Actively Recruiting
Rehabilitation by Multifactorial Approach After a Latarjet Procedure
Led by Clinique Générale dAnnecy · Updated on 2026-04-06
52
Participants Needed
1
Research Sites
182 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Kinesiophobia (fear of physical movement) is common after a previous shoulder dislocation and persists after one year, regardless of the occurrence of a recurrence. This kinesiophobia is associated with a lower level of physical activity and a lower return to sport. Increased kinesiophobia, combined with other psychological factors such as depression and fear of re-injury in patients with shoulder instability, results in poor outcomes after treatment. Given that there is currently no postoperative protocol that takes this psychological component into account, a new rehabilitation protocol focused on reducing kinesiophobia was recently designed as part of an international consensus study based on the method Delphi. This protocol includes a core set of evidence-based interventions aimed at regaining functional stability of the shoulder and reducing fear of recurrent dislocation and kinesiophobia. The goal of this study is to determine if we can reduce kinesiophobia in patients who have undergone stabilization surgery for anterior shoulder instability using this new rehabilitation protocol.
CONDITIONS
Official Title
Rehabilitation by Multifactorial Approach After a Latarjet Procedure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Primary or recurrent traumatic anterior dislocation of the shoulder
- Indication of abutment according to Latarjet (arthroscopic or open sky)
- Age between 18 and 67 years
- Understanding of the French language spoken and written
- Written informed consent according to ICH-GCP guidelines
You will not qualify if you...
- Posterior or multidirectional instability of the shoulder (Beighton score >5)
- Age under 18 or over 67 years
- Additional rotator cuff tear
- History of surgery on either shoulder
- Connective tissue disorders (e.g., Ehler-Danlos syndrome)
- Current anxiety disorders or use of anxiolytic medications (e.g., antipsychotics)
- Neurological disorders or systemic disease
- Inflammatory disease, rheumatoid arthritis, or active malignancy
- Previous hospitalization for shoulder pain
- Upper tubercle fracture
- Motor neurological deficit
- Pregnant or breastfeeding
- Patient protected under protective measure
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Clinique Générale d'Annecy
Annecy, France, 74000
Actively Recruiting
Research Team
G
Geert Alexander Buijze, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here