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RecruitingNCT05996497RnDysUpdated Mar 3, 2025

Evaluation of Speech Rhythm Training in Dyslexic Readers Aged 7 to 9 Years

An interventional study of behavioral measures and Electrophysiological measures in Dyslexia, sponsored by Institut Pasteur. Recruiting at 1 site in France. Open to participants aged 7 Years to 9 Years. Per ClinicalTrials.gov, last updated 2025-03-03.

Sponsored by Institut Pasteur · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Primary completion was expected by Jan 2026, 10 months ago, but the record still lists the study as recruiting.
  • Started Oct 2023; still recruiting 3 years 1 month later.
Phase
Not applicable
Study type
Interventional
Enrollment
160
Allocation
Randomized
Ages
7 Years to 9 Years
Sex
All
01

Study summary

Studies of dyslexia have shown altered oscillatory activity in the low gamma band (\~25-35 Hz) in the left auditory cortex. Neural oscillations around 30 Hz constitute the basic sampling rate of speech, from which the ability to form specific phonemic categories on which reading learning is based is derived. An alteration of the oscillatory activity at 30 Hz could therefore influence the ability of children to learn to read, and explain the reading deficit observed in children with a specific written language disorder. The objective of our study is to determine whether intensive rhythmic auditory stimulation applied during 30 sessions of 15 minutes spread over 6 weeks (5 sessions per week) can correct neural oscillations in the gamma-low band, allowing an improvement of phonemic categorization abilities, and thus the reading abilities of dyslexic readers aged 7 to 9 years. The long-term objective of this study is to test the therapeutic potential of auditory stimulation with speech rhythms for the treatment of reading disorders.

Read the detailed description

Longitudinal cross-over study carried out on 4 experimental groups to compare the effect of two rhythmic auditory trainings (30 Hz and low frequencies) compared to the effect of a grapho-phonological correspondence training (GraphoGame).

The study begins with a recruitment and inclusion period after diagnosis of dyslexia. During this study, 4 assessments are performed and include behavioral measures in the care setting and electrophysiological measures in the research setting:

  • at time T1 before any remediation,
  • at T2 after the first training,
  • at T3 at most 7 days after the 2nd training session,
  • at T4 seven weeks after T3.

After the T1 assessment, participants were randomized into 4 different groups (training 1 then training 2):

Group 1 : Auditory Rhythmic at 30 Hz then GraphoGame Group 2 : GraphoGame then Rhythmic Auditory at 30 Hz Group 3 : Auditory Rhythmic at low frequencies then GraphoGame Group 4 : GraphoGame then Auditory Low Frequency Rhythmic The first training period (total duration 6 weeks) according to the assigned group begins and takes place at the speech therapist's office and at home.

After the T2 evaluation, the 2nd training period (total duration 6 weeks) according to the assigned group begins and takes place at the SLP's office as well as at home.

The post-training evaluations T3 and T4 take place, respectively, 1 week and 7 weeks after the last training.

02

Conditions studied

  • Dyslexia

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03

In context

Dyslexia

127 studies on the registry are indexed under Dyslexia; 27 are open to participants now.

This study's planned enrollment of 160 is above the median of 71 across 106 interventional studies indexed under Dyslexia.

Browse Dyslexia studies →

Lead sponsor

Institut Pasteur is the lead sponsor of 99 studies on the registry; 41 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
7 Years to 9 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • between 7 and 9 years old
  • in regular schooling
  • have a diagnosis of dyslexia
  • have a non-verbal intelligence assessment within the norm. Inclusion assessments must show a major reading disability without associated cognitive deficits.
  • be equipped with a PC at home
  • have given their assent and whose parents/legal guardians have given their oral consent

Exclusion criteria

Exclusion Criteria:

  • have any other diagnosis of language impairment
  • have a neurological disorder (visual, auditory, executive)
  • have an associated psychiatric disorder
  • have a developmental delay.
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
160 participants (estimated)

