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UnknownNCT05749796

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

Status
Unknown
Phase
Study type
Observational
Enrollment
32 (estimated)
Sponsor
Tokat Gaziosmanpasa University · Academic / Other
Sex
All
Age
7 Months – 16 Months
Healthy volunteers

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.

Conditions

Timeline

Start date
2023-03-01
Primary completion
2024-04-30
Completion
2024-05-31
First posted
2023-03-01
Last updated
2023-09-13

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05749796. Inclusion in this directory is not an endorsement.

Investigation of the Relationship Between Development, Neurological Assessment and Object Permanence in High Risk Infant (NCT05749796) · Clinical Trials Directory