- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03494192
Effects of Exercise Trainings on Pain, Function and AHD in Patients With SPS
Utilizing Scapula Retraction Exercises With or Without Glenohumeral Rotational Exercises With a Gradual Progression: A Double-Blind Randomized Controlled Trial for Subacromial Pain Syndrome
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.
Study Overview
Status
Conditions
Detailed Description
Coordinated motion between the humerus and scapula is required for pain-free arm movement. Rotator cuff and scapulothoracic muscles dynamically control the subacromial space or acromiohumeral distance (AHD).Scapulothoracic muscles need to provide stability and control in a synchronized fashion to facilitate normal scapulohumeral movement. Scapular upward rotation and posterior tilt is essential to maintain the AHD.Therefore, the force couple function of the rotator cuff muscles play an critical role in opposing the superior migration force that is generated by deltoid muscle and, to maintenance the subacromial space.
Abnormal reduction of the AHD has been considered as one of the possible mechanisms in the aetiology of subacromial impingement 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.
he 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.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Ankara, Turkey, 06100
- Hacettepe University, Faculty of Health Sciences, Dept. of Physiotherapy and Rehabilitation
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: scapula retraction exercise group
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physiotherapy program consists of manual therapy, supervised stretching and scapulothoracic muscles strengthening exercises and home exercise programme including stretching and strengthening exercises will be applied two times a week total 24 sessions. After 24 sessions completed, patients will proceed to reduced exercise program until the 6-month follow-up.
Other Names:
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Experimental: Scapula Retraction +Glenohumeral Rotational Exercise Group
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physiotherapy program consists of manual therapy, supervised stretching and scapulothoracic and also rotator cuff muscles strengthening exercises and home exercise programme including stretching and strengthening exercises will be applied two times a week total 24 sessions. After 24 sessions completed, patients will proceed to reduced exercise program until the 6-month follow-up
Other Names:
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No Intervention: Control Group
Age-sex and hand-dominancy matched healthy controls will be included as a control group (CG) for acromiohumeral distance (AHD) normative data
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional Level
Time Frame: ffrom baseline to twelve week after treatment sessions
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Functional level will be assessed by using Shoulder Pain and Disability Index (SPADİ).
All assessment will be recorded at baseline, at the end of the 12-week treatment sessions and 6-month follow-up.
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ffrom baseline to twelve week after treatment sessions
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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pain assessment
Time Frame: from baseline to 6-month follow up
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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.
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from baseline to 6-month follow up
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Acromiohumeral Distance Measurement
Time Frame: from baseline to 6-month follow up
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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.
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from baseline to 6-month follow up
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Patient Satisfaction
Time Frame: at 12 week and 6-month follow ups
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Patient Satisfaction will be assessed by simple questions consisting of self- recovery rate and patients expectation
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at 12 week and 6-month follow ups
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KA-180018
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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