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Taste Perception and Chronic Disease Risk

2014年5月21日 更新者:Tufts University

Relationship Between Variations in Taste Perception and Chronic Disease Risk Factors as a Function of Age

The purpose of the Taste Perception Study is to assess variations in the ability to taste and perceive sensations from various stimuli in younger (18-49 years) and older (50-85 years) volunteers. The study's goal is to determine how these sensations influence what one likes to eat, and what one chooses to eat, and whether there is an association with dietary intake, body composition and chronic disease. Another objective of the study is to determine the association between variations in oral sensations and genes mediating sensory perception and dietary behaviours.

研究概览

详细说明

The objective of the Taste Perception Study is to assess variations in oral sensations in younger (18-49 years; n=35) relative to older (50-85 years; n=35) subjects, and determine the association between variations in oral sensations and measures of chronic disease risk factors, body composition, habitual dietary intake and selected genes mediating sensory perception and dietary behaviors. Subjects who are participating in the Glycemic Index study (IRB #7196) will be asked for voluntarily participation in the proposed study. These volunteers will undergo 1-2 hours of standardized testing. These tests will involve tasting or smelling certain foods/beverages or ingredients in foods/beverages and rating the degree of liking/disliking, intensity and flavor or odor using a validated general Labeled magnitude scale. Volunteers will also be asked to complete a food preference survey and eating inventory questionnaire, as well as provide a DNA sample from a cheek swab or blood sample. These data will then be merged with the measures of chronic disease risk factors, body composition and habitual dietary intake data generated from the Glycemic index study in order to better understand if variations in oral sensations influence food preferences and patterns and subsequently chronic disease risk.

研究类型

观察性的

注册 (实际的)

90

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

    • Massachusetts
      • Boston、Massachusetts、美国、02111
        • Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University

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 85年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Community Sample

描述

Inclusion Criteria:

  • men and women;
  • aged 18 to 85 years old;
  • free of known chronic disease;
  • BMI < 35 kg/ m2.

Exclusion criteria:

  • BMI ≥ 35 kg/m2;
  • renal or liver disease;
  • untreated hypertension;
  • irritable bowel syndrome;
  • malabsorptive, esophageal and gastrointestinal motility disorders;
  • chronic pancreatitis, or history of acute pancreatitis within the last year;
  • hypothyroidism or hypothyroidism, as defined as screening TSH outside of normal ranges;
  • anemia, as defined by screening hematocrit of 34% for women and 38% for men;
  • smoking within the past 6 months;
  • diabetes;
  • fasting glucose ≥ 125 mg/dL;
  • pregnancy or breastfeeding;
  • history of polycystic ovary syndrome;
  • history of autoimmune or other connective tissue disorders associated with chronic inflammation, such as rheumatoid arthritis; alcohol consumption > 7 drinks/ week;
  • use of medications known to affect glucose or lipid metabolism;
  • established CVD (myocardial infarction, stroke, heart failure, coronary artery bypass, graft, stenosis > 50%, peripheral arterial disease);
  • unwillingness to adhere to study protocol;
  • weight gain or loss of more than 15 lbs within 6 months prior to enrollment and other abnormal screening laboratory analysis results.

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

  • 观测模型:队列
  • 时间观点:横截面

队列和干预

团体/队列
18-49 years
Younger
50-85 years
Older

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Sensory/hedonic rating
大体时间:1 - 2 hours
1 - 2 hours

次要结果测量

结果测量
大体时间
Genetic Variation
大体时间:1- 2 hours
1- 2 hours

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:Nirupa R Matthan, Ph.D.、HNRCA at Tufts University

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

2008年7月1日

初级完成 (实际的)

2010年3月1日

研究完成 (实际的)

2010年3月1日

研究注册日期

首次提交

2009年11月30日

首先提交符合 QC 标准的

2009年12月1日

首次发布 (估计)

2009年12月2日

研究记录更新

最后更新发布 (估计)

2014年5月23日

上次提交的符合 QC 标准的更新

2014年5月21日

最后验证

2014年5月1日

更多信息

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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