RecruitingNot ApplicableNCT06133426

Evaluation of the Role of Connected Scales in the Therapeutic Care of Hematology Patients


Sponsor

Assistance Publique - Hôpitaux de Paris

Enrollment

30 participants

Start Date

Sep 4, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

In this research, we will evaluate the feasibility of following by remote monitoring, using a connected scale, in hematology patients suffering from myeloma or lymphoma and requiring treatment with chemotherapy. 30 patients will be included in the research and will all use a connected scale for the duration of their participation (7 weeks +/- 1 week). During their participation, patients will be asked to weigh themselves once a day, ideally at a set time. Patient data will be accessible by the medical team via a remote monitoring platform. Alerts will be generated in the event of abnormal development of certain clinical parameters (weight, heart rate, etc.) allowing early treatment to be implemented by the medical team. At the end of their participation, we will evaluate patients' support and perception of this tool, as well as the healthcare consequences of the alerts generated by the remote monitoring platform.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether using a smart connected scale (a scale that sends data to a care team remotely) can help monitor weight changes and improve care for patients with aggressive non-Hodgkin lymphoma or multiple myeloma who are receiving chemotherapy. Weight changes can be an early warning sign of complications, and smart monitoring may allow faster intervention. **You may be eligible if...** - You are 18 or older with aggressive non-Hodgkin lymphoma or multiple myeloma - You are starting or have recently started (within 2 cycles) systemic chemotherapy, or are preparing for a stem cell transplant - You can be contacted by phone and can return home after initial hospitalization - You read and understand French **You may NOT be eligible if...** - Your expected survival is less than 3 months - You have moderate-to-severe cognitive impairment - You have a pacemaker - You are in another interventional clinical trial - You are pregnant - You are under legal protection Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEConnected scale "Body Comp Pro" from Withings

Use once a day from inclusion to week 7.


Locations(1)

Cochin Hospital

Paris, France

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NCT06133426


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