Micronutrients and traumatic brain injury: a feasibility study

niversity of Canterbury Foundation- donations given to the principal investigator0 个研究点目标入组 15 人开始时间: 2019年9月2日最近更新: 2020年2月10日

适应症

试验速览

暂无简介。

•1) Between 6 and 13 years, 2) must be children or young people with a Traumatic Brain Injury more than a year old, and 3) meet the criteria for emotional dysregulation as defined by the Affective Reactivity Scale. Participants will be assessed on the ARI- P (parent scale). Those scoring more than 3 will be considered eligible.

•1) A known allergy to any of the ingredient used in the intervention, 2) any known abnormality of mineral metabolism (e.g., Wilson's disease, haemochromatosis – assessed via blood tests), 3) ingestion of any medications with primarily central nervous system activity, including mood stabilizers, atomoxetine or stimulants. Participants must have been off their medications for a minimum of four weeks prior to the trial. Participants will not be encouraged to come off their medications in order to participate.

发起方

niversity of Canterbury Foundation- donations given to the principal investigator