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OpenTrials
Completed

NCT Number: NCT02366572

PERFECT Project - Part 1 - Study 2

The objectives are to test the acute effects of different cereals containing pulse ingredients on: 1) post-prandial blood glucose, insulin and appetite for two hours, and 2) food intake two hours following consumption of pulse products.

We hypothesize that cereals containing pulse ingredients will lead to lower blood glucose, insulin, appetite and food intake responses compared to non-pulse cereals.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Normoglycemic (<5.6 mmol/L) and normotensive (systolic blood pressure <140 mm Hg and diastolic blood pressure below < 90 mm Hg)
  • BMI of 18.5-29.9 kg/m2

Exclusion criteria

  • Restrained eaters
  • Regularly skip breakfast
  • Smokers
  • Competitive sports or athletic training at a high intensity
  • Those on medications that may influence study outcomes or have experienced any gastrointestinal related health conditions/surgeries over the past year.
  • Those unable to walk for an hour continuously

Treatment and study plan

Control

Other

Non pulse extruded cereal

Pea protein

Other

Pulse extruded cereal

Pea Starch

Other

Pulse extruded cereal

Pea fibre + pea starch

Other

Pulse extruded cereal

Pea protein + pea starch

Other

Pulse extruded cereal

Pea fibre + pea starch + pea protein

Other

Pulse extruded cereal

Primary outcomes

  1. Plasma Glucose and Insulin Concentrations

    Time frame: 0 - 200 min

    Glucose will be determined by automated methods using Abbot Spectrum CCX Analyzer, and Insulin will be measured by commercially available RIA kits

  2. Food Intake

    Time frame: at 120 min

    Measured by VAS questionnaire

  3. Subjective Appetite

    Time frame: 0-200 min

    Motivation-to-eat VAS questionnaire

Secondary outcomes

  1. Palatability of treaments and meal

    Time frame: 5 and 140 minutes

    Measured by VAS questionnaire

  2. Physical comfort

    Time frame: 0 - 200 min

    Measured by VAS questionnaire

  3. Energy/fatigue

    Time frame: 0-200 min

    Measured by VAS questionnaire

Sponsors and collaborators

Lead sponsor

University of Manitoba

Other

Collaborators

  • Alberta Pulse Growers
  • Saskatchewan Pulse Growers

Registry information

Official study title

Pulse EnRiched Food and Exercise Clinical Trials (PERFECT Project): Part 1 - Acute Effects of Pulse Ingredients in Snack Products on Appetite, Blood Glucose, and Food Intake in Adults - Study 2

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Feb 19, 2015
Registry last updated
Jan 23, 2023

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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