Role of Kinesiotape Over Dorsi Flexors Muscles on Balance in Children With Spastic Diplegia

January 26, 2020 updated by: Samar Samy Ibrahim Hegazy, Cairo University

Role of Kinesiotape Over Dorsi Flexors Muscles on Balance in Children With Spastic Diplegia (Using Biodex Balance System)

To detect the effect of kinesio -tape on balance in children with spastic diplegia.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The use of Kinesio Taping might influence the cutaneous receptors of the sensory motor system, resulting in the improvement of voluntary control and coordination in a physiotherapy program for children with CP. (Yasukawa et al., 2006).

The study will be conducted To investigate the effect of kinesiotape applied on dorsi fexors muscles on improving balance in spastic diplegic children .

Study Type

Interventional

Enrollment (Actual)

30

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

      • Cairo, Egypt
        • Cairo Univeristy

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

4 years to 10 years (CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • • Thirty children with spastic diplegia of both genders participated in this study.

    • Theywere selected from the out-patient clinic, faculty of physical therapy, Cairo University.
    • Children height not less than 1 meter to be able to see the screen of the biodex balance system.
    • Their agehad ranged from 4 to 8 years.
    • All patients have mild spasticity according to modified Aschwar scale grade 1 &1+ (Alhusaini, 2010) presented in (Appendix I).
    • All patients wereable to stand alone GMFM presented in (Appendix II).
    • They could understand and follow instructions.
    • All Children used Ankle Foot Orthosis.

Exclusion Criteria:

  • • Children with visual or auditory problems.

    • Children with positive sensitivity to kinesiotape.
    • Children with irrivisable muscle contracture at the calf muscles.

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: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
ACTIVE_COMPARATOR: control group
15 diplegic children received regular exercise program including balance exercise
apply kinesio taping on dorsi flexors muscles
EXPERIMENTAL: study group
15 diplegic children recieved regular exercise program plus putting kinesiotape
apply kinesio taping on dorsi flexors muscles

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
effect of K-Tape on balance
Time Frame: three months
effect of using K-Tape on dorsi flexors to see its effect on balance
three months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: I, Cairo 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)

February 10, 2019

Primary Completion (ACTUAL)

August 11, 2019

Study Completion (ACTUAL)

October 13, 2019

Study Registration Dates

First Submitted

January 22, 2020

First Submitted That Met QC Criteria

January 26, 2020

First Posted (ACTUAL)

January 28, 2020

Study Record Updates

Last Update Posted (ACTUAL)

January 28, 2020

Last Update Submitted That Met QC Criteria

January 26, 2020

Last Verified

December 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • peadiatrics 123

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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