Combined Effects of Sequential Variety and Portion Size on Meal Intake of Women

September 21, 2023 updated by: Barbara J. Rolls, Penn State University
The primary purpose of this study is to investigate the combined effects of sequential meal variety and portion size on food intake at a meal. Additionally, other individual characteristics will be examined for their influence on the effects of simultaneous variety and portion size on meal intake.

Study Overview

Study Type

Interventional

Enrollment (Actual)

52

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Pennsylvania
      • University Park, Pennsylvania, United States, 16802
        • Laboratory for the Study of Human Ingestive Behavior, The Pennsylvania State University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Be willing and able to travel to Penn State University Park campus weekly for meals
  • Be fully vaccinated against COVID-19
  • Be a woman 20 - 65 years old
  • Regularly eat 3 meals/day
  • Be willing to refrain from drinking 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
  • Must not have taken prescription or non-prescription drugs that may affect appetite or food intake within the last 3 months
  • Must not dislike or be unable to eat the test foods (because of allergies, intolerance, or dietary restrictions)
  • Must not have a high variability in liking of the test foods
  • Must not be currently dieting to gain or lose weight
  • Must not have a health condition that affects appetite
  • Must not 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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Sequential Variety, Small Portion
3 different foods served in a small portion in 3 successive courses
3 different foods served in 3 successive courses
Small meal portion size
Experimental: Sequential Variety, Large Portion
3 different foods served in a large portion in 3 successive courses
3 different foods served in 3 successive courses
Large meal portion size
Experimental: Single-Food, Small Portion
1 food served in a small portion in 3 successive courses
Small meal portion size
1 food served in 3 successive courses
Experimental: Single-Food, Large Portion
1 food served in a large portion in 3 successive courses
Large meal portion size
1 food served in 3 successive courses

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in intake by weight
Time Frame: Weeks 1, 2, 3, 4
Weight (grams) of all meal components consumed
Weeks 1, 2, 3, 4
Change in energy intake
Time Frame: Weeks 1, 2, 3, 4
Energy intake (kilocalories) of all meal components consumed, calculated from weight and energy density
Weeks 1, 2, 3, 4

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in bite count
Time Frame: Weeks 1, 2, 3, 4
The number of bites of food during the meal
Weeks 1, 2, 3, 4
Change in active eating time
Time Frame: Weeks 1, 2, 3, 4
Duration of the time spent eating in minutes
Weeks 1, 2, 3, 4
Change in mean eating rate
Time Frame: Weeks 1, 2, 3, 4
Mean food intake per minute (grams/minute), calculated by dividing meal food intake by meal duration
Weeks 1, 2, 3, 4
Change in mean bite size
Time Frame: Weeks 1, 2, 3, 4
Mean food intake per bite (grams/bite), calculated by dividing meal food intake by bite count
Weeks 1, 2, 3, 4
Change in sip count
Time Frame: Weeks 1, 2, 3, 4
The number of sips of water during the meal
Weeks 1, 2, 3, 4
Change in mean drinking rate
Time Frame: Weeks 1, 2, 3, 4
Mean water intake per minute (grams/minute), calculated by dividing meal water intake by meal duration
Weeks 1, 2, 3, 4
Change in mean sip size
Time Frame: Weeks 1, 2, 3, 4
Mean water intake per sip (grams/sip), calculated by dividing meal water intake by sip count
Weeks 1, 2, 3, 4
Change in switching between bites and sips
Time Frame: Weeks 1, 2, 3, 4
The number of switches between bites and sips during the meal
Weeks 1, 2, 3, 4
Change in rating of pleasantness of the taste of food samples
Time Frame: Weeks 1, 2, 3, 4
Measured on a 100-mm visual analogue scale ranging from not at all pleasant (0 mm) to extremely pleasant (100 mm). This will be used to calculate Sensory-Specific Satiety
Weeks 1, 2, 3, 4
Change in rating of desire to eat food samples
Time Frame: Weeks 1, 2, 3, 4
Measured on a 100-mm visual analogue scale ranging from not at all strong (0 mm) to extremely strong (100 mm), in answer to "How strong is your desire to eat [this food] right now?". This will be used to calculate Sensory-Specific Satiety.
Weeks 1, 2, 3, 4
Change in rating of hunger
Time Frame: Weeks 1, 2, 3, 4
Measured on a 100-mm visual analogue scale ranging from not at all hungry (0 mm) to extremely hungry (100 mm)
Weeks 1, 2, 3, 4
Change in rating of thirst
Time Frame: Weeks 1, 2, 3, 4
Measured on a 100-mm visual analogue scale ranging from not at all thirsty (0 mm) to extremely thirsty (100 mm)
Weeks 1, 2, 3, 4
Change in rating of nausea
Time Frame: Weeks 1, 2, 3, 4
Measured on a 100-mm visual analogue scale ranging from not at all nauseated (0 mm) to extremely nauseated (100 mm)
Weeks 1, 2, 3, 4
Change in rating of fullness
Time Frame: Weeks 1, 2, 3, 4
Measured on a 100-mm visual analogue scale ranging from not at all full (0 mm) to extremely full (100 mm)
Weeks 1, 2, 3, 4
Change in rating of prospective consumption
Time Frame: Weeks 1, 2, 3, 4
Measured on a 100-mm visual analogue scale ranging from nothing at all (0 mm) to a large amount (100 mm), in answer to "How much food do you think you could eat right now?".
Weeks 1, 2, 3, 4

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 6, 2022

Primary Completion (Actual)

April 3, 2023

Study Completion (Actual)

April 7, 2023

Study Registration Dates

First Submitted

July 28, 2022

First Submitted That Met QC Criteria

July 29, 2022

First Posted (Actual)

August 3, 2022

Study Record Updates

Last Update Posted (Actual)

September 22, 2023

Last Update Submitted That Met QC Criteria

September 21, 2023

Last Verified

September 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • FoodVariety104

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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