Reciprocal Electrical Stimulation Versus Kinesio Taping

March 7, 2024 updated by: Basma Elsaid Mahmoud Bakr

Effect Of Reciprocal Electrical Stimulation Versus Kinesio Taping On Hand Functions In Hemiparetic Cerebral Palsy Children

This study will be conducted to:

  1. evaluate the effect of kinesio taping on hand functions in hemiplegic cerebral palsy children
  2. compare between the effects of reciprocal electrical stimulation and kinesio taping on hand functions in hemiplegic cerebral palsy children.

Study Overview

Status

Completed

Conditions

Detailed Description

A. Patients preparation All the children demographic and outcome measures data will be collected in specially well-designed sheets1. Evaluation of fine motor skills using PDMS-2 Evaluation of hand function using Besta scale

. The traditional exercise program (given to both groups):

  1. Treatment protocol in Group A, Reciprocal electrical stimulation protocol

    • The device has two channels that can stimulate two opposing groups of muscles alternatively (reciprocate).
    • During ES, the child sits in a chair with his treated forearm resting on a pillow placed on the bed in front of him.
    • The electrodes will be placed as follows:
    • Channel 1 (stimulates wrist and hand extensors) electrodes placed over the dorsum of the forearm as follows: the active electrode is placed over the common extensor origin, while in different over the motor point of extensor pollicis longus, abductor pollicis longus, and extensor indices.
    • Channel 2 (stimulates wrist and hand flexors) electrodes placed on the palmar side of the forearm are as follows: the negative electrode is placed between the finger flexors and wrist flexors. The positive electrode is placed over the tendonportion of the forearm,
    • The treatment duration will be 20 minutes.
    • The treatment protocol will be repeated 3 times per week for 12 weeks.
  2. Treatment protocol in Group B, Kinesio taping protocol:

    • Kinesio taping will be applied on both sides of the upper limb.
    • The applied area will be from the proximal one-third of the forearm to the wrist and then will be split into 5 straps into the distal interphalangeal joint of fingers.
    • On the dorsal side, KT will be applied on the forearm, wrist, and fingers extensors for improvement of wrist and fingers extension.
    • On the plantar side, KT will be applied on the forearm, wrist, and fingers flexors for inhibition of wrist and fingers flexion.
    • Taping will be applied for 6 days, 24 h a day, on the affected upper limb, and it will be removed for only one day per week.

Study Type

Interventional

Enrollment (Actual)

68

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

    • Kafrelsheikh
      • Kafr Ash Shaykh, Kafrelsheikh, Egypt
        • Physical Therapy

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 6 years (Child)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • A medical diagnosis of spastic hemiplegic CP made by paediatricians or pediatric neurologists.
  • Children with spasticity grades ranged from 1 to 1+ according to MAS.
  • Their age range from 4 to 6 years.
  • Children who can sit on the chair with good balance and recognize and follow verbal orders and commands included in both testing and training techniques

Exclusion Criteria:

  • They had a permanent deformity (bony or soft tissue contractures).
  • Children having visual or auditory defects.
  • Children with intelligence quotient less than 70.
  • Children who had Botox application to the upper extremity in the past 6 months or had undergone a previous surgical intervention to wrist and hand.
  • A history of epileptic seizure and any diagnosed cardiac or orthopaedic disability that may prevent the use of assessment methods.
  • Children who are absent in two taping change sessions

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 Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Group (A)
will receive RES in addition to the traditional exercise program.
the device has 2 channels ,4 electrodes with multiple ems programs
Active Comparator: Group (B)
will receive KT in addition to the traditional exercise program.
kinesio tape a therapeutic tape that's applied strategically to the body to provide support, lessen pain, reduce swelling, and improve performance

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Fine motor skills
Time Frame: 3 months
we will use Peabody developmental motor scale-2 to assess fine motor skills
3 months

Collaborators and Investigators

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

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 15, 2023

Primary Completion (Actual)

October 15, 2023

Study Completion (Actual)

October 30, 2023

Study Registration Dates

First Submitted

March 3, 2023

First Submitted That Met QC Criteria

April 3, 2023

First Posted (Actual)

April 5, 2023

Study Record Updates

Last Update Posted (Actual)

March 12, 2024

Last Update Submitted That Met QC Criteria

March 7, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

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.

Clinical Trials on Cerebral Palsy

Clinical Trials on electrical stimulation device

Subscribe