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Evaluating the effect of Tecar therapy in patients with frozen shoulder

Not Applicable
Conditions
M75.0
Frozen shoulder.
Adhesive capsulitis of shoulder
Registration Number
IRCT20191130045550N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
30
Inclusion Criteria

Male and female patients with Frozen Shoulder between 41 and 72 years of age
Shoulder pain and movement limitation of minimum 3 months duration
Restriction of passive external rotation more than 30° in the glenohumeral joint compared to the contralateral side
Restriction of passive motion of at least a second plane of movement more than 30° in the glenohumeral joint compared to the contralateral side
Have enough ability to fill out the questionnaire

Exclusion Criteria

Bilateral Frozen shoulder
Systemic inflammatory joint disease like Rheumatoid arthritis, psoriasis arthritis and ...
Malignancies
Medical conditions such as cardiac diseases, infections and coagulation disorders
Full thickness tear of rotator cuff
History of shoulder joint surgery
Neurological disorders of the upper limb
Osteoarthritis of the glenohumeral joint
Fractures of upper limb
Cervical radiculopathy
Impaired sensation of hot and cold
Subjects who had a cardiac pacemaker
Pregnancy
Subjects who had physiotherapy treatment in the past 6 weeks
Taking analgesic or anti-inflammatory drugs

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Shoulder joint passive range of motion. Timepoint: Before treatment, 1 days after last session, 4 weeks after treatment. Method of measurement: Digital inclinometer.;Shoulder Pain and Disability Index. Timepoint: Before treatment, 1 days after last session, 4 weeks after treatment. Method of measurement: shoulder pain and disability index Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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