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Heart FailureFOOD-HFNCT06115369

Food Supplementation Delivered Conditionally vs Not Among Patients With Heart Failure

A study testing Medically Tailored Meals Delivered Conditionally, Medically Tailored Meals Delivered Unconditionally and Produce Boxes delivered Conditionally in people with Heart Failure, run by University of Texas Southwestern Medical Center at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The current study proposes to investigate if the provision of healthy food can improve outcomes following discharge after HF hospitalization. To investigate this in an efficient and pragmatic manner, a factorial randomized control trial design will be utilized to simultaneously investigate two separate, important… Read more about this study

Who is it for?
Ages 18 to 100 years
Conditions the study is for
Heart Failure
What is being tested?
Medically Tailored Meals Delivered Conditionally, Medically Tailored Meals Delivered Unconditionally and Produce Boxes delivered Conditionally
Could I receive a placebo?
No, everyone receives an active treatment
How many people
150 participants
Where
1 siteUnited States
Study dates
15 Apr 2024to 30 Oct 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 100 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Adults over 18 years age with a recent hospitalization for acute decompensated HF

Who cannot join

  • Baseline hyperkalemia with K > 5.5 mEq/L or history of hyperkalemia requiring hospitalization for urgent treatment,
  • Receipt of a heart transplant or left ventricular assist device,
  • Use of inotropic therapy at hospital discharge,
  • Discharge to a skilled nursing facility or long-term care facility that provides prepared patient meals, comorbidity with expected survival < 6 months, and
  • Inability to provide an address to receive produce shipments (including unhoused individuals or individuals residing in temporary housing shelters).
  • Pregnancy

Trial locations and contacts

1 site in 1 country.

United States1 site
  • UT Southwestern Medical Center

    Dallas, Texas, 75235

Other trials in United States

About this study

Official title: Examining the Impact of Medically Tailored Meals vs Produce Supplements Delivered Conditionally vs Not on Health Engagement and Health Outcomes Among Patients With Heart Failure

The current study proposes to investigate if the provision of healthy food can improve outcomes following discharge after HF hospitalization. To investigate this in an efficient and pragmatic manner, a factorial randomized control trial design will be utilized to simultaneously investigate two separate, important food-related questions:

  • Does the provision of 90 days of either medically-tailored meals or fresh produce boxes improve 90-day patient outcomes among those with HF relative to a control group not receiving food supplements and instead receiving an equivalent monetary supplement?
  • Does receipt of the supplement in a conditional fashion, where the supplement is continued only if the participant attends follow-up visits or fills prescribed medications at the pharmacy, have more impact than providing unconditional supplementation?
Read the detailed description

Eating a nutritious diet is important for maintaining health. However, getting healthy foods can be a challenge for many individuals whose food shopping is limited by finances, location, or physical limitations from pre-existing health problems. For such in-need individuals, providing supplemental healthy meals can improve their diet and potentially improve their health outcomes. Additionally, getting food supplements can also be a powerful incentive to encourage healthy behaviors.

Individuals with heart failure (HF) present a unique population to assess the value of food supplementation both for its nutritional value and as a health engagement incentive. HF is a common, high-cost public health problem in the United States. Hospitalizations for HF are associated with high rates of mortality, readmission, worsened quality of life, and burgeoning healthcare expenditures. During the post-discharge period, patients are exceptionally vulnerable to a wide variety of adverse health events due to multi-system physiologic impairments. Roughly 20% of all patients with Medicare are readmitted within 30 days, and many are readmitted for different causes than the principal diagnosis of the index admission. While multifactorial, frequent contributing causes of HF readmission include dietary indiscretion, failure to take medications, and failure to follow up with healthcare providers.

Prior studies demonstrate that patients with HF often have food insecurity and non-ideal diets. Nationally, food insecurity among those patients with cardiovascular diseases has increased. Those with HF specifically had some of the highest rates of food insecurity, and the prevalence of food insecurity rose from 11.3% in 1999-2000 to 45.3% in 2017-2018.

