Actively Recruiting
Eccentric or Concentric Contralateral Training in Rehabilitation After Shoulder Surgery With Elbow Immobilization
Led by Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer · Updated on 2026-04-13
42
Participants Needed
1
Research Sites
69 weeks
Total Duration
On this page
Sponsors
C
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Lead Sponsor
S
Sainte-Anne Military Teaching Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to find out if exercising the non-immobilized arm can help maintain muscle strength and mass in patients recovering from shoulder surgery who have their arm immobilized at the elbow. This is important because immobilization, while necessary to protect the shoulder, often causes muscle loss and weakness that can delay recovery. The study compares two types of exercise—eccentric (muscle lengthening) and concentric (muscle shortening)—against standard care without such training to see which best preserves muscle function during recovery. Participants are divided into three groups: one receiving standard rehabilitation care, one doing eccentric training, and one doing concentric training with their non-immobilized arm. Training happens three times a week during a 4 to 6 week immobilization period, with specific exercises involving elbow flexion and extension performed in sets and repetitions at controlled intensity and timing. The study includes four visits: before surgery, at the end of immobilization, six weeks after immobilization, and 17 weeks after immobilization, with repeated assessments at each visit. Participants will undergo various tests measuring muscle strength, arm circumference, muscle size with ultrasound, handgrip strength, and functional scores related to arm and shoulder use. Researchers will also monitor pain, perceived exertion, joint position sense, and muscle stiffness. The primary outcome is the strength of the immobilized arm before and after immobilization. Follow-up visits continue for several months to track recovery progress and the effects of the different training methods.
CONDITIONS
Brief Title
Eccentric or Concentric Contralateral Training in Rehabilitation After Shoulder Surgery With Elbow Immobilization
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patient (18 years or older) undergoing shoulder surgery such as Bankart procedure, rotator cuff repair, or arthroplasty
- Expected immobilization period of 4 to 6 weeks after surgery
- No neurological diseases
- Provided informed consent before participation
You will not qualify if you...
- Medical reasons preventing participation in physical or sports activities
- Expected change in physical activity of the non-immobilized limb during the study
- Injury to upper limbs within the last 6 months
- Previous surgery on upper limbs
- Pregnant, giving birth, or breastfeeding women
- Known cognitive impairments
- Under legal guardianship or similar protective measures
- Not covered by health insurance
- Any other condition that may interfere with study evaluations as judged by the investigator
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) during pre-surgical consultation for information and consent
Duration - Within 7 days before surgery
Participants undergo baseline assessments including strength, muscle size, arm circumference, handgrip strength, and functional scores before surgery.
1 visit (in-person) before surgery
Duration - 4 to 6 weeks
Participants have their arm immobilized for 4 to 6 weeks after surgery and are randomly assigned to receive standard care alone or with eccentric or concentric training of the non-immobilized arm.
Participants attend rehabilitation sessions three times per week; training sessions for exercise groups occur 3 times weekly with rest periods between sets and repetitions
Duration - At the end of immobilization (4 to 6 weeks post-surgery)
Participants repeat the same strength, muscle size, arm circumference, handgrip strength, and functional assessments as before surgery to evaluate recovery after immobilization.
1 visit (in-person) for assessments
Duration - Up to 17 weeks after immobilization
Participants return for follow-up visits to repeat strength and functional assessments at 6 weeks and 17 weeks after immobilization to monitor ongoing recovery.
2 visits (in-person) at 6 weeks and 17 weeks post-immobilization
Trial Site Locations
Total: 1 location
1
Hôpital National d'Instruction des Armées Sainte-Anne
Toulon, Var, France, 83000
Actively Recruiting
Research Team
M
Magali Cesana
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
3
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