Clinical Trial: Exercise and Manual Therapy for Shoulder Subacromial Impingement Syndrome
Study Status: Completed
Recruit Status: Completed
Study Type: Interventional
Official Title: Effectiveness of Rehabilitation for Subacromial Impingement Syndrome
Brief Summary:
The purposes of this study are to:
- 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;
- 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:
- the rehabilitation treatment program will result in significant changes in pain and quality of life
- 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.
Detailed Summary: 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.
Sponsor: Virginia Commonwealth University
Current Primary Outcome: Shoulder disability [ Time Frame: 6 week and 3, 6, 12 months ]
Original Primary Outcome: Same as current
Current Secondary Outcome:
- 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 ]
Original Secondary Outcome: Same as current
Information By: Virginia Commonwealth University
Dates:
Date Received: March 3, 2008
Date Started: January 2008
Date Completion:
Last Updated: December 18, 2015
Last Verified: December 2015