Health Condition 1: M708- Other soft tissue disorders related to use, overuse and pressure
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Both male and female participants aged twenty to fifty years clinically diagnosed with shoulder impingement syndrome by an orthopedic surgeon or based on positive clinical tests such as Neer and Hawkins Kennedy. Participants with shoulder pain duration more than four weeks and pain score greater than four on numeric pain rating scale. Participants willing to actively participate and comply with the intervention protocol.
Exclusion criteria
Exclusion criteria: Participants currently taking non steroidal anti inflammatory drugs or with a positive drop arm test indicating full thickness rotator cuff tear. Participants with neurological or psychological conditions affecting posture motor control or ability to follow instructions. Participants with a history of shoulder surgery trauma or dislocation involving the affected shoulder within the past one year.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain intensity measured using Numeric Pain Rating Scale and shoulder function measured using Shoulder Pain and Disability IndexTimepoint: Every 2 weeks, Pain intensity measured using Numeric Pain Rating Scale and shoulder function measured using Shoulder Pain and Disability Index | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient satisfaction measured using Likert scaleTimepoint: Post intervention at 6 weeks;Adherence to intervention measured by number of sessions attendedTimepoint: Throughout intervention period | — |
Countries
India
Contacts
Amity institute of Health and Allied Sciences