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Comparison the effectiveness of mobilization and mobilization with movement on range of motion and acromiohumeral distance in patients with chronic shoulder impingement syndrome

Comparison the effectiveness of mobilization and mobilization with movement on range of motion and acromiohumeral distance in patients with chronic shoulder impingement syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230722058881N1
Enrollment
30
Registered
2023-08-14
Start date
2023-09-23
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

chronic shoulder impingement syndrome. Other synovitis and tenosynovitis, unspecified site

Interventions

Intervention 1: first intervention group: In this research, both groups will receive routine physiotherapy consists of: 1- lifestyle correction 2- Pectoral muscles stretching 3-posterior capsule stret

Sponsors

Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1-Unilateral shoulder pain more than 6 months 2-No history of systemic illness 3-Not using NSIDs and anti-inflamatory drugs before and after assessment 4-No history of cortico-steroid injection on shoulder region in the past year 5-No history of fracture and surgery on neck and shoulder 6-No history of physical therapy in for the neck and shoulder in the past three months 7-Positive one sub acromial impingent tests including: neer test-hawkins kennedy test-jobe test

Exclusion criteria

Exclusion criteria: Failure to complete physiotherapy sessions by patients Non participation of patients in physiotherapy sessions The occurrence of unforeseen events for each of the participants in the study Increased pain or other symptoms of patients

Design outcomes

Primary

MeasureTime frame
Acromiohumeral distance. Timepoint: before physical therapy sessions-after physical therapy sessions. Method of measurement: ultrasonography.;Pain intensity. Timepoint: before and after physical therapy sessions. Method of measurement: VAS.;Upper limb function. Timepoint: before and after treatment period. Method of measurement: DASH questionare.;Range of motion. Timepoint: before and after treatment period. Method of measurement: electrogoniometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ahmadreza Askari Ashtiani

Zahedan University of Medical Sciences

ahmadaskary@gmail.com+98 54 3329 5836

Outcome results

None listed

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