Prehabilitation with physiotherapy and mechanical stimulation before LD flap breast reconstruction
Official title: Randomized, Multicentre Study Evaluating the Impact of Pre-habilitation Using Physiotherapy and Mechanical Stimulation on Shoulder Pain and Mobility in Patients Undergoing Breast Reconstruction Using a Latissimus Dorsi Flap
Run by Institut du Cancer de Montpellier - Val d'Aurelle · NCT07418060 · Data updated 2026-11-12
This study tests whether prehabilitation with physiotherapy and mechanostimulation improves shoulder pain and mobility for women undergoing breast reconstruction with a latissimus dorsi flap.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 96 (estimated) |
| Sponsor | Institut du Cancer de Montpellier - Val d'Aurelle Academic / other |
| Locations | 2 sites (Bordeaux, Aquitaine and 1 other locations) |
| Status | Recruiting |
| Started | August 28, 2026 |
| Main results expected | July 2030 |
| Study ends | July 2030 |
| Registry record updated | September 15, 2026 |
| Trial ID | NCT07418060 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adult women (18 years or older) scheduled for breast reconstruction with a latissimus dorsi flap after breast cancer.
✕Probably not a fit
Individuals with pre-existing shoulder pathology or other factors excluding them from the study may not experience benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Patients scheduled for breast reconstruction using a latissimus dorsi flap are randomized to receive a structured prehabilitation program with physiotherapy and mechanostimulation versus standard care without prehabilitation. The trial aims to determine if the preparatory rehabilitation reduces postoperative shoulder pain and improves range of motion and function. Procedures are conducted in France at multiple centers, enrolling adults who meet eligibility criteria and can understand French. The intervention is non-pharmacologic and focused on preoperative optimization of shoulder health. Outcomes likely include pain scores, mobility measures, and patient-reported function.
Why it matters
Potential benefit: If successful, patients may experience less shoulder pain and better shoulder mobility after reconstruction, improving recovery and quality of life.
How similar studies have gone: Previous surgical rehabilitation studies suggest rehabilitation approaches can improve postoperative shoulder function, but this exact prehabilitation with mechanostimulation before LD flap reconstruction is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Female patient aged 18 years or older * Scheduled for breast reconstruction with a latissimus dorsi flap following breast cancer * Patient has been informed and has signed the informed consent form * Affiliated with a social security system Exclusion Criteria: * Patient with pre-existing shoulder pathology (Constant score \< 80/100) * Patient with uncontrolled psychiatric or mental disorders * Patient unable to understand French * Patient under guardianship or safeguard of justice * Pregnant or breastfeeding women
Where it's running
-
Institut régional du Cancer de Montpellier
Montpellier, Herault, France Recruiting -
Institut Bergonié
Bordeaux, Aquitaine, France Not yet recruiting
Study contacts
- Study coordinator: Aurore MOUSSION
- Email: drci-icm105@icm.unicancer.fr
- Phone: 0467613102
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.