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Use of Bedside Imaging and Community Health Workers for Early Screening and Referral of Pre-symptomatic Stage B Heart Failure in the Emergency Department

StatusCompleted
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

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  1. Trial completed
    • Primary completion date changed from estimate of Jun 30, 2026 to Aug 1, 2026
    • Eligibility criteria expanded, about 6 words
    • Site details revised
  2. Trial status: Not Yet Recruiting to Recruiting
    • Site details revised
    v5
  3. Start date: Jul 2025 to Oct 13, 2025v4 Show 4 more changesShow less
    • Primary completion date: Jun 2026 to Jun 30, 2026
    • Study completion date: Sep 2026 to Sep 30, 2026
    • Site contact updated
    • Collaborators expanded, about 9 words
  4. Re-verified, no change to tracked fieldsv3
  5. Eligibility criteria shortened, about 39 wordsv2
  6. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 learn if using point-of-care ultrasound (POCUS) can increase participant engagement and changes in behavior among adults with risk factors for pre-symptomatic heart failure presenting to the emergency department. The main questions it aims to answer are: 1. Does POCUS increase understanding of heart failure and the likelihood to improve diet, exercise, and follow up? 2. Does POCUS improve diet, exercise, follow up, and self-efficacy at three months post-intervention? Researchers will compare an educational intervention with versus without POCUS to see if POCUS works to improve outcomes. Participants will: Receive either the educational intervention alone or an educational intervention plus POCUS. They will report the difference in their understanding and likelihood to improve diet, exercise, and follow up immediately post-intervention. They will also report changes in diet, exercise, follow up, and self-efficacy at three months post-intervention.
Trial Details
NCT Number NCT06769880
Lead Sponsor Rush University Medical Center
Collaborators: National Institute on Minority Health and Health Disparities (NIMHD)
Conditions
(from sponsor)		 Heart Diseases
Related terms Heart Diseases
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov