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OpenTrials
Completed

NCT Number: NCT03066713

Post-prandial Glucose Response From Phytochemical Rich Potato Products

Assess the impact of high antioxidant potato products on postprandial glycemic response and subsequent appetite and food intake.

Completed

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Purdue University

West Lafayette, Indiana, 47906, United States

About this study

Preliminary results from anthocyanin rich potato products suggest that a reduced postprandial glycemic response might be expected from certain types of potato products and that phenolic antioxidants may play a critical role in predicting the physiological response from potato products. Further, if consumed early in the day, such as at breakfast, a reduced glycemic response may serve to mitigate appetite and food consumption later in the day. Investigators aim to better understand how characteristics of commercial potato products (i.e. frozen potato products) with different phenolic profiles and content, may alter postprandial glycemic response and subsequent appetitive behavior. Specifically, investigators will assess the glycemic response from a serving of potato products in the morning using continuous glucose monitoring. Further, appetite and subsequent food consumption later in the day will be assessed through appetite logs and continuous glucose monitoring.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • BMI 18.5-25, male or female

Exclusion criteria

  • BMI outside 18.5-25

Treatment and study plan

Skin Off French Fry

Other

Skin Off French Fries will be provided at breakfast and lunch

Skin On French Fry

Other

Skin On French Fries will be provided at breakfast and lunch

Hash brown

Other

Hash brown potatoes will be provided at breakfast and lunch.

Carbohydrate Control

Other

A pancake will be provided at breakfast, and pretzels will be provided at lunch.

Primary outcomes

  1. Change in Blood Glucose over 24 hours

    Time frame: 24 hours

    Samples taken every 5 minutes for 24 hours by a continuous glucose monitor

Secondary outcomes

  1. Appetite

    Time frame: Every hour for 24 hours

    Questionnaire on hunger, fullness, desire to eat, prospective consumption, thirst taken hourly on the same day as the feeding intervention

Sponsors and collaborators

Lead sponsor

Purdue University

Other

Collaborators

  • USDA Beltsville Human Nutrition Research Center

Registry information

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Feb 28, 2017
Registry last updated
Jan 18, 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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