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Heart FailureMutton-HFNCT06675331

Mutton Heart Failure Food is Medicine Pilot

A study testing Medically Tailored Meal Program with Traditional Navajo Foods in people with Heart Failure, run by University of Pennsylvania 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

Study subjects with heart failure will receive either pre-prepared, home-delivered DASH/SRD-compliant meals incorporating local Navajo traditional foods or usual care for 30 days (14 meals weekly). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Heart Failure
What is being tested?
Medically Tailored Meal Program with Traditional Navajo Foods
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 siteUnited States
Study dates
7 Oct 2024to 1 May 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 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age >=18 years
  • ICD I50* diagnosis
  • Clinical encounter in last 12 months
  • Primary care physician at the two IHS sites
  • Hospitalization (any-cause) within last 12 months

Who cannot join

  • Hospice care
  • Living in acute rehabilitation or skilled nursing facility
  • Living outside the Gallup Service Unit (outside 50-mile catchment area)

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Tohatchi Health Clinic

    Tohatchi, New Mexico, 87325

Other trials in United States

About this study

Official title: Medically Utilized Tailored Traditional Meals to Optimize Nutrition in Heart Failure Pilot Trial

Study subjects with heart failure will receive either pre-prepared, home-delivered DASH/SRD-compliant meals incorporating local Navajo traditional foods or usual care for 30 days (14 meals weekly).

Read the detailed description

The American Indian and Alaska Native population has experienced significant cardiovascular health disparities compared with other racial and ethnic groups in the U.S. [1] Heart failure, in particular, causes significant morbidity and mortality in Navajo Nation. For many Navajo patients, similar to other American Indian populations, food insecurity is a major driver of health disparities. [2][3] In fact, qualitative data from our heart failure patient advisory committee have found that 89% of patients with heart failure believe nutrition insecurity is a major barrier to optimal health. Dietary factors are believed to be an important cause of hospitalizations in patients with heart failure and cardiovascular outcomes. There is increasing evidence that direct dietary support, such as produce prescription or provision of medically tailored meals may improve cardiovascular outcomes and disease-specific quality of life. Furthermore, there has been an increased focus in Indigenous communities to reclaim traditional indigenous foods to improve health. However, more evidence of the benefit of traditional Indigenous foods for cardiovascular health is needed.

We, therefore, in discussion with community members and tribal partners at two Indian Health Service (IHS) sites in Navajo Nation, will implement and evaluate the effectiveness of a medically and Native-sourced culturally tailored meal delivery program to improve outcomes in heart failure in rural Navajo Nation. This study will include two phases, with a phase I pilot feasibility study, followed by phase II-a comparativeness effectiveness randomized controlled trial to compare the implementation of our medically and culturally tailored meal delivery program compared to usual care. For phase I, we will conduct a one-arm pilot trial of the MUTTON-HF intervention to determine 1) feasibility of the intervention and outcome assessment and 2) acceptability of the intervention and 3) fidelity of the intervention. We will enroll 20 patients to receive medically tailored meals (14 meals weekly) for 30 days to inform the phase II comparativeness effectiveness trial.

Phase I outcomes will include implementation outcomes such as feasibility and acceptability of the intervention including the various delivery mechanisms and meals as measured by quantitative (i.e. % meals delivered and % meals received by patient) and qualitative methods, of outcome assessment including surveys and laboratory evaluation (% with completed outcome assessment), and fidelity of intervention as measured by quantitative (% meals consumed). We will additionally measure feasibility and acceptability of supporting local food systems by measuring % meals with locally sourced produce and meat, and % sourced from Navajo farmers and ranchers specifically. We will also explore implementation outcomes with community partners including farmers, growers, ranchers, food pantry.

Conditions
Heart Failure
Being tested
Medically Tailored Meal Program with Traditional Navajo Foods
Keywords
indigenous, food is medicine, Traditional Foods, Nutrition Security, Navajo
Medical subject headings
Heart Failure

What participants receive

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

  • Medically Tailored Meal Program with Traditional Navajo FoodsOther

    Patients will receive medically-tailored meals incorporating local traditional Navajo foods

Study groups in NCT06675331
Study groupRoleWhat they receive
Meal delivery programExperimentalPatients will receive 2 meals daily (14 meals weekly) of medically-tailored meals incorporating traditional Navajo foods, followed by a cooking class at the end of the meal program (meals provided for 4 weeks)
Receives: Other: Medically Tailored Meal Program with Traditional Navajo Foods

What is being measured

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

  1. Feasibility: Percentage of meals successfully received by the patient

    Proportions of meals that were successfully picked up or received by the patient. We have determined that >70% would count as success/feasibility of the intervention.

