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Study identifier: NCT06847165 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Trigeminal Nerve Stimulation for Children With Prenatal Alcohol Exposure

Condition: Fetal Alcohol Spectrum Disorders · Attention Deficit Hyperactivity Disorder  ·  Sponsor: University of California, Los Angeles

PhaseNA
Planned participants30
Who can joinAll sexes, 8 Years to 12 Years
Healthy volunteersNo

About this study

This is an open-label trial of trigeminal nerve stimulation (TNS) for children aged 8-12 years with attention deficit hyperactivity disorder (ADHD) putatively due to prenatal alcohol exposure (PAE). TNS has been successful in treating pediatric ADHD generally and it is US Food and Drug Administration (FDA)-cleared for this condition. But this will be the first time it is tried for ADHD specifically associated with PAE. In TNS, a weak electric current is applied to the child's forehead overnight while sleeping to gently stimulate the brain. TNS is administered at home by the parent to the child. TNS is safe and well tolerated. Efficacy of TNS in ADHD is \~50%. The purpose of the present pilot study is to determine the feasibility of TNS for children with PAE and ADHD. Feasibility means safety (any serious side effects?), tolerability (do children comply with TNS? are they comfortable with it?), and a rough idea of efficacy (does TNS seem to work in most kids?) A secondary goal of the study is to get a more precise idea of brain mechanisms of TNS with magnetic resonance imaging (MRI). Families who participate will make three clinic visits: eligibility (4-5 hours), pre-TNS (2-3 hours including MRI), and post-TNS (2-3 hours including MRI). Children will receive TNS, applied by the parent, for 8 hours every night while sleeping for 4 weeks. Four weeks after treatment, families will take part in a telephone follow-up, to see whether any improvements made last.

This description comes directly from the study's public registry record.

Talk to the study team

Jennifer M Korthas, BS  ·  (310) 267-2710  ·  ChildBrainStudy@mednet.ucla.edu

Joseph O'Neill, PhD  ·  (310) 825-5709  ·  joneill@mednet.ucla.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of California Los Angeles Semel Institute Division of Child & Adolescent PsychiatryLos Angeles, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06847165