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Transitional Care Model Evaluation 2020

Evaluation of the Multisite Replication of the Transitional Care Model

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04212962
Acronym
TCM2020
Enrollment
962
Registered
2019-12-30
Start date
2020-07-07
Completion date
2026-12-01
Last updated
2026-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CHF - Congestive Heart Failure, COPD, Pneumonia

Brief summary

The study is a randomized controlled trial to estimate the effects of the transitional care model (TCM) on hospital admissions and patients' experience during the year following the patient's qualifying discharge. The University of Pennsylvania, where TCM was developed, will be the coordinating center for the implementation. The study will be conducted in three large health systems spread throughout the U.S., drawing patients from seven hospitals in those systems. Eligible patients are older adults (age 65 and older) admitted to a participating hospital with symptoms of heart failure (HF), chronic obstructive pulmonary disease (COPD), or pneumonia (PNA). The evaluation will be conducted by Mathematica.

Detailed description

The Transitional Care Model (TCM) is an advanced practice registered nurse (APRN) led, team-based, care management strategy designed to improve the care and outcomes of high-risk older adults transitioning from hospital to home. Eligible patients who agree to participate in the study will be randomly assigned to either the intervention group, which receives the TCM intervention, or the control group, which receives usual care (standard hospital discharge planning and post-hospital follow up services). The target sample size for the study is close to 1000, evenly divided into intervention and control groups, with 250 to 270 patients derived from each of UCSF and Trinity health systems, and another 450 recruited from the two VHA hospitals combined. Data will be collected at intake, prior to randomization, by enrollment coordinators at each of the participating hospitals. Followup data will be collected in a survey of patients conducted 90 days after discharge, and from claims data obtained from Medicare, Medicare Advantage plans, and the VHA.

Interventions

BEHAVIORALTransitional care model (TCM)

Patient education about post-discharge self-care and medications, arrangement of needed social services, coordination of information from medical providers interacting with patient

BEHAVIORALUsual care

usual hospital discharge and post-discharge care

Sponsors

Mathematica Policy Research, Inc.
Lead SponsorOTHER
University of Pennsylvania
CollaboratorOTHER
Arnold Ventures
CollaboratorOTHER
Veterans Health Administration--St. Louis and Cleveland
CollaboratorUNKNOWN
Trinity Health System
CollaboratorINDUSTRY
Providence St. Joseph Health-Swedish Health Services (Swedish)
CollaboratorUNKNOWN
University of California, San Francisco
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Advance practice registered nurses provide care management and education to intervention group patients prior to discharge and during the 90 days after transitioning to home.

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 65 years and older * Admitted from home with Pneumonia OR with a history of HF or COPD with symptoms of HF or COPD exacerbation or whose symptoms suggest a new HF or COPD diagnosis * English and non-English speaking, able to respond to questions * Reachable by telephone after discharge * Resides within the geographic service area * Consent to participation

Exclusion criteria

* Enrolled in Medicare's Hospice or End-Stage Renal Disease programs * Presence of active and untreated psychiatric conditions (ICD10: F10-F29) * Long-term care resident * Undergoing active cancer treatment * Currently enrolled in another RCT

Design outcomes

Primary

MeasureTime frameDescription
Number of hospital admissions12 monthsnumber of times admitted to the hospital during 12 months after initial discharge
Costs12 monthsCosts of medical care paid for by Medicare, Medicare Advantage plan, or Veterans Health Administration

Secondary

MeasureTime frameDescription
30-day readmission30 dayswhether readmitted to a hospital during the 30 days after initial discharge
emergency department visits12 monthsnumber of times treated in an emergency department after initial discharge
length of time to death or hospital admission12 months after initial dischargenumber of days between initial discharge and either death or readmission to hospital
Skilled nursing facility days12 months after initial dischargeNumber of days spent in a skilled nursing facility
Mortality12 months after initial dischargewhether died after initial discharge
Edmonton Symptom Assessment Scale90 days after initial dischargemeasures post-hospital symptoms, range 0-100, high score is bad
Patient-Reported Outcomes Measurement Information System Physical Functioning (SF10a)90 days after initial dischargefunctional status, range 10-50, high score is good
Patient Health Questionnaire for Depression and Anxiety (PHQ-4)90 days after initial dischargeindex of depression and anxiety, range 0-12, high score is bad

Countries

United States

Contacts

STUDY_DIRECTORArkadipta Ghosh, PhD

Mathematica Policy Research, Inc.

PRINCIPAL_INVESTIGATORRandall S Brown, PhD

Mathematica Policy Research, Inc.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 9, 2026