Effectiveness of Video-Based Rehabilitation Program on Pain, Functionality and Quality of Life in the Treatment of Rotator Cuff Tears
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Rotator Cuff Tear
- Sponsor
- Istanbul University
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Shoulder Range of Motion (ROM)
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
The aim of this study was to investigate the efficacy of the video-based rehabilitation program on pain, functionality and quality of life in the conservative treatment of partial tears of the rotator cuff whether it was as successful as the physiotherapist-supervised rehabilitation program.
Detailed Description
In our study a common exercise program, which can be used in conservative treatment of a partial rotator cuff tear, is applied with two different methods; a video-based rehabilitation program and physiotherapist-supervised rehabilitation program. Video-based rehabilitation program was developed to investigate whether this program is effective on pain, functionality and quality of life and as successful as a physiotherapist-supervised rehabilitation program.
Investigators
Ezgi Türkmen
Research Assistant
Istanbul University
Eligibility Criteria
Inclusion Criteria
- •Forty years of age or older patients that had been diagnosed for a partial rotator cuff tear that was unrelated to trauma by a specialist orthopedist with MRI and physical examination and no other shoulder problems on the diagnosed shoulder were included into this study.
Exclusion Criteria
- •Patients that had been diagnosed for a full-thickness or massive rotator cuff tear, operated previously, had frozen shoulder or glenohumeral instability
- •Younger than 40-year-old, and athletic patients with acute tear symptom were excluded from this study.
Outcomes
Primary Outcomes
Shoulder Range of Motion (ROM)
Time Frame: Shoulder range of motion evaluation was performed first time at baseline and second time after 6 weeks rehabilitation program. After treatment "change" was assessed.
The shoulder flexion, abduction, internal and external rotation ROM were evaluated with goniometer while the patient was in supine position.
Secondary Outcomes
- Short Form 12 (SF-12)(Evaluation was performed before treatment and after 6 weeks rehabilitation program.)
- Visual Analogue Scale (VAS)(Evaluation was performed before treatment and after 6 weeks rehabilitation program. Patients were asked to evaluate their pain status with a 10-point scale and high scores are positively correlated with pain.)
- Disabilities of the Arm, Shoulder and Hand (DASH) Questionnaire(Evaluation was performed before treatment and after 6 weeks rehabilitation program.)
- ASES (The American Shoulder and Elbow Surgeons Standardized Shoulder Assessment) Form(Evaluation was performed before treatment and after 6 weeks rehabilitation program.)
- Global Rating of Change (GRC) Scale(Evaluation was performed after 6 weeks rehabilitation program.)