Digital Remote Home Monitoring for Heart Failure
Stopped early · Not applicable
Conditions studied: Heart Failure, Systolic
In brief
We will enroll 150 adult participants with systolic heart failure into the ADHERE-HF trial. The study will randomize participants in a 1:2 fashion to usual care or usual care plus the American Heart Association's Digital Solution for 90 days. This wearable device and careplan package is hypothesized to improve rates of guideline directed heart failure medical care for participants.
Key facts
- Study ID
- NCT05988749
- Run by
- University of Texas Southwestern Medical Center
- People needed
- 15
- Starts
- 2024-12-13
- Expected to finish
- 2025-11-30
- Last updated by the study team
- 2026-02-18
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- ≥18-year-old adults with a clinical diagnosis of heart failure AND a left ventricular ejection fraction ≤40% by transthoracic echocardiogram or cardiac MRI within 12 months prior to enrollment.
You may not qualify if…
- Patients who are pregnant.
- Patients who do not have a smartphone or access to the Internet
- Prisoners or refugees.
- Patients who are homeless or have unstable housing.
- Unable or unwilling to consent or use study related materials.
- On-going cocaine, methamphetamine, opioid, alcohol, or other illicit substance abuse as determined by the study PI.
- Not fluent in English or Spanish.
- Students or trainees at UT-Southwestern or Parkland Health System.
- Enrolled or considering hospice.
- Recent or home inotropic therapy, or heart transplant evaluation.
- Survival anticipated <6 months.
- End-stage renal disease, receiving dialysis or eGFR ≤30 mL/min/1.73m2
- Non-Texas resident
Where it is running
- Parkland Health & Hospital System — Dallas, Texas, United States
- UT Southwestern Medical Center — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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