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临床试验/NCT04896619
NCT04896619已完成不适用

Cholesterol Effects of Kori-tofu Proteins

Wageningen University and Research2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2021年9月7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
48
试验地点
2
主要终点
Change in total cholesterol levels

研究概览

简要总结

The study is a randomized, cross-over, double-blind, controlled trial in which participants with mildly elevated levels of cholesterol will receive two 4-week interventions (e.g. kori-tofu or control), with a wash-out period of 4 weeks in between. During the intervention periods, subjects will eat 3 slices of bread per day, representing a Kori-tofu dose of 34.5 grams or a matched reference. Fasting total and LDL cholesterol will be determined at the start and end of each of the two intervention periods.

详细描述

There are several types of tofu, an example of a specific type of tofu is called Kori-tofu. Kori-tofu literally means frozen tofu. The production process of Kori-tofu leads to the formation of a higher high molecular weight fraction (HMF) content of the soy proteins. Several studies describe the effects of Kofi-tofu on health. In this study the aim is to investigate the effect of repetitive consumption of Kori-tofu on blood cholesterol levels and other lipid metabolism related measures, in research subjects with mildly elevated levels of cholesterol.

The primary objective is to assess the effect of repetitive consumption of Kori-tofu on blood total and LDL cholesterol levels. The secondary objective is to assess the effect of repetitive consumption of Kori-tofu on other markers of lipid metabolism, glucose metabolism and blood pressure.

The study is a randomized, cross-over, double-blind, controlled trial in which participants will receive two 4-week interventions (e.g. kori-tofu or control), with a wash-out period of 4 weeks in between. During the intervention periods, subjects will eat 3 slices of bread per day, representing a Kori-tofu dose of 34.5 grams or a matched reference (whey protein, soy oil and maltodextrin/cellulose). Research subjects will visit our research unit before and after each intervention period for a test day. During these test days fasting blood samples will be collected and blood pressure measurements will be performed.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
40 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 40-70 years;
  • BMI between 18.5-35 kg/m2;
  • Total cholesterol levels >5 mmol/L or LDL >3 mmol/L

排除标准

  • Use of medication/supplements/food items that may influence the study results, such as cholesterol lowering medication, Becel ProActiv (judged by our research physician);
  • Total cholesterol levels >7 mmol/L;
  • LDL cholesterol levels >5 mmol/L;
  • Reported slimming, medically prescribed or other extreme diets;
  • Reported weight loss or weight gain of >5 kg in the month prior to pre-study screening;
  • Not willing to give up blood donation during the study;
  • Current smokers;
  • Alcohol intake ≥4 glasses of alcoholic beverages per day;
  • Pregnant, lactating or wishing to become pregnant in the period of the study (self-reported);
  • Abuse of soft and/or hard drugs;
  • Food allergies or intolerances for products that we use in the study;
  • Participation in another clinical trial at the same time; NL75320.081.20 CHOKO Version number: 4, April 2021 15 of 34
  • Being an employee of the Food, Health & Consumer Research group of Wageningen Food & Biobased Research.

结局指标

主要结局

Change in total cholesterol levels

时间窗: 0 weeks, 4 weeks, 8 weeks and 12 weeks

under fasting conditions

Change in LDL cholesterol levels

时间窗: 0 weeks, 4 weeks, 8 weeks and 12 weeks

under fasting conditions

次要结局

  • Change in systolic blood pressure levels(0 weeks, 4 weeks, 8 weeks and 12 weeks)
  • Change in diastolic blood plessure levels(0 weeks, 4 weeks, 8 weeks and 12 weeks)
  • Change in triglycerides levels(0 weeks, 4 weeks, 8 weeks and 12 weeks)
  • Change in leptin levels(0 weeks, 4 weeks, 8 weeks and 12 weeks)
  • Change in adiponectin levels(0 weeks, 4 weeks, 8 weeks and 12 weeks)
  • Change in plasma insulin levels(0 weeks, 4 weeks, 8 weeks and 12 weeks)
  • Change in HDL cholesterol levels(0 weeks, 4 weeks, 8 weeks and 12 weeks)
  • Change in glucose levels(0 weeks, 4 weeks, 8 weeks and 12 weeks)
  • Change in fructosamine levels(0 weeks, 4 weeks, 8 weeks and 12 weeks)
  • Change in HbA1c levels(0 weeks, 4 weeks, 8 weeks and 12 weeks)

研究者

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

Diederik Esser

Project leader clinical trials

Wageningen University and Research

研究点 (2)

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