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Benefits of a Higher Protein, 'Egg-cellent' Breakfast in the Classroom

Benefits of a Higher Protein, 'Egg-cellent' Breakfast in the Classroom

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03536676
Enrollment
91
Registered
2018-05-25
Start date
2018-04-24
Completion date
2020-07-01
Last updated
2022-01-10

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

Conditions

Breakfast, Eating Behavior, Mood, Obesity

Keywords

Breakfast, Obesity, Mood, Eating Behavior, Cognitive Function

Brief summary

This study will test whether whether the implementation of and Egg-cellent 'Breakfast in the Classroom' improves school breakfast participation and breakfast consumption in middle school adolescents; whether the implementation of 'Breakfast in the Classroom' improves appetite control, mood, cognitive performance, and unhealthy snacking behavior in middle school adolescents when compared to a traditional school breakfast program.

Detailed description

The investigators propose an 4-week cross-over design breakfast study in children enrolled in 6-8th grade within the Center School District in the Kansas City, Missouri. This school will begin their 'Breakfast in the Classroom' program on March 26, 2018. Prior to the start of 'Breakfast in the Classroom', baseline data will be collected on the students who wish to participate in the study. Baseline data includes anthropometric assessments; demographics; current eating habits; cognitive performance; appetite; and mood. Following baseline, the students will be provided a breakfast that meets all the requirements for a reimbursable school breakfast with the addition of two eggs for 3-weeks: At 4 weeks (3 weeks after initiation of the program), the study participants will complete a similar outcomes to those completed at baseline.

Interventions

OTHER'Egg-cellent' Breakfast in the Classroom

Includes the additional 2 eggs per day

Receives the standard meal for Breakfast in the Classroom

Sponsors

Egg Nutrition Center
CollaboratorOTHER
Purdue University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
10 Years to 16 Years
Healthy volunteers
Yes

Inclusion criteria

* All students from the Center Middle School in Kansas City, MO who choose to participate and whose parent/legal guardian (excluding Wards of the State) signs the consent will be included.

Exclusion criteria

* Wards of the State will be excluded from this study.

Design outcomes

Primary

MeasureTime frameDescription
School Breakfast Program Participation3-weeks prior to program initiation and 3-weeks of programParticipation at during the traditional school breakfast program and throughout the Breakfast in the Classroom program will be determined by the electronic school meal tracking system that logs student participation each day for breakfast and lunch.

Secondary

MeasureTime frameDescription
Benefits of Breakfast QuestionnaireBaseline and 3-weeks after beginning the interventionDuring one day, a questionnaire asking the participants what happens when participants consume breakfast and skip breakfast will be administered. They will be given a list of choices (multiple selections are allowed) and the units for analysis will be binary (they chose it or did not choose it).
Snacking QuestionnairesBaseline and 3-weeks after beginning the interventionDuring one day, questionnaires assessing typical snacking behavior will be completed once. Participants will be asked to think about what they ate during the past week. They will be asked how many times they ate a variety of foods throughout this week. The students will complete these on their respective Chromebook laptops or will be provided paper copies (if their Chromebook is not available).
Cognitive Performance AssessmentBaseline and 3-weeks after beginning the interventionDuring one day, cognitive performance assessments will occur once between 120 min and 180 min after breakfast using the online CNS Vital Signs neurocognitive assessment system during one day. The CNS Vital Signs system contains a battery of computerized tests to assess attention, memory, executive function, and cognitive flexibility. The assessment will occur outside of classroom learning activities.
Habitual Breakfast Habits QuestionnaireBaseline and 3-weeks after beginning the interventionDuring one day, a questionnaire assessing previous breakfast habits will be given to participants. This questionnaire asks how many days per week they consume various breakfast foods.
Mood State QuestionnairesBaseline and 3-weeks (Post-study)Questionnaires assessing tiredness, sleepiness, energy, irritability/agitation, etc.) will be completed during the following times for 1 day immediately before lunch. The questions are worded as how strong is your feeling of or how strong is your desire with anchors of not at all to extremely. The students will complete these on their respective Chromebook laptops or will be provided paper copies (if their Chromebook is not available). All results will be a number from 0 (not at all) to 100 (extremely) with the unit of out of 100.
Breakfast in the Classroom Participation QuestionnaireBaseline and 3-weeks after beginning the interventionQuestionnaires assessing whether they ate breakfast or skipped breakfast and what types of foods they ate (if they ate breakfast) will be completed for 5 consecutive days during baseline.
Appetite QuestionnairesBaseline and 3-weeks after beginning the interventionQuestionnaires, assessing hunger, fullness, prospective food consumption, and eating initiation, will be completed during the following times for 1 day immediately before lunch. The questions are worded as how strong is your feeling of or how strong is your desire with anchors of not at all to extremely. The students will complete these on their respective Chromebook laptops or will be provided paper copies (if their Chromebook is not available). All results will be a number from 0 (not at all) to 100 (extremely) with the unit of out of 100.

Countries

United States

Outcome results

None listed

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