Benefits of a 6-month, Individualized, Hybrid, "Real-life" Adapted Physical Activity Program on the Quality of Life of Patients Treated for Multiple Myeloma
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Adapted physical activity.
- Кому может быть актуально
- Состояния в реестре: Multiple Myeloma (MM). Базовые параметры: от 61 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Франция
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
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
Обзор
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).
Вмешательства
- Процедура 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.
Первичные конечные точки
- compare EORTC-QLQ-C30 summary score at 6 months between both groups [Срок оценки: 6 months post inclusion]
Вторичные конечные точки (11)
- compare functional and symptomatic dimension of EORTC-QLQ-C30 at 3 and 6 months between both groups [Срок оценки: 3 and 6 months after inclusion]
- study the effect of 6 months intervention on objective and subjective level of physical activity [Срок оценки: 3 months and 6 months after inclusion]
- study effect of 6 months of intervention on bone pain (FACT-Bone) evolution [Срок оценки: 3 and 6 months post inclusion]
- Study effect of 6 months intervention on muscular mass [Срок оценки: 6 months post inclusion]
- study the effect of 6 months intervention on osteolytic lesion [Срок оценки: 6 months post inclusion]
- faisability of the intervention in population of interest [Срок оценки: from frist intervention day to 6 months]
- study the effect of 6 months intervention on patient tolerance to immunomodulators [Срок оценки: from inclusion to end of intervention]
- study effect of 6 months intervention on immunomodulators treatment response [Срок оценки: 3 and 6 months after inclusion]
- Identification of the factors mediating the improvement in quality of life following the intervention [Срок оценки: 0 and 6 months of intervention]
- safety of the intervention [Срок оценки: from 0 to 6 months]
- study effect of 6 months of intervention on disease-specific patient's reported outcomes (FACT-MM) [Срок оценки: 3 and 6 months post inclusion]
Критерии участия
Критерии включения
- 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
Критерии исключения
- 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
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Открытое
- Основная цель
- Лечение
Центры проведения
Франция · 2 центра
- CH Annecy Genevois — Annecy
- CH Métropole Savoie — Chambéry
Идентификаторы
NCT: NCT07547007 · CHMS25006 · 2025-A01123-46