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Medically Tailored Meals to Support Recovery After a Hospital Stay for Heart Failure

Tests meals designed for medical needs in adults recovering from heart failure.

Plain-language title generated from the registry record
Registry title: Pilot Study Exploring the Feasibility, Acceptability, and Impact of Medically Tailored Meals on Post-Discharge Recovery in Patients With Heart Failure

Key facts

Where
Philadelphia, United StatesSee the site

Where in United States

  • Penn MedicinePhiladelphia, United StatesNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University of Pennsylvania
Trial code
NCT07251894
Record updated
17 August 2026
Original description
The goal of this interventional pilot study is to evaluate the feasibility, acceptability, and impact of medically tailored meals (MTM) on post-discharge recovery in patients with heart failure for Penn Medicine patients in Philadelphia and Lancaster through two pilots.Read full original descriptionShow less

HF-MTM Pilot: Pilot Study Exploring the Feasibility, Acceptability, and Impact of Medically Tailored Meals on Post-Discharge Recovery in Patients With Heart Failure

The goal of this interventional pilot study is to evaluate the feasibility, acceptability, and impact of medically tailored meals (MTM) on post-discharge recovery in patients with heart failure for Penn Medicine patients in Philadelphia and Lancaster through two pilots.

Inclusion: Age ≥ 18 years old; Have a primary diagnosis of health failure based on ICD code I50* with active hospitalization at time of enrollment; Must be insured by Medicaid or Medicare or dual eligible; Ability to read and speak English; Ability to provide informed consent.

Exclusion: Are undergoing evaluation for advanced HF treatments including heart transplant or ventricular assist devices; Are on hospice care or reside in an acute or skilled nursing facility; Are unable to complete data collection due to cognitive decline or disability (based on the electronic health record or referring provider assessment).

ClinicalTrials.gov NCT07251894