The purposes of this study are to: 1. determine if a rehabilitation program that consists of exercise and manual therapy reduces pain and improves quality of life in patients with shoulder subacromial impingement syndrome; 2. determine which patients are likely to respond to this rehabilitation program and which patients are not likely to respond to this rehabilitation program The hypotheses are: 1. the rehabilitation treatment program will result in significant changes in pain and quality of life 2. there will be items from the history and examination that will identify those patients who respond favorably and those who do not respond favorably to rehabilitation at 6 weeks, 3, 6 and 12 months.
Subacromial impingement syndrome (SAIS) is the most frequent cause of shoulder pain. A variety of non-surgical treatments have been advocated to correct the impairments associated with SAIS. Clinical trials support the use of therapeutic exercise and joint mobilizations to improve pain and functional disability associated with SAIS. However, not all patients in these trials had a favorable outcome. Moreover, the effect sizes in these trials were small to moderate. Thus the purposes of this study are to 1. determine the effect of a multi-modal rehabilitation program consisting of strengthening, stretching, manual therapy to the shoulder and spine, patient education, posture, and functional re-training; and 2. identify those patients who are and who are not likely to respond to rehabilitation at the start of care.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
162
Exercise, manual therapy, patient education, posture, home exercise program
Virginia Commonwealth University
Richmond, Virginia, United States
Shoulder disability
Time frame: 6 week and 3, 6, 12 months
Patient satisfaction
Time frame: 6 weeks and 3, 6, 12 months
Quality of life
Time frame: 6 weeks and 3, 6, 12 months
Pain with rest, normal activities, and strenuous activities
Time frame: 6 weeks and 3, 6, 12 months
Patient perceived global rating of effect
Time frame: 6 weeks and 3 months
Additional healthcare utilization and medication use
Time frame: 6 weeks and 3, 6, 12 months
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