None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1 clinically diagnosed supraspinatus tendinitis confirmed through ultrasound or MRI 2 pain duration more than 6 weeks 3 positive Jobe test 4 age 40 to 50 years 5 giving valid informed consent
Exclusion criteria
Exclusion criteria: 1 full thickness rotator cuff tear 2 history of shoulder surgery or fractures 3 neurological or systemic conditions affecting shoulder movements 4 no compliance or unwillingness to participate 5 lactating females and pregnant women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The study seeks to furnish evidance based insights on the efficacy of conventional physiotherapy alone compared to conventional physiotherapy in conjunction with advanced manual techniques for the treatment of supraspinatus tendinitis in blue collar workersTimepoint: 3 to 6 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1 to evaluate the efficacy of CPT alone verses CPT combined with advanced manual techniques in diminishing pain intensity assessed by VAS 2 to evaluate the enduring effects of rehabilitation on functional recovery and persistent pain alleviation over a six month period 3 to determine the psychosocial impact of supraspinatus tendinitis and its therapy on mental health indicators including stress anxiety and depression through DASS 21 scale 4 to evaluate the impact of rehabilitation on occupational health specifically regarding return to work rates and decrease in absenteeismTimepoint: 3 to 6 weeks;NILTimepoint: NIL | — |
Countries
India
Contacts
GMC Jammu