Actively Recruiting

Phase Not Applicable
Age: 7Years - 18Years
All Genders
Healthy Volunteers
NCT05414903

Reading Outcomes in Children With Vestibular Loss

Led by Father Flanagan's Boys' Home · Updated on 2025-12-23

90

Participants Needed

1

Research Sites

212 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Vestibular loss can co-occur with hearing loss causing dual sensory deficits. This project examines vestibular loss as a contributing factor to reading difficulties for children with hearing loss, where previously only the effects of hearing loss and subsequent language difficulties have been considered. These results are expected to influence the identification and habilitation of vestibular loss in children with hearing loss.

CONDITIONS

Official Title

Reading Outcomes in Children With Vestibular Loss

Who Can Participate

Age: 7Years - 18Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Children with nonverbal problem-solving or intelligence scores within 1.5 standard deviations of the mean (77 to 123)
  • Children with normal hearing must have hearing thresholds less than or equal to 20 dB HL from 0.25 to 8 kHz
  • Children with hearing loss must have pure-tone averages greater than 65 dB HL
Not Eligible

You will not qualify if you...

  • Children who fail a vision screen at 20/30
  • Children diagnosed with autism, blindness, other optic disorders, cerebral palsy, significant neurological conditions, uncorrectable vision problems, or intellectual disability
  • Children with nonverbal problem-solving or intelligence scores below 77 or above 123
  • Children taking medications known to cause eye movement slowing, such as anti-depressants, vestibular suppressants, or sedatives

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Boys Town National Research Hospital

Omaha, Nebraska, United States, 68131

Actively Recruiting

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Research Team

K

Kristen L Janky, PhD

CONTACT

J

Jessie N Patterson, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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