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NCT02636998 Clinical Trial

Nutrition and Cognitive Function in Preadolescents

Healthy Children Clinical Trial

Official title:
Nutrition and Cognitive Function in Preadolescents

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT02636998
Other study ID # 204071
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date June 2015
Est. completion date December 2024

Study information
Verified date December 2023
Source Arkansas Children's Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is designed to evaluate cognitive function in preadolescents who have different body mass indexes.

Description:

The investigators plan to document differences between normal weight and obese preadolescents on psychological and neurocognitive measures of executive function controlling for factors known to influence brain function and behavior not considered in previous studies.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 116
Est. completion date December 2024
Est. primary completion date June 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 9 Years to 11 Years
Eligibility Inclusion Criteria: - Normal weight (BMI: <85th percentile) or obese (BMI: >95th percentile) - Right hand dominance - Report eating breakfast at least 4 days/week - Able to hear at least 20 dB stimulus - Visual acuity must be at least 20/40 - Arithmetic Computation Task - Biological mother available to attend the enrollment study visit Exclusion Criteria: - Full Scale IQ <80 - Children taking medications or having chronic illnesses/disorders that may independently affect study outcome measures (as determined by the PI)

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Arkansas Children's Nutrition Center Little Rock Arkansas

Sponsors (1)
Lead Sponsor Collaborator
Arkansas Children's Hospital Research Institute

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Psychological assessments Standardized assessments 9-10 years
Primary Neurocognitive measures Brain Lab Recordings 9-10 years
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