dynamic posterior humeral head subluxation pre-osteoarthritis pre-osteoarthritis of the shoulder
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients diagnosed with Walch B0 and Walch B1 primary glenohumeral arthritis are eligible for inclusion in this study. Patients that are eligible for enrollment in this study are those that meet the following inclusion criteria: • History of shoulder pain without a previous shoulder dislocation • At least findings on physical shoulder examination: o Restricted glenohumeral internal rotation in abduction as compared to the contralateral side. o Posterior glenohumeral instability based on eighter a positive Jerk test or Posterior thumb test. o Reduced strength of the infraspinatus and teres minor muscle as compared to the contralateral shoulder without the suspicion of a rotator cuff tear • Primary osteoarthritis with the exception of Walch B1 primary osteoarthritis • Absence of rotator cuff tears based on physical examination and CT scan
Exclusion criteria
Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: • Inability to understand, read or write the Dutch language. • Current exercise treatment for the shoulder • Previous corticosteroid injection of the shoulder in the last 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To measure the effectiveness of the personalized physiotherapy program, daily assessment of a patient functioning is measured using the Patient Specific Functional Scale on a daily basis. | — |
Secondary
| Measure | Time frame |
|---|---|
| • Shoulder functioning using the Patient Specific Functional Scale daily • Pain of the shoulder in rest and during activities using the Visual Analogue Scale daily • Pain acceptability daily • Training log-book, each training sessionDuring training sessions: • Muscle strength using a dynamometer • Shoulder functioning using Constant-Murley score • Glenohumeral passive range of motion using a goniometer • Adverse training responseat baseline, 3, 6 and 12 months. • Shoulder functioning using the Patient Specific Functional Scale • Pain of the shoulder in rest and during activities using the Visual Analogue Scale • Quality of life using the EQ-5D-5L • Shoulder functioning using the DASH and Oxford shoulder score • Adherence to therapy: Nr of sessions attended, Nr of exercises performed at appropriate intensity, numer of unsupervised sessions • Volumetric quantification of the rotator cuff on CT • Force vector analysis | — |
Countries
Netherlands
Contacts
VieCuri Medisch Centrum