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Completed

NCT Number: NCT03128684

The Effects of Lentil-containing Food Products on Satiety and Food Intake

The Lentil Satiety study will examine the effects of replacing wheat and rice with two types of lentils within food products (muffins and chilies) on satiety and food intake in healthy adults.

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Human Nutraceutical Research Unit

Guelph, Ontario, N1G 2W1, Canada

About this study

The Lentil Satiety study will examine the effects of replacing wheat and rice with two types of lentils (small green Eston and red split) within food products (muffins and chilies) on satiety and food intake in healthy adults, for a total of 6 study treatments. A total of 3 to 6 study visits (corresponding to consuming all muffins and/or all chilies) will take place where participants will consume one of the study treatments and subsequently complete satiety questionnaires over 180 minutes to measure satiety as subjective appetite sensations (hunger, fullness, desire to eat, and prospective food consumption). At 180 minutes, participants will receive ad libitum pizza and bottled water to consume until they are comfortably full for a measure of weighed food intake. At the end of each study visit, participants will be given a food scale and instructed to weigh and record all food and drink consumed for the remainder of the day for a measure of 24-hour energy intake.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy males and females
  • Age 18 to 40 years old
  • BMI 20-30 kg/m2

Exclusion criteria

  • Blood pressure greater than 140/90 mmHg
  • Major medical condition including a history of AIDS or hepatitis
  • Medical or surgical event requiring hospitalization within 3 months of randomization
  • Any medication use except stable dose (3 months) of oral contraceptives, blood pressure or statin medications
  • Tobacco use
  • Probiotic supplement use
  • Dietary fibre supplement use
  • Natural health products (NHPs) used for glycemic control (all other NHPs are ok, as long as stable for 3 months)
  • Pulse consumption greater than 4 servings per week
  • Food allergy or non-food life threatening allergy
  • Pregnant or breastfeeding
  • Alcohol consumption of greater than 14 drinks per week or greater than 4 drinks per sitting
  • Recent or intended significant weight loss or gain (greater than 4kg in previous 3 months)
  • Elite athletes
  • Shift workers
  • Breakfast skippers
  • Score greater than 11, 9, or 8 on the Three Factor Eating Questionnaire (TFEQ) Cognitive Restraint, Disinhibition, and Hunger scales, respectively
  • Dislike of frozen pizza

Treatment and study plan

Small Green Lentil Muffin

Other

Consumption of small green lentil muffin; consumption of ad libitum pizza test meal after 180 minutes

Split Red Lentil Muffin

Other

Consumption of split red lentil muffin; consumption of ad libitum pizza test meal after 180 minutes

Wheat Muffin

Other

Consumption of wheat muffin; consumption of ad libitum pizza test meal after 180 minutes

Small Green Lentil Chili

Other

Consumption of small green lentil chili; consumption of ad libitum pizza test meal after 180 minutes

Split Red Lentil Chili

Other

Consumption of split red lentil chili; consumption of ad libitum pizza test meal after 180 minutes

Rice Chili

Other

Consumption of rice chili; consumption of ad libitum pizza test meal after 180 minutes

Primary outcomes

  1. Satiety

    Time frame: Acute: 0, 15, 30, 45, 60, 90, 120, 150, and 180 minutes after treatment consumption

    Satiety will be measured using 100mm visual analog scales (VAS) rating appetite sensations of hunger, fullness, desire to eat, and prospective consumption

  2. Food Intake

    Time frame: Acute: 180 minutes following consumption of treatment

    Food intake will be measured as kilocalories using an ad libitum cheese pizza test meal

Secondary outcomes

  1. 24-hour Energy Intake

    Time frame: Acute: 24 hours

    24-hour energy intake will be measured by providing electronic food scales to participants to weigh and record all food and drink consumed for the rest of the day after leaving the study visit

Sponsors and collaborators

Lead sponsor

University of Guelph

Other

Collaborators

  • Agriculture and Agri-Food Canada
  • Pulse Canada
  • Saskatchewan Pulse Growers

Registry information

Official study title

The Effects of Lentil-containing Food Products on Satiety and Food Intake in Healthy Adults

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Apr 25, 2017
Registry last updated
Dec 19, 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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