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Effect of Soy Protein and Colorado Diet on Weight Loss and Maintenance

2018年11月6日 更新者:University of Colorado, Denver

The Effect of Incorporating Soy Protein Foods in the Colorado Diet for Weight Loss and Maintenance.

Dietary protein is a key element of most effective weight loss regimens. This study will investigate the effects of consuming soy protein on body composition and cardiometabolic health within the context of an effective weight loss and maintenance program called the Colorado Diet.

研究概览

详细说明

This is a randomized study involving 60 study subjects (30 per arm). Investigators plan to enroll 72 subjects (36 per arm) in order to allow for any potential drop outs with the goal of 60 study completers. Investigators will compare the efficacy of inducing weight loss of two treatment arms all based on the Colorado Diet. Subjects will be randomly assigned to one of two study arms and instructed to follow the Colorado Diet by participating in weekly Colorado Diet group classes (State of Slim class). There will be 4 classes of 18 subjects each (two classes for each treatment group). Subjects will be followed in the study for 12 months. Subjects will be randomized into one of two treatment groups as follows:

  • Group 1 will participate in a State of Slim group class, receive a State of Slim book (describing the Colorado Diet), and will then purchase food items allowed in the Colorado Diet from the lists of acceptable foods in the State of Slim book.
  • Group 2 will participate in a State of Slim class, receive the State of Slim book, and be provided soy protein foods to be consumed as part of the Colorado Diet (subjects will receive up to 3 foods with approximately 20g of soy protein each, per day).

研究类型

介入性

注册 (实际的)

71

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Colorado
      • Aurora、Colorado、美国、80045
        • University of Colorado Denver, Anschutz Health and Wellness Center

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 55年 (成人)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Males and females ages 18 - 55 years
  2. BMI between 27-40
  3. Weight stable (have not lost or gained more than 10 pounds in the last 3 months)
  4. Generally healthy
  5. Able to exercise 70 minutes per day at moderate intensity
  6. Willing and able to participate in a State of Slim group class for the first 16 weeks of the study and willing to participate in 5 study visits over the 12 month study period.

Exclusion Criteria:

  1. Pregnant or trying to become pregnant.
  2. Diagnosis of type 1 or type 2 diabetes
  3. Individuals following a vegetarian only diet
  4. Food allergies (to soy, dairy, wheat/gluten, eggs, or peanuts)
  5. Taking medications that could cause weight loss or weight gain or alter plasma lipids (such as steroids, tricyclic antidepressants, chemotherapy, antipsychotics, prescribed or over-the-counter weight loss agents, statins, fibrates, niacin, etc). Oral contraceptives can be used as long as subject agrees to not change use of these during the study. Multivitamins containing niacin can be used as long as subject agrees to not change use of these during the study.
  6. Known renal disease
  7. hypothyroidism
  8. Current alcohol or drug abuse or dependence (Subjects who have quit smoking in the last 6 months will be excluded. Smokers whose smoking habits have been stable for the last 6 months and which remain stable during the study can be included).
  9. Any medical condition for which following a diet and/or 70 minutes of exercise daily would be inadvisable
  10. LDL cholesterol levels above 190 mg/dl or triglycerides above 400 mg/dl.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Soy Group
Subjects in the soy group were asked to participate in the Colorado Diet program and to consume 3 soy food items per day.
其他:Non-soy Group
Subjects in the non-soy group were asked to participate in the Colorado Diet program and to avoid soy food products.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Change from baseline in % body weight at the end of a 16 week period
大体时间:at month 4
at month 4
Change from baseline in body fat at the end of 16 week period
大体时间:at month 4
at month 4
Change from baseline in % body weight at the end of a 52 week period
大体时间:at month 12
at month 12
Change from baseline in body fat at the end of a 52 week period
大体时间:at month 12
at month 12
Change from baseline in lipid panel results at end of 16 week period (total cholesterol)
大体时间:at month 4
at month 4
Change from baseline in lipid panel results at end of 52 week period (total cholesterol)
大体时间:at month 12
at month 12
Change from baseline in lipid panel results at end of 16 week period (LDL)
大体时间:at month 4
at month 4
Change from baseline in lipid panel results at end of 52 week period (LDLl)
大体时间:at month 12
at month 12
Change from baseline in lipid panel results at end of 16 week period (HDL)
大体时间:at month 4
at month 4
Change from baseline in lipid panel results at end of 52 week period (HDL)
大体时间:at month 12
at month 12
Change from baseline in lipid panel results at end of 16 week period (triglycerides)
大体时间:at month 4
at month 4
Change from baseline in lipid panel results at end of 52 week period (triglycerides)
大体时间:at month 12
at month 12

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:James O Hill, PhD、University of Colorado, Denver

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2015年3月10日

初级完成 (实际的)

2016年10月29日

研究完成 (实际的)

2016年10月29日

研究注册日期

首次提交

2017年8月9日

首先提交符合 QC 标准的

2017年8月11日

首次发布 (实际的)

2017年8月14日

研究记录更新

最后更新发布 (实际的)

2018年11月7日

上次提交的符合 QC 标准的更新

2018年11月6日

最后验证

2018年11月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • 14-1666

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

IPD 计划说明

Banked blood samples may be shared with other researchers (with subject consent)

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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