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Cross-Training and Locomotor Abilities in Cerebral Palsy

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06750081
Enrollment
40
Registered
2024-12-27
Start date
2023-08-01
Completion date
2024-12-15
Last updated
2024-12-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Palsy (CP), Spastic Hemiparesis

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.

Interventions

OTHERPhysical Therapy

Exercises to improve locomotor abilities of children with CP

Program of exercises to enhance abilities

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
6 Years to 8 Years
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

Design outcomes

Primary

MeasureTime frame
active ankle dorsiflexion range of motion (AROM)Baseline and at the end - through study completion, an average of 1 year
10-meter walking testBaseline and at the end - through study completion, an average of 1 year

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026