Understanding how heart failure patients follow remote monitoring guidelines
Description of Patient Adherence to Heart Failure Remote Monitoring and Its Determinants
This study looks at how well heart failure patients follow remote monitoring guidelines after being hospitalized to see what helps or hinders their adherence.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 150 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier Régional Metz-Thionville Academic / other |
| Locations | 2 sites (Metz and 1 other locations) |
| Trial ID | NCT06723509 on ClinicalTrials.gov |
What this trial studies
This observational cohort study aims to assess patient adherence to remote monitoring protocols for heart failure after hospitalization. It involves retrospective data collection and prospective semi-structured interviews with patients who have received telemonitoring since 2020 at the CHR Metz-Thionville. The study will gather socio-demographic and clinical data from patient records and telerecording software, while also exploring factors influencing adherence through interviews. Patients will be monitored for 12 months or until their follow-up is terminated.
Who should consider this trial
Good fit: Ideal candidates include adults diagnosed with heart failure who have participated in telemonitoring at the CHR Metz-Thionville.
Not a fit: Patients who have not received telemonitoring for heart failure or who refuse to participate in the study will not benefit.
Why it matters
Potential benefit: If successful, this study could enhance the effectiveness of remote monitoring for heart failure patients, potentially improving their health outcomes.
How similar studies have performed: Previous studies have shown that remote monitoring can improve outcomes for heart failure patients, indicating potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Major patient * Heart failure * Having received telemonitoring for heart failure from the CHR * Patient clearly informed about the research in progress * Gave oral consent for telephone interview Exclusion Criteria: * Refusal to reuse data for the study
Where this trial is running
Metz and 1 other locations
- CHR Metz Thionville Hopital de Mercy — Metz, France (Recruiting)
- CHR Metz-Thionville Hopital Bel Air — Thionville, France (Recruiting)
Study contacts
- Study coordinator: Arpiné EL NAR, PhD
- Email: projet-recherche-clinique@chr-metz-thionville.fr
- Phone: 0033387557766
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.