Clinical Trials Directory

Trials / Completed

CompletedNCT01554462

The Effects of EPA/DHA Supplementation on Cognitive Control in Children With ADHD

The Effects of Eicosapentaenoic Acid (EPA)/ Docosahexaenoic Acid (DHA) Supplementation on Cognitive Control in Children With Attention Deficit Hyperactivity Disorder (ADHD)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
79 (actual)
Sponsor
Unilever R&D · Industry
Sex
Male
Age
8 Years – 12 Years
Healthy volunteers
Accepted

Summary

Forty children with and 40 children without Attention deficit Hyperactivity Disorder (ADHD) receive Docosahexaenoic Acid (DHA) and Eicosapentaenoic Acid (EPA) or placebo via a dietary intervention. Cognitive control functions are measured with functional Magnetic Resonance Imaging (MRI) before and after the intervention. Behavioural change is monitored with behavioural scales.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTEicosapentaenoic acid / Docosahexaenoic acid650 mg EPA + 650 mg DHA daily
DIETARY_SUPPLEMENTPlacebo dietary intervention (MUFA) in ADHD groupPlacebo contains mono-unsaturated fatty acids (MUFA) in stead of poly-unsaturated fatty acids (PUFA), same energy value
DIETARY_SUPPLEMENTEicosapentaenoic acid / Docosahexaenoic acid650 mg EPA and 650 mg DHA daily
DIETARY_SUPPLEMENTPlacebo dietary intervention (MUFA) in healthy control groupPlacebo contains MUFA in stead of PUFA, same energy value

Timeline

Start date
2009-01-01
Primary completion
2013-01-01
Completion
2013-01-01
First posted
2012-03-15
Last updated
2013-12-11

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT01554462. Inclusion in this directory is not an endorsement.