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Completed

NCT Number: NCT03045354

Dietary Carbohydrate Consumption at Breakfast on Food Intake, Glycemic Response, and Subjective Appetite

The purpose of this study is to determine the effect of carbohydrates of familiar breakfast meals on glycemic response, subjective appetite, and food intake in normal weight (NW) and overweight or obese (OW/OB) children.

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Key information

Age range

9 year–14 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

School of Nutrition, Ryerson University

Toronto, Ontario, M5B 2K3, Canada

About this study

Regular breakfast eating NW and OW/OB children, 9-14 years of age, will participate in the experiment. Four isocaloric (450 kcal) breakfasts (eggs with a side of French fries, mashed potatoes, or beans, and control breakfast of milk, cereal and toast) and breakfast skipping will be examined. On five separate mornings, 7 days apart and after a 12 hour overnight fast, each participant will receive one of the four breakfasts or skip breakfast, in a randomized counterbalanced order. Participants will be given an ad libitum lunch 3 hours after breakfast and parents will report the rest of day food record for food intake analysis. Blood glucose will be measured via finger-prick at baseline, and 30, 60, 120, and 180 minutes after breakfast consumption. Subjective appetite will be measured with a visual analogue scale at baseline and every 15 minutes for 1 hour, and every hour for 3 hours.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • be between 9 and 14 years of age
  • be healthy, and have been born at term
  • not be taking any medications
  • not have allergies or sensitivities to potatoes, eggs, gluten, dairy, or beans
  • NW (between the 5th and 85th BMI percentile for age and gender)
  • OW/OB (>85th BMI percentile for age and gender)

Exclusion criteria

  • food sensitivities, allergies, or dietary restrictions
  • health, learning, emotional, or behavioural problems
  • receiving any medications

Treatment and study plan

Mashed potatoes

Other

Isocaloric (450 kcal) breakfast treatments of eggs with a side of mashed potatoes

Traditional breakfast

Other

Isocaloric (450 kcal) control breakfast treatments of cereal, milk, toast and jam

Breakfast skipping

Other

No breakfast

French fries

Other

Isocaloric (450 kcal) breakfast treatments of eggs with a side of French fries

Beans

Other

Isocaloric (450 kcal) breakfast treatments of eggs with a side of beans

Primary outcomes

  1. Short-term food intake (kcal)

    Time frame: 3 hours after breakfast

    Participants will consume an ad libitum lunch 3 hours post breakfast consumption.

Secondary outcomes

  1. Subjective appetite

    Time frame: Baseline, at 15 or 60 minutes intervals for 3 hours

    Participants will complete subjective ratings on appetite and well-being

  2. Blood glucose

    Time frame: Baseline, 30, 60, 120 and 180 minutes after breakfast

    Finger prick capillary blood glucose will be collected

  3. Rest of day food record

    Time frame: 8-12 hours

    Parents/guardians will record participants' food intake until the end of the day

Sponsors and collaborators

Lead sponsor

Toronto Metropolitan University

Other

Registry information

Official study title

The Effect of Carbohydrate-Containing Foods at Breakfast on Food Intake, Glycemic Response, and Subjective Appetite in Normal Weight and Overweight/Obese Children

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Feb 7, 2017
Registry last updated
Jul 23, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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