- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06858566
Impact of the Kaligo Solution on Learning to Write in Children Aged 6 to 11 With Handwriting Disorders : KALIGO+ (KALIGO+)
Impact of the Kaligo Solution on Learning to Write in Children Aged 6 to 11 With Handwriting Disorders: a Multiple Baseline Online SCED Study
Writing is a fundamental skill, crucial to a child's success at school and the development of independence. Around 30% of children present difficulties in learning to write, and for some of them (10%), these difficulties persist for a long time. Adapted learning can improve their handwriting. Initial studies into the use of new technologies (tablets, virtual reality headsets) have shown that they can help children learn to write. Attractive to children, these interfaces make it possible to apply new paradigms (e.g. enrichment of feedback [sonification], variation of writing media) that have proved effective, mainly with children with 'typical' development. The Kaligo+ solution is based on the latest scientific advances to offer an innovative approach to learning to write, particularly for children with significant difficulties in this area. This study proposes to test the benefits of the Kaligo+ solution on 15 children with writing difficulties.
The main objective of this pilot study is to demonstrate improved writing performance following use of the Kaligo+ solution in children aged 6 to 11 with writing difficulties, using a Single Case Experimental Design (SCED) methodology.
Study Overview
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Manon LE GOFF
- Phone Number: +33 0298028308
- Email: manon.legoff@ildys.org
Study Contact Backup
- Name: Matthieu PICHELIN
- Phone Number: +33 0298293915
- Email: matthieu.pichelin@ildys.org
Study Locations
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-
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Brest cedex 2, France, 29218
- Recruiting
- Fondation ILDYS
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Contact:
- Manon LE GOFF
- Phone Number: 0298028308
- Email: manon.legoff@ildys.org
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Contact:
- Ludovic MIRAMAND
-
Contact:
- Christelle PONS BECMEUR
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Children with writing difficulties (who may or may not be receiving care in this area)
- Age: 6 - 11 years
- Score > 1 standard deviation on the BHK deterioration score
Exclusion Criteria:
- Contraindication to the use of the tablet or virtual reality
- Moderate, severe or profound intellectual disability (Total Intelligence Quotient below 55 on an intellectual efficiency scale such as WISC-V or K-ABC-II).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Children with handwriting difficulties
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The Kaligo + Score will be taken twice a week during baseline and intervention and once a week during follow-up.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Composite score brings together a set of parameters defining writing efficiency (static, kinematic and pressure) : Kaligo +
Time Frame: This assessment will be carried out twice a week up to 19 weeks during the baseline and intervention and once a week up to 1 month after the interventiona
|
Static parameters: density, height, width and length Kinematic parameters: Time (in air and on paper), speed, number of speed inversion, median frequency of the speed, jerk and acceleration. Pressure: Median, 60th percentile, median frequency of the pressure change. The score is normalized between 0 (worst) and 1 (best). |
This assessment will be carried out twice a week up to 19 weeks during the baseline and intervention and once a week up to 1 month after the interventiona
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessing the ecological impact and its generalisation
Time Frame: This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention.
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Movement Assessment Battery for Children | Second Edition (M-ABC-II).
Questionnaire to assess motor skills in everyday situations, comprising 3 parts: part A "movement in a static and/or predictable environment", part B "movement in a dynamic and/or non-static environment", part C "non-motor factors that can affect movement".
A raw score is obtained for each of these parts, as well as a total motricity score (A + B).
|
This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention.
|
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Assessing the ecological impact and its generalisation
Time Frame: This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention
|
Handwriting Proficiency Screening Questionnaire for Children (HPSQ-C).
Questionnaire to assess motor skills in everyday situations, comprising 3 parts: part A "movement in a static and/or predictable environment", part B "movement in a dynamic and/or non-static environment", part C "non-motor factors that can affect movement".
A raw score is obtained for each of these parts, as well as a total motricity score (A + B).
|
This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention
|
|
Assessing the ecological impact and its generalisation
Time Frame: This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention.
|
Concise Assessment Scale for Children's Handwriting (BHK).