Studies have also investigated whether providing food supplements to patients with HF can potentially also improve health outcomes. In a recent cohort study, Medicare Advantage patients with acute heart failure (HF) were given up to 4 weeks of post-hospitalization home-delivered meals. Compared with historical controls, those receiving these meals were significantly less likely to have all-cause readmission and death. In contrast, a recent randomized clinical trial found that providing 10 weeks of medically tailored meals to patients with chronic diseases hospitalized during the COVID-19 pandemic did not lead to reductions in risk of 90-day readmission. However, in an exploratory sub-analysis, patients with HF who had the medically tailored meal intervention had significant reductions in readmissions. While these data are supportive of the hypothesis, they are not definitive, and a prospective randomized trial among patients with HF is needed to rigorously support the efficacy of food support in the post-discharge period to reduce readmission. There is also limited information on the type and means of food supplementation may affect its efficacy.

Based on this background, the current study proposes to investigate if the provision of healthy food can improve outcomes following discharge after HF hospitalization. To investigate this in an efficient and pragmatic manner, a factorial randomized control trial design will be used that will simultaneously investigate two separate important food-related questions. The first factorial design question will evaluate the direct impact of two nutritional supplementation strategies on rehospitalizations and ED visits for HF. Specifically, those hospitalized for HF will be randomized at hospital discharge to either 90 days of healthy medically tailored full meals (MTM) (n=50) or 90 days of a weekly fresh produce box (n=50) or to a control arm (usual care receiving no food supplements with dietary education only) (N=50).

The second factorial intervention will determine whether food supplements can be used as an incentive to increase patient engagement in their own care (i.e., attending a follow-up clinic visit and filling their prescriptions). Specifically, participants receiving food supplementation will be randomized 1:1 to receive their food supplements (MTMs or produce box) in an unconditional or conditional fashion based on the participant successfully attending their clinic visits and filling their medication.

Conditions
Heart Failure
Being tested
Medically Tailored Meals Delivered Conditionally, Medically Tailored Meals Delivered Unconditionally, Produce Boxes delivered Conditionally, Produce Boxes Delivered Unconditionally
Keywords
Heart Failure, Produce, Medically Tailored Meals, Patient Participation
Medical subject headings
Heart Failure, Patient Participation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Medically Tailored Meals Delivered ConditionallyDietary supplement

    Season Health, our food intervention partner, will provide participants with weekly deliveries of twice-daily prepared medically tailored meals (MTM). Participants will receive this supplement conditioned on continued participation and engagement in their healthcare, including attending all scheduled office visits and refilling prescription medications. If participants do not refill their prescriptions or do not attend their office visits, the shipments of medically tailored meals will be paused. These will be restarted when the participant's appointment is rescheduled or when the participant's prescription is refilled.

  • Medically Tailored Meals Delivered UnconditionallyDietary supplement

    Season Health, our food intervention partner, will provide participants with weekly deliveries of twice-daily prepared medically tailored meals (MTM). Participants will receive this supplement unconditionally for the entire study duration.

  • Produce Boxes delivered ConditionallyDietary supplement

    Season Health, our food intervention partner, will provide participants with weekly deliveries of fresh produce and pantry staples. Participants will receive this supplement conditioned on continued participation and engagement in their healthcare, including attending scheduled office visits and refilling prescription medications. If participants do not refill their prescriptions or do not attend their office visits, the shipments of medically tailored meals will be paused. These will be restarted when the participant's appointment is rescheduled or when the participant's prescription is refilled.

  • Produce Boxes Delivered UnconditionallyDietary supplement

    Season Health, our food intervention partner, will provide participants with weekly deliveries of fresh produce and pantry staples. Participants will receive this supplement unconditionally throughout the entire study period.

