Heart Patients' remote monitoring habits under the microscope
NCT ID NCT06723509
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at 179 heart failure patients who used remote monitoring after a hospital stay. Researchers tracked how long patients kept using the system and interviewed some who stopped to understand why. The goal is to learn what helps or hinders sticking with remote monitoring, which could lead to better support for heart failure patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help doctors understand why patients stop using remote monitoring and find ways to keep them engaged, potentially improving heart failure management.
- What could go wrong
- This is an observational study, not a treatment trial. It only describes what happened in one hospital, so results may not apply to all patients or settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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179 people
The number who actually took part.
- Started
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Jul 2024
- Finished
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Oct 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Heart failure patients
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
CHR Metz Thionville Hopital de Mercy
Metz, 57085, France
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CHR Metz-Thionville Hopital Bel Air
Thionville, 57100, France
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Other studies related to the condition(s) this trial covers.
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