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Preparing FIM-BCS - A Lifestyle Modification for African-American Breast Cancer Survivors

Study acronym: FIM-BCS
StatusCompleted
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Trial completed Final enrollment: 14 participants (planned 24) · Primary completion date changed from estimate of Jun 2026 to May 1, 2026 · Eligibility criteria expanded, about 8 words Show 3 more changesShow less
    • Final enrollment: 14 participants (planned 24)
    • Primary completion date changed from estimate of Jun 2026 to May 1, 2026
    • Eligibility criteria expanded, about 8 words
  2. Trial status: Recruiting to Completed Enrollment target: estimated 24 to confirmed 14 · Primary completion date changed from estimate of Jun 2026 to May 1, 2026 · Study completion date changed from estimate of Jun 2026 to Jun 1, 2026 · 2 more Show 5 more changesShow less
    • Enrollment target: estimated 24 to confirmed 14
    • Primary completion date changed from estimate of Jun 2026 to May 1, 2026
    • Study completion date changed from estimate of Jun 2026 to Jun 1, 2026
    • Eligibility criteria expanded, about 10 words
    • Site details revised
  3. Trial status: Suspended to Recruiting Primary endpoint revised · Primary completion date: Jan 2026 to Jun 2026 · Eligibility criteria revised · 1 morev3 Show 4 more changesShow less
    • Primary endpoint revised
    • Primary completion date: Jan 2026 to Jun 2026
    • Eligibility criteria revised
    • Site details revised

    See this version in full on ClinicalTrials.gov ↗

  4. Trial status: Recruiting to Suspended Sponsor's reason: Awaiting IRB approval for modifications Primary completion date: Nov 2024 to Jan 2026 · Completion date: Jan 2025 to Jun 2026 · Site details revisedv2 Show 3 more changesShow less
    • Primary completion date: Nov 2024 to Jan 2026
    • Completion date: Jan 2025 to Jun 2026
    • Site details revised
  5. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Hypertension and obesity are both major risk factors for cardiovascular disease (CVD), a leading cause of death for Black women in the United States. The investigators propose examining the feasibility and acceptability of the 12-week RN-CHeFRx (Real Nourishment and Cooking Healthy Food is Rx) intervention \- grocery delivery, cooking classes, and nutrition education - for Black women with hypertension and obesity to improve nutritious eating habits and blood pressure control.
Trial Details
NCT Number NCT06504914
Lead Sponsor University of Illinois at Chicago
Conditions Hypertension, Obesity, Nutrition, Healthy
Enrollment 14 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov