Relation Between Scapular Dyskinesia, Rotator Cuff Strength And Subacromial Space In Asymptomatic Scapular Dyskinesia
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: asymptomatic scapular dyskinesia group.
- Who it may be relevant to
- Registry conditions: Scapular Dyskinesis. Basic parameters: 18 years — 40 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
This study will be conducted to investigate the relationship between scapular dyskinesia and rotator cuff muscle strength and acromiohumeral distance in asymptomatic individuals.
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
Interventions
- Other asymptomatic scapular dyskinesia group
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.
Primary outcome measures
- subacromial space [Time frame: up to one day]
Secondary outcome measures (3)
- shoulder internal rotator muscles strength [Time frame: up to one day]
- shoulder external rotator muscles strength [Time frame: up to one day]
- scapular dyskinesis [Time frame: up to one day]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07593963 · P.T.REC/012/006147