- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06729281
The Effect of Kinesio Taping on Posture in Healthy Young Adults
Healthy young adults who are health care workers at Haydarpasa Numune Training and Research Hospital will be included in the study considering the inclusion and exclusion criteria. Demographic data such as age, gender, height, weight will be recorded. Thoracic kyphosis and lumbar lordosis angles of the participants will be recorded with Goniometer pro application at the beginning. Spinal muscle thickness including the back extensor muscle group will be measured from the thoracic and lumbar regions with ultrasound by a specialist with clinical experience for ultrasound. Measurement will be made at T8 level for thoracic region and L3 level for lumbar region. They will be evaluated with the Nottingham health profile.
A total of 78 people will be included in the study and will be randomly divided into two groups as intervention + exercise and exercise only group. Randomization will be done by closed envelope method. Kinesiobanting will be applied to the intervention group for 4 weeks, with the posture correction technique on Mondays, and the kinesiobant application will be applied once a week for 4 sessions in total, to be removed on Friday. Both groups will be given a 40-minute posture exercise program based on clinical experience, to be performed every other day, i.e. 4 times a week for 12 weeks. Patients will be given an exercise follow-up chart and will be called once a week and followed up for 12 weeks. In the intervention group, thoracic kyphosis and lumbar lordosis angle measurements with Goniometer pro application will be examined at 30.minute at baseline, Week 4 and Week 12, while in the exercise only group they will be examined at baseline, Week 4 and Week 12. Ultrasound measurement of spinal muscle thickness will be performed at baseline and at Week 12 in both groups. Nottingham Health Profile will be performed at baseline, Week 4 and Week 12 in both groups. Differences within and between groups will be analyzed statistically.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
İstanbul, Turkey
- Haydarpaşa Numune Training and Research Hospital Physical Medicine and Rehabilitation Clinic
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Health workers
- Over 18 and under 40
- Visual analog scale (VAS) < 4 for muscle pain
- Inactive (category 1) and minimally active (category 2) according to the international physical activity survey
- Healthcare workers without cognitive deficits who can take verbal instructions
Exclusion Criteria:
- Diagnosed disc herniation with or without spinal deformity
- Bone abnormality and peripheral symptoms
- Infectious or inflammatory arthropathies
- History of joint replacement surgery,
- History of spinal surgery
- Need for assistive devices for ambulation
- irregular hypertension
- Uncontrolled diabetes mellitus
- Presence of neurological disease
- History of malignancy
- Uncontrolled cardiopulmonary disease
- Pregnancy
- Morbid obesity (Body mass index > 35)
- Having fibromyalgia syndrome
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: exercise
Regular exercise is also among the factors affecting the formation of posture.
A regular and systematic exercise program can change the curvatures of the spine in the sagittal plane.
|
|
|
Other: exercise and kinesio taping
Regular exercise is also among the factors affecting the formation of posture.
A regular and systematic exercise program can change the curvatures of the spine in the sagittal plane.
+ Kinesiotaping
|
The application of kinesio tape is a relatively new method, first developed in 1973 by Kenzo Kase in Japan, also known as elastic bandage, which has become popular in the last 10 years following announcements at major events such as the Olympic Games.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Thoracic kyphosis and lumbar lordosis measurements with Goniometer Pro Application
Time Frame: 1. month and 3. month
|
Thoracic kyphosis and lumbar lordosis angle measurements with Goniometer pro application will be examined at 30 minutes at baseline, Week 4 and Week 12, whereas only in the exercise group will be examined at baseline, Week 4 and Week 12.
|
1. month and 3. month
|
|
Spinal muscle thickness measurements with Ultrasound
Time Frame: 1. month and 3. month
|
Ultrasound measurement of spinal muscle thickness will be performed with Mindray brand ultrasound in both groups at baseline and at week 12, with measurements indicated in millimetres.
|
1. month and 3. month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Nottingham Health Profile
Time Frame: 1.month and 3. month
|
Nottingham Health Profile will be performed at baseline, Week 4 and Week 12 in both groups.
Differences within and between groups will be analyzed statistically
|
1.month and 3. month
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- E-62977267-903.99-23331179
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
product manufactured in and exported from the U.S.
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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