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Language impairment in the 22q11 deletion syndrome

Language impairment in the 22q11 deletion syndrome - Language impairment in 22q11DS

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON54844
Enrollment
210
Registered
2017-10-01
Start date
2019-01-02
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

developmental language disorder developmental language impairment

Interventions

None listed

Sponsors

Universiteit Utrecht
Lead Sponsor

Eligibility

Age
2 Years to 15 Years

Inclusion criteria

Inclusion criteria:  Age: 3-6,5 years Growing up in monolingual, Dutch-speaking families Patient groups: a diagnosis of 22q11 deletion syndrome OR Specific Language  Impairment (which is not strictly a medical condition) Control group: healthy, typically developing children; confirmed absence of any  of the above conditions. 

Exclusion criteria

Exclusion criteria:  severe hearing loss (35 dB or worse) growing up in a family in which one or more other languages in addition to  Dutch are regularly used to communicate with the child 

Design outcomes

Primary

MeasureTime frame
(1) Similarity/ difference in developmental language profiles of children with 22q11DS and children with SLI, in comparison to neurotypical (typically developing) controls. (2a) Similarity / difference of the 22q11DS and SLI groups with respect to neurocognitive mechanisms hypothesized to be critical for language acquisition: short-term/working memory, executive function, and implicit learning. (2b) The degree of association between neurocognitive performance and language outcomes in the 22q11DS and SLI groups.

Countries

Netherlands

Contacts

Public ContactJR Wignand

Universitair Medisch Centrum Utrecht

3tonderzoek@uu.nl0302535753

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)