Actively Recruiting

Age: 18Years +
All Genders
NCT05417490

Factors Influencing Participation in PRADO and Telemedicine Interventions in Heart Failure

Led by University Hospital, Montpellier · Updated on 2026-04-15

700

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Patients with heart failure (HF), after hospitalization, present a marked fragility. Interventions improving the coordination of care actors at the time of discharge from hospitalization have been tested and have shown, in preliminary studies, a reduction in rehospitalizations for heart failure and all-cause mortality. Among these promising devices, two have recently been deployed nationwide. * The return home program for IC patients (PRADO IC), set up by the Health Insurance, aims to facilitate the return and stay at home after hospitalization. It offers assistance with the initiation of outpatient medical follow-up, nursing follow-up for 2 to 6 months depending on the severity of the patient, and a follow-up log facilitating the exchange of information. * At the same time, as part of the ETAPES (Telemedicine experiments for the improvement of healthcare pathways) program of the Health Insurance, the deployment of telemedicine for remote monitoring of heart failure pursues a comparable objective of reducing rehospitalizations. These two systems are widely deployed on a national scale, and are intended to be universal. Our hypothesis is that adherence to care transition and telemedicine programs, and therefore their effectiveness, may depend on their association, as well as socio-demographic, cultural, and geographical factors.

CONDITIONS

Official Title

Factors Influencing Participation in PRADO and Telemedicine Interventions in Heart Failure

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patient
  • Patient hospitalized for cardiac decompensation or a condition where heart failure is a key factor
  • Patient agrees to participate in the research (consent given)
Not Eligible

You will not qualify if you...

  • Refusal to participate
  • Pregnant or breastfeeding women
  • Patients unable to provide protected adult consent or considered vulnerable
  • Individuals deprived of liberty by judicial or administrative decision

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital, Montpellier

Montpellier, France

Actively Recruiting

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Research Team

F

François ROUBILLE, PUPH

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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