Transitional Care Model Evaluation 2020 (TCM2020)

Mathematica Policy Research

Status: Active, not recruiting

Conditions: CHF - Congestive Heart Failure; Pneumonia; COPD

Treatments: Behavioral: Usual care; Behavioral: Transitional care model (TCM)

Study type: Interventional

Funder types: Other

Identifiers

NCT04212962

MathematicaPR

Details and patient eligibility

About

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.

Full 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.

Enrollment: 962 patients

Sex: All

Ages: 65+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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962 participants in 2 patient groups

Treatment group

Experimental group

Description:

The treatment group receives the TCM intervention while in the hospital and during the first 90 days after returning to the community.

Treatment:

Behavioral: Transitional care model (TCM)

Control group

Experimental group

Description:

The control group receives usual discharge planning and post-discharge care.

Treatment:

Behavioral: Usual care