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Clinical Trials/NCT05957549
NCT05957549RecruitingNot Applicable

Tracking Early Emergence of Sound Perception Impairments in FXS With Multimodal fNIRS/EEG- Preschool Age

Children's Hospital Medical Center, Cincinnati1 site in 1 country90 target enrollmentStarted: October 4, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
90
Locations
1
Primary Endpoint
Changes in tympanometric pressure profile in the inner ear

Study Overview

Brief Summary

Individuals with Fragile X Syndrome show differences in how they understand and learn language from infancy. They frequently have lifelong delays in speech and language as well. In addition, they experience other auditory symptoms, including being very sensitive to certain sounds as well as being more sensitive than others to loud sounds. The underlying brain activity for sound perception and speech learning in Fragile X is not well understood, especially in the infant, toddler, and preschool years. This study uses behavioral assessment of speech and language abilities, neuroimaging, and hearing tests to understand how speech and hearing are different in children with Fragile X Syndrome.

Detailed Description

Fragile X Syndrome (FXS) is the leading monogenic cause of intellectual disability and autism and is associated with extremely high risk for early delays in speech and language. While early childhood is essential for speech and language development, neural mechanisms for language impairments have been studied entirely in older children and adults with FXS. Therefore, markers for speech and language impairments are unavailable in young children with FXS to predict severity, test potential mechanisms, and track response to intervention. The investigators have identified a hallmark brain-based phenotype of hyperresponsiveness to sounds in adolescents and adults with FXS. This fundamental alteration in cortical responses to sound could influence early language delays, but this phenotype has not been explored in infants or toddlers with FXS.

Specifically, in this study the investigators will use simultaneous EEG/fNIRS during presentation of simple speech, stories, and nonspeech sounds to quantify and localize auditory hypersensitivity and neural differentiation in 30 preschoolers with FXS. The investigators will assess specificity through comparison with 30 typically developing controls and 30 mental-age matched children with a history of premature birth and language delays.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
24 Months to 4 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Diagnoses of Fragile X Syndrome, Typical Development, or History of Premature Birth
  • •able to sit independently
  • •English is spoken at home

Exclusion Criteria

  • •For all participants: no seizures in the past 6 months
  • •For typical development group and Fragile X group: not born prior to 32 weeks gestation

Arms & Interventions

Speech Sounds

Experimental

Participants listen to speech sounds while the investigators measure electrical and hemodynamic changes in the brain.

Intervention: Speech discrimination (Other)

Outcomes

Primary Outcomes

Changes in tympanometric pressure profile in the inner ear

Time Frame: at single study visit between ages of 2-4 years inclusive

Wide Band Tympanometry is completed to measure variability in tympanometric pressure for left and right ears that may affect hearing profile.

Change in Mullen Scales of Early Learning

Time Frame: at single study visit between ages of 2-4 years inclusive

change in Mullen Scales scores (age-corrected) from baseline on all subscales, including Expressive Language, Receptive Language, FIne Motor, Gross Motor, and Visual Reception. T-Scores from the Mullen Scales of Early Learning (MSEL) have a mean of 50 and a standard deviation of 10. Range=20-80. Higher scores indicate more advanced developmental skills.

Changes in oxygenated and deoxygenated hemoglobin concentration in response to sounds in language regions of the brain

Time Frame: at single study visit between ages of 2-4 years inclusive

Relative increase in oxygenated versus deoxygenated hemoglobin for no sounds, low intensity sounds, and medium intensity sounds. Measured via functional Near Infrared Spectroscopy with optodes placed over frontal, temporal, and parietal language regions.

Changes in amplitude of mismatch negativity response during sound discrimination

Time Frame: at single study visit between ages of 2-4 years inclusive

Electroencephalography is measured over the scalp while participant listens to speech sounds with infrequent "oddball" stimuli. Amplitude of the P100 for all stimuli as well as amplitude of the mismatch negativity response (frequent minus infrequent response) as well as change in these metrics over development are tracked in all groups.

Changes in hearing thresholds

Time Frame: at single study visit between ages of 2-4 years inclusive

Hearing thresholds in dB as assessed using Conditioned Play Audiometry (CPA) or Visual Reinforced Audiometry (VRA) dependent on child age and developmental ability.

Otoacoustic Emissions (OAEs)

Time Frame: at single study visit between ages of 2-4 years inclusive

Signals produced by excitation of hair cells in cochlea are measured for a range of frequencies.

Secondary Outcomes

  • Sensory profile 2 Auditory Processing subtest(at single study visit between ages of 2-4 years inclusive)
  • Sensory Profile 2 Attentional subtest(at single study visit between ages of 2-4 years inclusive)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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