Actively Recruiting

Phase 2
Phase 3
Age: 3Years - 8Years
All Genders
NCT06872736

Wereables for Upper Limb Functionality in Hemiparesis

Led by Universidade da Coruña · Updated on 2025-03-12

40

Participants Needed

1

Research Sites

132 weeks

Total Duration

On this page

Sponsors

U

Universidade da Coruña

Lead Sponsor

C

Complexo Hospitalario Universitario de A Coruña

Collaborating Sponsor

AI-Summary

What this Trial Is About

The project is configured as a national interventional study that aims to determine the effectiveness of an intervention strategy using wearable technology, tailored to improve function (WeFun-wearable), on the spontaneous use of the affected upper extremity, activities of daily living and the participation in children with unilateral cerebral palsy.

CONDITIONS

Official Title

Wereables for Upper Limb Functionality in Hemiparesis

Who Can Participate

Age: 3Years - 8Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of unilateral cerebral palsy (UCP).
  • Children aged between 3 and 8 years old.
  • Manual Ability Classification System (MACS) levels I to III.
Not Eligible

You will not qualify if you...

  • Botulinum toxin injection or surgical interventions in the upper limb within 6 months prior to study entry.
  • Uncontrolled medical complications interfering with participation (e.g., uncontrolled epilepsy).
  • Predominantly athetoid or dystonia movement patterns.
  • Insufficient cognitive level to follow instructions.
  • Non-corrected marked visual impairments.
  • Families not collaborating or assisting with weekly sessions after starting.
  • Wearable activity recordings less than 20% of expected.
  • Families not providing feedback about daily sessions through the app or registration sheet.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Universidade da Coruña

A Coruña, A Coruña, Spain, 15006

Actively Recruiting

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Research Team

V

Verónica Robles García, PhD

CONTACT

I

Irene González Eiroa, MsC

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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