Can a music and Brain-Training app boost reading in kids with dyslexia?
NCT ID NCT06592911
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed study tested a digital app called Poppins Clinical in 306 children with dyslexia or other reading/writing learning disabilities. The app combines musical and cognitive exercises with reading training. One group used the app plus bi-monthly speech therapy, while the control group had weekly speech therapy alone. The goal was to see if the app could match standard therapy in improving reading skills.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Poppins Clinical (a digital app providing cognitive and musical training)
- What this could lead to
- If successful, this app could offer a convenient, at-home supplement to speech therapy, potentially reducing the need for frequent clinic visits while maintaining reading improvements.
- What could go wrong
- This is a non-inferiority trial, meaning it aims to show the app is not worse than standard care, not necessarily better. The study is completed but results are not yet widely available, so real-world benefits remain unconfirmed.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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306 people
The number who actually took part.
- Started
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Dec 2024
- Finished
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Jan 2026
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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7 to 11 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Diagnosis of SLD with reading deficit, based on a speech-language assessment. SLD with reading deficit is defined in the Diagnostic and Statistical Manual of Mental Disorders (DSM-5-TR, 2022). The speech-language assessment should consist of at least three reading and/or transcription tests with a SD (standard deviation) of at least - 1.4 or a result below the 20th percentile or two reading and/or transcription tests with a SD of at least - 2 SD or a results below the 10th percentile; * Subject aged between 7 and 11, enrolled from CE1 to CM2; * Subject receiving speech and reading therapy for less than 2 years, receiving speech and reading therapy for written language for less than 2 years, with a maximum treatment frequency of one session per week, either for at least 3 months for children followed for more than 3 months, or for the duration of the treatment for children followed for less than 3 months.; * French mother tongue or French bilingualism at home and more than 3 years schooling in France; * Tablet or smartphone available at home; * Subject affiliated to the French National Insurance (Sécurité Sociale); * Subject and parental/legal guardians consent to participate, and commitment to follow the protocol. Exclusion Criteria: * Subject has previously used Poppins Clinical or a previous version (Mila-Learn); * Unstabilized chronic illness (at investigator's discretion); * Participants with autism spectrum disorders or documented intellectual disabilities; * Vision or Hearing difficulties preventing the use of the tablet or smartphone; * Any condition that, in the opinion of the investigator, may prevent the patient from participating in the trial * Participant actively participating in an interventional study that may affect results. * Concurrent participation of any other family member in the same clinical trial
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hôpital Henri Laborit Poitiers, 86000
Poitiers, 86000, France
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Hôpital Pitié-Salpêtrière, Paris, Paris 75013
Paris, 75013, France
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Other studies related to the condition(s) this trial covers.
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