Arthroscopic rotator cuff repair. Rotator cuff tear or rupture, not specified as traumatic
Conditions
Interventions
Intervention 1: Control group: Patients of both groups use immobilizer in the first two weeks of surgery, and after one to two weeks of surgery, their treatment begins. The duration of treatment in bo
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients over 18 years old Two weeks after RC Repair surgery Patients with rotator cuff tears except subscapularis Since this operation is usually performed along with other restorative operations such as Subacromial Decompression and Distal clavicle resection and biceps tendon tenotomy, in order to increase the generalizability to the society in this study, these operations may also have been performed together with surgery. People with an education level higher than a diploma
Exclusion criteria
Exclusion criteria: History of cervical radiculopathy Referred chest and neck pain Bankart surgery History of fracture, dislocation Traumatic rupture caused by direct impact
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of the study is pain intensity. Timepoint: Before the intervention, immediately after the end of the intervention (2 weeks after the start of the intervention). Method of measurement: Visual Analogue Scale (VAS) is used to evaluate the outcome of pain intensity. In this scale, there is a horizontal segment where the left end of the segment indicates the absence of pain and the right end of the segment indicates the maximum possible pain intensity experienced by the patient. | — |
Secondary
| Measure | Time frame |
|---|---|
| Passive range of motion. Timepoint: Before the intervention, immediately after the end of the intervention (2 weeks after the start of the intervention). Method of measurement: Passive range of motion is measured with a goniometer. It has been reported that the range of motion measured by the goniometer has high reliability.;Shoulder disability. Timepoint: Before the intervention, immediately after the end of the intervention (2 weeks after the start of the intervention). Method of measurement: The Shoulder Pain and Disability Index (SPADI) is used to evaluate the shoulder disability. This questionnaire contains 13 questions in two sections: pain (5 questions) and disability (8 questions). The overall score is calculated out of 100 and the higher the score, the greater the pain intensity and disability level of the patient. The Persian version of this questionnaire has been confirmed in terms of cultural compatibility, reliability and responsiveness.;Shoulder disability. Timepoint: Before the intervention, immediately after the end of the intervention (2 weeks after the start of the intervention). Method of measurement: The Shortened Disability of Arm, Shoulder, Hand (Quick DASH) questionnaire is used to evaluate the shoulder disability. This questionnaire includes questions about the degree of difficulty in performing various activities due to shoulder, arm and hand disorders (8 questions), the intensity of pain and weakness during various activities (4 questions), as well as questions related to the effect of this problem on social activities, work. And a person's idea of ??himself (4 questions). Each question has a score between 1 and 5, and finally the scores of all these subscales are added together and a number between zero (no limitation and disability) and (100 severe disability) is obtained. The Persian version of this questionnaire has been confirmed in terms of cultural compatibility, reliability and responsiveness.;Kinesiophobia. Timepoint: Before the i | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNeda Mostafaee
Mashhad University of Medical Sciences
Outcome results
None listed