Status:
ACTIVE_NOT_RECRUITING
A Post-treatment Program to Identify and Manage Complications Related to Oncology or Hematology Treatments in Cancer Survivors.
Lead Sponsor:
Centre Leon Berard
Collaborating Sponsors:
Malakoff-Humanis
Fondation Apicil
Conditions:
Late Effects
Testicular Germ Cell Tumor Mixed
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
INTRODUCTION: Approximately 44% of cancer survivors experience a deteriorated quality of life 5 years after diagnosis due to late onset of complications related to cancer treatments. The objective of ...
Eligibility Criteria
Inclusion
- males and females aged 18-65 years;
- Diagnosis and management at CLB for one of the following cancers: Hodgkin's lymphoma, aggressive non-Hodgkin's lymphoma, acute myeloid leukemia and primary non metastatic invasive breast cancer (BC), TGCT, or Sarcoma (Soft Tissue Sarcoma, Osteosarcoma, and Ewing's Sarcoma);
- receiving first-line intensive chemotherapy;
- with a complete response status at the end of the last treatment, which may include chemotherapy (excluding maintenance and hormone therapy), radiotherapy or adjuvant surgery, depending on the last scheduled treatment;
- No contraindications to adapted physical activity (APA) at inclusion;
- no medical, social, family, or psychological barriers against study participation.
- Patients will be excluded if they have a history or coexistence of another primary cancer (except basal cell skin cancer), are participating in another study affecting the primary outcome, are deprived of liberty, or reside outside the Auvergne-Rhône-Alpes region or the Saône-et-Loire department.
Exclusion
Key Trial Info
Start Date :
December 24 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 24 2029
Estimated Enrollment :
500 Patients enrolled
Trial Details
Trial ID
NCT04671693
Start Date
December 24 2020
End Date
April 24 2029
Last Update
September 5 2025
Active Locations (1)
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1
Centre Leon Berard
Lyon, France, 69373