- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04425811
The Effect of Kinesiological Taping Applied to the Tibialis Anterior Muscle on Gait Parameter in Stroke Patients
The Effect of Kinesiological Taping Applied to the Tibialis Anterior Muscle on Gait Parameter in Stroke Patients: Sham Controlled Study
Study Overview
Detailed Description
Objective: The aim of this study was to compare the immediate effect of kinesiological and / or sham taping to the tibialis anterior muscle on walking parameters in stroke individuals.
Methods: The study included 28 adults stroke patients . The subjects who received scores of 7 or more in the Hodkinson Mental Test and 3 and above in the Functional Ambulation Classification with subjects who gastrocnemius muscle spasticity 2 and below points according to Modified Ashworth Scale were included in the study. The walking parameters of the participants were evaluated with the BTS G-Walk Spatio-Temporal Walking Analysis System. The walking parameters of the participants who were selected by randomization method were evaluated separately by applying kinesiological taping and sham taping or without any taping or interference on a 10 meter track.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Denizli, Turkey, 20100
- Pamukkale University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 28 stroke individuals (hemiplegic / hemiparetic) who were treated in the Adult
- Neurological Rehabilitation Unit of Pamukkale University Medical Faculty Hospital were included in the study.
- Being between the ages of 25-70
- Volunteers with written consent
- With a 1-year history of stroke
- Who had a stroke for the first time
- Having a lesion in one brain hemisphere
Exclusion Criteria:
- Having neurological or orthopedic comorbid disease
- Patients with a gastrocnemius spasticity greater than 2 according to the modified ashworth scale
- Patients with communication problems
- Patients with cognitive functions below 7 points according to the Hodkinson Mental Test
- Patients with ambulation level below 3 according to Functional Ambulation Classification
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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No Intervention: No tape applied
Walking parameters were evaluated without any intervention.
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Experimental: Kinesiological Tape
Walking parameters were evaluated after kinesiological taping on the tibialis anterior muscle
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The kinesiological banding applied to the tibialis anterior muscle was applied to improve walking parameters and compared to sham control.
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Sham Comparator: Sham taping
Walking parameters were evaluated after sham taping on the tibialis anterior muscle
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The kinesiological banding applied to the tibialis anterior muscle was applied to improve walking parameters and compared to sham control.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
non-taping walking parameter measurement
Time Frame: 2 hours
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The dominant side lower extremity of the participants was determined as the first preferred lower limb to take steps when walking.
Walking parameters of the participants included in the study were evaluated with BTS G-Walk Spatio-Temporal Gait Analysis System.
Before the banding applications of the patients, walking parameters were measured by asking them to walk with a shoe that they always use daily with the command "walk normally" on a 10-meter course, and stop with the command "stop" after 10 meters.
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2 hours
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
With kinesiological taping walking parameter measurement
Time Frame: 2 hours
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Kinesiological taping or sham taping was performed by a certified physiotherapist 2 hours after the measurement of walking parameters without any intervention.
Kinesiological banding for the tibialis anterior muscle was performed using muscle technique (stimulation).
The taping was performed with the patients lying on a stretcher in the supine position.
The kinesiological band was cut in the shape of I considering the participant's muscle length, the edges were ovalized, and the skin was purified from moisture, hair and oil.
While applying the muscle technique (stimulation), the tibialis anterior muscle was stretched in the plantar flexion and eversion position.
It was then activated by applying heat along the band.
After the band was activated, the walking parameters of the participant were measured again with the BTS G-Walk device.
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2 hours
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With sham taping walking parameter measurement
Time Frame: 2 hours
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The sham taping was applied to the participants a week or a week before the application of the kinesiological tape.
Sham taping application was applied to the same area as kinesiological taping application, but no technique was used.
After the Sahm taping application, the walking parameters of the participants were measured again with the BTS G-Wlak device.
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2 hours
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Emre Baskan, Phd, Pamukkale 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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- pamukkaleU
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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