Study groups in NCT06115369
Study groupRoleWhat they receive
Medically Tailored MealsExperimentalSeason Health, our food intervention partner, will provide participants with weekly deliveries of twice daily prepared medically tailored meals (MTM; 14 total per week). Study participants will be able to select choices for these in conjunction with a dietician. The study team will work with Season Health to create customizations to allow for the incorporation of patient dietary preferences. Study team members will assist patients in setting up their Season Health accounts.
Receives: Dietary Supplement: Medically Tailored Meals Delivered Conditionally; Dietary Supplement: Medically Tailored Meals Delivered Unconditionally
Fresh ProduceExperimentalWe will work with Season Health, our food intervention partner to provide participants with weekly deliveries of a large box full of fresh produce and pantry staples. The study participants will be able to select choices for these from a large selection of health options in conjunction with a dietician. The study team will work with Season Health to create customizations to allow for the incorporation of patient dietary preferences. Study team members will assist patients in setting up their Season Health accounts.
Receives: Dietary Supplement: Produce Boxes delivered Conditionally; Dietary Supplement: Produce Boxes Delivered Unconditionally
Control armNo interventionThis control arm will receive dietary education only with usual heart failure care.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of participants with a readmission or emergency department visit for HF

    Total readmissions or visits to the emergency department for HF

    Measured: 90 days

Secondary outcomes (5)
  1. Hierarchical Composite Endpoint

    Win-ratio based endpoint with the following hierarchy: (1) mortality, (2) readmission or ED visit for HF (total), (3) ≥10 point improvement in Kansas City Cardiomyopathy Questionnaire (KCCQ) - Clinical Summary Score (CSS). The KCCQ clinical summary score ranges from 0 to 100, where higher scores indicating better quality of life.

    Measured: 90 days

  2. Between group change in Kansas City Cardiomyopathy Questionnaire - Clinical Summary Score

    The KCCQ clinical summary score ranges from 0 to 100, where higher scores indicating better quality of life.

    Measured: The survey will be assessed at baseline and at 90 days at the conclusion of the study.

  3. Medication adherence

    Morisky Medication Adherence Score. Scores are summed from 0 to 8, with higher scores meaning better adherence.

    Measured: 90 days

  4. Attendance to scheduled clinic appointments

    Percent from 0-100%, calculated by the number of attended visits divided by the number of scheduled visits after excluding cancelled visits (either cancelled by provider or participant)

    Measured: 90 days

  5. Filling of outpatient medication prescription

    Percent from 0-100%, calculated by percent of new prescriptions filled at pharmacy divided by number of prescriptions sent to pharmacy by providers

    Measured: 90 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Nov 2023
  2. Study start15 Apr 2024
  3. Primary completion15 Oct 2025
  4. Study completion30 Oct 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Factorial
Model description
The study will be designed as a 2 x 2 factorial randomized clinical trial. First, study patients will be randomized 1:1:1 to receive weekly medically tailored meals (MTM) for twice daily consumption (N = 50) vs. weekly fresh produce box (N = 50) vs. a control arm (usual care with dietary counseling only) (N=50). In the second factorial intervention, participants will be randomized 1:1 to receive their food supplements in a conditional fashion, based on whether they attend clinic visits and fill their medications (N =50) vs. receiving the intervention unconditionally (N =50). The intervention will be initiated within a week of hospital discharge and will continue for a period of 90 days.
Masking
None (open label)
Enrolment
150 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06115369
Sponsor's protocol ID
STU-2023-0978
Acronym
FOOD-HF
Status last verified
Nov 2025
First submitted
24 Oct 2023
Last updated
18 Nov 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Pandey A, Keshvani N, Coellar JD, Jain AK, Segar MW, Bustillo-Rubio M, Rizvi SK, Peterson ED. Food Supplementation in Patients Hospitalized for Heart Failure: A Randomized Clinical Trial. JAMA Cardiol. 2026 Jun 1;11(6):564-573. doi: 10.1001/jamacardio.2026.0435.

    PubMed 41949846

Questions about this trial

What is this clinical trial studying?

A study testing Medically Tailored Meals Delivered Conditionally, Medically Tailored Meals Delivered Unconditionally and Produce Boxes delivered Conditionally in people with Heart Failure, run by University of Texas Southwestern Medical Center at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of participants with a readmission or emergency department visit for HF (time frame: 90 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06115369, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Nov 2025.

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FOOD-HF Clinical Trial NCT06115369 | AzTrials