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Clinical Trials/NCT05314036
NCT05314036
Completed
Not Applicable

Establishment of a Standard Operating Procedure for Screening of the Pathologies Associated With Prediabetes and Diabetes -The Wellness Transformation Network Pilot Study.

SciMar Ltd.1 site in 1 country15 target enrollmentJanuary 17, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non-Diabetic
Sponsor
SciMar Ltd.
Enrollment
15
Locations
1
Primary Endpoint
Establishment of proposed Wellness Transformation Network clinical trial procedures.
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The purpose of the study is to establish a Standard Operating Procedure (SOP) for the screening of pathologies associated with prediabetes and type 2 diabetes.

Detailed Description

The proposed study will enable screening of pathologies associated with cardiometabolic diseases (i.e., hypertension, prediabetes, insulin resistance, diabetes, and obesity). The Meal-Induced Insulinemia and Glycemia (MIG) score will correlate with those dysfunctions that are components of the Absence of Meal-Induced Insulinemia (AMIS) syndrome. Overall the study aims: 1. To establish an SOP for screening pathologies associated with cardiometabolic diseases using a combination of biometrics and metabolomics. 2. To compare a participant's MIG score and hepatalin levels following consumption of a standardized test meal containing macronutrients, and the measurement of several indices of organ health associated with diabetes (i.e., body composition, handgrip strength, spirometry, blood pressure, and heart rate variability). The study will involve 2 study visits: Visit 1 - Screening and Visit 2 - Intervention (Test meal administration and postprandial blood collection).

Registry
clinicaltrials.gov
Start Date
January 17, 2022
End Date
April 5, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adults (males and females)18 years of age or older.
  • Able to understand and communicate in English.
  • Willing to answer a questionnaire on lifestyle and health status.
  • Willing to undergo measurements of height, weight, waist circumference, hip circumference, blood pressure, heart rate and heart rate variability, body mass index, handgrip strength (handgrip dynamometry) testing, and pulmonary function (spirometry) testing.
  • Willing to fast for 12 hours prior to two in-person study visits.
  • Willing to consume a standardized test meal containing food ingredients.
  • Willing to provide a urine sample.
  • Willing to take a pregnancy test (female participants of childbearing potential).
  • Willing to provide the research team with a listing of all current medications and Natural Health Products(NHPs).
  • Willing to complete an online eDiary, including a 3-day food record.

Exclusion Criteria

  • Individuals diagnosed with diabetes.
  • Women with confirmed pregnancy or who are breastfeeding.
  • Individuals with allergy or sensitivity to any component of the standardized test meal (i.e., dextrose, lecithin, soy protein).
  • Individuals with a fasting blood glucose of 7.0 mmol/L or higher.
  • Individuals with abnormal glucose in their urine.
  • Individuals who are related to or working for the clinic site, research staff, and study sponsor.

Outcomes

Primary Outcomes

Establishment of proposed Wellness Transformation Network clinical trial procedures.

Time Frame: 2 Weeks

Practical feasibility of the proposed Wellness Transformation Network clinical trial procedures (Yes/No)

Secondary Outcomes

  • Time course and curve analysis of serum glucose response after the test meal administration.(Test: Baseline, every 30 minutes up to 2 hours after test meal administration)
  • Time course and curve analysis of Meal Induced Glycemia (MIG) scores response after the test meal administration.(Test: Baseline, every 30 minutes up to 2 hours after test meal administration)
  • Time course and curve analysis of serum insulin response after the test meal administration.(Test: Baseline, every 30 minutes up to 2 hours after test meal administration)
  • Time course and curve analysis of plasma hepatalin response after the test meal administration.(Test: Baseline, every 30 minutes up to 2 hours after test meal administration)
  • Time course and curve analysis of serum triglycerides response after the test meal administration.(Test: Baseline, every 30 minutes up to 2 hours after test meal administration)

Study Sites (1)

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