Frozen shoulder. Adhesive capsulitis of shoulder
Conditions
Interventions
Intervention 1: First intervention group: Group A: The patient is in a sitting position on a chair with his arm hanging at his side. We place the linear probe transversely on the posterior part of the
Sponsors
Babol University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Persistent shoulder pain for at least three months Persistent limitation of shoulder movement for at least three months Stages 1 and 2 of the Kisner and Colby classification system
Exclusion criteria
Exclusion criteria: Known systemic diseases such as rheumatoid arthritis, History of recent trauma or surgery or known chronic disease (such as rotator cuff lesions) Pivacaine, any known systemic disease Osteoarthritis Midclavicular joint, cervical radiculopathy Brachial plexopathy, neoplasm Pregnancy Diabetes Opioid addiction
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Shoulder Pain and Disability Index. Timepoint: 3 primary outcome assessments (at baseline, after surgery, after 6 months of surgery). Method of measurement: Shoulder Pain and Disability Index Questionnaire.;Pittsburgh Sleep Quality Index. Timepoint: 3 primary outcome assessments (at baseline, after surgery, after 6 months of surgery). Method of measurement: Pittsburgh Sleep Quality Index Questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Shoulder Internal Rotation Movement Scale score. Timepoint: Before the intervention, 6 weeks and 6 months after the intervention. Method of measurement: Score obtained based on the goniometer device.;Shoulder external rotation movement scale score. Timepoint: Before the intervention, 6 weeks and 6 months after the intervention. Method of measurement: Score obtained based on the goniometer device.;Shoulder abduction range of motion score. Timepoint: Before the intervention, 6 weeks and 6 months after the intervention. Method of measurement: Score obtained based on the goniometer device.;Shoulder flexion movement scale. Timepoint: Before the intervention, 6 weeks and 6 months after the intervention. Method of measurement: Score obtained based on the goniometer device. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactYasin Sharifzadeh
Babol University of Medical Sciences
Outcome results
None listed