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Life sciences · Interventional Study
ClinicalTrials.gov · October 13, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07439081). This is a study registration, not published results. Lead sponsor: Médipôle Lyon-Villeurbanne. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 504 participants (ACTUAL). Conditions: Heart Failure, Acute Heart Failure (AHF). Interventions: DEVICE: Satelia® Cardio Remote Patient Monitoring System. Primary outcome measures: Number of Cardiac Rehospitalizations , 1 year before enrollment and 1 year after enrollment. Brief summary: Heart failure is a leading cause of hospitalization and readmission, particularly among older adults with multiple comorbidities. Traditional outpatient follow-up may be insufficient to detect early clinical deterioration in this vulnerable population. Remote patient monitoring (RPM) using non-invasive symptom and weight tracking has been proposed to enhance ambulatory care, but its effectiveness appears to depend on integration within structured care pathways. The OPTIMUM study evaluated the real-world implementation of an integrated ambulatory heart failure care pathway combining non-invasive RPM with multidisciplinary follow-up in routine clinical practice. Patients enrolled after a recent heart failure hospitalization were managed using the Satelia® Cardio monitoring system, nurse-led therapeutic education, and a planned cardio-geriatric day-hospital reassessment. The study aimed to describe pathway implementation and assess associations with rehospitalizations, mortality, alert activity, and patient and healthcare professional satisfaction in an older, frail population.