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Clinical Trials/NCT06750081
NCT06750081CompletedNot Applicable

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

Cairo University1 site in 1 country40 target enrollmentStarted: August 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
active ankle dorsiflexion range of motion (AROM)

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
6 Years to 8 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

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

Arms & Interventions

Experimental

Experimental

receive an experimental intervention

Intervention: Designed rehabilitation program (Other)

Control

Active Comparator

another therapy used to treat the same condition

Intervention: Physical Therapy (Other)

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tamer Mohamed El-Saeed

Associate Professor

Cairo University

Study Sites (1)

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