The Morning Coffee Study

  • STATUS
    Recruiting
  • participants needed
    30
  • sponsor
    University of Guelph
Updated on 19 February 2024

Summary

The liking of a breakfast meal has been shown to influence food choice throughout the day. This study will investigate the effects that liking of different coffee beverages has on daily food intake.

Description

This is a postprandial acute meal crossover blinded study in which 30 fasted young healthy women will consume one of two butter-rich coffees, or black coffee, in random order, at each of three study sessions separated by at least 4 days. Participants will rate the coffee characteristics and complete paper visual analogue scale ratings of alertness, fatigue, nausea, satiety, and comfort for 180 minutes and consume a pasta lunch meal.

Details
Condition Appetitive Behavior
Age 20-35 years
Treatment Coffee with water, Coffee with butter-I, Coffee with butter-II
Clinical Study IdentifierNCT04250740
SponsorUniversity of Guelph
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Generally healthy women
-35 yrs
BMI of 18.5-26.1 kg/m2 and waist circumference <88cm
Non-smoking
Non to moderate alcohol drinkers
Regular coffee consumers
Regularly consumes dairy products
Pre-menopausal with regular monthly periods
Stable medication use
Have not gained or lost significant weight during the past 3 months
Not pregnant or lactating
Enjoy and be willing to consume pasta with tomato sauce

Exclusion Criteria

Any food sensitivity or intolerance
Any anaphylactic allergy or gastrointestinal disorder
History of any major disease or medical condition
Elite or training athletes
Three Factor Eating Questionnaire restraint score >16
Taking any natural health products or dietary supplements, other than a multivitamin, that interfere with fat or caffeine digestion
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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