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Carbohydrate Intolerance Questionnaire Study

Not Applicable
Completed
Conditions
Carbohydrate Intolerance
Interventions
Dietary Supplement: TRUTOL Glucose Tolerance Beverage
Registration Number
NCT03138902
Lead Sponsor
Texas A&M University
Brief Summary

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

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
108
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Glucose Tolerance BeverageTRUTOL Glucose Tolerance Beverage75 g. of a fruit punch flavored oral glucose solution
Primary Outcome Measures
NameTimeMethod
Complete a Carbohydrate Intolerance Questionnaire (CIQ)1 day

Primary Outcome

Complete a 2 Hour Oral Glucose Tolerance Test (OGTT) to measure glucose response2 hours

Primary Outcome

Complete a 2 Hour Oral Glucose Tolerance Test (OGTT) to measure insulin response2 hours

Primary Outcome

Secondary Outcome Measures
NameTimeMethod
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