The Effect of an Evidence-based Physiotherapy Regimen for Patients With Rotator Cuff Tendinopathy
Sponsored by Bergen University College
About this trial
Last updated 7 years ago
Study ID
Status
Type
Phase
Placebo
Accepting
Not accepting
Trial Timing
Ended 3 years ago
What is this trial about?
What are the participation requirements?
Inclusion Criteria
Patients on need for surgery ( placed at surgical waiting list at hospital or referred to surgery by their GP ) 1. Typical history with difficulties working with arms elevated over the head, and pain located in the upper segment of C5 dermatome. 2. Symptom duration of minimum 3 months. 3. Three or more reproducible signs of rotator cuff tendinopathy / subacromial impingement: - Positive isometric abduction and/or lateral rotation (Ombregt, Bisschop & Veer, 2003) - Painful arc during active abduction (Ombregt, Bisschop & Veer, 2003) - Positive Neers sign (Neer, 1972 ; Tennent, Beach & Meyers, 2003) - Positive Jobes test (Jobe & Moynes, 1982 ; Tennent, Beach & Meyers, 2003) - Positive Hawkins-Kennedy impingement test (Hawkins & Kennedy, 1980)
Exclusion Criteria
1. Shoulder pain due to trauma, e.g. fall. 2. Reduced ROM consistent with adhesive capsulitis/frozen shoulder 3. History in combination with examination and tests (apprehension/relocation), giving reason to suspect pathological instability 4. Full thickness rupture of rotator cuff tendon 5. OA of the glenohumeral joint, Os acromiale with decreased space of the subacromial space, previous fractures in the shoulder complex or shoulder surgery on the symptomatic side. 6. Subjects with other comorbidity: Rheumatological or neurological disease, fibromyalgia or symptoms from the cervical spine 7. Subjects suffering from serious psychiatric illness. 8. Subjects unable to understand English or Norwegian. 9. Less than 3 positive reproducible sings of rotator cuff pathology / subacromial disease.