- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06723873
Effects of Kinesiology Taping in Stroke Patients
The Immediate Effects of Kinesiology Taping on the Trunk-Scapula-Shoulder Complex in Stroke Patients: A Placebo-Controlled Study
The goal of this clinical trial is to learn if kinesiology taping works to treat stroke patients. The main question it aims to answer is:
Is kinesiology taping effective in stroke patients? Researchers compare kinesiology taping to a placebo (visually similar but has no effects) to see if kinesiology taping works immediately to treat stroke patients.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study aimed to evaluate the immediate effects of kinesiology taping (KT) on trunk control, posture, proprioception, and upper limb function in stroke patients, specifically focusing on the trunk-scapula-shoulder complex. A total of thirty-seven stroke patients participated in this placebo-controlled trial, where they were randomly assigned to either the KT group (n=19) or a placebo-controlled sham KT group (n=18). The KT group received kinesiology taping applied using facilitation and inhibition techniques, while the control group received sham taping without therapeutic tension.
The application of kinesiology taping to the trunk-scapula-shoulder complex in stroke patients resulted in immediate enhancements in trunk control, shoulder posture, and proprioception. However, it did not significantly improve upper limb function in the short term.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul, Turkey
- Beykent University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Experienced a first-ever stroke
- Demonstrated a motor recovery level of Brunnstrom stages 3 or 4 in the affected upper limb
- No history of botulinum toxin-A therapy within the past three months
- Possess sufficient cognitive ability to understand and follow assessment instructions
Exclusion Criteria:
- Individuals with movement or functional limitations due to prior shoulder injuries
- Exhibited allergic reactions or skin sensitivities to taping
- Patients with any existing skin conditions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Kinesiology Taping Group
Each taping method was carefully designed to address the unique muscle imbalances and functional deficits commonly seen in stroke patients.
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The treatment group received Kinesiology Taping around the trunk extensors, lower and middle trapezius, supraspinatus, deltoid muscle group, and serratus anterior muscle.
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Sham Comparator: Placebo-Controlled Sham Group
Utilizing three 'I'-shaped strips placed superficially on the skin to ensure no therapeutic effects were achieved.
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In the control group, kinesiology tape was applied without tension and in a manner that did not target specific muscle groups or respect the anatomical origin and insertion points.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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The Trunk Impairment Scale
Time Frame: Change of trunk impairment from baseline at the end of 24 hours of each kinesiology taping intervention.
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The Trunk Impairment Scale (TIS) is a validated assessment tool designed to evaluate trunk function in stroke patients, measuring static sitting balance, dynamic sitting balance, and trunk coordination through a total of 17 items.
Each item is scored based on the patient's performance, with the highest score recorded from three repetitions.
The TIS provides a total score ranging from 0 to 23 points, where a higher score indicates better trunk function.
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Change of trunk impairment from baseline at the end of 24 hours of each kinesiology taping intervention.
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Posture Evaluation
Time Frame: Change of posture scores from baseline at the end of 24 hours of each kinesiology taping intervention.
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Posture was assessed using the Posture Screen Mobile (PSM) application, a reliable and valid software tool for posture analysis available on iOS and Android devices.
In this study, a physiotherapist utilized an iPad camera to capture sagittal plane photographs of each participant, which were then digitized by marking specific anatomical landmarks.
The PSM application calculated anterior and lateral translations, as well as angular displacements, overlaying a grid on the images to assist in accurate landmark placement.
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Change of posture scores from baseline at the end of 24 hours of each kinesiology taping intervention.
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Proprioception Evaluation
Time Frame: Change of proprioception scores from baseline at the end of 24 hours of each kinesiology taping intervention.
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Trunk and shoulder proprioception were evaluated using the inclinometer, with participants positioned at 30° forward flexion of the trunk for testing.
They were instructed to hold this position for 5 seconds and then return to a neutral position for another 5 seconds before attempting to reproduce the initial benchmark position, with up to five attempts allowed.
Shoulder proprioception was assessed at 75° and 90° flexion.
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Change of proprioception scores from baseline at the end of 24 hours of each kinesiology taping intervention.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Motor Assessment Scale
Time Frame: Change of upper-limb function scores from baseline at the end of 24 hours of each kinesiology taping intervention.
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The Motor Assessment Scale (MAS) was employed to evaluate upper-limb function in stroke patients, focusing specifically on three items: item 6 (upper-limb function), item 7 (hand movements), and item 8 (advanced hand activities).
Each item is scored on a scale from 0 to 6, with higher scores indicating better functional ability, resulting in a total score range of 0 to 18 for these three items.
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Change of upper-limb function scores from baseline at the end of 24 hours of each kinesiology taping intervention.
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Burcu Ersöz Hüseyinsinoğlu, Assoc.Prof., Marmara University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
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
- 108400987-244
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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