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Dynamic Taping in Symptomatic Rotator Cuff Tendinopathy

Not Applicable
Completed
Conditions
Rotator Cuff Tendinosis
Interventions
Other: Dynamic taping
Other: Kinesio taping
Other: Physiotherapy and Rehabilitation
Registration Number
NCT05029544
Lead Sponsor
Muğla Sıtkı Koçman University
Brief Summary

This study was conducted to compare the efficacy of two different therapeutic bands in symptomatic rotator cuff tendinopathy. One of the tapes was kinesio tape and the other was dynamic tape. The study was in a parallel group randomized controlled trial design.

Detailed Description

This study was planned to compare the effectiveness of dynamic taping and kinesio taping combined with a rehabilitation program on the symptomatic shoulder in patients with symptomatic rotator cuff tendinopathy (RCT). The study was carried out on 60 patients who applied to Muğla Training and Research Hospital Physical Therapy and Rehabilitation outpatient clinic with symptoms of RCT. The patients were divided into 3 groups by randomization method. Dynamic taping was applied to the symptomatic shoulder in the first group and kinesio taping was performed in the second group. The third group was the control group and no taping was done. A standard rehabilitation program was applied for the individuals in the whole group. Evaluations were made before and after treatment (6 weeks). Evaluation parameters were acromiohumeral distance (primary outcome), shoulder joint range of motion, muscle strength, proprioception measurements, and function evaluations. The acromiohumeral distance was measured by the radiologist, and all other measurements and treatments were performed by the physiotherapist. Standard goniometer was used for shoulder joint range of motion measurement, manual muscle dynamometer was used for muscle strength measurement, and digital inclinometer was used for proprioception measurement. Timed arm-shoulder function test was performed for function evaluation. The arm, shoulder, and hand disability (DASH) questionnaire and the Western Ontario Rotator Cuff Index (WORC) were used for the self-function report. The data obtained from the research will be analyzed using the SPSS program. Statistical significance level will be accepted as p\<0.05. In the statistical difference analysis between groups, one-way ANOVA test will be used for parametric data and Kruskal-Wallis test will be used for non-parametric data.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Those with a diagnosis of RCT
  • Those with subacromial pain
  • At least two of the three impingement tests are positive (empty-can test, Hawkins-Kennedy test, modified Neer test)
  • 18-65 years old
Exclusion Criteria
  • Those with open wounds at the taping area
  • Those who have allergic reactions to taping
  • Those who have had shoulder surgery before
  • Those with total rotator cuff tendon rupture
  • Those with a history of fractures in the upper extremity or glenohumeral joint subluxation -- Presence of adhesive capsulitis (those with more than passive shoulder joint motion loss 70%)
  • Presence of congenital or acquired deformity involving the upper extremity
  • Those with rheumatic or neurologic disease
  • Those with cervical radiculopathy
  • Those with a history of neoplasm or cognitive impairment (MMSE<24)
  • Those who received corticosteroid injection to the shoulder region in the last 3 months
  • Those who received physiotherapy treatment in the last 3 months

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
intervention group 1Dynamic tapingdynamic taping and standard rehabilitation program
intervention group 2Kinesio tapingKinesio taping and standard rehabilitation program
Control groupPhysiotherapy and RehabilitationNo taping on shoulder, only standard rehabilitation program
intervention group 1Physiotherapy and Rehabilitationdynamic taping and standard rehabilitation program
intervention group 2Physiotherapy and RehabilitationKinesio taping and standard rehabilitation program
Primary Outcome Measures
NameTimeMethod
Acromiohumeral Distance (AHD)Change in acromiohumeral distance at 6 week

Measurement of the distance between the humeral head and the inferior acromion by ultrasound to determine the subacromial space

Secondary Outcome Measures
NameTimeMethod
Lateral Scapular Slide TestChange in scapular position at 6 week

Background: The Lateral Scapular Slide Test is a static test used in clinical settings to assess medio-lateral inferior angle displacement and scapular asymmetry at three different degrees of shoulder abduction.

Muscle StrengthChange in shoulder muscle strength at 6 week

shoulder muscle strength measurement (flexion, abduction, internal and external rotation) with a manual dynamometer

Shoulder Range of MotionChange in shoulder range of motion at 6 week

Shoulder range of motion (painless and full) measurement (flexion, abduction, internal and external rotation)

Timed Functional Arm and Shoulder TestChange in shoulder function at 6 week

The test includes 3 steps. 1) Hand to head and back: this test is timed for 30 seconds. Each time the patient touches the back of his or her head, it counts as 1 repetition. 2) Wall wash outward and inward: this test is timed for 60 seconds in each direction. 3) Gallon-jug lift: this test is timed for 30 seconds. Starting counter height should be 36 inches, and the shelf should be 20 inches above the counter (56 inches off the floor). Begin with a full gallon jug on the counter. Lift the jug to touch the shelf and return to start. Every time the jug touches the shelf, it counts as 1 repetition. Record the score.

Western Ontario Rotator Cuff (WORC) IndexChange in WORC scores at 6 week

the WORC Index, is a disease-specific quality of life questionnaire, evaluating the change in symptoms and functional ability, specific to a RC tendinopathy. Each question uses a visual analogue scale (VAS) - which is a straight line, representing a 100-point scale, ranging from 0-100. The maximum score (21items) is 2100 (worst possible symptoms). Zero (0) represents no symptoms at all. To make the final score more clinically friendly, some minor math is involved. The score can be reported as a percentage by subtracting the total from 2100, dividing by 2100, and multiplying by 100. This give an overall percentage. Total final WORC scores can, therefore, range from 0% ( lowest functional status level) to 100% (the highest functional status).

ProprioceptionChange in proprioception at 6 week

Measurement with digital inclinometer with active reposition repetition method in shoulder flexion of 30 and 60 degrees

The Disabilities of the Arm, Shoulder and Hand (DASH)Change in DASH scores at 6 week

DASH questionnaire is a 30-item questionnaire that looks at the ability of a patient to perform certain upper extremity activities. This questionnaire is a self-report questionnaire that patients can rate difficulty and interference with daily life on a 5 point Likert scale. In DASH higher scores indicate a greater level of disability and severity, whereas, lower scores indicate a lower level of disability. The score ranges from 0 (no disability) to 100 (most severe disability).

Trial Locations

Locations (1)

Muğla Sıtkı Koçman University

🇹🇷

Muğla, Turkey

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