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Evaluation of a PREHABilitation Protocol Using Adapted Physical Activity (APA) for Multiple Myeloma Patients Eligible for Intensive Autologous Stem Cell Transplantation Treatment (PREHAB-APA)

C

Centre Hospitalier Henri Duffaut - Avignon

Status

Not yet enrolling

Conditions

Multiple Myeloma

Treatments

Other: Adapted exercises
Behavioral: Physical activity questionnaire
Behavioral: Physical condition
Behavioral: Quality of Life questionnaire
Behavioral: Questionnaire of Fatigue
Other: No intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06789003
PREHAB-APA

Details and patient eligibility

About

Adapted physical activity for patients with haematological malignancies generally has positive effects on quality of life, fatigue and physical condition. However, some studies show little or no effect.

This may be explained by inefficient protocols, but also by low rates of patient acceptability regarding the proposed exercises.

The multiplicity of APA protocols and the fluctuation of their results mean that validity, methodology and effects on patients need to be verified before they can be considered for implementation in healthcare services. A program must prove its feasibility, but patients must also adhere to it.

Acceptability can be measured by adherence, which represents the number of validated sessions in relation to the number of planned sessions, and by attrition, which corresponds to the number of stops or drop-outs for any reason. The various APA programs offered in the context of intensive auto or allograft treatment are limited, notably by adherence, which can fall by as much as 24%, and attrition, which can be as high as 67%. Optimization of the proposed exercises and follow-up methods is therefore necessary in order to propose an APA program that will be feasible, effective and acceptable to a maximum number of patients.

To meet these objectives for patients with multiple myeloma eligible for autologous stem cell transplantation, the protocol for this study took into consideration the various recommendations of previous publications and the guidelines from HAS (French National Authority for Health).

The ultimate goal of this study is to validate, in terms of effectiveness and acceptability, the methodology and in particular the use of new specific tools for optimizing an APA program. It will subsequently be offered to all patients with multiple myeloma eligible for autologous stem cell transplantation, independently of their age or physical condition, while respecting their rhythm and physical condition.

Enrollment

120 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 18 years old.
  • CML patient in chronic phase, eligible for oral therapy.
  • Diagnosis of multiple myeloma.
  • Patient eligible for autologous stem cell transplantation.
  • Patient capable to read, understand and complete a questionnaire in french.
  • WHO less than or equal to 2.
  • Patient affiliated with french social security.
  • Patient with a medical prescription for APA.

Exclusion criteria

  • Patient with previous cancer within the previous 3 years (except basal cell and squamous cell skin cancers, carcinomas in situ of any type that have been previously resected, and stable prostate or breast cancers more than 3 years old and undergoing adjuvant hormone therapy).
  • Medical contraindications to APA (heart failure, angina, unbalanced hypertension, bone metastases, severe osteoporosis, etc.)
  • Sensory or motor neuropathy.
  • Patient deprived of liberty, under guardianship or curatorship.
  • Patient considered socially or psychologically unfit to be enrolled in a study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

120 participants in 2 patient groups

APA group
Experimental group
Treatment:
Behavioral: Questionnaire of Fatigue
Behavioral: Quality of Life questionnaire
Behavioral: Physical condition
Behavioral: Physical activity questionnaire
Other: Adapted exercises
Control group
Active Comparator group
Treatment:
Other: No intervention
Behavioral: Questionnaire of Fatigue
Behavioral: Quality of Life questionnaire
Behavioral: Physical condition
Behavioral: Physical activity questionnaire

Trial contacts and locations

1

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Central trial contact

Emmanuelle Guilie, APA; Marilyne Grinand, PhD

Data sourced from clinicaltrials.gov

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