The effect of acquired brain dysfunction on visuomotor integration in neonatal critically ill childre

Completed

• Conditions: anatomical congenital malformation; neonatal critical illness; 10027664; 10029305; 10028920

• Registration Number: NL-OMON46243
• Lead Sponsor: Erasmus MC, Universitair Medisch Centrum Rotterdam

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 70

Inclusion Criteria

Patient group: children aged 9 to 16 years that have had birth defects, including CDH or OA, and have been treated with or without ECMO. Control group: children without birth defects and/or ECMO treatment

Exclusion Criteria

Serious neurological and/or visual co-morbidity.
Diagnosed with attention and/or concentration deficits such as AD(H)D

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Parameters to quantify eye- and hand movements, such as the reaction time and<br /><br>velocity of eye-hand movements, and the accuracy of both movements.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Motor performance-test<br /><br>Parents perceived motor competence of their child-checklist<br /><br>Participation of the child<br /><br>Motor competence (child)<br /><br>Sustained attention of the child<br /><br>Motor-free Visual Perception Test<br /><br>Wechsler Intelligence Scale for Children-3-NL (WISC)<br /><br>VMI: test of Visual Motor Integration<br /><br>behavioral symptoms</p><br>