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Clinical Trials/NCT06999369
NCT06999369Enrolling By InvitationNot Applicable

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

Sutter Health1 site in 1 country180 target enrollmentStarted: February 25, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
180
Locations
1
Primary Endpoint
Blood Pressure

Study Overview

Brief Summary

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

Detailed Description

The goal of this research clinical trial is to learn understand or learn whether a guideline-based nutrition application (app) called MedChefs can help heart failure patients adopt and sustain an evidence-based dietary patterns.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to 89 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •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 Criteria

  • •• 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.

Arms & Interventions

Control

No Intervention

Patients in the control arm will be asked to complete a baseline survey questionnaire and a final survey questionnaire 6 months after they enroll. During enrollment or (if not obtained at baseline) up to 1 month after, patients will be asked to provide their baseline BP and weight measurements. Study team members will contact patients at month 3 and 6 to ask how they are doing and get follow up BP and weight measurements.

Intervention: MedChefs

Experimental

Once patients have been randomized to the MedChefs arm, they will be contacted by the research team and sent an email link to use the MedChefs app During enrollment or up to 1 month after, patients will be contacted to provide their baseline BP and weight measurements. Patients will be contacted at month 3 and 6 by the research team to see how they are doing, about their app use, get their BP and weight measurements and will be sent a final survey 6 months after they first log into MedChefs.

Intervention: MedChef App (Other)

MedChefs plus Instacart Food Voucher

Experimental

Once patients have been randomized to the MedChefs arm and voucher arm, they will be contacted by the research team and sent an email link to use the MedChefs app. Patients will also be given a $100 voucher to buy food recommended by the app. Vouchers will be provided once a month for the 6 months of the study. During enrollment or up to 1 month after, patients will be asked to provide their baseline BP and weight measurements. At month 3 and 6 the research team will contact the patients to see how they are doing and ask for patients follow up BP and weight measurements. Patients will also be asked to complete a final survey 6 months after they first log into MedChefs.

Intervention: MedChef App (Other)

MedChefs plus Instacart Food Voucher

Experimental

Once patients have been randomized to the MedChefs arm and voucher arm, they will be contacted by the research team and sent an email link to use the MedChefs app. Patients will also be given a $100 voucher to buy food recommended by the app. Vouchers will be provided once a month for the 6 months of the study. During enrollment or up to 1 month after, patients will be asked to provide their baseline BP and weight measurements. At month 3 and 6 the research team will contact the patients to see how they are doing and ask for patients follow up BP and weight measurements. Patients will also be asked to complete a final survey 6 months after they first log into MedChefs.

Intervention: MedChefs and Instacart food voucher (Other)

Outcomes

Primary Outcomes

Blood Pressure

Time Frame: Baseline and 6 months

Blood pleasure will be measure by mmHg

Secondary Outcomes

  • Weight(Baseline and 6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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