Human Factor Validation of Pediatric Mobility Device

Status Completed

Clinical Trial Summary

The purpose of this study is to validate the user interface of a pediatric power mobility device by establishing that the product is safe and effective use for the intended users.

Clinical Trial Description

The purpose of this study is to validate the user interface of a pediatric power mobility device by establishing that the product is safe and effective use for the intended users. The human factors validation study will be conducted in children with mobility impairments as categorised by Hays (1987) in the age range of 6 months to 36 months under realistic use conditions.The study is an open label, un-blinded, non-randomized study which consists of one visit. ;

Study Design

Related Conditions & MeSH terms

Disability Physical

Clinical Trial Details

NCT number	NCT03714256
Study type	Interventional
Source	Permobil, Inc.
Contact
Status	Completed
Phase	N/A
Start date	September 21, 2018
Completion date	November 19, 2018

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