    Measured: 30 days

Secondary outcomes (30)
  1. Cultural Connectedness Scale-California

    The Cultural Connectedness Scale (CCS) was developed in Canada by First Nations/Indigenous persons for First Nations/Indigenous persons. The 29-item CCS consists of three sub-scales: identity, traditions, and spirituality. This scale ranges from 0-40, with 40 indicating higher levels of cultural connectiveness.

    Measured: Baseline, 30 Days

  2. Kansas City Cardiomyopathy Questionnaire (KCCQ-12)

    This is a validated score for evaluating quality of life and symptom measures in heart failure patients. Score ranges from 0-100, with 0 meaning very poor quality of life/symptoms and health status, 100 meaning excellent quality of life/symptom burden/health status.

    Measured: Baseline, 30 Days

  3. USDA Adult Food Security: Six Item short Form survey

    The six-item short form of the survey module and the associated Six-Item Food Security Scale were developed by researchers at the National Center for Health Statistics in collaboration with Abt Associates Inc.

    Measured: Baseline, 30 Days

  4. Hospitalization or Emergency Department Visit

    Hospitalization or Visit to Emergency Department (All-cause)

    Measured: 90 Days

  5. Laboratory Biomarker Data

    Albumin, prealbumin, creatinine, NT-proBNP, HbA1c, Total cholesterol, LDL-C, HDL-C, Triglycerides, CRP

    Measured: Baseline, 30 Days

  6. Weight/Body Mass Index

    weight and BMI

    Measured: Baseline, 30 Days

  7. Emergency Room Visits

    ER visits: All cause

    Measured: 90 Days

  8. ER visits or hospitalizations

    All cause

    Measured: 180 days

  9. ER visit for Heart Failure

    ER visit for volume overload or HF symptoms

    Measured: 90 Days

  10. Heart Failure Hospitalizations

    Hospitalizations for heart failure specifically

    Measured: 90 days

  11. Feasibility: Percentage of meals delivered successfully to the Gallup Food Pantry

    Proportions of meals that were successfully delivered to the Gallup Food Pantry by our community partner and Native-run Kitchen

    Measured: 30 days

  12. Feasibility of Intervention: Delivery/Pick-Up

    We will survey patients post-intervention with question to assess feasibility: "I would rate getting the meals (either picking up or delivery): Very easy, Somewhat easy, Neither easy nor difficult, Somewhat difficult, Very difficult.

    Measured: 30 days

  13. Acceptability of the Intervention (AIM) Measure

    We will evaluate acceptability of the intervention among the patients through quantitative assessment using the validated acceptability of the intervention (AIM) measure

    Measured: 30 days

  14. Net Promoter Score

    We will also assess acceptability of the intervention through assess the Net Promoter Score (i.e. how likely is it that you would recommend this program to a community member?"), which is a scale 1 (highly unlikely) to 10 (highly likely).

    Measured: 30 days

  15. Fidelity: Consumption

    Patients will also rate meals from 1-5 and the amount of the meal they consumed (none [or only a few bites], less than half, about half, most, or all)

    Measured: 30 days

  16. Acceptability: Taste

    Patients will also be surveyed post-intervention the following questions to assess acceptability: How would you rate the meals overall, in terms of taste (excellent, good, average, below average, bad?"

    Measured: 30 days

  17. Qualitative measures of feasibility and acceptability

    We will also perform semi-structured interviews of patients to assess feasibility and acceptability through qualitative methods. Semi-structured interviews will be guided by the Consolidated Framework for Implementation Research (CFIR), and we will explore multiple constructs within each CFIR domain that are hypothesized by the study team and based on existing literature to be relevant to acceptability and feasibility of the program

    Measured: 30 days

  18. Feasibility of Supporting Local Food Systems

    We will assess feasibility among our community partners by assessing the validated feasibility of the intervention measure (FIM) among our food pantry partners.

    Measured: 30 days

  19. Feasibility: Local Food Sourcing

    We will also assess the % of meals that include locally sourced ingredients, % of meals sourced by Native suppliers/farmers (produce), % of meals soured by Native ranchers (meat)

    Measured: 30 days

  20. Feasibility of Outcome Assessment

    We will determine the proportion of patients that completes baseline, as well as post-implementation survey and laboratory data.

