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Effects of Acromioclavicular joint mobilization in Frozen Shoulder Syndrome

: Effects of Acromioclavicular joint mobilization on symptoms and functional disability in patients with Frozen Shoulder Syndrome: A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100605004104N7
Enrollment
56
Registered
2019-01-06
Start date
2018-12-22
Completion date
Unknown
Last updated
2019-01-29

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

Conditions

Frozen shoulder. Adhesive capsulitis of shoulder

Interventions

Intervention 1: Intervention group: Acromioclavicular joint mobilization techniques will be performed in the form of passive accessory inferior ,posterior to anterior & anterior to posterior glides( g

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age between 18 to 60 years Unilateral frozen shoulder Normal shoulder Xray and normal neurological examination At least two months passing from the onset of symptoms

Exclusion criteria

Exclusion criteria: Inflammatory or infectious shoulder joint disease Neurological deficit such as stroke which is due to shoulder muscle dysfunction Poor controlled diabetes Neoplastic disorder of shoulder region A recent history of fracture, dislocation or subluxation of shoulder complex A history of steroid injection of glenohumeral joint, subdeltoid burse or acromiocalvicular joint within the previous 6 months or surgery A feeling of instability at the glenohumeral joint Shoulder pain referred from the severe cervical radiculopathy.

Design outcomes

Primary

MeasureTime frame
Ability to manage in everyday life. Timepoint: before treatment, immediately after treatment. Method of measurement: Shoulder Pain and Disability Index Questionnaire.;Range of motion of shoulder joints. Timepoint: before treatment and immediately after treatment. Method of measurement: Goniometer.;Pain severity. Timepoint: Before treatment, immediately after treatment. Method of measurement: Visual Analogue Scale with grading from zero to 10 centimeters.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSepideh Ranjbar

Tabriz University of Medical Sciences

Sepideh_R_k@yahoo.com+98 41 3336 1928

Outcome results

None listed

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