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
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData 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