Subacromial Impingement Syndrome Clinical Trial
Official title:
Effectiveness of Functional Massage of the Teres Major Muscle in Patients With Subacromial Impingement Syndrome. A Randomized Controlled Pilot Study
Verified date | February 2015 |
Source | Jordi Gol i Gurina Foundation |
Contact | n/a |
Is FDA regulated | No |
Health authority | Spain: Catalan Health Institut |
Study type | Interventional |
Purpose: Subacromial impingement syndrome is the most common shoulder condition. Myofascial
trigger points in teres major muscle can be associated with this syndrome. The investigators
objective is to find out if adding manual therapy specifically for teres major trigger
points can produce better results in these patients.
Method: A randomized controlled pilot study was carried out. Fifty people were randomly
assigned to one of two groups: intervention group or control group. Both groups received a
protocolized physical therapy treatment while the intervention group additionally received
manual therapy for teres major trigger points.
Status | Completed |
Enrollment | 58 |
Est. completion date | March 2014 |
Est. primary completion date | March 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age 18 years and over - Clinical diagnosis of Subacromial Impingement Syndrome. - Detectable trigger points in teres major muscle. - Sign informed consent form. Exclusion Criteria: - Presence of wounds or cutaneous alterations in the shoulder region - Previous surgery in the shoulder - Presence of acute inflammatory process in the shoulder (< 7 days), - Being involved in litigation or compensation processes - Not having a domain of the language that could make the informed consent not understandable. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Jordi Gol i Gurina Foundation |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Pain Intensity (visual analogue scale) | Using a Visual analogue scale | Change from baseline to 3 weeks | Yes |
Secondary | Change in Function (Abbreviated Constant-Murley score) | Using the Abbreviated Constant-Murley score | Change from baseline to 3 weeks | Yes |
Secondary | Change in Active Range of Motion | Flexion, extension, abduction, external rotation and internal rotation | Change from baseline to 3 weeks | Yes |
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