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Portion Size and To-go Container on Dinner Intake

The Influence of the Provision of a To-go Container on the Portion Size Effect in Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03502096
Enrollment
58
Registered
2018-04-18
Start date
2016-10-31
Completion date
2017-12-31
Last updated
2018-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eating Behavior, Obesity

Keywords

portion size, food intake, energy intake, food choice

Brief summary

This study investigated whether the provision of a to-go container influenced the portion size effect at a meal. Following a screening visit, women came to the lab once a week for 4 weeks to eat a meal of multiple foods. At each visit, the portion size of the meal was varied in a counterbalanced order. Prior to their first meal, women were randomly assigned to one of two groups: a group that would have their leftovers packaged to go (to-go group) and a group that did not have leftovers packaged (control group). Women were instructed to eat ad libitum at the meals. They also answered questions about hunger and fullness as well as food characteristics before and after each meal. Following the final meal, subjects completed a series of questionnaires assessing subject characteristics as well as food characteristics. It was hypothesized that the effect of portion size on intake would be attenuated in subjects who received a to-go container with the meal. In addition, we aimed to identify any subject characteristics that moderated or exacerbated the portion size effect. It was also of interest to determine whether the portion size effect on individual foods were influenced by food characteristics such as perceived value.

Interventions

BEHAVIORALTo-Go container

Subjects were provided a to-go container in which leftover foods would be packaged

OTHERControl

Subjects were not provided a to-go container with the meal

Sponsors

United States Department of Agriculture (USDA)
CollaboratorFED
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
Jenny Craig, Inc.
CollaboratorINDUSTRY
Penn State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

The two factors were meal portion size and provision of a to-go container. The portion size factor was within-subjects (crossover). All subjects received each of the 4 portions served (the order in which portions were served was counterbalanced). The container factor was between-subjects. Subjects were randomly assigned to 1 of 2 groups: one group had uneaten food packaged to take home, the other group (control) did not.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Regularly eats 3 meals/day * Willing to avoid alcohol the day before and during test days * Likes foods offered at test meals * Body mass index 18 - 36 (kg/m\*m)

Exclusion criteria

* Smokes * Athlete in training * Pregnant or breastfeeding * Taking medication that may affect appetite or food intake * Food allergies or dietary restrictions * Currently have or recently been diagnosed with disease or disorder known to affect appetite

Design outcomes

Primary

MeasureTime frameDescription
Change in the weight of food consumedWeeks 1, 2, 3, and 4Change in the weight of food consumed (in grams) across experimental conditions and intervention groups.
Change in energy intakeWeeks 1, 2, 3, and 4Change in energy intake (in kcal) across experimental conditions and intervention groups.

Secondary

MeasureTime frameDescription
Changes in post-meal measures of satietyWeeks 1, 2, 3, and 4Changes in post-meal measures of satiety across experimental conditions and intervention groups using 100-mm visual analog scales.
Change in energy density consumedWeeks 1, 2, 3, and 4Change in food energy density consumed (in kcal/g) across experimental conditions and intervention groups.
Changes in ratings of food propertiesWeeks 1, 2, 3, and 4Changes in post-meal ratings of food properties across experimental conditions and subject groups using 100-mm visual analog scales.
Changes in post-meal ratings of meal characteristicsWeeks 1, 2, 3, and 4Changes in post-meal ratings of meal characteristics across experimental conditions and between subject groups using 100-mm visual analog scales.
Change in intake of individual foodsWeeks 1, 2, 3, and 4Change in both the weight (g) and energy (kcal) consumed of individual foods served at the meal across experimental conditions and intervention groups.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026