Actively Recruiting

Age: 2Years - 18Years
All Genders
NCT06403891

The Effect of a Comprehensive Rehabilitation Program Using Robotic Walking and Functional Electrical Stimulation Technologies on Balance and Walking in Children With Cerebral Palsy

Led by Ankara City Hospital Bilkent · Updated on 2024-05-08

30

Participants Needed

1

Research Sites

113 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study was to investigate the effect of a comprehensive rehabilitation program using robotic walking and functional electrical stimulation technologies on balance and gait in children with cerebral palsy. This study was planned as a prospective observational study. A total of 30 patients in two groups were planned to be included in the study. Patients in both groups were planned to receive a 6-week conventional rehabilitation program that was prepared to meet the requirements of their clinical conditions, including neurophysiological exercises, balance-coordination and posture exercises. The case group was planned to consist of patients who received a comprehensive rehabilitation program using high-tech devices including functional electrical stimulation (FES) and robotic rehabilitation applications in addition to the conventional rehabilitation program.

CONDITIONS

Official Title

The Effect of a Comprehensive Rehabilitation Program Using Robotic Walking and Functional Electrical Stimulation Technologies on Balance and Walking in Children With Cerebral Palsy

Who Can Participate

Age: 2Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 2 and 18 years
  • Diagnosis of cerebral palsy
  • Able to walk independently with or without an assistive walking device
  • Gross Motor Function Classification System (GMFCS) score between 1 and 3
  • No history of seizures
  • Legal guardian has signed informed consent to participate in the study
Not Eligible

You will not qualify if you...

  • Presence of contracture in lower extremities
  • Received botulinum toxin treatment within one month before or during the 6-week treatment period
  • Unable to cooperate with clinical assessments

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Ankara Bilkent City Hospital

Ankara, Turkey (Türkiye), 06800

Actively Recruiting

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Research Team

B

Berat M Alkan, Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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