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

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
France
Cochin Hospital
RECRUITING
Paris
Contact Information
Primary
Rudy BIRSEN, Dr
rudy.birsen@aphp.fr
01.58.41.42.90
Backup
Elodie LEMADRE, Mrs
elodie.lemadre@aphp.fr
01.44.84.17.34
Time Frame
Start Date: 2025-09-04
Estimated Completion Date: 2026-05
Participants
Target number of participants: 30
Treatments
Other: Cohort group
Patients will be used a connected scale during the duration of their participation in the study.~Patients will be invited to use the scale once a day. Patient's data will be accesible by medical team via a specific remote plateform.~Alert will be generated according to the evolution of clinical data, permetting a early patient management by the medical team.
Related Therapeutic Areas
Sponsors
Collaborators: Withings
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov

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