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临床试验/NCT02557334
NCT02557334已完成不适用

Effects of Freeze Dried Strawberry Powder Supplementation on Vascular Function and Blood Markers of Cardiovascular Risk

Penn State University1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2015年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
1
主要终点
LDL-C

研究概览

简要总结

The purpose of this study is to evaluate the effects of freeze dried strawberry powder on LDL cholesterol, central and peripheral blood pressure, indices of arterial stiffness, and other lipid and lipoprotein concentrations. The investigators hypothesize that the bioactive compounds in freeze dried strawberry powder may elicit beneficial effects on LDL cholesterol, as well as blood pressure and arterial health.

详细描述

The proposed study design is a 3-period randomized crossover dose-response study to evaluate the effect of freeze dried strawberry powder supplementation on LDL-C and vascular health. Research participants will be overweight or obese (BMI 25-39 kg/m^2) but otherwise healthy adults with moderately elevated LDL-C (>116 mg/dL or >3.0mmol/L), blood pressure <160/100 mmHg, total cholesterol below 273 mg/dL for men and below 284 mg/dL for women, and triglycerides below 350 mg/dL. Subjects will be randomly assigned to three supplementation periods: 1) low dose freeze dried strawberry powder (13 g/d); 2) high dose freeze dried strawberry powder (40 g/d); and 3) a placebo powder. Each powder will be provided for 4-6 weeks, separated by a 2-week washout period between treatment periods. Baseline and endpoint testing will include blood collection and vascular testing.

研究设计

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

入排标准

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

入选标准

  • •Men and women 35-65 years of age
  • •BMI ≥ 25 and ≤ 39 kg/m^2
  • •LDL-C > 116 mg/dL
  • •Total Cholesterol below 273 mg/dL for men and below 284 mg/dL for women
  • •Triglycerides below 350 mg/d
  • •Non-smokers
  • •Blood pressure < 160/100 mmHg

排除标准

  • •History of acute or chronic inflammatory conditions or heart disease, kidney disease, liver disease, autoimmune disorders, or thyroid disease (unless controlled by medication and blood results within the previous 6 months are provided)
  • •History of diabetes mellitus (and/or a fasting glucose > 126 mg/dL at screening)
  • •Stage II hypertension (blood pressure ≥ 160/100 mmHg)
  • •Lactation, pregnancy, or desire to become pregnant during the study
  • •Unwillingness to discontinue nutritional supplements, herbs, or vitamins, unless approved by investigator
  • •Use of medications/supplements for elevated lipids, blood pressure, or glucose
  • •Chronic use of non-steroidal anti-inflammatory or immunosuppressant medication
  • •Conditions requiring the use of steroids
  • •Unwillingness to refrain from blood donation prior to and during the study
  • •Any medical condition or abnormal laboratory value that is judged clinically significant by an investigator
  • •Allergy or sensitivity to strawberries or any ingredient in the study powders

研究组 & 干预措施

Low Dose Strawberry Powder

Experimental

40 g composed of 13 g freeze dried strawberry powder + 27 g placebo powder

干预措施: Low Dose Strawberry Powder (Dietary Supplement)

High Dose Strawberry Powder

Experimental

40 g freeze dried strawberry powder

干预措施: High Dose Strawberry Powder (Dietary Supplement)

Placebo Powder

Placebo Comparator

40 g color and taste matched placebo powder

干预措施: Placebo Powder (Dietary Supplement)

结局指标

主要结局

LDL-C

时间窗: Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage

LDL-C values calculated using the Friedewald equation

次要结局

  • Peripheral Blood Pressure(Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage)
  • HDL-C(Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage)
  • Total Cholesterol(Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage)
  • Central Blood Pressure(Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage)
  • Augmentation Index(Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage)
  • Pulse Wave Velocity(Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage)
  • Triglycerides(Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage)
  • Oxidized LDL (oxLDL)(Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage)
  • Malondialdehyde (MDA)(Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage)
  • High Sensitivity C Reactive Protein (hs-CRP)(Change from baseline after 4 week treatments of low dose, high dose, and placebo strawberry beverage)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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