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Clinical Trials/NCT06750081
NCT06750081
Completed
Not Applicable

Effect of Cross-Training on Locomotor Abilities in Children with Spastic Hemiparesis

Cairo University1 site in 1 country40 target enrollmentAugust 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cerebral Palsy (CP)
Sponsor
Cairo University
Enrollment
40
Locations
1
Primary Endpoint
active ankle dorsiflexion range of motion (AROM)
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose was to investigate the effect of cross-training as a method of unilateral motor priming on locomotor abilities in children with spastic unilateral cerebral palsy.

Detailed Description

Thirty children with spastic unilateral cerebral palsy were recruited from different rehabilitation centers. They were assigned randomly into two groups. Children in the control group (A) were engaged in a selected physical therapy program while those in the experimental group (B) received cross-training program followed by application of the same selected physical therapy program received by group (A). The treatment programs were conducted five times per week for six successive weeks. Measurements obtained included active ankle dorsiflexion range of motion (AROM), and the speed of walking obtained by 10-meter walking test. These measures were recorded two times: pre- and post-treatment.

Registry
clinicaltrials.gov
Start Date
August 1, 2023
End Date
December 15, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Tamer Mohamed El-Saeed

Associate Professor

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Spasticity grade 1 to 1+, according to the Modified Ashworth Scale.
  • Can stand and walk autonomously.
  • Able to follow verbal commands and instructions.

Exclusion Criteria

  • Fixed musculoskeletal deformities
  • significant cognitive disorders
  • significant perceptual disorders
  • significant auditory disorders
  • significant visual disorders

Outcomes

Primary Outcomes

active ankle dorsiflexion range of motion (AROM)

Time Frame: Baseline and at the end - through study completion, an average of 1 year

10-meter walking test

Time Frame: Baseline and at the end - through study completion, an average of 1 year

Study Sites (1)

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