About this trial
The purpose of this study will be to investigate if there is any correlation between shoulder dysfunction and the lateral alignment of the spine, scapular dyskinesia, pelvic tilting angle, Shoulder height angle, and trunk side bending (strength and mobility) in the frontal plane in patients with unilateral SIS.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Non-athletic patients of both sexes.
referred by an orthopedic surgeon with a diagnosis of unilateral SIS (Stage I, or II).
Patients aged between 20 to 40 years.
BMI between 18.5 to 29.9 kg/m2.
Disqualifiers
Systematic illnesses
Pregnancy
Any degenerative disorder or disc lesion affection of the spine
A history of upper limb or spinal surgery
Trial population
Thirty four (34) patients with unilateral SIS. Male and female subjects will be included between 20 and 40 years of age with a BMI between 18.5 to 29.9 kg/m2.
Trial design
Other
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Thoracolumbar lateral deviation
will be measured using a scoliometer
Scapular dyskinesia
will be measured using lateral scapular slide test (LSST)
The pelvic tilting angle and shoulder height angle
will be evaluated using Kinovea software
Trunk side bending ROM
will be evaluated using a bubble inclinometer
Sponsors and contacts
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