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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02199808
Other study ID # 14-0198
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 2014
Est. completion date May 2016

Study information

Verified date December 2020
Source University of North Carolina, Chapel Hill
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Purpose: To examine the effect of the omega-6 to omega-3 fatty acid ratio on age-related changes in executive functions in children and older adults. Participants: Eighty-four typically-developing 7-to 12-year-old children. Procedure (methods): Participants and a caregiver will participate in 4 sessions. Three sessions will consist of the screening. These sessions will be telephone calls to collect 24-hour diet information that will be used to determine whether they are eligible for the fourth session. Approximately 120 participants will be screened to find 84 participants who are eligible for the fourth session, in which participants will complete a series of tests on the Cambridge Neuropsychological Test Automated Battery (CANTAB) - a touch-screen device that provides computerized versions of standardized cognitive tests. They will also complete a maze task in which they figure out a path through the maze by walking on the correct squares. Brain activity will be recorded using a portable near-infrared spectroscopy (NIRS) system.


Recruitment information / eligibility

Status Completed
Enrollment 79
Est. completion date May 2016
Est. primary completion date May 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 7 Years to 12 Years
Eligibility Inclusion Criteria: - Typically-developing children 7-12 years old Exclusion Criteria: - Children or parents who do not speak English - Any diagnosis of a psychological illness - History of seizures - History of tobacco exposure during gestation - History of alcohol exposure during gestation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States UNC-Chapel Hill's Nutrition Research Institute Kannapolis North Carolina

Sponsors (2)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill Sigma Xi

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Error (count) and latency (in milliseconds) measures from executive function tasks For one specific aim, the omega-6 to omega-3 fatty acid ratio will be determined by summing the omega-6 and omega-3 fatty acid levels in plasma and dividing omega-6 fatty acids by omega-3 fatty acids. The calculated ratio will be used to predict error and latency scores on executive function tasks.
For a second specific aim, the oxygenated and deoxygenated hemoglobin concentrations from near-infrared spectroscopy (NIRS) measurements will be used to predict the error and latency measures from executive function tasks.
One time with children who are 7-12 years old
Secondary Oxygenated and deoxygenated hemoglobin concentrations from near-infrared spectroscopy (NIRS) Plasma levels of omega-6 and omega-3 fatty acids will be used to predict oxygenated and deoxygenated hemoglobin concentrations from near-infrared spectroscopy (NIRS) measurements in children who are 7-12 years old. One time with children who are 7-12 years old.
Secondary Performance on the Maze as measured by Noldus Ethovision Performance on the Maze as measured by Noldus Ethovision tracking system will be compared to performance on standardized measures of planning and spatial working memory. One time with children who are 7-12 years old
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