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Clinical Trials/NCT03409601
NCT03409601TerminatedNot Applicable

The Role of Satiety in the Effect of Portion Size on Intake

Penn State University2 sites in 1 country14 target enrollmentStarted: April 2, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
14
Locations
2
Primary Endpoint
Differences in intake by weight

Study Overview

Brief Summary

The study uses a crossover design in which the portion size of food is varied at each meal. Across four test meals, subjects will be served four different portions of food, and intake will be determined from pre- and post-meal food weights. The first visit will be a screening visit, at which subjects will complete the consent form, have their height and weight measured, and rate the taste of the study food. Test meals will be scheduled once a week for four weeks. At visits 2-5, subjects will eat lunch and rate characteristics of the meal. At visit 6, subjects will complete various questionnaires. The objective of this study is to determine whether any individual characteristics related to satiety influence the effect of portion size on intake.

Study Design

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

Eligibility Criteria

Ages
20 Years to 65 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 - 60 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-squared
  • Be willing to refrain from eating after 10 pm the evening before test sessions

Exclusion Criteria

  • An athlete in training
  • 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)
  • 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

Arms & Interventions

100% Portion Size

Experimental

Test meal consists of baseline (100%) portion size of meal.

Intervention: 100% Portion Size (Other)

125% Portion Size

Experimental

Test meal consists of food portion size that is 125% the size of baseline portion.

Intervention: 125% Portion Size (Other)

150% Portion Size

Experimental

Test meal consists of food portion size that is 150% the size of baseline portion.

Intervention: 150% Portion Size (Other)

175% Portion Size

Experimental

Test meal consists of food portion size that is 175% the size of baseline portion.

Intervention: 175% Portion Size (Other)

Outcomes

Primary Outcomes

Differences in intake by weight

Time Frame: Weeks 1, 2, 3, and 4

Weights (grams) of all foods consumed

Differences in energy intake

Time Frame: Weeks 1, 2, 3, and 4

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

Secondary Outcomes

  • Sensory-specific satiety(Weeks 1, 2, 3, and 4)
  • Ratings of meal characteristics(Weeks 1, 2, 3, and 4)
  • Eating rate(Weeks 1, 2, 3, and 4)
  • Ratings of hunger and satiety(Weeks 1, 2, 3, and 4)
  • Ratings of sensory characteristics of the food(Weeks 1, 2, 3, and 4)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Barbara J. Rolls

BJR

Penn State University

Study Sites (2)

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