The key objective of the Leuven growing-into-deficit (GID) follow-up-study is to test the hypothesis that children with a congenital heart disease (CHD) show more neurocognitive impairment at the second follow-up at 7 years old than at the first follow-up at the age of 4, compared to healthy controls.
Study Type
OBSERVATIONAL
Enrollment
172
Dept Intensive Care Medicine
Leuven, Vlaams Brabant, Belgium
reaction time (RT) and error rates of inhibitory control (Response Organization Objects, ROO) (Amsterdam Neuropsychological Tasks, ANT)
Time frame: one testpoint at age of 7 years
reaction time (RT) and error rates of cognitive flexibility (ROO, ANT) and working memory (Memory Search - Objects 2 Keys, ANT)
Time frame: one testpoint at age of 7 years
Mean RT + standard deviation (SD) of RT on computerized alertness task (Baseline Speed, ANT)
Time frame: one testpoint at age of 7 years
Number of taps on computerized tapping tasks (ANT)
Time frame: one testpoint at age of 7 years
IQ measures (Revised Wechsler Preschool and Primary Scale of Intelligence, WPPSI-R)
Time frame: one testpoint at age of 7 years
Visual-Motor Integration total standard score (VMI)
Time frame: one testpoint at age of 7 years
Child Behavior CheckList T-scores for internalizing and externalizing problems
Time frame: one testpoint at age of 7 years
Pediatric Quality of Life Inventory - Generic Score Scales (PedsQL) to quantify quality of life
Time frame: one testpoint at age of 7 years
Behavior Rating Inventory of Executive Function (BRIEF) to measure executive functions (parent and teacher version)
Time frame: one testpoint at age of 7 years
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Teacher Report Form (TRF) T-scores for internalizing and externalizing problems at school
Time frame: one testpoint at age of 7 years
Incidence of medical problems (e.g. head trauma), interventions and operations since first follow-up
Time frame: one testpoint at age of 7 years