The clinical effect of enhancing adductor co-contraction in Subacromial Pain Syndrome. A prospective single-centre randomised controlled trial - CoCon trial

eids Universitair Medisch Centrum0 个研究点目标入组 80 人开始时间: 待定最近更新: 2024年4月15日

试验速览

暂无简介。

•In order to participate in this study, a subject must meet all of the following
•- Chronic shoulder pain (>3months).
•- Suspicion of subacromial origin of pain (e.g. combination of positive painful
•arc test, Hawkins-Kennedy test and empty can test).
•- Presence of conventional ultrasonography.
•- Presence of conventional radiographs.

•- Younger than 18 years of age;
•- History of fracture or dislocation of the shoulder;
•- History of surgery around the shoulder;
•- Clinical and/or radiographic signs of comorbidities or alternative diagnoses
•of the affected shoulder (glenohumeral instability,
•glenohumeral/acromioclavicular osteoarthritis or arthritis, rheumatic disorder,
•history of trauma of the affected shoulder, capsulitis adhesiva, full thickness
•rotator cuff rupture, cervical radiculopathy, plexus lesions).
•- Tendinitis calcarea >3mm, although part of saps; requires different treatment
•- Symptomatic cervical spine pathology;
•- Neoplasms;
•- Pregnancy;
•- Cognitive impairment;
•- Electronic implants (e.g. Implantable Cardioverter Defibrillator, pacemaker);
•- Insufficient Dutch language skills;
•- Refusing physical therapy treatment (for example, due to the absence of
•reimbursement);
•- Refusing ultrasound guided subacromial corticosteroid injection;
•- No informed consent.

发起方