Clinical Trial

Effects of Phosphatidylserine and DHA on Cognitive Performance in Children With ADHD

Study acronym: PS-DHA-ADHD
Completed
View on ClinicalTrials.gov →
Summary
This study aimed to evaluate the effects of different phosphatidylserine (PS) formulations, with or without docosahexaenoic acid (DHA), on cognitive performance in children diagnosed with attention-deficit/hyperactivity disorder (ADHD) or presenting with clinically significant subthreshold ADHD symptoms. A total of 45 medication-naïve children aged 10-14 years were randomly assigned to one of four groups: placebo, PS capsule (PS + DHA), PS sachet (PS without DHA), or PS Plus capsule (higher-dose PS + DHA). The intervention period was eight weeks. Cognitive performance was assessed at baseline and after the intervention using the MOXO continuous performance test and the Stroop test. The study aimed to compare the effects of different PS formulations on attention, impulsivity, hyperactivity, and executive function.
Trial Details
NCT Number NCT07521449
Lead Sponsor Çağlar Charles Daniel Jaicks
Conditions Attention Deficit Hyperactivity Disorder (ADHD), ADHD
Enrollment 45 participants
Start Date 2023-12-30
Primary Completion 2024-06-01 (estimated)
Study Completion 2025-06-01 (estimated)
Updated on ClinicalTrials.gov 2026-04-13