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Recruiting Not applicable

Personalization of Visual Characters and Text-to-Speech (TTS) to Support Learning in Students With Reading Difficulties

NCT06947512 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2023-02-16
Last updated
2026-11-05

Condition(s) studied

Developmental DyslexiaReading Problem

Investigational drug(s) / intervention(s)

Seleggo Test

Seleggo Test: Seleggo Test is a computerized procedure to identify the personalized visual and auditory parameters facilitating reading and writing for each participant. By applying these parameters to the visualization and to the TTS software during reading of school texts, the participants are expected to be facilitated in reading and understanding the text.

Study summary

Previous research has shown the importance of font type, size and spacing to facilitate text reading in dyslexia. A special automatized procedure was designed to select the most favorable parameters for both text visualization and text-to-speech (TTS) conversion to be used by students with reading difficulties. The validation of its outcomes will be carried out through a systematic comparison of the use of the personalized versus standard fonts and voices in reading and writing tests.

Eligibility

Sex
ALL
Min age
7 Years
Max age
15 Years
Healthy volunteers
Accepted
Inclusion Criteria (for TD group): * age 7-15 years * no history of reading difficulties * attends school in Italy Exclusion Criteria (for TD group): * special educational needs or diagnosis of neurodevelopmental disorders Inclusion Criteria (for DD group): * age 7-15 years * diagnosis of Developmental Dyslexia or Specific Reading Disorder * Attends school in Italy Exclusion Criteria (for DD group): * diagnosis of Intellectual Disability Inclusion Criteria (for SEN group): * age 7-15 years * reported by school to have significant difficulties in reading and writing * Attends school in Italy (at least 6 months continued schooling and exposure to the Italian language) Exclusion Criteria (for SEN group): * diagnosis of Intellectual Disability

Primary outcome measure(s)

  • Reading facilitation (speed), i.e. the advantage in reading performance (speed) produced by personalized parameters as compared to standard parameters — Intervention will take place at day 1 assessment and will last about 1,5 hours (comparison between personalized and standard parameters during the same assessment session)
    difference between reading speed (seconds to read the text displayed by the software) with personalized and with standard visual parameters
  • Reading facilitation (accuracy), i.e. the advantage in reading performance (accuracy) produced by personalized parameters as compared to standard parameters — Intervention will take place at day 1 assessment and will last about 1,5 hours (comparison between personalized and standard parameters during the same assessment session)
    difference between reading accuracy (number of errors in reading the text displayed by the software) with personalized and with standard visual parameters
  • Comprehension facilitation, i.e. the advantage in auditory comprehension performance produced by personalized TTS parameters as compared to standard parameters — Intervention will take place at day 1 assessment and will last about 1,5 hours (comparison between personalized and standard parameters during the same assessment session)
    difference between writing accuracy (number of errors in writing a pre-defined list of nonwords) for stimuli dictated with personalized and with standard auditory parameters in the TTS device

Trial sites (3)

FacilityCityRegionStatus
IRCCS E. Medea, polo di Bosisio Parini Bosisio Parini LC Recruiting
IRCCS E.Medea, polo di Conegliano Conegliano TV Recruiting
Associazione La Nostra Famiglia Treviso TV Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06947512 on ClinicalTrials.gov ↗ ← All trials in Italy