Using biofeedback and electrical stimulation to help children with hemiplegia
Official title: Combined Effect of Biofeedback and Functional Electrical Stimulation on Upper Limb Functions in Children With Hemiplegia
Run by Cairo University · NCT06729190 · Data updated 2026-11-12
This study is testing if a mix of biofeedback and electrical stimulation can help children with hemiplegia cerebral palsy improve their arm movement and skills.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 5 Years to 10 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Giza) |
| Status | Recruiting |
| Started | December 2024 |
| Main results expected | March 2025 |
| Study ends | March 2025 |
| Registry record updated | December 20, 2024 |
| Trial ID | NCT06729190 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are children aged 5 to 10 years with hemiplegia and specific functional limitations.
✕Probably not a fit
Patients with loss of sensation, visual or auditory impairments, or other significant upper limb issues may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study involves 40 children aged 5 to 10 years with hemiplegia cerebral palsy, recruited from an outpatient clinic. The intervention combines functional electrical nerve stimulation and biofeedback to evaluate their combined effects on improving upper limb function. Participants will be assessed based on their ability to follow instructions and their spasticity levels. The goal is to enhance motor skills and functional abilities in these children.
Why it matters
Potential benefit: If successful, this approach could significantly improve upper limb function in children with hemiplegia.
How similar studies have gone: While the combination of biofeedback and electrical stimulation is a recognized approach, the specific application in this pediatric population is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Their age will range from 5 to 10 years. * Spasticity grade range from 1+ to 2, according to Modified Ashworth Scale (MAS) (Bohannon and Smith, 2011). * Their UL ability function will be at level II according to Manual Ability Classification System (MACS) (Penta et al., 2001). * They will be able to follow instructions. Exclusion Criteria: * Loss of sensation * The presence of visual or auditory impairments. * Musculoskeletal problems or fixed deformities in the upper extremities. * Seizures. * Surgical interference in upper limbs. * Botulinum toxin injections in the last 6 months.
Where it's running
-
Cairo University
Giza, Egypt Recruiting
Study contacts
- Study coordinator: Alaa T Ramadan, M.SC
- Email: dr.alaataha@yahoo.com
- Phone: 01019320008
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.