CClinicalTrials.gg
CompletedNCT00465686Updated May 9, 2008

Effect of Ergonomic Classroom Furniture on the Printing Legibility of Elementary Students With Cerebral Palsy

A Phase 1 interventional study of ergonomic chair and desk (Q-Learn Classic Chair and Q-Learn Desk) and ergonomic desk and chair (Q-Learn Desk) in Cerebral Palsy, sponsored by Holland Bloorview Kids Rehabilitation Hospital. Completed at 1 site in Canada. Open to participants aged 6 Years to 8 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2008-05-09.

Sponsored by Holland Bloorview Kids Rehabilitation Hospital · Phase 1, Interventional, and Supportive care

Phase
Phase 1
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
6 Years to 8 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Cerebral Palsy

Browse trials for

Keywords

  • handwriting
  • child
  • primary school
  • posture
  • assistive device
03

In context

Cerebral Palsy

1,853 studies on the registry are indexed under Cerebral Palsy; 435 are open to participants now.

This study's enrollment of 30 is close to the median of 33 across 1,368 interventional studies indexed under Cerebral Palsy.

Browse Cerebral Palsy studies →

Lead sponsor

Holland Bloorview Kids Rehabilitation Hospital is the lead sponsor of 62 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Years to 8 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • primary diagnosis of cerebral palsy
  • functional status of Gross Motor Function Classification System Level I or II

Exclusion criteria

Exclusion Criteria:

  • genetic disorder;
  • attention-deficit hyperactivity disorder; or,
  • pervasive developmental disorder
05

Study design

Phase
Phase 1
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    A

    Device: ergonomic chair and desk (Q-Learn Classic Chair and Q-Learn Desk) · Device: ergonomic desk and chair (Q-Learn Desk)

Interventions

  • Deviceergonomic chair and desk (Q-Learn Classic Chair and Q-Learn Desk)

    ergonomic school chair and desk adjusted to fit the child user as per the manufacturer's instructions

    Also known as: Q-Learn Classic Chair and Q-Learn Desk

  • Deviceergonomic desk and chair (Q-Learn Desk)

    child sits on chair and desk for 5 minutes, then provides handwriting sample at one desk, then repeats this for the other desk

    Also known as: Q-Learn Desk

06

What researchers measure

Primary outcomes

  1. Minnesota Handwriting Assessment

    Time frame: 5-10 minutes

07

Study locations

1 site
  • Bloorview Research Institute, Bloorview Kids Rehab
    Toronto, Ontario M4G 1R8, Canada
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 9, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00465686
Lead sponsor
Holland Bloorview Kids Rehabilitation Hospital
First posted
Apr 25, 2007
Start date
Feb 2007
Primary completion
May 2008
Completion
May 2008
Last update
May 9, 2008

Study contacts

Stephen E Ryan, MSc, PEng
principal investigator · Bloorview Research Institute, Bloorview Kids Rehab

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2008. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion