Assessment of Upper Limb Function in Children
Development of New Multifactorial Functional Assessment Protocols and Related Indices for Pediatric Age -Functional Assessment Protocol for the Upper Limb
This study tests a new way to measure how well children with conditions like cerebral palsy and brain injuries can use their arms to help improve their treatment and rehabilitation.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 6 Months to 65 Years |
| Sex | All |
| Sponsor | IRCCS Eugenio Medea Academic / other |
| Locations | 1 site (Bosisio Parini, Lecco) |
| Trial ID | NCT06400667 on ClinicalTrials.gov |
What this trial studies
This study evaluates upper limb functionality in children with conditions like cerebral palsy and acquired brain injuries using a novel kinematic assessment protocol. Participants will perform specific tasks while their movements are captured with an optoelectronic system, allowing for detailed analysis of motion patterns. The goal is to improve understanding of upper limb motor behavior and its abnormalities, which can enhance clinical diagnosis and treatment outcomes. The study aims to provide objective data that can inform rehabilitation strategies and interventions.
Who should consider this trial
Good fit: Ideal candidates include children with unilateral cerebral palsy or acquired brain injuries who are eligible for specific rehabilitation therapies.
Not a fit: Patients with behavioral, visual, or auditory problems, or those experiencing pain in the upper limbs may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved rehabilitation techniques for children with upper limb impairments, enhancing their quality of life.
How similar studies have performed: Other studies utilizing kinematic assessments for upper limb function have shown promise, indicating that this approach is both relevant and potentially effective.
Eligibility criteria
Show full inclusion / exclusion criteria
For healthy group: Inclusion Criteria: - absence of functional impairments in the upper limbs Exclusion Criteria: * behavioral, visual or auditory problems * presence of pain in the upper limbs For pathological group: Inclusion Criteria: * Unilateral PCI candidates for CIMT (Constraint Induced Movement Therapy) treatment; * Acquired brain injury candidates for CIMT or Bimanual treatment; * Ability to understand and follow test instructions. Exclusion Criteria: * behavioral, visual or auditory problems * presence of pain in the upper limbs
Where this trial is running
Bosisio Parini, Lecco
- IRCCS E. Medea — Bosisio Parini, Lecco, Italy (Recruiting)
Study contacts
- Principal investigator: Giuseppe Andreoni — IRCCS E. Medea - La Nostra Famiglia
- Study coordinator: Giuseppe Andreoni
- Email: giuseppe.andreoni@lanostrafamiglia.it
- Phone: 031877350
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.