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Recruiting NCT07531706

Cortical Tracking of Speech in the First Year of Life

Observational Language Development Language Development Disorders Infant Development Infant Developmental Assessment

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In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Electrophysiological recording, Behavioral Assessment.
Who it may be relevant to
Registry conditions: Language Development, Language Development Disorders, Infant Development, Infant Developmental Assessment. Basic parameters: 30 Weeks — 34 Weeks · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Cortical Tracking of Speech in the First Year of Life: a Window Into (a)Typical Language Acquisition

Overview

The goal of this observational study is to investigate early neural mechanisms underlying the processing of spoken language, specifically the phenomenon of cortical tracking, and to determine whether these mechanisms can serve as early predictors of later language development outcomes in infants, including both typical and atypical trajectories. The main questions it aims to answer are: * How do infants with and without a familial history of language and learning impairments differ in their neural ability to track speech and non-speech auditory stimuli at an early stage of development (around 8 months of age)? * To what extent do early cortical tracking mechanisms predict later language abilities, including both receptive and expressive skills, measured at approximately 18 months of age? Researchers will compare infants with a familial risk for language and learning impairments (FH+) to infants without such risk (FH-) to determine whether differences in early neural processing of auditory stimuli are associated with later language outcomes. Participants will: * undergo a neurophysiological assessment involving non-invasive electroencephalographic (EEG) recording while being exposed to auditory stimuli, including: speech stimuli (pre-recorded simple stories in Italian, presented in infant-directed speech); non-speech stimuli (musical sounds matched for rhythmic and acoustic properties) * take part in a developmental assessment at approximately 8 months of age, including standardized measures of cognitive and early linguistic abilities * be involved in a follow-up assessment approximately 10 months later (around 18 months of age), during which standardized tests will evaluate language comprehension and production abilities * have additional background information collected, including family history of language and learning disorders and socio-demographic characteristics, to better understand potential risk and protective factors The study follows a longitudinal design and uses non-invasive procedures that do not require active responses from the infant.

Interventions

  • Other Electrophysiological recording
    Investigation of early neural markers using electrophysiology at 8 months
  • Behavioral Behavioral Assessment
    Behavioral Assessment at 8 months with Bayley-III Scales of Infant and Toddler Development.

Primary outcome measures

  • Communicative Development [Time frame: Age 18 months]
Secondary outcome measures (1)
  • Global Development [Time frame: Age 18 months]

Eligibility criteria

Inclusion criteria

  • Healthy infants aged between 7 and 8 months
  • Infants with and without familial risk for language disorders (Infants are assigned to the group with familial risk for language disorders if at least one first-degree relative had a certified (clinical) diagnosis of language and/or learning disorders).
  • Both parents are native-Italian speakers

Exclusion criteria

  • Gestational age < 37 weeks and/or birth-weight < 2500 grams
  • APGAR scores at birth at 1' and 5' < 7
  • Bayley Cognitive Score < 7
  • Presence of certified diagnosis of intellectual deficiency, attention-deficit disorder, sensorial and neurological disorders or autism within first-degree relatives.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Italy · 1 center
  • IRCCS Eugenio Medea Associazione La nostra famiglia — Bosisio Parini

Identifiers

NCT: NCT07531706 · 78/24

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