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Internet-based, randomized, controlled trial of omega-3 fatty acids for hyperactivity in autism
Stephen Bent1, Robert L Hendren1, Tara Zandi2
1University of California, San Francisco.
Insights
Omega-3 fatty acids showed a trend toward reducing hyperactivity in children with autism spectrum disorder (ASD). An internet-based trial design proved feasible for evaluating therapies in ASD, though larger studies are needed.
Area of Science:
- Neuroscience
- Pediatrics
- Clinical Trials
Background:
- Preliminary evidence suggests omega-3 fatty acids may alleviate hyperactivity in children with autism spectrum disorder (ASD).
- Evaluating novel therapies for ASD requires efficient and accessible clinical trial designs.
Purpose of the Study:
- To assess the feasibility of an Internet-based clinical trial for evaluating omega-3 fatty acids in children with ASD.
- To examine the efficacy of omega-3 fatty acids in reducing hyperactivity symptoms in children with ASD.
Main Methods:
- A 6-week, Internet-based randomized controlled trial involving 57 children (aged 5-8 years) with ASD.
- Participants received either omega-3 fatty acids or a placebo, with outcomes measured via parent and teacher ratings of hyperactivity.
Main Results:
- The study demonstrated the feasibility of Internet-based recruitment and data collection for ASD clinical trials.
- While the omega-3 group showed a greater reduction in hyperactivity, the difference was not statistically significant.
- Adverse events were infrequent and not linked to omega-3 supplementation; participant feedback was positive.
Conclusions:
- Internet-based trials are a feasible and cost-effective method for evaluating therapies in children with ASD.
- A larger sample size is necessary to confirm the efficacy of omega-3 fatty acids for hyperactivity in ASD.
- This study design offers a promising model for future research in pediatric neurodevelopmental disorders.
Objective:
Preliminary evidence suggests that omega-3 fatty acids may reduce hyperactivity in children with autism spectrum disorder (ASD). We sought to examine the feasibility of a novel, Internet-based clinical trial design to evaluate the efficacy of this supplement.
Method:
E-mail invitations were sent to parents of children aged 5 to 8 years enrolled in the Interactive Autism Network. All study procedures, including screening, informed consent, and collection of outcome measures took place over the Internet. The primary outcome measures were parent- and teacher-rated changes in hyperactivity on the Aberrant Behavior Checklist (ABC-H).
Results:
During the 6-week recruitment period, 57 children from 28 states satisfied all eligibility criteria and were randomly assigned to 1.3 grams of omega-3 fatty acids or an identical placebo daily for 6 weeks. Outcome assessments were obtained from all 57 participants and 57 teachers, and the study was completed in 3 months. Children in the omega-3 fatty acid group had a greater reduction in hyperactivity (-5.3 points) compared to the placebo group (-2.6 points), but the difference was not statistically significant (1.9-point greater improvement in the omega-3 group, 95% CI = -2.2 to 5.2). Adverse events were rare and not associated with omega-3 fatty acids. Participant feedback was positive.
Conclusion:
Internet-based, randomized controlled trials of therapies in children with ASD are feasible and may lead to marked reductions in the time and cost of completing trials. A larger sample size is required to definitively determine the efficacy of omega-3 fatty acids. Clinical trial registration information-Omega-3 Fatty Acids for Hyperactivity Treatment in Autism Spectrum Disorder; http://clinicaltrials.gov; NCT01694667.
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