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Vitamin D and omega-3 fatty acid supplements in children with autism spectrum disorder: a study protocol for a factorial randomised, double-blind, placebo-controlled trial

机译:自闭症谱系障碍儿童的维生素D和omega-3脂肪酸补充剂:一项因子随机,双盲,安慰剂对照试验的研究方案

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Background There is strong mechanistic evidence to suggest that vitamin D and omega-3 long chain polyunsaturated fatty acids (n-3 LCPUFAs), specifically docosahexaenoic acid (DHA), have the potential to significantly improve the symptoms of autism spectrum disorder (ASD). However, there are no trials that have measured the effect of both vitamin D and n-3 LCPUFA supplementation on autism severity symptoms. The objective of this 2?×?2 factorial trial is to investigate the effect of vitamin D, n-3 LCPUFAs or a combination of both on core symptoms of ASD. Methods/design Children with ASD living in New Zealand ( n =?168 children) will be randomised to one of four treatments daily: vitamin D (2000?IU), n-3 LCPUFAs (722?mg DHA), vitamin D (2000?IU)?+?n-3 LCPUFAs (722?mg DHA) or placebo for 12?months. All researchers, participants and their caregivers will be blinded until the data analysis is completed, and randomisation of the active/placebo capsules and allocation will be fully concealed from all mentioned parties. The primary outcome measures are the change in social-communicative functioning, sensory processing issues and problem behaviours between baseline and 12?months. A secondary outcome measure is the effect on gastrointestinal symptoms. Baseline data will be used to assess and correct basic nutritional deficiencies prior to treatment allocation. For safety measures, serum 25-hydroxyvitamin D 25(OH)D and calcium will be monitored at baseline, 6 and 12?months, and weekly compliance and gastrointestinal symptom diaries will be completed by caregivers throughout the study period. Discussion To our knowledge there are no randomised controlled trials assessing the effects of both vitamin D and DHA supplementation on core symptoms of ASD. If it is shown that either vitamin D, DHA or both are effective, the trial would reveal a non-invasive approach to managing ASD symptoms. Trial registration Australian New Zealand Clinical Trial Registry, ACTRN12615000144516 . Registered on 16 February 2015.
机译:背景技术有很强的机械证据表明,维生素D和omega-3长链多不饱和脂肪酸(n-3 LCPUFAs),特别是二十二碳六烯酸(DHA),具有显着改善自闭症谱系障碍(ASD)症状的潜力。然而,尚无试验测量维生素D和n-3 LCPUFA补充剂对自闭症严重程度症状的影响。这项2××2析因试验的目的是研究维生素D,n-3 LCPUFA或两者的组合对ASD核心症状的影响。方法/设计居住在新西兰的ASD儿童(n = 168名儿童)将被随机分配至以下四种治疗方法之一:维生素D(2000?IU),n-3 LCPUFAs(722?mg DHA),维生素D(2000 ?IU)?+?n-3 LCPUFA(722 mg DHA)或安慰剂治疗12个月。所有研究人员,参与者及其照护者都将不知情,直到数据分析完成为止,所有提及的参与者都将隐瞒活性/安慰剂胶囊的随机性和分配情况。主要的结果指标是社交沟通功能,感觉处理问题和问题行为在基线与12个月之间的变化。次要结果指标是对胃肠道症状的影响。在分配治疗之前,基线数据将用于评估和纠正基本营养不足。为安全起见,将在基线,第6和12个月时监测血清25-羟基维生素D 25(OH)D和钙,并且在整个研究期间,护理人员应完成每周的依从性和胃肠道症状日记。讨论据我们所知,尚无评估维生素D和DHA补充对ASD核心症状影响的随机对照试验。如果证明维生素D,DHA或两者均有效,则该试验将揭示一种非侵入性方法来治疗ASD症状。试验注册澳大利亚新西兰临床试验注册中心(ACTRN12615000144516)。 2015年2月16日注册。

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