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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
53
This programme will include the practice of general physical activity and the implementation of nutritional and psychological support. Each patient will have 8 Oncorehabilitation Transdisciplinary Evaluations (OTE): * 2 OTE will be performed before the surgery, * 6 OTE will be performed after the surgery. During the program (at each OTE), patients will also be asked to complete the QLQ-C30 questionnaire.
Institut Universitaire du Cancer de Toulouse - Oncopole
Toulouse, France
RECRUITINGRate of patients with a MSTS score (Musculoskeletal Tumor Rating Scale) greater than 75% at 24 months post-surgery.
Time frame: 26 months for each patient.
Quality of life using the Quality Of Life Questionnaire Core 30 (QLQ-C30).
Quality of life will be evaluated from OTE1 to OTE8.
Time frame: 26 months for each patient.
Anxiety using the Hospital Anxiety and Depression Scale (HADS).
Seven item subscale. Each item is scored on a 4-point scale. Anxiety will be evaluated from OTE1 to OTE8.
Time frame: 26 months for each patient.
Depression using the Hospital Anxiety and Depression Scale (HADS).
Seven item subscale. Each item is scored on a 4-point scale. Depression will be evaluated from OTE1 to OTE8.
Time frame: 26 months for each patient.
The patient functionality will be evaluated using the Tinetti's test from OTE1 to OTE8.
Time frame: 26 months for each patient.
The patient functionality will be evaluated using the 6-min walk test from OTE1 to OTE8.
Time frame: 26 months for each patient.
The patient functionality will be evaluated using the New Functional Ambulation Classification test from OTE1 to OTE8.
Time frame: 26 months for each patient.
The patient functionality will be evaluated using the Box and Block Test from OTE1 to OTE8.
Time frame: 26 months for each patient.
The patient functionality will be evaluated using the Frenchay Arm Test from OTE1 to OTE8.
Time frame: 26 months for each patient.
The patient functionality will be evaluated using the Visual Analog Scale from OTE1 to OTE8.
Time frame: 26 months for each patient.
The patient functionality will be evaluated using the Ricci and Gagnon's Score from OTE1 to OTE8.
Time frame: 26 months for each patient.
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