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Clinical Trials/NCT01023906
NCT01023906
Completed
Not Applicable

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

Tufts University1 site in 1 country90 target enrollmentJuly 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiovascular Disease
Sponsor
Tufts University
Enrollment
90
Locations
1
Primary Endpoint
Sensory/hedonic rating
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

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.

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
July 2008
End Date
March 2010
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • men and women;
  • aged 18 to 85 years old;
  • free of known chronic disease;
  • BMI \< 35 kg/ m
  • Exclusion criteria:
  • BMI ≥ 35 kg/m2;
  • renal or liver disease;
  • untreated hypertension;
  • irritable bowel syndrome;
  • malabsorptive, esophageal and gastrointestinal motility disorders;

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Sensory/hedonic rating

Time Frame: 1 - 2 hours

Secondary Outcomes

  • Genetic Variation(1- 2 hours)

Study Sites (1)

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