- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05858073
Investigation of Immediate Efficacy of Kinesiology Taping in Individuals With Scapular Dyskinesia
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: HAZAL genç
- Phone Number: 05413204291
- Email: hazaloksuz@gmail.com
Study Locations
-
-
None Selected
-
Istanbul, None Selected, Turkey, 34353
- HAZAL genç
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Scapular Dyskinesia
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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