- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07593963
Relation Between Scapular Dyskinesia, Rotator Cuff Strength And Subacromial Space In Asymptomatic Scapular Dyskinesia (ASD)
May 17, 2026 updated by: Aya Mostafa Mohamed Sayed, Cairo University
This study will be conducted to investigate the relationship between scapular dyskinesia and rotator cuff muscle strength and acromiohumeral distance in asymptomatic individuals.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
When the scapula moves in an abnormal way, a condition known as scapular dysfunction (SD) occurs, leading to shoulder pain and dysfunction.
It is possible for patients with SD to experience no symptoms at all.
SD symptoms can include a combination of the following anterior shoulder pain, Posterosuperior scapular pain, Superior shoulder pain, shoulder impingement syndrome, rotator cuff dysfunction, and shoulder instability.Things like early scapular elevation, abrupt downward rotation, and a prominent medial edge and inferior angle of the scapula are seen during shoulder motions.
It has been suggested that impaired scapulothoracic musculature function might lead to changes in shoulder kinematics, which in turn can increase the risk of injury.Individuals with SD often experience pathologies such as scapula-humeral rhythm disturbance, glenoid labrum difficulties, glenohumeral instability, rotator cuff syndrome, subacromial impingement syndrome, and glenoid labrum abnormalities.
In individuals suffering from RC tendinopathy, a decline in RC muscle performance is associated with lower health-related quality of life and patient-rated function.
In order to determine which patients with scapular dyskinesis may benefit most from a rehabilitation program aimed at enhancing muscular performance, clinicians may find it useful to gather data on shoulder strength.
A portable dynamometer is an easy, cheap, and valid way to get these kinds of data.
to fill that gap in literature by Finding an association between scapular dyskinesia and the acromiohumeral distance and rotator cuff muscle strength in individuals with asymptomatic scapular dyskinesia
Study Type
Observational
Enrollment (Estimated)
51
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Aya mostafa, master
- Phone Number: 01142667586
- Email: ayaphysicaltherapy2020@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Fifty-one subjects with asymptomatic scapular dyskinesia, their ages ranging from eighteen to forty years.
subjects showed an opposite result on lateral scapular slide test and with a visual-based palpation method
Description
Inclusion Criteria:
- Both genders.
- Those experiencing asymptomatic scapular dyskinesia
- The average age of the population ranges from eighteen to forty years.
- Individuals who showed appositive result on lateral scapular slide test and with a visual-based palpation method
- Type 2 and 3 scapular dyskinesia
Exclusion Criteria:
- any type of injury or pain affecting the neck, shoulders, or cervical region
- Participating in any form of formal athletic training or fitness program with their express written approval
- If they had previously suffered an injury to their upper limbs, such as a dislocation, fracture, or strain
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
asymptomatic scapular dyskinesia group
fifty-one asymptomatic scapular dyskinesia subjects will be included
|
From both genders, fifty-one asymptomatic scapular dyskinesia subjects were included in this group.
their ages from eighteen to forty years.
Subjects showed an opposite result on the lateral scapular slide test.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
subacromial space
Time Frame: up to one day
|
The subacromial space will be measured by ultrasonography device with mm or cm. it was defined as the linear perpendicular distance between the top surface of the humeral head and the lower surface of the acromion
|
up to one day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
shoulder internal rotator muscles strength
Time Frame: up to one day
|
shoulder internal rotator muscles strength will be measured by active force 2 device
|
up to one day
|
|
shoulder external rotator muscles strength
Time Frame: up to one day
|
shoulder external rotator muscles strength will be measured by the Active Force 2 device
|
up to one day
|
|
scapular dyskinesis
Time Frame: up to one day
|
lateral scapular slide test (LSST) will be used to assess scapular dyskinesis.
examined the distance between the scapular inferior angle and the corresponding spinous process in three different positions using the lateral scapular slide test (LSST) to evaluate scapular stability in both the right and left scapula.
The subject's arms were relaxed at his sides, lying on his hips, with his shoulders internally rotated and abducted 45 degrees, and fully internally rotated and abducted 90 degrees.Kibler has stated that a 1.5 cm discrepancy on both sides should be considered abnormal scapular asymmetry.
|
up to one day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
May 20, 2026
Primary Completion (Estimated)
July 20, 2026
Study Completion (Estimated)
July 20, 2026
Study Registration Dates
First Submitted
May 12, 2026
First Submitted That Met QC Criteria
May 12, 2026
First Posted (Actual)
May 18, 2026
Study Record Updates
Last Update Posted (Actual)
May 20, 2026
Last Update Submitted That Met QC Criteria
May 17, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- P.T.REC/012/006147
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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