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Clinical Trials/NCT03886428
NCT03886428CompletedNot Applicable

Lunch Feeding Study for Men and Women

Penn State University1 site in 1 country50 target enrollmentStarted: May 21, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
50
Locations
1
Primary Endpoint
Change in intake by weight

Study Overview

Brief Summary

The purpose of this study is to gain a better understanding of the satiation measures that influence human eating behavior in regard to intake of large portion sizes at a meal. The investigators hypothesize that satiation measures will influence the magnitude of the portion size effect at a meal. Additionally, other individual characteristics will be examined for their influence on the portion size effect. The portion size effect will be measured by serving a test meal once a week for four weeks in which the portion size of the entree will be varied.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Be willing and able to travel to Penn State University Park campus weekly for meals
  • •Be a man or woman 18 - 70 years old
  • •Regularly eat 3 meals/day
  • •Be willing to avoid alcohol the day before and during test days
  • •Have a body mass index between 18.0 and 35.0 kg/m*m
  • •Be willing to refrain from eating after 10 pm the evening before test sessions
  • •Be willing to participate in all study procedures

Exclusion Criteria

  • •Must not be a smoker
  • •Must not be an athlete in training
  • •Must not be pregnant or breastfeeding at the time of screening
  • •Have taken prescription or non-prescription drugs that may affect appetite or food intake within the last 3 months
  • •Dislike or be unable to eat the test foods (because of allergies, intolerance, or dietary restrictions)
  • •Must not be currently dieting to gain or lose weight
  • •Have a health condition that affects appetite
  • •Have participated in a similar study in our lab in the past year
  • •Must not be a student, faculty, or staff member in nutritional sciences or psychology

Arms & Interventions

100% Portion Size

Experimental

Test meal with portion size 100% of baseline

Intervention: 100% portion size (Other)

125% Portion Size

Experimental

Test meal with portion size 125% of baseline

Intervention: 125% portion size (Other)

150% Portion Size

Experimental

Test meal with portion size 150% of baseline

Intervention: 150% portion size (Other)

175% Portion Size

Experimental

Test meal with portion size 175% of baseline

Intervention: 175% portion size (Other)

Outcomes

Primary Outcomes

Change in intake by weight

Time Frame: Weeks 1, 2, 3, 4

Weights (grams) of all foods consumed

Change in energy intake

Time Frame: Weeks 1, 2, 3, 4

Calculated energy intake (kcal) based on weight and energy density of food consumed

Secondary Outcomes

  • Change in mean bite rate(Weeks 1, 2, 3, 4)
  • Change in meal duration(Weeks 1, 2, 3, 4)
  • Change in rating of the pleasantness of the taste of the entree sample(From before the test meal to after the test meal in weeks 1, 2, 3, 4)
  • Change in rating of prospective consumption of the entree sample(From before the test meal to after the test meal in weeks 1, 2, 3, 4)
  • Change in rating of thirst(From before the test meal to after the test meal in weeks 1, 2, 3, 4)
  • Change in ratings of prospective consumption(From before the test meal to after the test meal in weeks 1, 2, 3, 4)
  • Change in rating of fullness(From before the test meal to after the test meal in weeks 1, 2, 3, 4)
  • Change in bite count(Weeks 1, 2, 3, 4)
  • Change in mean bite size(Weeks 1, 2, 3, 4)
  • Change in mean eating rate(Weeks 1, 2, 3, 4)
  • Change in distribution of estimated bite size(Weeks 1, 2, 3, 4)
  • Change in sip count(Weeks 1, 2, 3, 4)
  • Change in rating of the pleasantness of the taste of food samples(From before the test meal to after the test meal in weeks 1, 2, 3, 4)
  • Change in rating of hunger(From before the test meal to after the test meal in weeks 1, 2, 3, 4)
  • Change in rating of prospective consumption of food samples(From before the test meal to after the test meal in weeks 1, 2, 3, 4)
  • Change in ratings of nausea(From before the test meal to after the test meal in weeks 1, 2, 3, 4)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Barbara J. Rolls

Professor of Nutrition and Director of the Laboratory for the Study of Human Ingestive Behavior

Penn State University

Study Sites (1)

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