The Effects of Breakfast on Neuropsychological Functioning

NCT01943604 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 195

Last updated 2015-04-29

No results posted yet for this study

Summary

This study is designed to examine healthy children who skip breakfast and the effects of fasting on their neuropsychological functioning and the potential benefits that a Balanced Breakfast may have on their learning abilities. It is expected that this study will provide new knowledge on how prolonged periods of 8 or more hours without food affect neurocognitive processes and thus learning how specific meals following this period of fasting, which most children experience, change those processes, potentially for the better.

The hypotheses for this study are:

1. Children who consume breakfast will demonstrate significantly higher levels of attention, greater concentration, and diminished impulsivity compared to children who do not consume breakfast.
2. Children who consume breakfast will demonstrate a significantly quicker reaction time and increased accuracy in correctly identifying target stimuli from an array compared to children who do not consume breakfast.
3. Children who consume breakfast will demonstrate increased freedom from distractibility and enhanced short-term memory compared to children who do not consume breakfast.
4. Children who consume breakfast will demonstrate increased cognitive processing speed compared to children who do not consume breakfast.
5. Children who consume breakfast will have improved verbal learning compared to children who do not consume breakfast.
6. Children who consume breakfast will have improved visual memory compared to children who do not consume breakfast.

Conditions

  • Neuropsychology

Interventions

OTHER

Nutella Breakfast

Breakfast composed of bread and Nutella, milk and apple slices

OTHER

Waffle Breakfast

Breakfast composed of waffles and syrup, milk, and apple slices

Sponsors & Collaborators

  • Ferrero Italy, Inc.

    collaborator INDUSTRY
  • Baylor College of Medicine

    lead OTHER

Principal Investigators

  • Theresa Nicklas, DrPH · Baylor College of Medicine

  • Isabella Iovino, PhD · Baylor College of Medicine

  • Janice Stuff, PhD · Baylor College of Medicine

Study Design

Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
8 Years
Max Age
10 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2014-11-30
Completion
2014-11-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01943604 on ClinicalTrials.gov