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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Eicosapentaenoic acid / Docosahexaenoic acid | 650 mg EPA + 650 mg DHA daily |
| DIETARY_SUPPLEMENT | Placebo dietary intervention (MUFA) in ADHD group | Placebo contains mono-unsaturated fatty acids (MUFA) in stead of poly-unsaturated fatty acids (PUFA), same energy value |
| DIETARY_SUPPLEMENT | Eicosapentaenoic acid / Docosahexaenoic acid | 650 mg EPA and 650 mg DHA daily |
| DIETARY_SUPPLEMENT | Placebo dietary intervention (MUFA) in healthy control group | Placebo 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.