Study arms

  • Other
    Auditory Rhythmic at 30 Hz then GraphoGame

    Training 1 with Auditory Rhythmic at 30 Hz (6 weeks) then Training 2 with GraphoGame (6 weeks)

    Behavioral: behavioral measures · Other: Electrophysiological measures · Other: Training 1 · Other: Training 2

  • Other
    GraphoGame then Rhythmic Auditory at 30 Hz

    Training 1 with GraphoGame (6 weeks) then Training 2 with Auditory Rhythmic at 30 Hz (6 weeks)

    Behavioral: behavioral measures · Other: Electrophysiological measures · Other: Training 1 · Other: Training 2

  • Other
    Auditory Rhythmic at low frequencies then GraphoGame

    Training 1 with Auditory Rhythmic at low frequencies (6 weeks) then Training 2 with GraphoGame (6 weeks)

    Behavioral: behavioral measures · Other: Electrophysiological measures · Other: Training 1 · Other: Training 2

  • Other
    GraphoGame then Auditory Low Frequency Rhythmic

    Training 1 with GraphoGame (6 weeks) then Training 2 with Auditory Rhythmic at Low Frequency Rhythmic (6 weeks)

    Behavioral: behavioral measures · Other: Electrophysiological measures · Other: Training 1 · Other: Training 2

Interventions

  • Behavioralbehavioral measures

    behavioral measures

  • OtherElectrophysiological measures

    Electrophysiological measures

  • OtherTraining 1

    Training 1

  • OtherTraining 2

    Training 2

06

What researchers measure

Primary outcomes

  1. Comparison of reading accuracy by measuring the percentage of correct responses in the isolated pseudoword reading task between rythmic auditory training condition vs. grapho-phonological mapping training (GraphoGame).

    Comparison of reading performance is assessed in terms of both accuracy and speed. High percentage of correct responses means that children improve their reading accuracy.

    Time frame: 2 years

  2. Comparison of reading speed by measuring reading time in the isolated pseudoword reading task between rythmic auditory training condition vs. grapho-phonological mapping training (GraphoGame).

    Comparison of reading performance is assessed in terms of both accuracy and speed. A short time means that children improve their reading speed.

    Time frame: 2 years

Secondary outcomes

  1. Measurement of reading accuracy (percentage of correct responses in the isolated pseudoword reading task) between multiple conditions.

    Reading accuracy compared between rhythmic auditory training then grapho-phonological mapping training vs. grapho-phonological mapping training then rhythmic auditory training and rhythmic auditory training at 30 Hz vs. rhythmic auditory training at 3.5 Hz

    Time frame: 2 years

  2. Measurement of reading speed (reading time in the isolated pseudoword reading task) between multiple conditions.

    Reading speed compared between rhythmic auditory training then grapho-phonological mapping training vs. grapho-phonological mapping training then rhythmic auditory training and rhythmic auditory training at 30 Hz vs. rhythmic auditory training at 3.5 Hz

    Time frame: 2 years

07

Study locations

1 of 1 sites recruiting
  • Institut de l'Audition
    Paris, France
    Recruiting
    • Diane Lazard, MD · Contact
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 3, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05996497
Lead sponsor
Institut Pasteur
Collaborators
Institut de l'Audition
Responsible party
Sponsor
First posted
Aug 18, 2023
Start date
Oct 5, 2023
Primary completion
Jan 1, 2026 (estimated)
Completion
Jul 1, 2026 (estimated)
Last update
Mar 3, 2025

Study contacts

Sophie Bouton, PhD
Contact
sophie.bouton@pasteur.fr
Anne-Lise Giraud, PhD
Contact
anne-lise.giraud-mamessier@pasteur.fr
+33176535054
Diane Lazard, MD
principal investigator · Institut Pasteur
Anne-Lise Giraud, PhD
study director · Institut Pasteur

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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