P. B. Kuld, N. Frielink, M. Zijlmans, C. Schuengel, P. J. C. M. Embregts
doi : 10.1111/jir.13036
People with severe or profound intellectual disabilities (IDs) are believed to experience low levels of self-determination, which negatively affects their quality of life. This systematic review describes existing interventions aimed to support self-determination or components thereof and synthesises evidence on the interventions' effects. Eight databases were searched, turning in 76 articles for the final inclusion.
F. M. MartÃnez-Arnau, R. Núñez-Cortés, J. M. Valderrama-MejÃa, C. Cruz-Montecinos, J. J. Carrasco, S. Cortés-Amador
doi : 10.1111/jir.13032
H. Takahashi, M. An, T. Sasai, M. Seki, T. Matsumura, Y. Ogawa, K. Matsushima, A. Tabata, T. Kato
doi : 10.1111/jir.13033
Individuals with Down syndrome (DS) exhibit deficits in static and dynamic balance abilities and maladaptive functions. This study aimed to determine the effectiveness of dance movement therapy (DMT) group intervention in individuals with DS.
D. Asano, M. Takeda, S. Nobusako, S. Morioka
doi : 10.1111/jir.13034
Analysis of the errors in the Raven's Coloured Progressive Matrices (RCPM) has been previously performed for children with intellectual disabilities but has not been investigated for those with cerebral palsy (CP). This study aimed to investigate whether the types and positions of errors made by individuals with CP differed from those made by typically developing (TD) controls.
W. H. Xu, L. J. Wang
doi : 10.1111/jir.13035
Meeting 24-h movement guidelines for children and adolescents has been associated with improved health indicators. However, the literature examining adherence to 24-h movement guidelines among Chinese children and adolescents with intellectual disability (ID) remains lacking. This study aims to investigate the prevalence of meeting the 24-h movement guidelines and its socio-demographic correlates for this population.
C. Meossi, A. Carrer, C. Ciaccio, M. Estienne, R. Silipigni, F. L. Sciacca, C. Pantaleoni, S. D'Arrigo, D. Milani
doi : 10.1111/jir.13038
Investigating copy number variations (CNVs) such as microdeletions or microduplications can significantly contribute to discover the aetiology of neurodevelopmental disorders. 15q11.2 genomic region, including NIPA1 and NIPA2 genes, contains a recurrent but rare CNV, flanked by the break points BP1 and BP2.
J. Finlayson, N. Roberts, T. Holt, J. Roast, M. McCardle, M. Parsonage, K. Slade, C. Sellers, V. Frighi
doi : 10.1111/jir.13030
People with intellectual disabilities (ID) are at high risk of developing respiratory health issues. The COVID-19 pandemic has compounded this, with serious consequences, and for some, death. Despite home-based oxygen saturation monitoring being recommended for people with ID, there is a stark lack of evidence in the literature on its feasibility.
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