- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04191291
Time for Lunch: The Impact of Lunch Time Constraints on Child Eating Behaviors
July 18, 2022 updated by: University of Illinois at Urbana-Champaign
Recent peer-reviewed observational evidence suggests that school children receive anywhere from 10-33 minutes of seated lunch time and that students with less time to eat discard higher amounts of milk, entrée (i.e. protein items), grains, and vegetables.
This waste is a missed nutritional and food security opportunity and also negatively impacts the environment.
The purpose of this study is to estimate the impact that lunch time constraints have on child food selection, consumption and waste behaviors using a crossover trial design, where the duration of seated lunch times are randomly allocated to be either 10 minutes or 20 minutes each day.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
39
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
-
-
Illinois
-
Urbana, Illinois, United States, 61801
- University of Illinois
-
-
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
7 years to 14 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Must be enrolled in local summer camp
Exclusion Criteria:
- None
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: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Shortened lunch period
The amount of seated lunch time will be 10 minutes.
|
We are randomly allocating a 10 minute or 20 period of seated lunch time.
|
|
Experimental: Longer lunch period
The amount of seated lunch time will be 20 minutes.
|
We are randomly allocating a 10 minute or 20 period of seated lunch time.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Food item selection
Time Frame: Ranges from 5 days to 20 days, depending upon how long each participant elects to enroll in the summer camp
|
The type and number of school meal components selected by students to eat for lunch.
|
Ranges from 5 days to 20 days, depending upon how long each participant elects to enroll in the summer camp
|
|
Food item consumption
Time Frame: Ranges from 5 days to 20 days, depending upon how long each participant elects to enroll in the summer camp
|
The weight of each school meal component that was consumed by each child during lunch.
Each measured in grams.
|
Ranges from 5 days to 20 days, depending upon how long each participant elects to enroll in the summer camp
|
|
Food item waste
Time Frame: Ranges from 5 days to 20 days, depending upon how long each participant elects to enroll in the summer camp
|
The weight of each school meal component that was discarded by each child during lunch.
Each measured in grams.
|
Ranges from 5 days to 20 days, depending upon how long each participant elects to enroll in the summer camp
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)
June 3, 2019
Primary Completion (Actual)
June 28, 2019
Study Completion (Actual)
June 28, 2019
Study Registration Dates
First Submitted
June 13, 2019
First Submitted That Met QC Criteria
December 6, 2019
First Posted (Actual)
December 9, 2019
Study Record Updates
Last Update Posted (Actual)
July 21, 2022
Last Update Submitted That Met QC Criteria
July 18, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- 19412
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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