Viewing Study NCT00465686



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Last Modification Date: 2024-10-26 @ 9:32 AM
Study NCT ID: NCT00465686
Status: COMPLETED
Last Update Posted: 2008-05-09
First Post: 2007-04-23

Brief Title: Effect of Ergonomic Classroom Furniture on the Printing Legibility of Elementary Students With Cerebral Palsy
Sponsor: Holland Bloorview Kids Rehabilitation Hospital
Organization: Holland Bloorview Kids Rehabilitation Hospital

Study Overview

Official Title: Ergonomic Classroom Furniture and the Printing Legibility of Elementary School Students With CP
Status: COMPLETED
Status Verified Date: 2008-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this pilot study is to gather the data needed to do a larger research study to determine whether children with cerebral palsy print better sitting at an ergonomically-designed custom-fitted school desk or at an oversized standard school desk
Detailed Description: This pilot study will allow us to gather information for a high-quality randomized controlled trial to study the efficacy of ergonomic school furniture as a remedial handwriting intervention for young students with cerebral palsy We will conduct the study in two parts In the first part 30 children with Gross Motor Function Classification System GMFCS Level I and II cerebral palsy will each provide manuscript handwriting samples using two different school furniture configurations A blinded assessor will score the legibility of handwriting samples using the Minnesota Handwriting Assessment MHA as a primary outcome measure In the second part seven occupational therapy experts will attend a focus group to help us determine the minimal clinically important difference score for the MHA We will use the data collected to determine the sample size requirements for a proposed randomized controlled trial

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None