跳至主要内容
临床试验/NCT02942888
NCT02942888已完成不适用

The Effects of NAD on Brain Function and Cognition

The University of Texas Health Science Center at San Antonio4 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2017年11月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
46
试验地点
4
主要终点
Change in Cognitive Assessment - Montreal Cognitive Assessment (MoCA) - from baseline at 10 weeks

研究概览

简要总结

The purpose of this study is to determine the effects of Niagen (nicotinamide riboside, vitamin B3), on NAD levels, brain function including cognition and blood flow in people diagnosed with mild cognitive impairment (MCI).

详细描述

Niagen is a patented formula which is the first and only commercially available form of Nicotinamide Riboside (NR). It has been proven in basic science studies as a highly effective NAD booster, but it also works as a vitamin B3 supplement. NAD helps pass energy from glucose to other pathways in the cell. Niagen (Nicotinamide Riboside, vitamin B3) is one of the most effective NAD+ precursors to support cellular health.

The purpose of this study is to determine the effects of Niagen (nicotinamide riboside, vitamin B3), on NAD levels, brain function including cognition and blood flow in people diagnosed with mild cognitive impairment (MCI).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Basic Science
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • Previously diagnosed with MCI based on inclusion criteria of Texas Alzheimer's Research Care and Consortium (TARCC) study (IRB: HSC20090535H). We are enrolling both genders, all races and ethnic groups.
  • Two week washout period for participants who were taking opioids or a dose of niacin over 200mg

排除标准

  • Previously considered as healthy individuals without a MCI or Alzheimer's disease diagnosis based on exclusion criteria of the TARCC study (IRB: HSC20090535H).
  • Neurological, psychiatric or active systemic medical disease
  • Moderate or severe depression and/or anxiety as determined the Geriatric Depression Scale (GDS) and the Geriatric Anxiety Scale (GAS), respectively
  • Diagnosis of dementia
  • Hearing, vision, motor or language deficits
  • Alcohol or drug abuse
  • Implantation of metal devices
  • Administration of Alzheimer's drugs, anticholinergics, neuroleptics, anticonvulsants, opiates, systemic steroids, and mood-stabilizers.
  • No opioid use while participating in study

结局指标

主要结局

Change in Cognitive Assessment - Montreal Cognitive Assessment (MoCA) - from baseline at 10 weeks

时间窗: 10 weeks

MoCA Value

次要结局

  • Change in endothelial function from baseline at 10 weeks(10 weeks)
  • Change in Cognitive Assessment - Test of Auditory Processing Skills (TAPS) - from baseline at 10 weeks(10 weeks)
  • Change in Physical Performance - Short Physical Performance Battery (SPPB) - from baseline at 10 weeks(10 weeks)
  • Change in cerebral blood flow from baseline at 10 weeks(10 weeks)
  • Change in plasma NAD from baseline at 10 weeks(10 weeks)
  • Change in Physical Performance - Instrumental Activities of Daily Living (IADLs) - from baseline at 10 weeks(10 weeks)
  • Change in Cognitive Assessment - Geriatric Depression Scale (GDS) - from baseline at 10 weeks(10 weeks)
  • Change in Cognitive Assessment - Geriatric Anxiety Scale (GAS) - from baseline at 10 weeks(10 weeks)
  • Change in Cognitive Assessment - Clock Drawing Task Protocol (CLOX) - from baseline at 10 weeks(10 weeks)
  • Change in Cognitive Assessment - Executive Interview (EXIT) - from baseline at 10 weeks(10 weeks)
  • Change in Physical Performance - Grip Strength - from baseline at 10 weeks(10 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

Loading locations...

相似试验