- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02797301
A Computerised Test for Assessing the Early Reading Skills
June 7, 2016 updated by: Annie France Frère Slaets, University of Mogi das Cruzes
A Computerised Test for Assessing the Early Reading Skills of Children With Mobility Limitations
This study was to develop a computerised test with an adapted peripheral to assess the emerging literacy knowledge of children with mobility difficulties.
The software was implemented using a game-like design controllable by a peripheral device without needing fine movements.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Conventional tests for assessing the early reading skills of preschool children on school entry are not accessible to children with mobility limitations.
This paper presents a game-like computerised test featuring an appealing scenario that is accessible to these children.
It was developed on a platform that creates 2D vector graphics and contains three phases of interactive content accessible through an adapted peripheral.
Conventional tests were also used to validate the effectiveness of the game.
The two types of tests had the same degree of predictive power when completed by thirty three preschool children without mobility impairment.
Study Type
Interventional
Enrollment (Actual)
40
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
4 years to 17 years (Child)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- G1 and G2: preschool children; no motor difficulties and normal school performance.
- G3: with moderate mobility impairment; similar cognitive ages and notions of writing to the participants of groups G1 and G2; children between seven and seventeen years old.
Exclusion Criteria:
- G1 and G2: children who often miss classes; children between four and seven years.
- G3: no moderate mobility impairment
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: synthetic test & computerised test
Seventeen preschool children (G1), with no motor impairments, from a private school.
The children in G1 performed the synthetic test before the computerised test.
|
The children performed the synthetic test with no time restriction.
The children performed the computerised test with no time restriction.
|
|
Experimental: computerised test & synthetic test
Sixteen preschool children (G2), with no motor impairments, from a private school.
The children in G2 performed the computerised test before the synthetic test.
|
The children performed the synthetic test with no time restriction.
The children performed the computerised test with no time restriction.
|
|
Experimental: computerised test
Seven volunteers (G3), two males and five females, with moderate mobility impairment, patients from the Physical Therapy and Rehabilitation Clinic.
|
The children performed the computerised test with no time restriction.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reading skills
Time Frame: 2 days
|
The tests determine whether children can differentiate between the letters of the alphabet and squiggles, numbers, and mathematical signs (first phase); can realise that the same word can be written using uppercase, lowercase, and cursive letters (second phase); know the correct number of letters required to graphically represent the sounds used in speech (third phase).
The numbers of incorrect choices made by children during the three phases of the computerised test (G1, G2 and G3) and the synthetic test (G1 and G2) are quantified.
|
2 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2010
Primary Completion (Actual)
September 1, 2010
Study Completion (Actual)
September 1, 2011
Study Registration Dates
First Submitted
June 2, 2016
First Submitted That Met QC Criteria
June 7, 2016
First Posted (Estimate)
June 13, 2016
Study Record Updates
Last Update Posted (Estimate)
June 13, 2016
Last Update Submitted That Met QC Criteria
June 7, 2016
Last Verified
June 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0135.0.237.000-10
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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