Peer-reviewed article
Risperidone for children with attention-deficit/hyperactivity disorder and severe behavioral dysregulation: a randomized placebo-controlled assessor-blinded trial.
Abbasi E, Abdi A, Eskandari R ·
Summary
Written by AI, not yet AICS's view · claude-haiku-4-5-20251001This randomized controlled trial tested whether the medication risperidone, added to behavioral therapy, could help children aged 3-12 with ADHD and severe behavioral problems like aggression and defiance. Children receiving risperidone showed significantly greater improvement in ADHD symptoms and overall functioning compared to those receiving placebo. However, risperidone caused weight gain and increased prolactin levels, meaning it should only be used selectively in carefully monitored children with serious behavioral difficulties, not as routine treatment.
Key points
- Risperidone produced significantly greater reduction in ADHD-RS-IV scores than placebo (15.63 vs. 26.47 at week 48; p < 0.001)
- Clinical response rate was 70.8% with risperidone versus 21.7% with placebo (p < 0.001)
- Parent-rated Conners' scores improved more in the risperidone group (16.94 vs. 28.42 at week 48; p < 0.001)
- Most common adverse effects were somnolence and increased appetite
- Risperidone was associated with greater weight gain and prolactin elevation than placebo, but no serious adverse events occurred
Limitations
The study does not report the country or setting where the trial was conducted, limiting generalizability assessment. Long-term effects beyond 48 weeks and outcomes in different cultural or healthcare contexts are not examined.
Abstract
Background Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder in childhood, and treatment of children with severe behavioral dysregulation remains challenging. This study evaluated the efficacy and safety of adjunctive risperidone specifically in children with ADHD and clinically significant behavioral dysregulation - including irritability, impulsive aggression, and oppositional symptoms - refractory to behavioral intervention alone. Methods In this 48-week randomized, placebo-controlled, assessor-blinded trial, children aged 3-12 years with moderate-to-severe ADHD and significant behavioral dysregulation refractory to behavioral intervention alone were allocated to risperidone (n = 48) or matched placebo (n = 46), both in addition to ongoing structured behavioral intervention and parental psychoeducation. The primary outcome was change in clinician-rated ADHD-RS-IV score from baseline to week 48. Secondary outcomes included parent-rated Conners' scores, Children's Global Assessment Scale (CGAS), treatment response, adverse events, and metabolic parameters. Results Risperidone produced a significantly greater reduction in ADHD-RS-IV scores than placebo over time (baseline: 28.85 ± 2.62 vs. 28.70 ± 2.50; week 48: 15.63 ± 1.82 vs. 26.47 ± 2.92; p < 0.001). Parent-rated Conners' scores also improved more in the risperidone group (week 48: 16.94 ± 1.81 vs. 28.42 ± 3.04; p < 0.001). Functional improvement was greater with risperidone, with higher CGAS scores and a higher clinical response rate (70.8% vs. 21.7%; p < 0.001). The most common adverse effects were somnolence and increased appetite. Risperidone was associated with greater weight gain and prolactin elevation than placebo, but no serious adverse events occurred. Conclusion In this study, risperidone was associated with improvement in ADHD symptom severity and global functioning in carefully selected children with ADHD and prominent behavioral dysregulation. However, treatment was also associated with clinically relevant metabolic and endocrine adverse effects. These findings support selective use as a pharmacological adjunct to behavioral intervention in closely monitored patients with significant behavioral comorbidity, and do not justify routine use for uncomplicated ADHD.
Findings the Hub has extracted
Each claim below is labelled by its type of design and links back to this report.
- Intervention
- Adjunctive risperidone medication added to ongoing structured behavioral intervention and parental psychoeducation
- Population
- Children aged 3-12 years with moderate-to-severe ADHD and significant behavioral dysregulation refractory to behavioral intervention alone (n=94 total: 48 risperidone, 46 placebo)
Key finding
ADHD-RS-IV scores reduced more with risperidone than placebo (difference of 10.84 points at week 48; p < 0.001)