Carbohydrate Intolerance Questionnaire Study

NCT ID: NCT03138902

Last Updated: 2017-05-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

108 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-06-01

Study Completion Date

2013-12-31

Brief Summary

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The purpose of this study is to evaluate the validity of using a carbohydrate intolerance questionnaire (CIQ) and/or other health markers as a means of predicting response to insulin sensitivity as determined by an oral glucose tolerance test (OGTT).

Detailed Description

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This study will utilize a carbohydrate intolerance questionnaire (CIQ). Responses to a CIQ will be correlated with diet inventories, baseline body composition and health assessments, a standard metabolic panel, fasting glucose and insulin levels, a homeostatic insulin resistance model (HOMA), a two hour oral glucose tolerance test (OGTT), and a carbohydrate sensitivity symptom questionnaire administered during the OGTT.

Conditions

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Carbohydrate Intolerance

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Glucose Tolerance Beverage

75 g. of a fruit punch flavored oral glucose solution

Group Type EXPERIMENTAL

TRUTOL Glucose Tolerance Beverage

Intervention Type DIETARY_SUPPLEMENT

A caffeine-free, non-carbonated, glucose tolerance beverage

Interventions

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TRUTOL Glucose Tolerance Beverage

A caffeine-free, non-carbonated, glucose tolerance beverage

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Participant is female
* Participant is between the ages of 18 and 60

Exclusion Criteria

* Participant is pregnant or nursing
* Participant is diabetic or pre-diabetic
* Participant has a Body Mass Index (BMI) \< 22
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Curves International

INDUSTRY

Sponsor Role collaborator

Texas A&M University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Richard B Kreider, PhD

Role: PRINCIPAL_INVESTIGATOR

Texas A&M University

Other Identifiers

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IRB2013-0401

Identifier Type: -

Identifier Source: org_study_id

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