- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03313245
Diet Quality and Cognitive Control Function in Early Childhood: A Pilot Study
October 9, 2018 updated by: Naiman Khan, University of Illinois at Urbana-Champaign
This study aims to study the relationship between diet and cognitive function among 4-5-year-olds.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Children's ability for optimal cognitive function is critical for their long-term capacity to learn and achieve scholastic success.
However, there is a gap in the knowledge pertaining to the selection of appropriate cognitive tasks for studying relationships between diet and cognitive control, particularly among young children.
Accordingly, this study aims to study the relationship between diet and cognitive function using a standardized neuropsychological assessment and a modified cognitive task battery.
Study Type
Observational
Enrollment (Anticipated)
104
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Naiman A Khan, PhD, RD
- Phone Number: 2173002197
- Email: nakhan2@illinois.edu
Study Locations
-
-
Illinois
-
Urbana, Illinois, United States, 61801
- Recruiting
- Department of Kinesiology and Community Health
-
Contact:
- Naiman A Khan, PhD, RD
- Phone Number: 217-300-2197
- Email: nakhan2@illinois.edu
-
Principal Investigator:
- Naiman A Khan, PhD, RD
-
Sub-Investigator:
- Anne Walk, PhD
-
-
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
4 years to 5 years (Child)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
4 and 5-year-olds
Description
Inclusion Criteria:
- Parental consent
- Child Assent
- 4 and 5 years of age
- Absence of neurological disorders
- Normal or corrected-to-normal vision
Exclusion Criteria:
- Younger than 4 and older than 5 years of age
- Presence of neurological disorders
- Uncorrected vision
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Early Cognitive and Academic Development
Time Frame: Once at laboratory visit
|
Woodcock Johnson IV eCAD
|
Once at laboratory visit
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Attention
Time Frame: Once at laboratory visit
|
2-stimulus Oddball task
|
Once at laboratory visit
|
Cognitive Flexibility
Time Frame: Once at laboratory visit
|
Hearts and Flowers Task
|
Once at laboratory visit
|
Diet Quality
Time Frame: 7-day average following first laboratory visit
|
Healthy Eating Index
|
7-day average following first laboratory visit
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
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)
August 1, 2016
Primary Completion (Anticipated)
December 31, 2018
Study Completion (Anticipated)
December 31, 2018
Study Registration Dates
First Submitted
October 13, 2017
First Submitted That Met QC Criteria
October 13, 2017
First Posted (Actual)
October 18, 2017
Study Record Updates
Last Update Posted (Actual)
October 10, 2018
Last Update Submitted That Met QC Criteria
October 9, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Other Study ID Numbers
- 16484
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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