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FIM+DASH: Food is Medicine Intervention to Promote Healthy Eating and Blood Pressure Control

Study acronym: FIM+DASH
StatusRecruiting
PhasePhase 2
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Primary completion pushed from Mar 2029 to Jun 30, 2030 Primary endpoint(s) modified · Recruitment opened · Completion pushed from Jun 2029 to Sep 2030 · 4 morev2 Show 7 more changesShow less
    • Primary endpoint(s) modified
    • Recruitment opened
    • Completion pushed from Jun 2029 to Sep 2030
    • Start date changed from estimate of Mar 1, 2026 to May 22, 2026
    • Eligibility criteria expanded, about 6 words
    • Secondary endpoints revised (3)
    • Study sites revised (4)

    See this version in full on ClinicalTrials.gov ↗

  2. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this clinical trial is to treat both hypertension and obesity in adults using a food is medicine framework. Participants will be randomized 1:1 to FIM+DASH or usual-care control. The 24-week trial includes a 12-week FIM+DASH intervention followed by a 12-week maintenance period and leverages existing partnerships with community-based organizations for home food delivery and culinary skill-skill building. The main questions it aims to answer are: (1) What is the effect of FIM+DASH vs. usual care control on blood pressure? (2) What is the effect of FIM+DASH vs. usual care control on DASH diet adherence (diet quality), body weight, and waist circumference? (3) How to identify factors associated with the sustainability and scalability of FIM+DASH in real-world settings?
Trial Details
NCT Number NCT07332741
Lead Sponsor University of Illinois at Chicago
Conditions Hypertension, Hypertension (HTN), Obesity & Overweight
Enrollment 150 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov