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临床试验/NCT01911299
NCT01911299已完成2 期

Choline Supplementation in Children With Fetal Alcohol Spectrum Disorders

San Diego State University2 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2013年5月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
55
试验地点
2
主要终点
Changes in cognitive function as measured by performance on neuropsychological tasks of learning/memory, executive functions, and attention

研究概览

简要总结

The purpose of this study is to determine whether choline supplementation can improve cognitive functioning of children with prenatal alcohol exposure.

详细描述

Despite the known damaging effects of alcohol on the developing fetus and the presence of warning labels on alcoholic beverages, many pregnant women continue to drink alcohol. The consequences include a range of physical, neurological, and behavioral effects referred to as fetal alcohol spectrum disorders (FASD). Unfortunately, there are currently no comprehensive treatments for individuals with FASD. This pilot study will examine whether a nutritional intervention could reduce the severity of cognitive deficits associated with prenatal alcohol exposure. Choline is an essential nutrient, necessary for brain and behavioral development. Animal studies have shown that prenatal or early postnatal choline supplementation can lead to long-lasting cognitive enhancement. Similarly, choline supplementation improves cognitive outcomes among rats exposed to alcohol during development, even when administered postnatally and after alcohol exposure has occurred. The present experiment translates these findings to a clinical population of individuals exposed to heavy prenatal alcohol exposure. Subjects will be randomly assigned to receive daily choline supplementation or placebo control for a period of 6 weeks (approximately 20 subjects per group). Performance on neuropsychological tasks that measure cognitive functioning will be measured prior to treatment and at 6 weeks. These data will provide important information regarding a potential nutritional intervention for fetal alcohol spectrum disorders.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
5 Years 至 10 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Confirmed histories of prenatal alcohol exposure (by review of medical, legal, or social service records or maternal report, if available; information about levels and timing of exposure will be inquired, but not necessary for inclusion)
  • English as primary language

排除标准

  • Significant physical (e.g., uncorrected visual impairment, hemiparesis) or psychiatric (e.g., psychosis) disability that would prohibit participation
  • History of neurological condition (e.g., epilepsy)

结局指标

主要结局

Changes in cognitive function as measured by performance on neuropsychological tasks of learning/memory, executive functions, and attention

时间窗: Baseline and 6 weeks

次要结局

  • Children's Behavior Checklist (CBCL), Behavioral Rating Inventory of Executive Function (BRIEF)(Baseline and 6 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jennifer Thomas

Associate Director - Center for Behavioral Teratology, San Diego State University

San Diego State University

研究点 (2)

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