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Comparative Impact of Protocolized Management, Intensive Rehabilitation Versus Long-term Classic Rehabilitation of Dyslexic Children.

Comparative Impact of Protocolized Management, Intensive Rehabilitation Versus Long-term Classic Rehabilitation of Dyslexic Children.

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05383937
Acronym
INTENS-DYS
Enrollment
3
Registered
2022-05-20
Start date
2022-10-10
Completion date
2024-04-15
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Children, Only, Dyslexia, Speech Therapy

Keywords

Dyslexia, Speech Therapy, Children, Intensive rehabilitation

Brief summary

Dyslexia is characterized by difficulties with accurate and/or fluent word recognition and by poor spelling and decoding abilities. In France, dyslexia is a public health disorder. Dyslexia is a real public health problem in France, affecting 6% of the general population. However, no clinical trial of a standardized rehabilitation has shown an impact on reading fluency. In the era of intensive rehabilitation, a new protocol based on the current data from the medical literature has been designed.

Interventions

OTHERSpeech Therapy INTENS-DYS

During the six research month, children included in the intensive arm will benefit of two daily hours speech therapy during two weeks. Those one will be carried out between the second and the fourth month.

Sponsors

Centre Hospitalier Universitaire de Besancon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Children from 8 to 12 years old, * Living in and around 50 kilometers from Besançon. * Diagnosis of dyslexia according to the DSM-V or CIM-10 requirements. * Consent form signed by the parental authority and the child, * Affiliation to a social security system.

Exclusion criteria

* Mother's medical history of pregnancy or delivery complications, * Patients's medical history of neurological infectious, vascular or tumoral events, * Patient's medical history of intellectual deficiency, * Patients's medical history of visual or hearing disorders, * Patient's medical history of psychiatric disorders (especially diagnosis of Attention Deficit / Hyperactivity Disorders (AD/HD)), * legal incapacity, * limited cooperation suspected by the investigator.

Design outcomes

Primary

MeasureTime frameDescription
Reading fluency to the Alouette test.Six month.Difference in the number of words read correctly in three minutes in the intensive and the conventional arm.

Secondary

MeasureTime frameDescription
Life Quality.6 month.Difference on the AUQUEI self questionnary, in the intensive and the conventional arm.
Rehabilitation adhesion.6 monthNumber of speech therapy session performed by patient in each arms.
Visual pattern.Six month.Difference in the number of errors to five visual pattern from the BALE and the EVALEO, in the intensive and the conventional arm.
Family and school evaluation.6 month.Difference to Visual Analog Scale (VAS) regarding the benefit of speech therapy rehabilitation, assessed by the family and the school teachers, in each arms.
Phonological processing tests.Six month.Difference in the number of errors in logatom repetition, which means phonological rules of a language corresponding of meaningless words, in the intensive and the conventional arm.
Speech langage rehabilitation cost.6 month.Differential cost/progress relation of intensive and classical rehabilitation.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026