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Cutting back on ultra-processed foods in people with heart failure

Looks at eating fewer ultra-processed foods in adults with heart failure.

Key facts

Who runs it
The Cleveland Clinic
Where
Cleveland, United StatesSee the site
Trial code
Registry title
Dietary Tracking in Heart Failure
Status
Not yet recruiting
People taking part
60 people, planned
Starts
Dec 2026
Expected to end
Dec 2040
Type of study
Observational
Treatments tested
  • Limiting Ultraprocessed Food (UPF) in Diet
Record updated
28 September 2026

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with heart failure (NYHA Class II-III) who can track their food with the Cronometer app and cook at home on their own. It tests a diet that cuts ultra-processed foods.

Age
18 years or older
Sex
All sexes can join.
Disease stage
Heart failure, NYHA Class II-III

Main reasons for not taking part

  • Past heart transplant or LVAD implant
  • Unable or unwilling to follow dietary coaching to cut ultra-processed foods
  • eGFR below 30 ml/kg/1.73m2

The registry criteria, word for word

Show all 5 criteriaShow less

Who can take part

  • Adults (≥18 years) with NYHA Class II-III HF
  • Able to use Cronometer to track dietary intake and able to prepare food at home independently (able to modify dietary intake)

Who cannot take part

  • History of heart transplant or LVAD implant
  • eGFR <30 ml/kg/1.73m2
  • Unable or unwilling to follow dietary coaching for UPF reduction

Where in United States

  • Cleveland Clinic - Main CampusCleveland, United StatesContact: Valesha Province, MSNot yet recruiting

About the trial

What the trial wants to find out

Emerging evidence links ultra processed foods (UPFs) to adverse cardiovascular outcomes. UPFs are often high in sodium, unhealthy fats and added sugars, while being low in essential nutrients and fiber. UPFs contribute to systemic inflammation, fluid retention, and metabolic dysfunction-key drivers of HF and kidney disease progression. Traditional dietary counseling often lacks specificity around food processing levels. Furthermore, the majority of nutrition studies relied on extensive self-reported dietary recall food frequency questionnaires (FFQ) that are subjective, often labor intensive, and difficult to implement practically in the clinical setting. As such, researchers have developed metabolite scores from blood and urine samples to help quantify UPF consumption, which has the promise to better guide dietary counseling and track process. Therefore, the aim of this study is to evaluate the feasibility and physiological impact of a structured UPF-reduction dietary intervention in patients with HF, leveraging both digital dietary tools (Cronometer) and biomarker assessments.

Treatments tested

  • Limiting Ultraprocessed Food (UPF) in Diet

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?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Dietary Optimization Through Tracking and Integrated Evaluation
Plain-language title
Cutting back on ultra-processed foods in people with heart failureGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Record updated
28 September 2026