Skip to content

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

Comparison of therapeutic effects of mobilization and mobilization with movement on acromiohumeral distance in athletes with shoulder primary impingement syndrome: A randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211101052934N1
Enrollment
51
Registered
2022-03-09
Start date
2021-12-22
Completion date
Unknown
Last updated
2022-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Shoulder impingement syndrome. Impingement syndrome of shoulder

Interventions

Intervention 1: Intervention group: Mobilization exercises (mobilization) for 6 sessions (3 times a week). In this group, mobilization techniques for the glenohumeral joint are performed by a training

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 35 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohreh Shokrian Tosi

Semnan University of Medical Sciences

zohreh_sh_pt@hotmail.com+98 11 3332 5586

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026