Effect of Kinesio Tape on Pain, Muscle Strength, Functionality and Kinesiophobia in Shoulder Impingement Syndrome

February 28, 2025 updated by: Yasemin Şahbaz, University of Beykent

The aim of the study is to compare the effects of different kinesiotape applications in addition to traditional physiotherapy on shoulder pain, joint range of motion, muscle strength, functionality and kinesiophobia in patients diagnosed with shoulder impingement syndrome within and between groups.

Subacromial space; At the bottom, it is the region limited by the humeral head and tuberculum major, acromion (anterior 1/3 of the acromion), coracoacromial ligament, coracoid process and acromioclavicular joint and acromioclavicular ligament. The rotator cuff muscles pass through this area and move within it. In anteroposterior radiographs taken with the shoulder in 0° abduction, the distance between the acromion and the humeral head is approximately 1.1 cm (1.0-1.5 cm). Between these two structures are the rotator cuff (mostly the supraspinatus tendon), the long head of the biceps muscle, the bursa, and the coracoacromial ligament.

When incompatibility is observed between the mentioned bone structures, it causes pressure on the subacromial structures. Subacromial impingement syndrome is one of the most common causes of shoulder pain. The complaint of the majority of patients is pain radiating to the shoulder and arm, especially during overhead movements.

Examples of overhead activities in these people include hanging curtains, reaching on a shelf, combing hair, or lifting an object. Subacromial impingement syndrome is a complex disease that occurs not only as a result of compression of the rotator cuff muscles under the acromion, but also due to a combination of external and internal causes. While the diagnosis of the disease can be made with a good history and physical examination, the diagnosis must also be supported by imaging methods.

Study Overview

Detailed Description

When applied to the skin and muscle, kinesiology tape affects the mechanoreceptors sensitive to tension, loading, pressure and shear forces by changing the length of the skin and superficial fascia and the tension of the muscle fibers.

This can lead to significant changes in muscle movement and tone. In particular, slow pressure stimulation on connective tissue alters the effect on mechanoreceptors and may affect gamma motor neuron firing and muscle tone regulation. Kinesio tape can be effective in increasing proprioceptive ability, especially in the middle of movement. In this range, muscle receptors are active while ligament mechanoreceptors are inactive. Understanding joint movement and position can be effective in improving proprioception by stimulating sensory afferent transmission.

Inhibition techniques are divided into two; Autogenic and reciprocal inhibition. It occurs when the contraction of certain muscles is inhibited due to activation of the Golgi tendon and muscle spindle. These two myotendinous proprioceptors, located in and around joints and muscles, help manage muscle control and coordination by responding to changes in muscle tension and length.

Although there are studies in the literature on traditional physiotherapy and kinesio taping in patients with shoulder impingement syndrome, no study has been found that includes different kinesio taping techniques and all evaluation parameters.

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • İstanbul, Turkey, 34500
        • Yasemin Şahbaz

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Diagnosed with subacromial impingement syndrome,
  • Between the ages of 45-65, without a history of shoulder injury other than subacromial impingement and/or shoulder symptoms requiring treatment for the last 1 year,
  • Those who have not had any shoulder surgery before,
  • Patients who agree to participate in the study will be included in the study.

Exclusion Criteria:

  • Those who do not meet the inclusion criteria and have a history of shoulder fracture, dislocation and/or cervical radiculopathy,
  • Presence of frozen shoulder, previous shoulder surgery,
  • Having received local corticosteroid injection/treatment to the shoulder joint in the last 3 months,
  • Presence of neuromuscular disease, pregnancy,
  • Those with a history of cancer, unstable angina, systemic inflammatory joint disease,
  • Situations where exercise is contraindicated,
  • Patients with orthopedic, rheumatic or congenital disease in the affected upper extremity and communication problems will be excluded from the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Sham Comparator: Grup A: Traditional Physiotherapy + Sham Kinesiotape

Traditional Physiotherapy: A total of 15 sessions of joint range of motion, stretching exercises and strengthening exercises will be applied 5 days a week for 3 weeks, each session lasting 45 minutes. Friction massage will be applied. In addition, ultrasound, TENS and cold packs will be applied to the patients according to their tolerance.

Sham Kinesiotape: 2 days a week, 6 times in total, following conventional physiotherapy for 3 weeks. Kinesio tape 10 cm I strips will be applied on the acromioclavicular joint in the sagittal plane and in the transverse plane from the distal deltoid without applying tension. The tape will be applied twice a week in total, remaining for 3 days and released one day after each application.

As exercise training, joint range of motion, flexion and abduction external cycle will be practiced with the gymnasts.

Circumference measurements will be taken for shoulder bone swelling and for atrophy.

Shoulder joint mobilizations will be applied (posterior cutting for flexion limitation, downward shifting and scapular mobilizations for abduction limitation).

Flexion and abduction will be stretched externally. Friction massage will be applied. Strengthening exercises for flexion, abduction and external rotation in the lower and upper segments of the shoulder with dumbbells and theraband, shoulder wheel and finger ladder will be practiced.

Codman exercises and staff exercises will be practiced.

