Health Economic Evaluation of an Adapted Physical Activity Program for Women With Breast Cancer

Recruiting now · Not applicable

Conditions studied: Breast Neoplasm

In brief

Adapted physical activity (APA) was recognized as a non-drug therapy by the French Health Authority (HAS) in 2011. Very few studies have examined the efficiency of APA programs during the active phase of treatment in cancer patients. The investigators assumed that non-drug therapy such as APA could improve the quality of life and reduces health costs. The main objective of this study is to assess the efficiency of a standardized APA program, as compared to conventional management including simple recommendations for the practice of physical activity in women in phase active breast cancer treatment.

Key facts

Study ID

NCT05949983

Run by

University Hospital, Toulouse

People needed

866

Starts

2024-12-23

Expected to finish

2027-12-01

Last updated by the study team

2025-12-31

Who can join

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

You may qualify if…

• women with breast cancer
• any type of breast cancer, all grades, all stages
• during treatment: surgery +/- chemotherapy +/- radiotherapy +/- hormone therapy

You may not qualify if…

• World Health Organization (WHO) 4
• Unstable angina
• Uncontrolled Atrial fibrillation
• Uncontrolled high blood pressure
• Recent myocardial infarction or myocarditis or pericarditis or thromboembolic disease (less than 3 weeks)
• Aortic stenosis or valve disease to operate
• Cardiac or respiratory failure, with dyspnea at rest
• Symptomatic anemia, thrombocytopenia
• Lytic or painful bone metastases, Severe osteoporosis
• Severe infectious syndrome,
• Surgery in the last 3 weeks
• Extreme fatigue, sharp pain, dizziness, disturbance of consciousness, severe undernutrition
• Contraindication to the practice of an adapted physical activity programme
• Currently involved or exclusion period of a interventional study or adapted Physical Activity program
• Patient with protective measures (guardianship, curators, and deprivation of liberty).
• Pregnancy or breastfeeding
• Patient with severe functional limitations

Where it is running

• Marie-Eve Rougé-Bugat — Toulouse, France (enrolling)

Full record on ClinicalTrials.gov

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