Heart Failure Food Intervention Trial: Impact of a Guideline-based Nutrition Digital Tool in Heart Failure Patient Clinical Outcomes

Enrolling by invitation · Not applicable

Conditions studied: Heart Failure

In brief

Measuring the impact of a guideline-based nutrition digital tool in heart failure patients

Key facts

Study ID: NCT06999369
Run by: Sutter Health
People needed: 180
Starts: 2025-02-25
Expected to finish: 2026-12-31
Last updated by the study team: 2025-05-31

Who can join

Age: 18 and older, up to 89. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

18-89 years old at time of enrollment
Any type of Heart failure diagnosis (e.g., I50.x) between 1/1/2023-present
Recent hospital admission (within a year)
Race/ethnicity: All race/ethnic groups
Location: patients have been treated in the Greater East Bay division and Greater Silicon Valley division areas.
Patients with have at least 1 office/outpatient visit with a primary care physician or cardiologist visit before index date

You may not qualify if…

• Patients with certain patient history (cognitive disabilities) and end stage renal or metastatic cancer diagnosis
Patients with active drug/substance use. Patients with heart failure who have active substance use are excluded from the study. HF patients with substance use require additional monitoring and follow up due to potential severe withdrawal symptoms, acute HF exacerbation and drug overdose or medication errors. Standard protocol includes additional monitor vital signs (e.g., blood pressure, heart rate) and HF symptoms (e.g., edema, dyspnea), and performing regular laboratory tests (e.g., renal function, electrolytes) which is beyond the clinical and logistical capabilities of this study.

Where it is running

2121 N. California Blvd., Suite 310 — Walnut Creek, California, United States

Full record on ClinicalTrials.gov

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