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临床试验/ACTRN12612000202864
ACTRN12612000202864尚未招募不适用

An investigation into the effects of glucose and caffeine on multitasking, mood and fMRI regional activation in healthy adults.

GlaxoSmithKline Nutritional Healthcare0 个研究点目标入组 40 人开始时间: 2012年2月17日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 55 Years(—)
性别
All

入选标准

  • People who meet the following inclusion criteria will be included in the trial:
  • 1. Male or female.
  • 2. Aged 18-55 years.
  • 3. Willing and able to provide written informed consent.
  • 4. Understands and is willing and able to comply with all study procedures.
  • 5. Are in good general health with no history of psychiatric disease.
  • 6. Regular caffeine consumers (between 1-4 cups of coffee per day or equivalent i.e. soft drinks, energy drinks)
  • 7. Must have corrected to normal vision
  • 8. Participants who take part in the fMRI subcomponent must be right handed. This is for ease of analysis of the neuroimaging data. There are hemispheric differences in terms of structure between right and left handed individuals that prove to be problematic when analysing the output. Given that this investigation will employ a method where participants need to press buttons as a response (in turn involving the motor cortex), it is wise to use an all right handed population.

排除标准

  • Participants who display any of the following will be excluded from the trial:
  • 1.Females who are pregnant, breast-feeding and/or not using a medically approved form of contraception.
  • 2. Individuals currently taking medication (other than the contraceptive pill – see section 4.5.2 for details).
  • 3.Any significant concurrent illness including any bleeding disorders, heart conditions, diabetes, glaucoma, high blood pressure or osteoporosis.
  • 4.Individuals who suffer from Diabetes Mellitus.
  • 5.Any known or suspected food allergies (this would cover all ingredients in the investigational product).
  • 6.Susceptible to any unwanted side-effects of caffeine, such as reduction in sleep quality.
  • 7.Smokers and users of recreational drugs (except alcohol and other food grade actives)
  • 8.Have participated in any other study involving an investigational product in the last 4 weeks.
  • 9.Have undergone an MRI scan within the previous 7 days.
  • 10.Those diagnosed with Phenyketonuria (PKU).

研究者

发起方
GlaxoSmithKline Nutritional Healthcare

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