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May 29, 2026npj Digital Medicine2 citationsOpen Access

Multicenter randomized trial of a digital therapeutic game for executive function in children with ADHD

SLSojung LeeYLYou Bin LimWCWooseok Choi

Key Points

  • This trial aims to assess the efficacy and safety of STAR RUCKUS, a digital therapeutic game for children with ADHD.
  • Multicenter, randomized, single-blind, sham-controlled design
  • Participated by 122 children aged 6-12 diagnosed with ADHD, assigned 1:1 to STAR RUCKUS or a sham intervention
  • Each child completed five daily game sessions for 4 weeks.
  • At Week 4, STAR RUCKUS reduced clinician-rated Korean ADHD rating scale scores more than sham (−7.50 vs. −4.00; p = 0.009)
  • Improvements in inattention (p = 0.024) and hyperactivity/impulsivity (p = 0.015) were observed
  • Statistically significant small-to-moderate improvements in ADHD symptoms with good adherence and tolerability.

Abstract

Abstract Significant executive function deficits mark attention-deficit/hyperactivity disorder (ADHD). Digital therapeutics (DTx) targeting cognitive control offer promising non-pharmacological options but require rigorous validation. We evaluated the efficacy and safety of STAR RUCKUS, an adaptive multitasking DTx designed to strengthen cognitive control in children with ADHD. In this multicenter, randomized, single-blind, sham-controlled trial, 122 children aged 6–12 years with DSM-5/ICD-10–diagnosed ADHD were assigned 1:1 to STAR RUCKUS or a visually matched driving-only sham intervention and completed five daily sessions for 4 weeks. The primary outcome was the change in clinician-rated Korean ADHD rating scale (K-ARS) scores. Of 122 randomized children, 114 completed the trial. At Week 4, STAR RUCKUS produced greater symptom reduction than sham (−7.50 vs. −4.00; p = 0.009), with improvements in inattention ( p = 0.024) and hyperactivity/impulsivity ( p = 0.015). These findings suggest statistically significant improvements of small-to-moderate magnitude ( ηp ² = 0.05) in clinician-rated ADHD symptoms, along with favorable adherence and tolerability. Trial registration: ClinicalTrials.gov (NCT07173439).

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Cite This Study

Lee et al. (2026) studied this question.

synapsesocial.com/papers/6a192ed7fab5b468c44181c8https://doi.org/10.1038/s41746-026-02721-3
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