Feasibility Assessment of Adapted Physical Activity in Patients Treated for a Brain Tumor

Starting soon · Not applicable

Conditions studied: Brain Tumor Adult

In brief

The goal of this clinical trial is to assess the feasibility of an adapted physical activity (APA) program in adult patients (≥18 years) with primary brain tumors, regardless of tumor type, grade, treatment stage, or the presence of motor, sensory, attention, concentration, or memory deficits. The main question it aims to answer is: What is the effective adherence rate to an APA program among eligible patients with primary brain tumors? Additional questions include: * What is the observance rate (number of sessions completed, intensity achieved, and duration) during the 3-month supervised APA program? * What is the retention rate (proportion of patients completing the program and continuing APA beyond the initial period)? * What is the impact of APA on quality of life, anxiety-depression, and cancer-related symptoms (measured via QLQ-BN20, HADS, and MFI-20 questionnaires at baseline, 3, and 4 months)? Participants will: * Undergo a 3-month supervised APA program (with possible continuation beyond this period). * Use connected watches to monitor physical activity (if they accept the general conditions of use). * Complete self-questionnaires (IPAQ, BREQ-2, QPP, QLQ-BN20, HADS, MFI-20) at inclusion, 3 months, and 4 months. * Be followed for a total of 4 months after inclusion.

Key facts

Study ID

NCT07570485

Run by

Center Eugene Marquis

People needed

90

Starts

2026-06-01

Expected to finish

2028-06-01

Last updated by the study team

2026-06-12

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Men or women ≥ 18 years old,
• Receiving medical oncology treatment at the CLCC Eugène Marquis,
• Diagnosed with a primary brain tumour, regardless of diagnosis, grade or treatment,
• Possible motor, sensory, attention, concentration, or memory deficits,
• Patients who accept the general terms of use for connected watches
• Patients affiliated with or covered by the French social security system,
• Patients who have received information and signed informed consent (or their legal representative),

You may not qualify if…

• WHO score ≥ 3
• Comprehension disorders that prevent participation in adapted physical activity
• Pregnant or breastfeeding women
• Patients without the necessary devices to use a smartwatch (smartphone, tablet or computer),
• Patients deprived of liberty, under guardianship, or curatorship, or subject to any other administrative safeguard measure.
• Patients unable to comply with the study schedule for social, medical, or psychological reasons.

Where it is running

• Centre Eugène Marquis — Rennes, France

Full record on ClinicalTrials.gov

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