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NCT06858566: KALIGO+

Impact of the Kaligo Solution on Learning to Write in Children Aged 6 to 11 With Handwriting Disorders : KALIGO+

Recruiting now NA Last updated 28 March 2025
What this trial tests

NA trial testing Kaligo + score in Writing Disorder in 15 participants. Currently enrolling.

Timeline
21 March 2025
Primary endpoint
24 February 2027
24 February 2027

Quick facts

Lead sponsorFondation Ildys
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Enrollment15
Start date21 March 2025
Primary completion24 February 2027
Estimated completion24 February 2027
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Fondation Ildys

Who can join

Adults 6 to 11, any sex, with Writing Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Fondation Ildys trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06858566.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing