Early Active Rehabilitation After Arthroscopic Rotator Cuff Repair
- Conditions
- Full Thickness Rotator Cuff Tear
- Registration Number
- NCT02915588
- Lead Sponsor
- Johannes Kepler University of Linz
- Brief Summary
The purpose of the study is to compare two different rehabilitation protocols after arthroscopic rotator cuff surgery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
- surgery of the rotator cuff after full thickness tear
- informed consent
- understanding german language
- previous surgery of the shoulder
- neurological or systemic diseases with impairment of shoulder function
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Change of Constant Murley Score up to 24 weeks Timepoints: Before surgery; 6, 12, 24 weeks after surgery
- Secondary Outcome Measures
Name Time Method Change of DASH Score up to 24 weeks Timepoints Before surgery; 6, 12, 24 weeks after surgery
Change of Active range of Motion (Flexion, Extension, Abduction, Internal Rotation, External Rotation) up to 24 weeks Timepoints: Before surgery; 6, 12, 24 weeks after surgery; Range of movement is measured by handheld goniometer
Change of Pain (max; average; rest) up to 24 weeks Timepoints: Before surgery; 6, 12, 24 weeks after surgery; Pain is measured by Visual Analogue Scale (0-100mm)
Change of Strength (abduction; external Rotation) up to 24 weeks Timepoints: Before surgery; 6, 12, 24 weeks after surgery; Measurement of Strength is evaluated using a BTE Simulator II Dynamometer (Peak torque in N).
Related Research Topics
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Trial Locations
- Locations (1)
Kepler University Hospital
🇦🇹Linz, Austria
Kepler University Hospital🇦🇹Linz, Austria