Rotator Cuff Tears Clinical Trial
Official title:
THE EFFECTS OF EARLY PERIOD KINESIO TAPE ON CLINICAL OUTCOMES IN PATIENTS WITH ARTROSCOPIC ROTATOR CUFF REPAIR
Verified date | August 2023 |
Source | Kirsehir Ahi Evran Universitesi |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this clinical trial is to the effects of kinesio tape application on pain, edema, range of motion and functionality . The main questions it aims to answer are: - Does kinesiotape application reduce pain and edema and improve quality of life in the early period in individuals undergoing arthroscopic rotator cuff repair? - Does kinesiotape application provide early restoration of functional activity level in individuals undergoing arthroscopic rotator cuff repair? Participants will receive kinesiotaping in addition to traditional physiotherapy programs. If there is a comparison group: Researchers will compare kinesiotape group, shamtape group and control group to see if kinesiotaping.
Status | Completed |
Enrollment | 45 |
Est. completion date | January 1, 2023 |
Est. primary completion date | December 29, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Be between the ages of 18-65, - Arthroscopic rotator cuff repair as a surgical method, - diagnosis of a small or medium-sized (<3 cm) rotator cuff tear by magnetic resonance imaging, - Having a score above 24 on the Mini Mental State Examination, - Volunteering to participate in the study. Exclusion Criteria: - Presence of diabetes mellitus, - Stage three and above according to the Goutallier fatty degeneration classification, - Presence of a neurological problem, - Presence of cervical disc herniation, - Past history of orthopedic disease on the affected side, - Presence of osteoarthritis, rheumatoid arthritis or other systemic inflammatory problem, - Corticosteroid injection for the affected side within 6 weeks before diagnosis. |
Country | Name | City | State |
---|---|---|---|
Turkey | Kirsehir Ahi Evran Universty | Kirsehir |
Lead Sponsor | Collaborator |
---|---|
Kirsehir Ahi Evran Universitesi |
Turkey,
Gulenc B, Yalcin S, Genc SG, Bicer H, Erdil M. Is Kinesiotherapy Effective in Relieving Pain and Reducing Swelling after Shoulder Arthroscopy? Acta Chir Orthop Traumatol Cech. 2019;86(3):216-219. — View Citation
Reynard F, Vuistiner P, Leger B, Konzelmann M. Immediate and short-term effects of kinesiotaping on muscular activity, mobility, strength and pain after rotator cuff surgery: a crossover clinical trial. BMC Musculoskelet Disord. 2018 Aug 22;19(1):305. doi — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain severity | Visual Analogue Scale (0-10, higher means worse) | 7 weeks | |
Primary | Edema | Diameter measurement was performed to evaluate the level of edema in the shoulder joint. Two reference points, the posterosuperior end of the acromion and the korkoid process, were used to measure the diameter of the shoulder. First, the distance between these points on the upper border of the deltoid muscle was measured with a tape measure and recorded. The second measurement was taken 1 cm lateral to the first measurement, over the middle deltoid and recorded. | 7 weeks | |
Secondary | Modified Constant-Murley score | The Modified Constant-Murley score is a 100-point scoring system that is divided into 4 subscales: pain, 15 points; activities of daily living (ADL), 20; range of motion (ROM), 40; and strength, 25. The pain and ADL subscales are self-reported by the patient. In the original version, the pain score was graded as none = 15, mild = 10, moderate = 5, and severe = 0. | 7 weeks | |
Secondary | REVISED OXFORD SHOULDER SCORE | REVISED OXFORD SHOULDER SCORE was developed to evaluate the functional parameters of the shoulder after surgery. It consists of a total of 12 questions. Each question has 5 answers ranging from 0 (bad score) to 4 (good score). The total score ranges from 0 to 48. 0 indicates the worst result, while the higher the score, the better the functionality. A score between 0-19 indicates severe disability, 20-29 indicates moderate disability, 30-39 indicates mild disability. A score between 40-48 indicates adequate functionality. | 7 weeks | |
Secondary | SHOULDER PAIN AND DISABILITY INDEX | The SPADI is a 13 item self-reported questionnaire assessing pain and functional status. Each item is measured on a 0-10 scale and a 0-100 score calculated. Higher scores represent greater levels of pain and disability. The SPADI has been shown to have good test-re-test reliability and be sensitive to change. | 7 weeks | |
Secondary | Western Ontario Rotator Cuff Index | WORC consists of 5 sections with 21 questions. The answer to each question is given on the VAS. The final score is between 0 and 2100. The higher the score, the lower the quality of life. | 7 weeks |
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