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Study identifier: NCT07649148 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Dietary Tracking in Heart Failure

Condition: Heart Failure · NYHA Class II Heart Failure · NYHA Class III Heart Failure  ·  Sponsor: The Cleveland Clinic

PhaseN/A
Planned participants60
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Valesha Province, MS  ·  216-636-6153  ·  provinv@ccf.org

Jennifer Wilcox  ·  216-636-6153  ·  kirsopj@ccf.org

Always discuss trial participation with your own doctor first.

Locations (1)

Cleveland Clinic Main CampusCleveland, Ohio, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07649148