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.
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.
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 group | Role | What they receive |
|---|---|---|
| Meal delivery program | Experimental | Patients 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.
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)
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
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
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
Hospitalization or Emergency Department Visit
Hospitalization or Visit to Emergency Department (All-cause)
Measured: 90 Days
Laboratory Biomarker Data
Albumin, prealbumin, creatinine, NT-proBNP, HbA1c, Total cholesterol, LDL-C, HDL-C, Triglycerides, CRP
Measured: Baseline, 30 Days
Weight/Body Mass Index
weight and BMI
Measured: Baseline, 30 Days
Emergency Room Visits
ER visits: All cause
Measured: 90 Days
ER visits or hospitalizations
All cause
Measured: 180 days
ER visit for Heart Failure
ER visit for volume overload or HF symptoms
Measured: 90 Days
Heart Failure Hospitalizations
Hospitalizations for heart failure specifically
Measured: 90 days
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
KCCW12-PL Physical Limitation Score
Subsection of KCCQ-12 Summary
Measured: 30 days
KCCQ12-PL Physical Limitation Score
Subsection of KCCQ12 looking at physical limitation
Measured: 30 days
KCCQ12-SF Symptom Frequency Score
Subsection of KCCQ-12 looking at frequency of symptoms
Measured: 30 Days
KCCQ-QL
Subsection of KCCQ-12 that looks at quality of life
Measured: 30 Days
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.
- First posted5 Nov 2024
- Study start7 Oct 2024
- Primary completion7 Feb 2025
- Study completion1 May 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Heart FailureStudies of the same condition, open and under way.
- More trials run by University of PennsylvaniaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- University of Pennsylvania
- Sponsor type
- University, hospital or other
- Collaborators
- Indian Health Service (IHS), Brigham and Women's Hospital, American Heart Association
- Responsible party
- Sponsor
- Investigators
- Lauren Eberly, MD, MPH, Principal investigator, Indian Health Service (IHS)
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
Study at a glance
From the registry record, last updated by the sponsor on 20 May 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Medically Utilized Tailored Traditional Meals to Optimize Nutrition in Heart Failure Pilot Trial
- ClinicalTrials.gov ID
- NCT06675331
- Acronym / sponsor ID
- Mutton-HF / 10072024
- Conditions
- Heart Failure
- Keywords
- indigenous, food is medicine, Traditional Foods, Nutrition Security, Navajo
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 20 participants (actual)
- Lead sponsor
- University of PennsylvaniaUniversity, hospital or other
- Collaborators
- Indian Health Service (IHS), Brigham and Women's Hospital, American Heart Association
- Study start
- 7 Oct 2024 (actual)
- Primary completion
- 7 Feb 2025 (actual)
- Study completion
- 1 May 2025 (actual)
- First posted
- 5 Nov 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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).
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Meal delivery program | Experimental | Other: Medically Tailored Meal Program with Traditional Navajo FoodsPatients 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) |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- 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
Key exclusion criteria (3 listed)
- Hospice care
- Living in acute rehabilitation or skilled nursing facility
- Living outside the Gallup Service Unit (outside 50-mile catchment area)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Medically Tailored Meal Program with Traditional Navajo FoodsPatients will receive medically-tailored meals incorporating local traditional Navajo foods | Other | Meal delivery program |
Primary outcome
Feasibility: Percentage of meals successfully received by the patient
Time frame: 30 days
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.
30 secondary outcomes
Cultural Connectedness Scale-California
Time frame: Baseline, 30 Days
Kansas City Cardiomyopathy Questionnaire (KCCQ-12)
Time frame: Baseline, 30 Days
USDA Adult Food Security: Six Item short Form survey
Time frame: Baseline, 30 Days
Hospitalization or Emergency Department Visit
Time frame: 90 Days
Laboratory Biomarker Data
Time frame: Baseline, 30 Days
Weight/Body Mass Index
Time frame: Baseline, 30 Days
Emergency Room Visits
Time frame: 90 Days
ER visits or hospitalizations
Time frame: 180 days
ER visit for Heart Failure
Time frame: 90 Days
Heart Failure Hospitalizations
Time frame: 90 days
Feasibility: Percentage of meals delivered successfully to the Gallup Food Pantry
Time frame: 30 days
Feasibility of Intervention: Delivery/Pick-Up
Time frame: 30 days
Acceptability of the Intervention (AIM) Measure
Time frame: 30 days
Net Promoter Score
Time frame: 30 days
Fidelity: Consumption
Time frame: 30 days
Acceptability: Taste
Time frame: 30 days
Qualitative measures of feasibility and acceptability
Time frame: 30 days
Feasibility of Supporting Local Food Systems
Time frame: 30 days
Feasibility: Local Food Sourcing
Time frame: 30 days
Feasibility of Outcome Assessment
Time frame: 30 days
Fidelity of Intervention
Time frame: 30 days
Adoption of Intervention
Time frame: 30 days
Diet Quality
Time frame: Baseline and 30 days
Physical Activity
Time frame: Baseline and 30 days
General Health Status
Time frame: Baseline and 30 days
KCCW12-PL Physical Limitation Score
Time frame: 30 days
KCCQ12-PL Physical Limitation Score
Time frame: 30 days
KCCQ12-SF Symptom Frequency Score
Time frame: 30 Days
KCCQ-QL
Time frame: 30 Days
KCCQ-SL Social Limitation Score
Time frame: 30 days
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 May 2025.
- Derived from this study: PubMed 41649816Eberly 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.
- Trial websiteLink provided by the sponsor.
- Individual participant dataSharing planned: No. Data is tribally owned data and is protected under Navajo Nation Human Research Review Board regulations.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Lauren Eberly, MD, MPH principal investigator
Indian Health Service (IHS)
1 site in 1 country: see every site and its status.
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.