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Effects of modafinil in children with attention-deficit/hyperactivity disorder: an open-label study

T A Rugino1, T C Copley

  • 1Department of Pediatrics, Helping Hands Development Center, Marshall University School of Medicine, Huntington, WV, USA. rugino@marshall.edu

Insights

Once-daily modafinil improved attention-deficit/hyperactivity disorder (ADHD) symptoms in children. This stimulant medication showed significant benefits in clinical and objective measures for pediatric ADHD treatment.

Area of Science:

  • Pediatric Neurology
  • Child Psychiatry
  • Pharmacology

Background:

  • Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder in children.
  • Current ADHD treatments often require multiple daily doses, posing adherence challenges.
  • Modafinil, a stimulant with a long duration of action, has potential for once-daily ADHD management.

Purpose of the Study:

  • To evaluate the efficacy of once-daily modafinil in treating the clinical features of ADHD in children.
  • To assess the impact of modafinil on objective measures of attention and behavior in pediatric ADHD.

Main Methods:

  • An open-label study involving 11 children (ages 5-15) diagnosed with ADHD.
  • Participants were assessed using the Conners Parent and Teacher Rating Scale-Revised (CPRS, CTRS), ADHD Rating Scale-IV, and Test of Variables of Attention (TOVA).
  • Assessments were conducted with and without once-daily modafinil treatment over an average of 4.6 weeks.

Main Results:

  • Significant improvements were observed in TOVA ADHD scores (2.43 SD, p = .0009).
  • CPRS and CTRS ADHD index T scores improved by 17.7 points (p = .001) and 14.1 points (p = .0009), respectively.
  • ADHD Rating Scale-IV scores improved from the 88th to the 75th percentile (p = .047); side effects were mild and manageable.

Conclusions:

  • Once-daily modafinil demonstrates potential as an effective treatment for ADHD in children.
  • The medication was generally well-tolerated, with mild side effects.
  • Further investigation with double-blind, placebo-controlled trials is warranted to confirm these findings.
Abstract

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