out to case managers at Pennsylvania Hospital and the study will be carried out over 18 months. To begin, 5 case managers will be randomized to receive training on the THRIVE clinical pathway. Following training they will be invited to begin offering referrals to the THRIVE clinical pathway. After 2 months the remaining 4 case managers will be trained on the THRIVE intervention and will be able to begin submitting referrals.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 99 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Medicaid insured
  • Residing in the state of Pennsylvania
  • Experienced a hospitalization at study hospital
  • Agrees to home care at partner home care setting.

Exclusion Criteria

  • Individuals under age 18

Arms & Interventions

THRIVE Intervention

Experimental

1 month intensive post discharge case management and care coordination.

Intervention: THRIVE Intervention (Behavioral)

Usual Care

No Intervention

Discharge to home without intensive post acute case management or care coordination.

Outcomes

Primary Outcomes

Rates of Referrals to Homecare

Time Frame: Through study completion, an average of 18 months

We will evaluate changes in home care referrals between case managers exposed to the intervention compared to those who were not.

Rates of Readmissions

Time Frame: 30 days following hospital discharge

We will evaluate the rate of readmissions over the course of the study for THRIVE participants compared to those receiving usual care.

Rates of Emergency Department Visit

Time Frame: 30 days following hospital discharge

We will evaluate the rate of ED visits over the course of the study for THRIVE participants compared to those receiving usual care.

Primary Care or Specialist Visit

Time Frame: 30 Days following hospital discharge

We will compare the rates of primary care provider and specialist visits within 30 days following discharge compared to those receiving usual care.

Secondary Outcomes

  • Feasibility, Acceptability, Appropriateness, Workload(Through study completion, an average of 18 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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