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Investigation of the Relationship Between Development, Neurological Assessment and Object Permanence in High Risk Infants.

Infant Development Clinical Trial

Official title:
Investigation of the Relationship Between Development, Neurological Assessment and Object Permanence in High Risk Infants.

Clinical Trial Summary

The aim of the study is to examine the relationship between development, neurological assessment and object permanence in risky infants aged 7-16 months. The sample of the study will consist of babies between 7-16 months at risk (preterm, low birth weight, asphyxia, hyperbillirubinemia, etc.). Inclusion criteria for the study: Between 7-16 months, having at least one risk factor. Exclusion criteria: Medical complications (eg, severe visual impairment) limiting participation in assessments; autism, down syndrome, or spinal cord injury; diagnosed uncontrolled seizure disorder; or a neurodegenerative disorder. Parents who agreed to participate in the study will be asked to fill out the demographic information questionnaire. Object permanence scale, Bayley III infant and toddler development scale and Hammersmith infant neurologic assessment will be applied to infants.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05749796
Study type Observational
Source Tokat Gaziosmanpasa University
Contact
Status Recruiting
Phase
Start date March 1, 2023
Completion date May 31, 2024
View Details
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