Music Effect on Concentration and Gait in Cerebral Palsy Children During Physical Therapy Sessions (NMT\CP)

June 3, 2026 updated by: Shrouk Mohamed Mahmoud Hussein, Cairo University

Effect of Physiotherapy With Auditory Cueing on Concentration and Gait in Children With Spastic Cerebral Palsy

  • To investigate the effect of music therapy as an additional intervention with physical therapy on concentration in children with spastic CP.
  • To investigate the effect of music therapy as an additional intervention with physical therapy on gait parameters for the children with spastic CP.

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Physical therapy only could be not attractive for child if it done by the traditional way; focus on motor part and no need to involve the sensory part through the rehabilitation.

Sense of hearing could be a unique one to stimulate for a better child attention during physical therapy session, even child with blindness could benefit from this idea.

Using music for attracting attention of the child as a therapeutic way so the child can walk properly regarding time and pace.

Singing as a live form of music could be more sensitive and interactive for child-therapist bond which is important to include the child as an active participant as child is being rehabilitated not just treatment.

Rehabilitation means to involve the child as a whole at this complicated process, not to move a passive limb.

Rehabilitation of CP:

  • A "temporal axis": Habilitation/rehabilitation should begin early and continuously - a minimum within the first years of child's life - and intensively - individually designed to meet child's needs.
  • A "spatial axis": where individual space, family, school, and social affair places must be all considered.
  • An "individual axis": Rehabilitation must observe the child as an active participant, not as a passive person of whom needs care.
  • A "relational axis": the standard of taking into consideration the relationship of the child and people who take care of him/her in different contexts of their life (Trabacca et al., 2016).

Study Type

Interventional

Enrollment (Estimated)

40

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 Contact

  • Name: Shrouk Mahmoud Mohamed researcher at Cairo university faculty of physical therapy, master
  • Phone Number: +201002952353
  • Email: shrouk.rere@gmail.com

Study Contact Backup

Study Locations

    • Giza Governorate
      • Dokki, Giza Governorate, Egypt, 02
        • Faculty of Physical Therapy Cairo 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

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • • The children age ranged from 5 to 7 years old (early childhood).

    • Spasticity degree ranges from 1 to 1+ as measured by the Modified Ashworth Scale
    • Children with lack of concentration according to MARS (Moss Attention Rating Scale)
    • Children can stand alone and walk.

Exclusion Criteria:

  • • Children with deafness.

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: MT and PT
music and physical therapy
Neurologic music therapy (NMT) Listening to music and moving rhythmically.
program for gait improvement ( Standing, balance and gait training)
Active Comparator: PT
Physical therapy
program for gait improvement ( Standing, balance and gait training)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
concentration as a cognitive function
Time Frame: pre intervention and 3 months post intervention
ability of child to pay attention during physical therapy sessions and be interactive with the therapist, measured by Moss Attention Rating Scale, score of 22 (minimum score) to less than 110 (maximum score), Higher scores indicate better attention.
pre intervention and 3 months post intervention
Gait
Time Frame: pre intervention and 3 months post intervention
improvement measured by Gross motor function measure 88 (gait section), 0 (minimum score) to 100 (maximum score) percentage %
pre intervention and 3 months post intervention
Kinovea, (Spatial and Temporal Parameters)
Time Frame: pre and 3 months post intervention
Kinovea, (Spatial and Temporal Parameters); Step length in centimeters (higher score better)
pre and 3 months post intervention
Kinovea, (Spatial and Temporal Parameters) ; stride length in centimeters (higher score better)
Time Frame: pre and 3 months post intervention
Kinovea, (Spatial and Temporal Parameters); stride length in centimeters (higher score better)
pre and 3 months post intervention
Gait (cadence)
Time Frame: pre and 3 months post intervention
Using Kinovea, cadence measured in steps\minute (lower score better).
pre and 3 months post intervention

Collaborators and Investigators

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

Investigators

  • Study Chair: Kamal El-sayed Shoukry, Doctorate, Professor of Physical Therapy for Pediatrics Faculty of Physical Therapy 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 (Estimated)

May 20, 2026

Primary Completion (Estimated)

December 15, 2026

Study Completion (Estimated)

May 15, 2027

Study Registration Dates

First Submitted

May 13, 2026

First Submitted That Met QC Criteria

June 3, 2026

First Posted (Actual)

June 4, 2026

Study Record Updates

Last Update Posted (Actual)

June 4, 2026

Last Update Submitted That Met QC Criteria

June 3, 2026

Last Verified

June 1, 2026

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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