Scapula Retraction Exercises in Subacromial Pain Syndrome
Primary Purpose
Rotator Cuff Impingement Syndrome
Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Exercise Intervention
Sponsored by
About this trial
This is an interventional treatment trial for Rotator Cuff Impingement Syndrome focused on measuring pain severity, functional status, acromiohumeral distance, shoulder pain
Eligibility Criteria
Inclusion Criteria:
Inclusion Criteria:
- aged between 18-45
- 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
- adhesive capsulitis.
Sites / Locations
- Hacettepe University, Faculty of Physical Therapy and Rehabilitation
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Intervention Group
Control Group
Arm Description
exercise program consists of progressive scapula retraction exercises will be applied three times a week total 24 sessions. Home exercise program will also advised two times a day.
Control group will not perform scapula retraction exercises. AHD values of the control group will be compared to intervention groups both retracted and non-retracted conditions.
Outcomes
Primary Outcome Measures
Acromiohumeral Distance (AHD) measurement
Acromiohumeral Distance will be recorded at 0°, 30°, 45°, 60° and 90° of shoulder abduction, and while they are doing scapular retraction with resistive elastic band at each shoulder position. All assessment will be recorded at baseline and at the end of the twelve week rehabilitation sessions
Secondary Outcome Measures
pain severity
pain severity will be assessed by using 100 millimeters Visual Analogue Scale at rest, at night and during activity.
All patients were asked to mark their pain level that corresponds to their pain intensity on the line between "0=no pain" and "100=the worst pain imaginable".
disability status
disability status will be assessed by using Shoulder Pain and Disability Index (SPADİ). All assessment will be recorded at baseline and at the end of the twelve week treatment sessions.
The questionnaire is scored on a 100-point scale, where 0 represents "no disabilities" and 100 represents "extreme disabilities"
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04956757
Brief Title
Scapula Retraction Exercises in Subacromial Pain Syndrome
Official Title
Investigating the Effect of Scapula Retraction Exercises on Acromiohumeral Distance Values and Symptoms (Pain and Disability) in Patients With SPS
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
July 30, 2021 (Actual)
Primary Completion Date
October 30, 2021 (Actual)
Study Completion Date
June 17, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hacettepe University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Scapula retraction exercises are often recommended as a part of the exercise programs. The primary aim of this study is to investigate the initial effect of the scapula retraction exercises on acromiohumeral distance (AHD) at varying shoulder abduction angles and to compare asymptomatic subjects. The secondary aim of this study is to investigate the effect of scapula retraction exercises on AHD values and symptoms (pain and disability) in patients with SPS.
Detailed Description
Subacmial pain syndrome (SPS) is a common cause of shoulder pain and dysfunction in the general population. Exercise interventions is thought as a primary choice in clinical settings. Scapula retraction exercises are commonly recommended as a part of the exercise programs. Applying scapula retraction exercises at varying shoulder abduction angles could restore balance between the scapulothoracic muscles. Since the scapulothoracic muscles dynamically control subacromial space, scapula retraction exercises could further help to maintain AHD during arm elevation.
The primary aim of this study is to investigate the initial effect of the scapula retraction exercises on acromiohumeral distance (AHD) at varying shoulder abduction angles and to compare asymptomatic subjects. The secondary aim of this study is to investigate the effect of scapula retraction exercises on AHD values and symptoms (pain and disability) in patients with SPS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rotator Cuff Impingement Syndrome
Keywords
pain severity, functional status, acromiohumeral distance, shoulder pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
42 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
exercise program consists of progressive scapula retraction exercises will be applied three times a week total 24 sessions.
Home exercise program will also advised two times a day.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Control group will not perform scapula retraction exercises. AHD values of the control group will be compared to intervention groups both retracted and non-retracted conditions.
Intervention Type
Other
Intervention Name(s)
Exercise Intervention
Intervention Description
Scapula retraction exercises at varying shoulder abduction angles will be applied
Primary Outcome Measure Information:
Title
Acromiohumeral Distance (AHD) measurement
Description
Acromiohumeral Distance will be recorded at 0°, 30°, 45°, 60° and 90° of shoulder abduction, and while they are doing scapular retraction with resistive elastic band at each shoulder position. All assessment will be recorded at baseline and at the end of the twelve week rehabilitation sessions
Time Frame
Acromiohumeral distance values will be recorded at baseline and 8-week follow-up
Secondary Outcome Measure Information:
Title
pain severity
Description
pain severity will be assessed by using 100 millimeters Visual Analogue Scale at rest, at night and during activity.
All patients were asked to mark their pain level that corresponds to their pain intensity on the line between "0=no pain" and "100=the worst pain imaginable".
Time Frame
pain severity will be recorded at baseline and 8-week follow-up
Title
disability status
Description
disability status will be assessed by using Shoulder Pain and Disability Index (SPADİ). All assessment will be recorded at baseline and at the end of the twelve week treatment sessions.
The questionnaire is scored on a 100-point scale, where 0 represents "no disabilities" and 100 represents "extreme disabilities"
Time Frame
PADI Score will be recorded at baseline and 8-week follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Inclusion Criteria:
aged between 18-45
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
adhesive capsulitis.
Facility Information:
Facility Name
Hacettepe University, Faculty of Physical Therapy and Rehabilitation
City
Ankara
ZIP/Postal Code
06100
Country
Turkey
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Scapula Retraction Exercises in Subacromial Pain Syndrome
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