Neurocognitive impairment cognitive problems, memory and concentration problems
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study, a participant must meet all of the following criteria:Does not meet the physical activity guideline (at least one hour of moderate-to-vigorous intensity physical activity daily, including muscle- and bone-strengthening activities at least three times per week);Has a neurocognitive functioning impairment (<5th percentile in at least 1 neurocognitive domain);Experiences neurocognitive problems as reported by parents;Is fluent in Dutch and inhabitant of the Netherlands. Specific for children with congenital heart disease:Underwent open-heart surgery before the age of one year;Is aged 6–18 years at the time of inclusion in the study;Has a physical cardiovascular fitness deficit (impaired exercise tolerance) as measured by VO2 max (< -1 SD).
Exclusion criteria
Exclusion criteria: A potential participant who meets any of the following criteria will be excluded from participation in this study:Absence or withdrawal of written informed consent;Contraindications for physical activity as assessed by treating physician;Inability to comprehend testing instructions;Patient had opt-out for re-use of clinical data for research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is neurocognitive functioning, measured in seven domains: Speed, Stability, Attention & Control, Memory, Verbal Working Memory, Visual Working Memory and Visuomotor Integration. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include physical cardiovascular fitness, physical activity, behavioural and emotional functioning, sleep quality and self-esteem. | — |
Countries
Netherlands
Contacts
Amsterdam UMC