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

Sponsor
Istanbul Medipol University Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05858073
Collaborator
(none)
70
1
2
6
11.6

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Kinesio Taping
  • Other: Placebo Kinesio Taping
N/A

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 Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Investigation of Immediate Efficacy of Kinesiology Taping in Individuals With Scapular Dyskinesia
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: Kinesio Taping.

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.

Other: 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.

Outcome Measures

Primary Outcome Measures

  1. Visual Analogue Scale (VAS) [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.

  2. Lateral Scapular Slip Test [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.

  3. New York Posture Scale [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.

  4. Proprioception Evaluation [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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 HAZAL genç Istanbul None Selected Turkey 34353

Sponsors and Collaborators

  • Istanbul Medipol University Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
hazal genc, Principal Investigator, Istanbul Medipol University Hospital
ClinicalTrials.gov Identifier:
NCT05858073
Other Study ID Numbers:
  • Scapular Dyskinesia
First Posted:
May 15, 2023
Last Update Posted:
May 15, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by hazal genc, Principal Investigator, Istanbul Medipol University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 15, 2023