Condition 1: Scapular Dyskinesia. Condition 2: Repetitive Shoulder Injuries. Other shoulder lesions, left shoulder Shoulder lesion, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Male and female aged 20 to 40 years Patients who had scapular dyskinesia positive by Modified SAT and LSST Patients who had pain score of 4 or more on the NPRS scale Patients who had pain, impaired ROM, and functional limitation secondary to repetitive shoulder injuries Patients who were willing to participate and filled the informed consent provided by the study protocol
Exclusion criteria
Exclusion criteria: Individuals with significant comorbidities affecting treatment, such as severe cardiovascular disease or neuromuscular disorders, shoulder dislocation, active infection, arthritis, fracture, and dislocation/subluxation were excluded Patients who had neurological injury such as Long Thoracic Nerve Injury Patients who had acute shoulder surgeries and winged scapula were excluded due to variations in recovery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Scapular Dyskinesia. Timepoint: before intervention and at 2 weeks after intervention (6 sessions total). Method of measurement: Ruler.;Pain. Timepoint: before intervention and at 2 weeks after intervention (6 sessions total). Method of measurement: NPRS Scale.;Shoulder and Scapular Range of Motion. Timepoint: before intervention and at 2 weeks after intervention (6 sessions total). Method of measurement: Goniometer and Digital Inclinometer. | — |
Secondary
| Measure | Time frame |
|---|---|
| Functional Limitation. Timepoint: before intervention and at 2 weeks after intervention (6 sessions total). Method of measurement: SPADI Questionnaire. | — |
Countries
Pakistan
Contacts
The University of Faisalabad, Pakistan