Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Female adolescents aged 13 to 19 years. Diagnosed with scapular dyskinesis based on a positive Scapular Dyskinesis Test performed by a qualified physiotherapist. Presence of unilateral or bilateral shoulder pain, discomfort, functional limitation, or shoulder dysfunction associated with scapular dyskinesis. School going or college going students who are able to attend the intervention sessions regularly. Willing to participate in the study and comply with the treatment protocol throughout the study period. Able to understand study procedures and provide written informed assent or consent parental or guardian consent will be obtained for participants below 18 years of age.
Exclusion criteria
Exclusion criteria: History of shoulder fracture, recurrent shoulder dislocation, or any significant traumatic injury to the shoulder complex that may affect shoulder function or interfere with the study outcomes. History of shoulder surgery within the previous 6 months, including arthroscopic or open surgical procedures, as postoperative recovery may influence pain, strength, and functional performance. Presence of neurological disorders affecting the upper limb or shoulder girdle, such as cervical radiculopathy, brachial plexus injury, stroke, peripheral nerve injury, or other neuromuscular conditions that may impair shoulder movement and function. Presence of severe musculoskeletal conditions involving the shoulder, including full-thickness rotator cuff tear, adhesive capsulitis, shoulder instability requiring surgical management, inflammatory joint disorders, or other conditions that may limit participation in the rehabilitation protocol. Known allergy, hypersensitivity, skin irritation, open wounds, dermatological conditions, or any contraindication to the application of kinesio tape in the shoulder or scapular region. Current participation in any other shoulder rehabilitation, physiotherapy, exercise program, or clinical trial targeting shoulder pain, function, or scapular dyskinesis during the study period. Any medical condition that, in the opinion of the investigator, may interfere with safe participation in the study, adherence to the intervention protocol, or interpretation of study outcomes.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Shoulder Pain And Disability (SPADI) Isometric Strength Test Scapula Dyskinesis Test Shoulder Range Of Motion Visual Analogue ScaleTimepoint: 4 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Ravi Nair Physiotherapy College, Datta Meghe Institute of Higher Education and Research (DU)