Home Based Adaptive Arm Training for Children

Status Terminated

Clinical Trial Summary

Twenty pediatric patients aged 5-17 years with Acquired Brain Injuries (ABI) will be randomized to receive either a bimanual-to-unimanual device home training program (10 subjects) or a conventional non-device home training program (10 subjects) for a period of 6 weeks. The specific aims of this proposal are to: Aim 1: Introduce home-based targeted upper limb training in children with hemiplegia from ABI (Acquired Brain Injuries) using a bimanual-to-unimanual training approach It is hypothesized that child-friendly home-based upper limb bimanual-to-unimanual training will lead to greater compliance and improved motor outcome on the Fugl Myer Scale compared to a conventional home training program. Aim 2: Improve the understanding of the pattern of recovery of isolated joint movements in the pediatric population with hemiplegia following ABI. It is hypothesized that individuals receiving device-based bimanual-to-unimanual training will show improvement in active range of motion across upper limb joints compared with a conventional home training program.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Hemiplegia

Clinical Trial Details

NCT number	NCT02751502
Study type	Interventional
Source	NYU Langone Health
Contact
Status	Terminated
Phase	N/A
Start date	January 2017
Completion date	February 9, 2021

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