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临床试验/NCT01244360
NCT01244360Unknown不适用

The Effects of Resveratrol Supplementation on Measurements of Health and Human Performance

Marywood University1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2010年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
44
试验地点
1
主要终点
Vascular function

研究概览

简要总结

The purpose of this study is to examine the effects of resveratrol on health and human performance. The study will evaluate cognitive function and several indicators of physical health before and after taking a resveratrol supplement or a placebo for three weeks.

详细描述

Measurements

  • blood laboratory parameters
  • cognitive assessment changes
  • body composition changes
  • vascular endothelial response

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
Double (Participant, Care Provider)

入排标准

年龄范围
45 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •men and women between 45 and 75 years of age
  • •Normal heart rate and Blood pressure
  • •Ability to use personal computer interface
  • •Successful completion of physical activity readiness questionnaire

排除标准

  • •Cardiovascular disease, uncontrolled hypertension, lung disease
  • •inability to tolerate exercise
  • •have taken grape related supplement in past 12 months
  • •current use of drugs or dietary supplements to enhance exercise performance
  • •allergy to wine, grape juice or grape seed supplements

研究组 & 干预措施

Sugar Pill

Placebo Comparator

Subject will take placebo for daily for 4 weeks, with optional additional 4 week treatment period.

干预措施: Placebo Comparator: Sugar Pill (Other)

Dietary Supplement: resveratrol

Active Comparator

Subject will take resveratrol supplement for 4 weeks, with optional additional 4 week treatment period.

干预措施: resveratrol (Dietary Supplement)

结局指标

主要结局

Vascular function

时间窗: 4 weeks, with option of additional 4 week treatment period

vascular response to stress will be measured using flow mediated dilation and ultrasound.

次要结局

  • Body fat percentage(4 weeks, with optional additional 4 week treatment period)
  • inflammation biomarkers(4 weeks, with optional additional 4 week treatment period)
  • cognitive function(4 weeks, with optional additional 4 week treatment period)

研究者

申办方类型
Other

研究点 (1)

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