Subacromial Impingement Syndrome Clinical Trial
Official title:
Utilizing Scapula Retraction Exercises With or Without Glenohumeral Rotational Exercises With a Gradual Progression: A Double-Blind Randomized Controlled Trial for Subacromial Pain Syndrome
Verified date | January 2022 |
Source | Hacettepe University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Abnormal reduction of the AHD has been considered as one of the possible mechanisms in the aetiology of subacromial pain syndrome. Maintenance of the AHD is crucial for prevention and rehabilitation of rotator cuff related disorders. The development of a rehabilitation treatment plan is based in part on the assessment of scapular motion and muscle deficits in patients with shoulder pain. Rehabilitation should be based on the identified impairments. The aim of this study is to investigate the effect of utilizing scapula retraction exercises with or without glenohumeral rotational exercises at gradual shoulder elevation angles into a scapular stabilization program on functionality, pain and AHD in patients with SPS and compare with health population.
Status | Completed |
Enrollment | 49 |
Est. completion date | February 15, 2021 |
Est. primary completion date | August 15, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 45 Years |
Eligibility | Inclusion Criteria: - painful arc of movement during flexion or abduction; - positive Neer or Kennedy-Hawkins impingement signs - pain on resisted lateral rotation, abduction or empty can test. Exclusion Criteria: - previous shoulder surgery; - shoulder pain reproduced by neck movement; - clinical signs of full-thickness RC tears; or - shoulder capsulitis. |
Country | Name | City | State |
---|---|---|---|
Turkey | Hacettepe University, Faculty of Health Sciences, Dept. of Physiotherapy and Rehabilitation | Ankara |
Lead Sponsor | Collaborator |
---|---|
Hacettepe University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | pain assessment | pain intensity will de assessed by using Visual Analog Scale at rest, activity and at night. All assessment will be recorded at baseline, at the end of the 12-week treatment sessions and 6-month follow-up. | from baseline to 6-month follow up | |
Other | Acromiohumeral Distance Measurement | Acromiohumeral Distance will be measured by 0°, 30°, 45°, 60° and 90° of shoulder abduction positions. All assessment will be recorded at baseline, at the end of the 12-week treatment sessions and 6-month follow-up. | from baseline to 6-month follow up | |
Other | Patient Satisfaction | Patient Satisfaction will be assessed by simple questions consisting of self- recovery rate and patients expectation | at 12 week and 6-month follow ups | |
Primary | Functional Level | Functional level will be assessed by using Shoulder Pain and Disability Index (SPADI). All assessment will be recorded at baseline, at the end of the 12-week treatment sessions and 6-month follow-up. | ffrom baseline to twelve week after treatment sessions |
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