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

Recruiting now · Not applicable

Conditions studied: Lymphoma, Non-Hodgkin, Myeloma Multiple

In brief

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.

Key facts

Study ID

NCT06133426

Run by

Assistance Publique - Hôpitaux de Paris

People needed

30

Starts

2025-09-04

Expected to finish

2026-05-01

Last updated by the study team

2025-09-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient aged 18 and over (male or female)
• Patient suffering from aggressive non-Hodgkin's lymphoma or multiple myeloma with a plan for systemic chemotherapy or having started two cycles or less or patient with the need for therapeutic intensification under the cover of autograft in the context of myeloma or lymphoma
• Patient who can be contacted by telephone during their participation in the research
• Patient able to return home at the end of their initial hospitalization
• Patient affiliated to social security
• Patient able to read and speak French
• Patient having signed free, informed and written consent

You may not qualify if…

• Patient with an estimated life expectancy < 3 months
• Patient with moderate to severe cognitive impairment (assessed by MMSE < 20)
• Patient with a psychiatric or physical disability that does not allow the use of the device
• Patient with a pacemaker
• Patient participating in another intervention research project
• Pregnant patient
• Patient deprived of liberty
• Patient under legal protection (guardianship or curatorship)

Where it is running

• Cochin Hospital — Paris, France (enrolling)

Full record on ClinicalTrials.gov

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