Investigation of the effect of repetition on kinematics and kinetics and pain and function of frozen shoulder

Not Applicable

Recruiting

Conditions: frozen shoulder.
Adhesive capsulitis of shoulder
M75.0

Registration Number: IRCT20220305054195N1

Lead Sponsor: Tarbiat Modares Univercity

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: 12

Inclusion Criteria

idiopathic (primary) frozen shoulder patients. Disease lasting at least 3 months and maximum 4 months.

Exclusion Criteria

Patients in age 45-70 years.
ln both gender (male and female).
Right shoulder involvement (dominant hand).
In the range of BMI 25-29.9 (overweight poeple) and Arm circumference is not greater than 27.9 cm.
Local pain in the entero-medial part of the shoulder that radiate distally (biceps muscle area) as well as laterally (deltoid area).
At least three months and at most four months have passed since the onset of symptoms (Frozen phase).
The onset of pain is spontaneous.
Pain during daily activities in the range of 3 to 5, in VAS scale.
Restrictions on active and passive movements (neither the patient nor the examiner is able to complete the range of motion).
Radiographs of AP and axillary views are normal.
Neir, Hawkin and Jobs clinical tests are negative.

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score. Timepoint: Before and 48 hours after the intervention. Method of measurement: shoulder pain and disability scale (SPADI) Questionnaire.;Shoulder joint kinematics. Timepoint: Before and 48 hours after the intervention. Method of measurement: vicon system motion analysis.;Shoulder muscles electromyography. Timepoint: Before and 48 hours after the intervention. Method of measurement: surface electromyograph electodes.;Shoulder joint kinetics. Timepoint: Before and 48 hours after the intervention. Method of measurement: vicon system motion analysis.;Disability score. Timepoint: Before and 48 hours after the intervention. Method of measurement: shoulder pain and disability scale (SPADI) Questionnaire.

Secondary Outcome Measures