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临床试验/NCT02061982
NCT02061982已完成2 期

A Non Invasive Intervention Study Performed by Subjects Themselves at Home; Evaluation of Study Infrastructure by Measuring the Effect of Caffeine on Attention and Alertness

TNO1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2013年11月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
70
试验地点
1
主要终点
Evaluate at home tests with controlled tests in experiment in metabolic ward

研究概览

简要总结

Subjects will perform experiments in an at home-setting. The effect of caffeine in coffee will be tested in subjects with computer tests on attention and alertness. Comparison of the results with published results from controlled experiments will indicate the effectiveness of home experiments.

详细描述

There is increasing interest in the general public in measuring health parameters at home, instead of in a medical setting. Many tests for measuring health parameters are commonly available in drug stores as well as online. When structured, this trend may also be used for performing a randomized intervention trial.

The current study is aimed to evaluate the procedure of performing a non invasive intervention study by subjects themselves performing the tests at home.

The study is designed as a randomized, placebo-controlled, double blind, crossover study.

Subjects have to consume a cup of coffee after an overnight fast. Coffee will be prepared from instant coffee containing either regular coffee or decaff coffee. Each intervention will be given twice.

Effects on alertness and attention will be established by three computerized tests provided by Quantified Mind. The tests will be performed by the subjects at t=0 (baseline, prior to coffee consumption) and t=1h, one hour after coffee consumption, in one go. Each test will be performed during 5 minutes. During the training session the participants will be instructed to get acquainted with the task.

研究设计

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

入排标准

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

入选标准

  • •Healthy as assessed by the:
  • •health and lifestyle questionnaire
  • •Adult age (>18y)
  • •Able to perform computerized tests
  • •Voluntary participation
  • •Having given written informed consent
  • •Willing to comply with the study procedures
  • •Moderate caffeine users
  • •Able to use a desk top or laptop with internet access at home
  • •Willing to accept use of all nameless data, including publication, and the confidential use and storage of all data 10 Willing to accept the disclosure of the financial benefit of participation in the study to the authorities concerned

排除标准

  • •Having a history of medical or surgical events that may significantly affect the study outcome, including attention (ADHD etc), psychological or psychiatric disorders
  • •Physical, mental or practical limitations in using computerized systems
  • •Use of concomitant medication including medication known for its effects on mood and/or attention (anti-depressives, sleep medication, etc)
  • •Alcohol consumption > 28 units/week for males and > 21 units (drinks)/week for females
  • •Personnel of TNO of location Zeist or of location Soesterberg, their partner and their first and second-generation relatives

研究组 & 干预措施

Caffeine

Experimental

Instant coffee with or without caffeine will be provided

干预措施: Coffee consumption (Dietary Supplement)

Coffee without caffeine

Placebo Comparator

Coffee without caffeine

干预措施: Coffee consumption (Dietary Supplement)

结局指标

主要结局

Evaluate at home tests with controlled tests in experiment in metabolic ward

时间窗: 1.5 hour

Compare results of cognitive tests in an at home setting versus the results of cognitive tests in a controlled setting in a metabolic ward. Each test costs 1.5h; there will be four test days. This evaluation will partly depend upon the actual number of subjects completing the tests in this at home set-up.

次要结局

  • The effect of coffee with and without caffeine on alertness and attention(1.5 hour on four test days)

研究者

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

W.J. Pasman

Principal Investigator

TNO

研究点 (1)

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