Investigation of Immediate Efficacy of Kinesiology Taping in Individuals With Scapular Dyskinesia

May 5, 2023 updated by: hazal genc, Istanbul Medipol University Hospital
Shoulder protraction is the forward tilt of the head with hyperextension of the cervical spine and is associated with lengthening of the sternocleidomastoid and scalene muscles. With the lengthening of the flexor muscles, the weakened and shortened trapezius, levator scapula, and serratus anterior muscles lead to extra flexor torque and sustained contraction.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Weakness in the rotator cuff muscles, especially infraspinatus and supraspinatus muscles, has been observed in individuals with scapular dyskinesia and who frequently use overhead movements in their daily lives. The most important point to be considered in the treatment of scapular dyskinesia is the effective evaluation and treatment of primary and secondary symptoms and conditions. The preference of shoulder rehabilitation programs in which the scapula is also included in the treatment program will provide great benefits to physiotherapists in terms of treatment. Effective treatment can be provided by taping, exercise and many other treatment methods.

Study Type

Interventional

Enrollment (Anticipated)

70

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 Contact

Study Locations

    • None Selected
      • Istanbul, None Selected, Turkey, 34353
        • HAZAL genç

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

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Those with neck pain
  • Being between 18-60 years old

Exclusion Criteria:

  • Hypertension
  • Cardiopulmonary disease
  • Pregnancy
  • malignancy
  • Operation, injection, etc. for the neck in the last 3 months. those with a history of treatment
  • Spine surgery
  • Psychological discomfort
  • Neurological and orthopedic deficits

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: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Kinesio Taping.

Standard 5 cm Kinesio Tex will be used. Initially, a Y-strip was paper-off (without tension) from the starting point to the insertion of the supraspinatus, while the participants were reaching with their upper extremities behind their backs and flexing their necks to the contralateral side. Second, an I-strip from the coracoid process will be applied around the posterior deltoid using approximately 50% to 75% downward flexion. Initially, the shoulder will be externally rotated without elevation, and then slightly horizontally adduction and forward elevation as the end of the band is applied without stretching. This I strip is shaped like a Y at the end of the tape.

Finally, a Y-strip will be applied using paper-off tension from the T10-T12 region to the medial border of the scapula to facilitate the lower trapezius muscle. For this technique, the shoulder was adducted horizontally and the middle tail was applied with the hands crossed over the chest.

Placebo Comparator: Placebo Kinesio Taping.
Standard placebo taping will be applied to the placebo Kinesio taping group with a standard 5 cm Kinesio Tex. Two tension-free strips will be applied separately to the acromioclavicular joint and lower trapezius muscle. Suspicious participants will be excluded from the study.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Visual Analogue Scale (VAS)
Time Frame: one day
In the measurement of neck pain severity, it was planned to use a standard, proven 10 mm VAS. Patients will be asked to determine a value between 0 and 10 for the VAS, with 0 in the absence of pain and 10 mm in the most severe pain.
one day
Lateral Scapular Slip Test
Time Frame: one day
Evaluation of Scapular Dyskinesia The Lateral Scapular Slip Test (LSST) was used for scapular dyskinesia. The LSST was used to determine the position of the scapula in the coronal plane at 0, 45, and 90° abduction of the arm. Evaluation was made for both sides of the scapula in 3 different positions (0°, 45° and 90° abduction). The distance between the inferior corner of the scapula and the spinous process was measured. For the test to be positive, there must be a difference of 1.5 cm or more between the right and left side measurements.
one day
New York Posture Scale
Time Frame: one day
Posture analysis is done while standing upright. Postures of the subjects participating in the study were evaluated with the New York Posture Scale. In this evaluation system, posture that can occur in 13 different parts of the body is evaluated. For scoring, a score of five was given if the person's posture was correct, three if it was moderately impaired, and one if it was severely impaired. The total score obtained with the test evaluation is a maximum of 65 and a minimum of 13. Standard evaluation criteria developed for this test were defined as "very good" if the total score was >=45, "good" if 40-44, "moderate" if 30-39, "poor" if 20-29, and "poor" if <=19. detected.
one day
Proprioception Evaluation
Time Frame: one day

An inclinometer is an instrument that records angular movements with respect to gravity. The inclinometer has many advantages such as precise measurement, digital display, and ease of use. In our study, inclinometer will be used to evaluate proprioception.

The patient is first brought to 30° shoulder flexion position 3 times while standing and asked to memorize this position. Then the patient is asked to find the same position with his eyes closed. The patient is asked to return to the upright position and find the 30° flexion position. The same procedure is repeated in sitting position at 30° flexion and 15° extension positions. This process is repeated 3 times and the results are recorded. The average of these 3 measurements will be used in the analysis of the data.

one day

Collaborators and Investigators

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

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 (Anticipated)

June 1, 2023

Primary Completion (Anticipated)

June 1, 2023

Study Completion (Anticipated)

December 1, 2023

Study Registration Dates

First Submitted

May 5, 2023

First Submitted That Met QC Criteria

May 5, 2023

First Posted (Actual)

May 15, 2023

Study Record Updates

Last Update Posted (Actual)

May 15, 2023

Last Update Submitted That Met QC Criteria

May 5, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • Scapular Dyskinesia

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

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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