Low Doses of Melatonin to Improve Sleep in Children with ADHD: An Open-Label Trial

Ana Checa-Ros1,2, Antonio Muñoz-Hoyos3, Antonio Molina-Carballo3

  • 1Grupo de Investigación en Enfermedades Cardiorrenales y Metabólicas, Departamento de Medicina y Cirugía, Facultad de Ciencias de la Salud, Universidad Cardenal Herrera-CEU, CEU Universities, Calle Santiago Ramón y Cajal s/n, Alfara del Patriarca, 46115 Valencia, Spain.

PubMed

Insights

Low-dose melatonin (1 mg) significantly increased total sleep time in pediatric patients with ADHD on methylphenidate. This treatment showed a good safety profile, suggesting potential benefits for sleep in this population.

Area of Science:

  • Pediatric Sleep Medicine
  • Neurodevelopmental Disorders
  • Pharmacology

Background:

  • Limited research exists on low-dose melatonin's sleep effects in children, especially those with ADHD.
  • Previous studies primarily focused on adult populations.

Purpose of the Study:

  • To investigate the impact of 1 mg melatonin (aMT) on the sleep patterns of pediatric patients diagnosed with ADHD and undergoing methylphenidate (MPH) treatment.
  • To assess changes in sleep duration, sleep onset latency, and sleep efficiency.

Main Methods:

  • A cohort of children and adolescents (7-15 years) with ADHD on extended-release MPH was enrolled.
  • Sleep diaries were collected over seven weeks, followed by a four-week treatment with 1 mg of aMT before bedtime.
  • Actigraphy was used for seven-day sleep assessments before and after the intervention.

Main Results:

  • Twenty-seven pediatric patients completed the study.
  • A statistically significant increase in total sleep time (TST) was observed after one month of aMT treatment (from 463 to 485 minutes; p < 0.040).
  • No significant improvements were noted in sleep onset latency (SOL) or sleep efficiency, with minor adverse effects reported.

Conclusions:

  • One milligram of melatonin effectively increases total sleep time in children and adolescents with ADHD receiving psychostimulant therapy.
  • The treatment demonstrated a favorable tolerability profile.
  • Further placebo-controlled studies are recommended to optimize aMT administration timing for potentially reducing SOL in this patient group.
Abstract

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