Dynamic Taping in Symptomatic Rotator Cuff Tendinopathy

Comparison of Effects of Kinesio Taping and Dynamic Taping Added to a Rehabilitation Programme for Patients With Symptomatic Rotator Cuff Tendinopathy: A Randomised Controlled Trial

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.

Study Overview

• Status: Completed
• Conditions: Rotator Cuff Tendinosis
• Intervention / Treatment: Other: Dynamic taping; Other: Physiotherapy and Rehabilitation; Other: Kinesio taping

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.

• Study Type: Interventional
• Enrollment (Actual): 60
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Turkey
  • Muğla, Turkey
    • Muğla Sıtkı Koçman University

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 16 years to 63 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

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 Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: intervention group 1; dynamic taping and standard rehabilitation program	Other: Dynamic taping; The intervention of this experimental study was therapeutic taping (dynamic tape) on the symptomatic shoulders of the participants.; Other: Physiotherapy and Rehabilitation; exercise, manuel therapy, mobilization, massage, sensorimotor control
Active Comparator: intervention group 2; Kinesio taping and standard rehabilitation program	Other: Physiotherapy and Rehabilitation; exercise, manuel therapy, mobilization, massage, sensorimotor control; Other: Kinesio taping; The intervention of this experimental study was therapeutic taping (kinesio tape) on the symptomatic shoulders of the participants.
Other: Control group; No taping on shoulder, only standard rehabilitation program	Other: Physiotherapy and Rehabilitation; exercise, manuel therapy, mobilization, massage, sensorimotor control

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Acromiohumeral Distance (AHD)	Measurement of the distance between the humeral head and the inferior acromion by ultrasound to determine the subacromial space	Change in acromiohumeral distance at 6 week

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Proprioception	Measurement with digital inclinometer with active reposition repetition method in shoulder flexion of 30 and 60 degrees	Change in proprioception at 6 week
Muscle Strength	shoulder muscle strength measurement (flexion, abduction, internal and external rotation) with a manual dynamometer	Change in shoulder muscle strength at 6 week
Shoulder Range of Motion	Shoulder range of motion (painless and full) measurement (flexion, abduction, internal and external rotation)	Change in shoulder range of motion at 6 week
Lateral Scapular Slide Test	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.	Change in scapular position at 6 week
Timed Functional Arm and Shoulder Test	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.	Change in shoulder function at 6 week
The Disabilities of the Arm, Shoulder and Hand (DASH)	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).	Change in DASH scores at 6 week
Western Ontario Rotator Cuff (WORC) Index	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).	Change in WORC scores at 6 week

Collaborators and Investigators

• Sponsor: Muğla Sıtkı Koçman University
• Investigators: Study Chair: Kılıçhan Bayar, Prof, Muğla Sıtkı Koçman University

Study record dates

Study Major Dates

• Study Start (Actual): March 1, 2021
• Primary Completion (Actual): June 12, 2021
• Study Completion (Actual): August 18, 2021

Study Registration Dates

• First Submitted: August 19, 2021
• First Submitted That Met QC Criteria: August 25, 2021
• First Posted (Actual): August 31, 2021

Study Record Updates

• Last Update Posted (Actual): August 31, 2021
• Last Update Submitted That Met QC Criteria: August 25, 2021
• Last Verified: August 1, 2021

More Information

Terms related to this study

• Keywords: Rehabilitation; Kinesiotaping; Proprioception; Dynamic taping; Shoulder pain; Rotatory cuff tendinopathy; Acromiohumeral distance
• Additional Relevant MeSH Terms: Wounds and Injuries; Musculoskeletal Diseases; Muscular Diseases; Rupture; Shoulder Injuries; Tendon Injuries; Rotator Cuff Injuries; Tendinopathy
• Other Study ID Numbers: interventional (Oncolys BioPharma Inc)

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No