Actively Recruiting
Description of Patient Adherence to Heart Failure Remote Monitoring and Its Determinants
Led by Centre Hospitalier Régional Metz-Thionville · Updated on 2024-12-09
150
Participants Needed
2
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a monocentric cohort study, with retrospective data collection and prospective semi-structured interviews. All patients who, since 2020, have received telemonitoring for heart failure after hospitalization at the CHR Metz-Thionville will be included. Patients will be informed of the study by e-mail, or by post if no e-mail is available. Data concerning their socio-demographic and clinical characteristics will be collected from the computerized patient record, and telerecording data will be extracted from the telerecording software. Patients whose follow-up is still in progress will be monitored (=simple data collection) for 12 months, or until follow-up is terminated if necessary. Patients whose follow-up has been interrupted for less than a month at the start of the study (to avoid memory bias) or during the course of the study will be contacted by telephone by the IPA carrying out the telemonitoring, and offered, after oral consent, a semi-structured interview to investigate the reasons for the interruption.
CONDITIONS
Official Title
Description of Patient Adherence to Heart Failure Remote Monitoring and Its Determinants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- Refusal to reuse data for the study
AI-Screening
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Trial Site Locations
Total: 2 locations
1
CHR Metz Thionville Hopital de Mercy
Metz, France, 57085
Actively Recruiting
2
CHR Metz-Thionville Hopital Bel Air
Thionville, France, 57100
Actively Recruiting
Research Team
A
Arpiné EL NAR, PhD
CONTACT
C
Céline PETITJEAN
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
0
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