Comparison of mobilization and mobilization with movement on acromiohumeral distance in athletes with shoulder primary impingement syndrome

Not Applicable

Recruiting

Conditions: Primary Shoulder impingement syndrome.
Impingement syndrome of shoulder
M75.4

Registration Number: IRCT20211101052934N1

Lead Sponsor: Semnan University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 51

Inclusion Criteria

Age between 20 to 35 years
Semi-professional athletes (who exercise an average of 3 to 6 hours per week)
Doing overhead exercises such as volleyball
primary impingement syndrome of shoulder
Patient consent to participate in the study

Exclusion Criteria

History of trauma, fracture, dislocation or surgery in the neck and shoulders
Osteoporosis
Tumor or neuromuscular disorders around the shoulder
Any subcutaneous inflammation
Inflammatory disorders such as rheumatoid arthritis
Adhesive capsules
Complete rupture of the rotator cuff tendon
Corticosteroid injections in shoulders in the past year
Received physical therapy for the shoulder or spine in the last 3 months

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Acromiohumeral distance (AHD). Timepoint: At baseline and after the end of treatment (2 week). Method of measurement: AHD measurement method using ultrasonography.;Functional Status and Symptom Severity of shoulder. Timepoint: At baseline and after the end of treatment (2 week). Method of measurement: Using Shoulder Pain and Disability Index (SPADI).;Pain severity. Timepoint: At baseline and after the end of treatment (2 week). Method of measurement: Visual Analogues Scale (VAS).

Secondary Outcome Measures