NCT06133426Recruiting
Evaluation of the Role of Connected Scales in the Therapeutic Care of Hematology Patients
Source: ClinicalTrials.gov · Last updated 15 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 30 (estimated)
- First submitted
- 30 Oct 2023
- Start date
- 4 Sept 2025
- Primary completion date
- May 2026
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Diseases
- Multiple myeloma
- NCT number
- NCT06133426
What you commit to
- Study type: Interventional
- Planned participants: 30
- From 4 Sept 2025 to the primary completion date, May 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- 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
Other
- Patient with an estimated life expectancy \< 3 months
- Patient with a pacemaker
- Patient participating in another intervention research project
- Pregnant patient
- Patient deprived of liberty
- Patient under legal protection (guardianship or curatorship)
Who the study is looking for
- 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
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Cochin Hospital Coordinator of this site? Confirm its status | Paris | France | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.