NCT06999369
Heart Failure Food Intervention Trial: Impact of a Guideline-based Nutrition Digital Tool in Heart Failure Patient Clinical Outcomes
Enrolling by Invitation
NAAges 18–89InterventionalHealth servicesSutter HealthInvestigator-initiated
~180 participants
Updated 2025-05-31 on ClinicalTrials.gov
What's tested:MedChef AppMedChefs and Instacart food voucher
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Blood Pressure
Measured over Baseline and 6 months
Conditions
NCT06999369
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
2121 N. California Blvd., Suite 310
Walnut Creek, Californiano site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Want this trial checked against your situation?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Eligibility criteria
Inclusion
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
Exclusion
• 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.
What this trial measures
- Blood PressureBaseline and 6 months
Blood pleasure will be measure by mmHg