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Prediction and Intervention in Developmental Dyslexia

Neuronal Markers of Grapheme-phoneme Training Response for Prediction of Successful Reading Acquisition in Children at Familial Risk for Developmental Dyslexia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02217696
Acronym
LEXI
Enrollment
110
Registered
2014-08-15
Start date
2013-07-31
Completion date
2018-07-31
Last updated
2014-08-15

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

Conditions

Developmental Dyslexia

Keywords

Electroencephalography (EEG), Magnetic Resonance Imaging (MRI), Multimodal Neuroimaging, Development, Prediction, Intervention

Brief summary

The long-term goal of this study is to improve prediction of poor reading outcome at preschool age by using a combination of behavioural and neuroimaging measures and to evaluate a specific computerized training program to support children with problems during reading acquisition.

Interventions

OTHERComputerized reading training

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
5 Years to 9 Years
Healthy volunteers
Yes

Inclusion criteria

for all groups: * Healthy, native (CH-) German speaking subjects, with an estimated non-verbal intelligence quotient (IQ) \>=80, without neurological and/or psychiatric disorder (except for attention deficit hyperactivity disorder, specific learning disorders, developmental language impairments) * Additional criteria for subgroups: * Recruitment of preschoolers (aged 5.5-7.5 years): * Healthy children with increased risk for developmental dyslexia in their second year at kindergarten * Recruitment of children in first grade (aged 6.5-8.5years): * Children showing impairments in learning to read (first/second grade). * Adults (aged 20-40 years): * Healthy, normal reading

Exclusion criteria

for all groups: * MRI contraindications * No history of premature delivery and/or maternal reports of severe prenatal, perinatal or postnatal complications.

Design outcomes

Primary

MeasureTime frameDescription
Changes in reading and spelling performanceParticipants will be tested at three times for the duration of the cross-sectional intervention, an expected average of 8 monthsPerformance in normed reading and/or spelling (standardized tests) as a result of reading acquisition and training

Secondary

MeasureTime frameDescription
Developmental and training induced changes in functional brain activation and brain structureParticipants will be tested after an expected average of 8, 12 and 16 monthsChanges in activation/structure of core language network regions assessed by EEG and MRI during development, learning and training
Accuracy of prediction on reading performance outcomeParticipants will be tested at T1 and on average 8 months laterAccuracy of prediction on reading performance (standardized tests) using behavioural and/or neuroimaging measures. Neuroimaging measures: EEG and MRI (functional activation, structural measures from white and/or grey matter, temporal information from event-related potential and/or frequency analyses)

Countries

Switzerland

Contacts

Primary ContactSilvia Brem, PhD
sbrem@kjpd.uzh.ch+41 43 499 2760

Outcome results

None listed

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