In the BHK [Brave Handwriting Kindergarten], the child is asked to copy a text for 5 minutes.
Blind double scoring is used (the scorer does not know when the child has copied the text).
A degradation score is calculated: the higher the score, the more "degraded" the quality of the child's handwriting.
The standardized score is taken into account for inclusion (to situate the child's performance in relation to his class), while the raw score is taken into account over the course of the intervention (allowing comparison of the subject with himself).
Psychometric qualities are documented in the test manual.
|
This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention.
|
|
Assessing the ecological impact and its generalisation
Time Frame: This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention.
|
NEPSY-II is the only single measure that allows clinicians to create tailored assessments across six domains, specific to a child's situation SUBTESTS - ORIENTATION SUBTEST - VISUO-MOTOR PRECISION SUBTEST - INHIBITION SUBTEST - FACE RECOGNITION
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This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention.
|
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Assessing the ecological impact and its generalisation
Time Frame: This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention.
|
Purdue Pegboard Test (PPT).
Test of manual dexterity and bimanual coordination.
The child must place rods in holes on a board as quickly as possible, using the dominant hand, the non-dominant hand, then both hands simultaneously.
In a final condition ("assembly"), the child must place a rod in one of the holes, then a washer, a tube and another washer, using both hands alternately.
Raw scores (number of correctly placed and assembled pieces) are taken into account.
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This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention.
|
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Assessing the ecological impact and its generalisation
Time Frame: This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention.
|
Written Language Analytical Battery (BALE).
In the BALE [Batterie Analytique du Langage Ecrit, Analytic test of the written language], the child is asked to write (under dictation) simple, complex and frequent irregular words from the French language, and to read regular and frequent irregular words.
For the purposes of this study, only raw scores will be taken into account, in order to compare the subject with himself.
|
This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention.
|
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- Evaluate the maintenance of performance over time after the end of the intervention
Time Frame: This assessment will be carried out at the end of the intervention and every week for a month.
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Evolution of the Kaligo + score.
Kaligo + Score: This composite score brings together a set of parameters defining writing efficiency (static, kinematic and pressure).
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This assessment will be carried out at the end of the intervention and every week for a month.
|
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Assessing the specific nature of the intervention
Time Frame: This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention
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Evolution of performance on an untrained task.
It will be demonstrated by the absence of as great an improvement in the control variable (face recognition task) compared with the improvement recorded in the primary endpoint
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This assessment will be conducted during the first week of the baseline, in the 10th week of the intervention, and once more one month after the intervention
|
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Assessing satisfaction with the intervention for the child and his or her family
Time Frame: during the last visit, 1 month after intervention
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The CSQ 8 is a short customer satisfaction questionnaire.
The CSQ8 is the benchmark questionnaire for assessing satisfaction among parents, children and teenagers.
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during the last visit, 1 month after intervention
|
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Assessing satisfaction with the intervention for the child and his or her family
Time Frame: during the last visit, 1 month after intervention
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10-point visual analogue scale to be completed by the child.
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during the last visit, 1 month after intervention
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Assessing the acceptability and usability of the solution for families and professionals
Time Frame: during the last visit, 1 month after intervention
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Mobile Application Rating Scale (MARS).
This validated questionnaire makes it possible to assess the quality of mobile healthcare applications in a way that is transparent for healthcare professionals and patients alike.
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during the last visit, 1 month after intervention
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Assessing the acceptability and usability of the solution for families and professionals
Time Frame: during the last visit, 1 month after intervention
|
System Usability Scale (SUS).
This questionnaire is currently the most widely used in the scientific community for measuring user satisfaction with a product, interactive system or service.
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during the last visit, 1 month after intervention
|
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Assessing the acceptability and usability of the solution for families and professionals
Time Frame: during the last visit, , 1 month after intervention
|
Carrying out qualitative interviews with families and professionals
|
during the last visit, , 1 month after intervention
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Christelle PONS BECMEUR, MP/PhD, Fondation ILDYS
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- RI2022_008
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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