The Effect of Kinesiological Taping Applied to the Tibialis Anterior Muscle on Gait Parameter in Stroke Patients

June 8, 2020 updated by: Muammer Çorum, Istanbul Rumeli University

The Effect of Kinesiological Taping Applied to the Tibialis Anterior Muscle on Gait Parameter in Stroke Patients: Sham Controlled Study

The effect of kinesiological taping applied to the tibialis anterior muscle on gait parameter in stroke patients: Sham controlled study

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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

Interventional

Enrollment (Actual)

28

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Denizli, Turkey, 20100
        • Pamukkale University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

25 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
No Intervention: No tape applied
Walking parameters were evaluated without any intervention.
Experimental: Kinesiological Tape
Walking parameters were evaluated after kinesiological taping on the tibialis anterior muscle
The kinesiological banding applied to the tibialis anterior muscle was applied to improve walking parameters and compared to sham control.
Sham Comparator: Sham taping
Walking parameters were evaluated after sham taping on the tibialis anterior muscle
The kinesiological banding applied to the tibialis anterior muscle was applied to improve walking parameters and compared to sham control.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
non-taping walking parameter measurement
Time Frame: 2 hours
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.
2 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
With kinesiological taping walking parameter measurement
Time Frame: 2 hours
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.
2 hours
With sham taping walking parameter measurement
Time Frame: 2 hours
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.
2 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Study Director: Emre Baskan, Phd, Pamukkale University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 14, 2018

Primary Completion (Actual)

July 22, 2019

Study Completion (Actual)

May 5, 2020

Study Registration Dates

First Submitted

June 4, 2020

First Submitted That Met QC Criteria

June 8, 2020

First Posted (Actual)

June 11, 2020

Study Record Updates

Last Update Posted (Actual)

June 11, 2020

Last Update Submitted That Met QC Criteria

June 8, 2020

Last Verified

June 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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