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Clinical Trials in France / NCT07547007
Recruiting Not applicable

Benefits of a 6-month, Individualized, Hybrid, "Real-life" Adapted Physical Activity Program on the Quality of Life of Patients Treated for Multiple Myeloma

NCT07547007 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-01-22
Last updated
2026-04-23

Condition(s) studied

Multiple Myeloma (MM)

Investigational drug(s) / intervention(s)

Adapted physical activity

Adapted physical activity: the intervention is a "real life"6 months adapted physical activity program which is individualised and hybrid (presential and distancial) . It includes a session in presential (at hospital) every 2 weeks for the first 3 months then once a month and 3 sessions par week for 6 months at home.

Study summary

The goal of this clinical trial is to evaluate the effect of a long-term, individualized, hybrid adapted physical activity program on the quality of life of patients with multiple myeloma. The main question it aims to answer are :

Does this logn term, individualized and hybrid adapted physical activity program improve quality of life in multiple myeloma patient ? What are the effects of this program on effort tolerance, pain, muscular mass, osteolytic lesions, tolerance to treatment, response to treatment? If there is a comparison group: Researchers will compare \[arm information\] to see if \[insert effects\].

Participants will be randomised in 2 groups.

* control group: patients will receive only advices about physical activities benefit
* interventional group: This group will be offered a program of adapted physical activities mixing sessions at home (remote) and sessions at the hospital (in person).

Eligibility

Sex
ALL
Min age
61 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * newly diagnosed or relapse multiple myeloma, \> 60 yo, not eligible to transplant * 1st to 4th line of treatment initiated during the last 3 months * receiving a systemic treatment that involved visit to the hospital at least twice a month durig the first 3 months and at least once a month the next 3 months Exclusion Criteria: * severe cardiac amyloidosis * absolute contraindication to physical activity * inability to comply with the protocol requirements * not french speaker * patient under guardianship or curatorship * pregnant or lactating women

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
CH Annecy Genevois Annecy France Recruiting
CH Métropole Savoie Chambéry France Recruiting

More Centre Hospitalier Metropole Savoie trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07547007 on ClinicalTrials.gov ↗ ← All trials in France