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Enrolling by invitation NCT07079488

Vestibular Function and Motor Development in Small Children

No phase Interventional Vestibular Disorder

For patients and families

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: Motor proficiency scales.
Who it may be relevant to
Registry conditions: Vestibular Disorder. Basic parameters: 5 months — 3 years · 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
Sweden
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

Motor Development in Infants and Toddlers Affected by Vestibular Impairment

Overview

Infants and toddlers with and without vestibular impairment will be tested blinded by pediatric physiotherapist with different age adequate motor scales in order to find out pathological motor patterns specifically associated to vestibular impairment.

Interventions

  • Diagnostic test Motor proficiency scales
    AIMS, PDMS-2, HINE

Primary outcome measures

  • Peabody Developmental Motor Scales II [Time frame: at enrollment and at 6 months]
  • Alberta Infant Motor Scales [Time frame: at enrollment and at 6 months]
  • Hammersmith Infant Neurological Examination checklist [Time frame: at enrollment and at 6 months]

Eligibility criteria

Inclusion criteria

vestibular impairment normal vestibular function -

Exclusion criteria

children unable to be tested with chield-friendly vestibular testing

\-

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

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Diagnostic

Study locations

Sweden · 1 center
  • Karolinska Univerisity Hospital — Stockholm

Identifiers

NCT: NCT07079488 · K2023-7366

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