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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

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Title
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
Published in
Trials, June 2016
DOI 10.1186/s13063-016-1428-8
Pubmed ID
Authors

Hajar Mazahery, Cathryn Conlon, Kathryn L. Beck, Marlena C. Kruger, Welma Stonehouse, Carlos A. Camargo, Barbara J. Meyer, Bobby Tsang, Owen Mugridge, Pamela R. von Hurst

Abstract

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. 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. 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. Australian New Zealand Clinical Trial Registry, ACTRN12615000144516 . Registered on 16 February 2015.

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Geographical breakdown

Country Count As %
France 1 <1%
Unknown 217 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 43 20%
Student > Master 27 12%
Researcher 20 9%
Student > Ph. D. Student 18 8%
Student > Postgraduate 14 6%
Other 38 17%
Unknown 58 27%
Readers by discipline Count As %
Medicine and Dentistry 51 23%
Nursing and Health Professions 31 14%
Psychology 15 7%
Biochemistry, Genetics and Molecular Biology 11 5%
Neuroscience 10 5%
Other 32 15%
Unknown 68 31%