    We will consider ≥ 80% completion rates as a success.

    Measured: 30 days

  21. Fidelity of Intervention

    We will assess fidelity of the intervention by evaluating:

    • We will have patients' complete food diaries for 3 days during week 1 and week 4 of the intervention.
    • % of meals consumed: Patients will also fill out meal cards weekly with percent consumed (None [or a few bites], ¼, ½, ¾, all [or nearly all]). § We will stratify meals consumed by whether the meal used traditional Diné ingredients or not.
    • We will additionally survey participants post-intervention the following:
    • In terms of leftovers, how much of the meals were not eaten and had to be thrown out? (all, most, about half, less than half, none).
    • We will consider ≥ 70% meals consumed (at least ½ or more of the meal) or ≥70% indicating they ate "most" or more of the meals as a success

    Measured: 30 days

  22. Adoption of Intervention

    We will survey participants post-intervention the following using a Likert scale:

    • How likely is it that this program will change your diet to be healthier moving forward? (very likely, somewhat likely, neither likely nor unlikely, somewhat unlikely, very unlikely)
    • How likely is it that you will add any of the meals or recipes from this program to your on-going diet in the future? (very likely, somewhat likely, neither likely nor unlikely, somewhat unlikely, very unlikely)

    Measured: 30 days

  23. Diet Quality

    We will assess diet quality using the 10-item DSQ [10] with an addition question to assess traditional Dine food intake (During the past month, how often did you eat traditional Diné foods (such as blue corn mush, steamed, roasted or dried corn, sumac berries, mutton, local varieties of squash or beans) at baseline and at the end of the intervention.

    Measured: Baseline and 30 days

  24. Physical Activity

    We will evaluate how much physical activity/exercise patients are participating in weekly at baseline, and at 30 days by asking patients to estimate the number of minutes weekly that they are participating in formal exercise or physical activity.

    Measured: Baseline and 30 days

  25. General Health Status

    We will evaluate patients' general health status using a single general health status question (would you say that in general your health is excellent, very good, good, fair, or poor) at baseline and post-intervention

    Measured: Baseline and 30 days

  26. KCCW12-PL Physical Limitation Score

    Subsection of KCCQ-12 Summary

    Measured: 30 days

  27. KCCQ12-PL Physical Limitation Score

    Subsection of KCCQ12 looking at physical limitation

    Measured: 30 days

  28. KCCQ12-SF Symptom Frequency Score

    Subsection of KCCQ-12 looking at frequency of symptoms

    Measured: 30 Days

  29. KCCQ-QL

    Subsection of KCCQ-12 that looks at quality of life

    Measured: 30 Days

  30. KCCQ-SL Social Limitation Score

    Subsection of KCCQ-12 looking at social limitation

    Measured: 30 days

Timeline

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

  1. First posted5 Nov 2024
  2. Study start7 Oct 2024
  3. Primary completion7 Feb 2025
  4. Study completion1 May 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
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
20 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06675331
Sponsor's protocol ID
10072024
Acronym
Mutton-HF
Status last verified
May 2025
First submitted
4 Nov 2024
Last updated
20 May 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Data is tribally owned data and is protected under Navajo Nation Human Research Review Board regulations.

Publications

  • Eberly LA, George C, Sandman S, Bex D, Chandra M, Shultz K, Tennison A, Wickre R, Wickre B, Morgan L, Gray L, Bolas M, Feliciano B, Damon-Mallette D, Lindsey E, Manche J, Detsoi-Smiley P, Mora P, Merino M, Shin SS. Feasibility of an Indigenous Food Is Medicine Program for Patients With Heart Failure in Rural Navajo Nation: The MUTTON-HF Nonrandomized Clinical Trial. JAMA Netw Open. 2026 Feb 2;9(2):e2556117. doi: 10.1001/jamanetworkopen.2025.56117.

    PubMed 41649816

Questions about this trial

What is this clinical trial studying?

A study testing Medically Tailored Meal Program with Traditional Navajo Foods in people with Heart Failure, run by University of Pennsylvania 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 5 inclusion and 3 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 20 May 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?

Feasibility: Percentage of meals successfully received by the patient (time frame: 30 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 NCT06675331, 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 20 May 2025.

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