Heart failure telemonitoring eligibility after program exclusion
Official title: Evaluation of Eligibility Criteria for Heart Failure Telemonitoring : Analysis of CARDIAUVERGNE's Cohort
Run by University Hospital, Clermont-Ferrand · NCT07278583 · Data updated 2026-11-12
This study tests whether patients who stop telemonitoring due to criteria no longer being met have a low risk of worse health outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 130 (estimated) |
| Sponsor | University Hospital, Clermont-Ferrand Academic / other |
| Locations | 1 site (Clermont-Ferrand) |
| Status | Recruiting |
| Started | December 5, 2025 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | July 30, 2026 |
| Trial ID | NCT07278583 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults who were enrolled in the CARDIAUVERGNE telemonitoring program between January 1, 2023 and December 31, 2024 and subsequently excluded due to not meeting eligibility criteria.
✕Probably not a fit
Patients who continue to experience heart failure progression or who develop new criteria indicating risk may not benefit from reduced monitoring.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study analyzes the prognosis of heart failure patients who were enrolled in a hospital-based telemonitoring program and subsequently excluded when they no longer met eligibility criteria. Patients were followed from January 1, 2023 to December 31, 2024, with follow-up assessments at 6 months and 1 year after exclusion. Data are drawn from medical records, including NYHA status, NT-proBNP levels, weight on connected scales, and any subsequent hospitalizations or changes in treatment. The study aims to determine if loss of eligibility correlates with favorable evolution and reduced need for remote monitoring resources. No intervention beyond standard telemonitoring and documentation of exclusions is described.
Why it matters
Potential benefit: If successful, clinicians may safely reduce monitoring for patients who no longer meet criteria, optimizing resource use without compromising outcomes.
How similar studies have gone: Prior telemonitoring programs have shown mixed results; this study addresses eligibility-based discontinuation to clarify safety of stopping remote monitoring.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * adults * able to read and understand french * included in CARDIAUVERGNE telemonitoring program from 1st january 2023 to 31st december 2024 such as defined by the french health authorithy criteria (heart failure within 12 months or dyspnea at least NYHA 2 associated with NTproBNP of at least 1000pg/mL) and excluded by medical decision as no longer presenting eligibillity criteria Exclusion Criteria: * Patients leaving telemonitoring for other reasons (choice, death, medical reason, relocation, inobservance)
Where it's running
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CHU Clermont-Ferrand
Clermont-Ferrand, France Recruiting
Study contacts
- Principal investigator: Clément RIOCREUX — University Hospital, Clermont-Ferrand
- Study coordinator: Lise Laclautre
- Email: promo_interne_drci@chu-clermontferrand.fr
- Phone: 334.73.754.963
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.