Using biofeedback and electrical stimulation to help children with hemiplegia
Combined Effect of Biofeedback and Functional Electrical Stimulation on Upper Limb Functions in Children With Hemiplegia
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
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 5 Years to 10 Years |
| Sex | All |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Giza) |
| Trial ID | NCT06729190 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates are children aged 5 to 10 years with hemiplegia and specific functional limitations.
Not a fit: Patients with loss of sensation, visual or auditory impairments, or other significant upper limb issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve upper limb function in children with hemiplegia.
How similar studies have performed: While the combination of biofeedback and electrical stimulation is a recognized approach, the specific application in this pediatric population is relatively novel.
Eligibility criteria
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 this trial is running
Giza
- Cairo University — Giza, Egypt (Recruiting)
Study contacts
- Study coordinator: Alaa T Ramadan, M.SC
- Email: dr.alaataha@yahoo.com
- Phone: 01019320008
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.