Actively Recruiting
Evaluation of the Role of Connected Scales in the Therapeutic Care of Hematology Patients
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-09-15
30
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
Sponsors
A
Assistance Publique - Hôpitaux de Paris
Lead Sponsor
W
Withings
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Evaluation of the Role of Connected Scales in the Therapeutic Care of Hematology Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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 will not qualify if you...
- Patient with an estimated life expectancy less than 3 months
- Patient with moderate to severe cognitive impairment (assessed by MMSE less than 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)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Cochin Hospital
Paris, France, 75014
Actively Recruiting
Research Team
R
Rudy BIRSEN, Dr
CONTACT
E
Elodie LEMADRE, Mrs
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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