Actively Recruiting
Efficacy of Pre-operative Prehabilitation in Patients With Limb Sarcoma
Led by Institut Claudius Regaud · Updated on 2025-09-15
53
Participants Needed
1
Research Sites
372 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This Phase II feasibility study, prospective, interventional, monocentric aiming to assess the interest of pre-operative rehabilitation in patients treated for bone or soft-tissue sarcoma of the limbs. This protocol will be based on the realisation of a surgical prehabilitation program adapted to the patient. This strategy will involve a team of several health professionals: rehabilitation doctor, physiotherapist, occupational therapist, specialised nurse, dietician and adapted physical activity teacher. The aim of an adapted surgical prehabilitation program is to improve the functional recovery of the treated limb and the patient's autonomy after surgery. Each patient will be followed until 24 months post surgery.
CONDITIONS
Official Title
Efficacy of Pre-operative Prehabilitation in Patients With Limb Sarcoma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 16 years or older
- Diagnosis of bone or soft-tissue sarcoma confirmed by the R�e9seau de Relecture en Pathologie Sarcomateuse (RRePS)
- Tumor localized in the lower or upper limb
- Localized or metastatic disease with optimal surgery planned for the primary tumor
- Indication for neoadjuvant treatment (radiotherapy and/or chemotherapy) decided by Multidisciplinary Concertation Meeting
- Inclusion before or during neoadjuvant treatment with surgery scheduled 6 to 10 weeks after inclusion
- Written informed consent provided; for minors, parental consent and patient assent obtained
- Affiliation to the French social security system
You will not qualify if you...
- Metastatic disease without optimal surgery planned for the primary tumor
- Any medical condition or disease interfering with study procedures or posing unacceptable risk as judged by the investigator
- Legal restrictions on freedom such as guardianship or curatorship
- Psychological, familial, geographic, or social situations preventing compliance with medical monitoring or study procedures
- Pregnancy or breastfeeding
AI-Screening
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Trial Site Locations
Total: 1 location
1
Institut Universitaire du Cancer de Toulouse - Oncopole
Toulouse, France
Actively Recruiting
Research Team
D
Dimitri GANGLOFF
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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