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

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 61
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
France
CH Annecy Genevois
RECRUITING
Annecy
CH Métropole Savoie
RECRUITING
Chambéry
Contact Information
Primary
Charlene DUPRE
charlene.dupre@ch-metropole-savoie.fr
+33479965910
Time Frame
Start Date: 2026-01-22
Estimated Completion Date: 2028-07-30
Participants
Target number of participants: 86
Treatments
No_intervention: Control group
patient will receive advices about benefit to practice physical activity, only once at the beginning of their treatment. Evaluation including 6 minutes walk test, chair stand test, gait-speed test, evaluation of maximum isometric strength of the quadriceps, quality of lif questionnaries, PRO, treatment tolerance, response evaluation will be held at inclusion, 3 months later and 6 months later.
Experimental: Experimental group
patient will follow an adapted physical activity program with presential (every 2 weeks the first 3 months, then once a month for 3 months) and distancial (3 times per week for 6 months) sessions.Evaluation including 6 minutes walk test, chair stand test, gait-speed test, evaluation of maximum isometric strength of the quadriceps, quality of lif questionnaries, PRO, treatment tolerance, response evaluation will be held at inclusion, 3 months later and 6 months later.
Related Therapeutic Areas
Sponsors
Leads: Centre Hospitalier Metropole Savoie

This content was sourced from clinicaltrials.gov