Research in developmental disabilities · 2013
Feasibility and preliminary efficacy data from a computerized cognitive intervention in children with chromosome 22q11.2 deletion syndrome.
Контролируемое клиническое исследованиеСтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Harrell Waverly, Eack Shaun, Hooper Stephen R, Keshavan Matcheri S, Bonner Melanie S, Schoch Kelly, Shashi Vandana
Аннотация
Children with chromosome 22q11.2 deletion syndrome (22q11DS) are significantly impaired in their academic performance and functionality due to cognitive deficits, especially in attention, memory, and other facets of executive function. Compounding these cognitive deficits is the remarkably high risk of major psychoses, occurring in 25% of adolescents and adults with the disorder. There are currently no evidence-based interventions designed to improve the cognitive deficits in these individuals. We implemented a neuroplasticity-based computerized cognitive remediation program for 12 weeks in 13 adolescents with 22q11DS, assessed feasibility, and measured changes in cognition before and after the intervention compared to a control group of 10 age- and gender-matched children with 22q11DS. Our results indicated that despite their cognitive impairments, this intervention is feasible in children with 22q11DS, with high rates of adherence and satisfaction. Our preliminary analyses indicate that gains in cognition occur with the intervention. Further study in a larger randomized controlled trial would enable assessment of efficacy of this novel intervention.
Предметные рубрики MeSH
Abnormalities, MultipleAdolescentAttentionChildChromosome DeletionChromosomes, Human, Pair 22CognitionCognitive Behavioral TherapyDiGeorge SyndromeExecutive FunctionFeasibility StudiesFemaleHumansMaleMemoryNeuronal PlasticityPilot ProjectsReproducibility of ResultsTherapy, Computer-AssistedTreatment Outcome