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Objective Neurocognitive assessment of young children with sickle cell disease by eye-tracking

Objective Neurocognitive assessment of young children with sickle cell disease by eye-tracking - ONSET

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON53538
Enrollment
100
Registered
2023-02-03
Start date
2023-04-06
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sickle cell anemia Sickle cell diseae

Interventions

None listed

Sponsors

Amsterdam UMC
Lead Sponsor

Eligibility

Age
No minimum to 11 Years

Inclusion criteria

Inclusion criteria: - Diagnosis of SCD (SCD group); - Age 6 - 24 months old; - Inhabitant of the Netherlands; - Written informed consent from parent/caretaker;

Exclusion criteria

Exclusion criteria: - Refused informed consent from parents/care-taker; - Diagnosis of visual impairment; - Diagnosis of a (co-morbid) congenital developmental condition - Any neurological condition, unrelated to SCD, that could affect the central nervous system, such as brain trauma, epilepsy and meningitis/encephalitis.

Design outcomes

Primary

MeasureTime frame
Early identification of children with SCD at risk of impaired neurocognitive development. Eye-tracking will be performed to assess neurocognitive development.

Secondary

MeasureTime frame
To identify determinants (risk and protective factors) and biomarkers of early neurocognitive deficits in children with SCD, by looking at socio-economic status and biomarkers. Next to this, the relationship between early neurocognitive functioning and adaptive daily life functioning later in life will be analysed, by looking at the quality of life, the behavioural and emotional functioning and general development.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)