Skip to main content
Clinical Trials/NCT03307681
NCT03307681CompletedNot Applicable

Effect of White Potatoes on Glycemic Response, Satiety and Food Intake in Children

Toronto Metropolitan University2 sites in 1 country14 target enrollmentStarted: December 21, 2018Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
14
Locations
2
Primary Endpoint
Ad libitum food intake (lunch, at 120 minutes)

Study Overview

Brief Summary

The purpose of the present study is to explore the influence of cooking methods on post-prandial glycaemia and its impact on satiety in children.

Detailed Description

Each of the 5 study sessions will be at least 7 days apart. Either meal skipping, or one of three treatments of white potatoes (a) baked (with skin), (b) mashed, (c) fried French fries, or white bread, prepared on the day of testing, will be served to healthy children (9-14 years). Participants will consume the equivalent to 1 medium sized potato (~280 kcal) or an equivalent amount of calories from white bread. Glycemic response, insulin, incretin hormones (glucagon-like peptide-1 (GLP-1), glucose-dependent insulinotropic peptide (GIP)), dipeptidyl peptidase 4 (DPP4), and cholecystokinin (CCK) will be measured for 2 h (0, 15, 30, 45, 60, 90 and 120 min) following meal consumption, as well as mood and subjective appetite. An ad libitum test meal will be provided at 120 min to assess food intake suppression.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
9 Years to 14 Years (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • be between 9 and 14 years of age
  • be healthy, and have been born at term
  • be a native English speaker
  • not be taking any medications
  • not have allergies to potatoes, rice, or beans.
  • normal body weight (between the 5th and 85th BMI percentile for age and gender)

Exclusion Criteria

  • anyone with food sensitivities or allergies to potatoes or potato-products,
  • diabetic or overweight/obese individuals.

Outcomes

Primary Outcomes

Ad libitum food intake (lunch, at 120 minutes)

Time Frame: at 120 minutes post morning meal consumption

Food intake will be determined by weighing the meal before and after serving. The net weight of the test meal will be converted to calories

Change from baseline glycemic response

Time Frame: 15, 30, 45, 60, 90, and 120 minutes after meal consumption

Blood glucose (mmol/L). Blood glucose will be measured in whole blood using YSI 2300 STAT PLUS (YSI Incorporated, Yellow Springs, OH)

Change from baseline insulin

Time Frame: 15, 30, 45, 60, 90, and 120 minutes after meal consumption

Blood insulin (pmol/L). Insulin concentration in serum will be determined in duplicate via enzyme-linked immunosorbent assay kits (ELISA; Millipore, Billerica, Massachusetts).

Secondary Outcomes

  • Change from baseline mood(15, 30, 45, 60, 90, and 120 minutes after meal consumption)
  • Change from baseline subjective appetite(15, 30, 45, 60, 90, and 120 minutes after meal consumption)
  • Change from baseline glucose-dependent insulinotropic peptide (GIP)(15, 30, 45, 60, 90, and 120 minutes after meal consumption)
  • Change from baseline glucagon-like peptide-1 (GLP-1)(15, 30, 45, 60, 90, and 120 minutes after meal consumption)
  • Change from baseline cholecystokinin (CCK)(15, 30, 45, 60, 90, and 120 minutes after meal consumption)
  • Change from baseline dipeptidyl peptidase 4 (DPP4)(15, 30, 45, 60, 90, and 120 minutes after meal consumption)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Nick Bellissimo

Associate Professor

Toronto Metropolitan University

Study Sites (2)

Loading locations...

Similar Trials