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Cross-syndrome comparison of real-world executive functioning and problem solving using a new problem-solving questionnaire

机译:使用新的问题解决问卷对现实世界中执行功能和问题解决的跨综合征比较

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摘要

BackgroundudIndividuals with neurodevelopmental disorders like Williams syndrome and Down syndrome exhibit executive function impairments on experimental tasks (Lanfranchi, Jerman, Dal Pont, Alberti, & Vianello, 2010; Menghini, Addona, Costanzo, & Vicari, 2010), but the way that they use executive functioning for problem solving in everyday life has not hitherto been explored. The study aim is to understand cross-syndrome characteristics of everyday executive functioning and problem solving.udMethodsudParents/carers of individuals with Williams syndrome (n = 47) or Down syndrome (n = 31) of a similar chronological age (m = 17 years 4 months and 18 years respectively) as well as those of a group of younger typically developing children (n = 34; m = 8 years 3 months) completed two questionnaires: the Behavior Rating Inventory of Executive Function (BRIEF; Gioia, Isquith, Guy, & Kenworthy, 2000) and a novel Problem-Solving Questionnaire.udResultsudThe rated likelihood of reaching a solution in a problem solving situation was lower for both syndromic groups than the typical group, and lower still for the Williams syndrome group than the Down syndrome group. The proportion of group members meeting the criterion for clinical significance on the BRIEF was also highest for the Williams syndrome group. While changing response, avoiding losing focus and maintaining perseverance were important for problem-solving success in all groups, asking for help and avoiding becoming emotional were also important for the Down syndrome and Williams syndrome groups respectively. Keeping possessions in order was a relative strength amongst BRIEF scales for the Down syndrome group.udConclusionudResults suggest that individuals with Down syndrome tend to use compensatory strategies for problem solving (asking for help and potentially, keeping items well ordered), while for individuals with Williams syndrome, emotional reactions disrupt their problem-solving skills. This paper highlights the importance of identifying syndrome-specific problem-solving strengths and difficulties to improve effective functioning in everyday life.
机译:背景 uds具有威廉姆斯综合症和唐氏综合症等神经发育障碍的人在实验任务上表现出执行功能障碍(Lanfranchi,Jerman,Dal Pont,Alberti和Vianello,2010; Menghini,Addona,Costanzo和Vicari,2010)迄今为止,他们尚未使用执行功能来解决日常生活中的问题。该研究的目的是了解日常执行功能和解决问题的综合症候群特征。 udMethods ud具有类似计时年龄的威廉姆斯综合征(n = 47)或唐氏综合症(n = 31)的个体的父母/照顾者(m =分别是17岁4个月和18岁)以及一组较年轻的典型发育中的儿童(n = 34; m = 8岁3个月)完成的两份问卷:执行功能行为评估量表(BRIEF; Gioia,Isquith (Guy和Kenworthy,2000)和一种新颖的问题解决问卷。 udResults ud这两个综合症组在解决问题的情况下达成解决方案的额定可能性均低于典型组,而在Williams综合征组中仍然更低比唐氏综合症组高。在Williams综合征组中,符合简报中临床意义标准的组成员比例也最高。在改变反应的同时,避免失去专注力和保持毅力对于所有组的问题解决成功都很重要,寻求帮助和避免变得情绪化对唐氏综合症和威廉姆斯综合症组也很重要。在唐氏综合症患者组中,保持财产秩序是BRIEF量表的相对优势。 udConclusion ud结果表明,唐氏综合症患者倾向于使用补偿性策略来解决问题(寻求帮助,并可能使物品井井有条)。患有威廉姆斯综合症的人,情绪反应破坏了他们的解决问题的能力。本文着重指出了识别特定于综合征的问题解决能力和改善日常生活中有效功能的困难的重要性。

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