Evaluating a tailored exercise program for breast cancer patients
Evaluation of the Interest of a Postural and Functional Analysis for the Follow-up of the Adapted Motor Activity of Patients Treated for Breast Cancer
This study is testing a personalized exercise program to see if it helps women recover better after surgery for non-metastatic breast cancer.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | GCS Ramsay Santé pour l'Enseignement et la Recherche Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Marseille) |
| Trial ID | NCT05677022 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to assess the acceptability of a tailored motor activity program for women who have recently undergone surgery for non-metastatic breast cancer. The study will follow participants over a 15-month period, with assessments conducted at four key points: before treatment, and at 3, 9, and 15 months post-initiation. The program is designed to support recovery through adapted physical activity, monitored through postural and functional analysis. The trial will take place at a single center, with patient recruitment occurring over 24 months.
Who should consider this trial
Good fit: Ideal candidates are adult women with non-metastatic breast cancer who are post-surgery and eligible for an adapted physical activity program.
Not a fit: Patients with contraindications to physical activity or those unable to understand or comply with the study protocol may not benefit.
Why it matters
Potential benefit: If successful, this program could enhance recovery and quality of life for breast cancer patients through tailored physical activity.
How similar studies have performed: While similar approaches have been explored, this specific evaluation of a tailored motor activity program in breast cancer patients is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult woman, having given her consent to participate in the study, * Patient with non-metastatic breast cancer, * Cancer to be treated by surgery with or without adjuvant treatment (radiotherapy and/or chemotherapy). Exclusion Criteria: * Contraindication to the practice of a physical activity, * Mental deficiency or any other reason that could hinder the understanding or the strict application of the protocol, * Patient not affiliated to the French social security system, * Patient under legal protection, guardianship or curatorship, * Patient already included in another therapeutic study protocol aimed at evaluating the benefits of adapted physical activity.
Where this trial is running
Marseille
- Clairval Hospital Center — Marseille, France (Recruiting)
Study contacts
- Study coordinator: Cyril FOA, MD
- Email: foacyril@club-internet.fr
- Phone: 04 91 17 14 83
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.