Experimental: Grup B: Kinesiotape with Facilitation Method + Traditional Physiotherapy
In addition to traditional physiotherapy, traditional physiotherapy will be applied 2 days a week, 6 times in total, followed by 3 weeks. Kinesio tape has been developed to reflect the properties of the skin, its thickness is similar to the epidermis layer of the skin, and its elasticity is similar to the elastic properties of human skin. Participants should be informed that the patch will remain for several days and will not be removed by bathing or swimming. Kinesio tape will be applied to the deltoid muscle with the starting point at 0 tension while the arm is in a relaxed position and will be slightly heated. It will be applied in addition to traditional physiotherapy 2 days a week for 3 weeks.
Kinesio tape will be applied with 0 tension at the starting point when the arm is in a relaxed position and will be slightly heated. Since the deltoid muscle is a three-headed muscle, it will be applied with 0 tension in the flexed position at the elbow, for the front part, the arm with the elbow in full extension, and for the middle part of the deltoid, the I tape will be applied along the muscle without applying tension.
Experimental: Grup C: Kinesiotape with Inhibition Method + Traditional Physiotherapy

In addition to traditional physiotherapy, traditional physiotherapy will be applied 2 days a week, 6 times in total, followed by 3 weeks.

Kinesio tape will be applied to the deltoid muscle with inhibition and mechanical correction technique, and to the supraspinatus muscle with inhibition technique twice a week, 3 days apart. First of all, it will be applied to the deltoid muscle with the inhibition technique. Y-shaped kinesio tape will be placed 3 cm below the humerus tuberculum deltoidea without stretching. During application, the shoulder will be in maximum extension and external rotation for the front arm of the Y strip, and in 45 degrees transverse flexion and horizontal adduction for the rear arm of the Y strip.

The Y-shaped kinesio tape will be placed on the deltoid muscle with inhibition and mechanical correction technique, and the Y-shaped kinesio tape will be placed on the supraspinatus muscle with inhibition technique, 3 cm below the humerus tuberculum deltoidea without tension. The Y tape will be applied along the outer edge of the anterior deltoid of the forearm with 15-25% light tension, and the posterior arm will be applied along the outer edge of the posterior deltoid with 15-25% light tension up to the lateral acromion. The last 3-5 cm of the tails will be applied to their permanent locations without tension. The shoulder will be held in maximum transverse extension and external rotation for the forearm of the Y support, and in 45 degrees transverse flexion and horizontal adduction for the posterior arm of the Y support. In addition, ultrasound, electrotherapy and cold application will be applied to the participants depending on their tolerance.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Joint Range of Motion (ROM)
Time Frame: 3 weeks
It refers to the measurement of the amount of movement around a particular joint. This measurement is usually made during a physical therapy evaluation. Physiotherapists measure joint range of motion with the help of a tool called a goniometer. The midpoint of the digital goniometer will be fixed by holding it with the hand, with the pivot point for movement of the shoulder joint placed on the greater tubercle of the humerus bone. A digital goniometer will be used to measure shoulder joint range of motion.
3 weeks
Muscle Strength
Time Frame: 3 weeks
The maximal power that can be generated by a specific muscle or muscle group. Muscular strength is the ability of the muscle to resist resistance. In assessing muscle strength, the force or torque applied during maximal voluntary contraction is measured. Evaluation is performed to detect peripheral muscle weakness before treatment, to plan a personalized resistance exercise training program, and to evaluate post-treatment effectiveness. Many methods including voluntary and involuntary contractions are used to measure muscle strength. The physiotherapist who will perform the application must choose the correct, sensitive and most reliable test appropriate to the clinical conditions.
3 weeks
Disabilities of the Arm, Shoulder and Hand (DASH)
Time Frame: 3 weeks

The questionnaire, which evaluates upper extremity functions and gives an idea about upper extremity functionality, consists of 3 parts: symptoms and daily living activities, sports and musician module. The questionnaire consists of 30 items assessing symptoms and activities of daily living. 21 questions in the survey evaluate difficulty in daily life activities, 5 questions evaluate body symptoms (pain, weakness, stiffness, numbness), and the remaining 4 questions evaluate work skills, sleep status, social function and the patient's self-confidence. A 5-grade system is used in scoring the survey. In the scoring scale from 1 to 5, 1 means "no difficulty" and 5 means "I cannot do it at all".

The time to complete the survey is 5-7 minutes and it is a survey that patients can easily answer on their own. The highest score is 100, and high scores indicate low patient functionality.

3 weeks
Visuel Analog Scale (VAS)
Time Frame: 3 weeks
Visuel analog scale is a scale where the intensity of pain is marked on a 10 cm horizontal/vertical line. The point "0" indicates no pain, and the point "10" indicates maximum pain. Participants will be asked to mark the point that represents their pain at the beginning and after treatment. The marked point will then be measured with a ruler and recorded in "cm". A higher value indicates more pain. The reliability of the assessment is r=0.79 and the retest validity is r=0.97.
3 weeks
Tampa Kinesiophobia Scale (TKS)
Time Frame: 3 weeks
The level of kinesiophobia will be assessed with the Tampa Kinesiophobia Scale (TKS). The scale consists of 17 questions. The scoring varies between 17-68, with higher scores indicating higher kinesiophobia.
3 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Yasemin ŞAHBAZ, Lecturer, Beykent University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 15, 2024

Primary Completion (Actual)

September 25, 2024

Study Completion (Actual)

September 30, 2024

Study Registration Dates

First Submitted

August 14, 2024

First Submitted That Met QC Criteria

August 14, 2024

First Posted (Actual)

August 19, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 28, 2025

Last Verified

August 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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