ADHD Clinical Trial
Official title:
The Efficacy of Cathodal Transcranial Direct Current Stimulation in Children and Adolescents With Attention-deficit Hyperactivity Disorder
The purpose of this study is to investigate the effectiveness of five sessions of cathodal tDCS over the left DLPFC on inhibitory control/response inhibition in children and adolescents with ADHD. Investigators hypothesize that multiple sessions of cathodal tDCS will induce a greater and long-term effect on inhibitory response in children and adolescents with ADHD.
Attention-deficit hyperactivity disorder (ADHD) is one of neural development disorder that
characterized by a persistent pattern of inattention, impulsivity and hyperactivity. This
disorder begins in childhood and often lasts into adulthood. Rates of ADHD diagnosis have
been rising in recent years, a prevalence estimates from 3-7% of childhood worldwide. A
recent national prevalence shows that 8.1% of Thai primary school-age children are affected
by ADHD . Pharmacological treatment used in ADHD is well-established, however, each patient
responds to medication differently and treatment in some of them are limited by side effect
and abuse of medication.
In the last decade, transcranial direct current stimulation (tDCS) has received a surge of
interest in clinical research since it could modulate cortical excitability and induce
plasticity in human brain. The device sends a constant low direct current (e.g. 1-2 mA)
delivered to the area of interest through the electrodes. This induces shifts in neuronal
resting membrane potential changing cortical excitability. Based on the polarity-specific
effects, anodal tDCS increases cortical excitability and cathodal tDCS decreases cortical
excitability. To change the cortical excitability, tDCS differs from other brain stimulation
techniques such as transcranial magnetic stimulation (TMS) in that it does not cause action
potentials in cortical neurons, but rather induces shifts in neuronal resting membrane
potential. This is considered to induce a lesser or no risk of a seizure. Given its
advantages such as painlessness, safety, easiness to use, and low-cost, a number of tDCS
studies has been increasing in the last decade particularly in motor rehabilitation and
neuropsychiatric disorders such as depression, autism and schizophrenia with a positive and
safety reports in adult and pediatric populations. Possible after-effect of tDCS has been
also reported in motor and psychological disorders that opens a way to use tDCS as a
therapeutic tool.
The most accepted theory of neural basis of ADHD is deficient of inhibitory control resulting
in executive dysfunction. Inhibitory control or response inhibition is key feature of
self-control and can be defined as ability to inhibit prepotent actions. Several evidences
reveal a physiological association between the prefrontal cortex and its subcortical
connection with the pathophysiology of ADHD. Neuroimaging studies demonstrate that regions of
the right dorso-lateral prefrontal cortex (DLPFC) play a role in the inhibition of motor
response. During preforming an inhibitory task that is usually used to evaluate the
efficiency of response inhibition such as stop-signal and go/no-go tasks, this area become
active in healthy individual, while in ADHD showed hypo-activation compared to control.
Evidences showed that the task performance in stop-signal and go/no-go tasks can be
influenced by tDCS application to the DLPFC in healthy subjects. It was recently reported
that a single session of cathodal tDCS, using a single session of 1.5 mA for 15 minutes over
the left DLPFC improved their ability to inhibit themselves by do not response to no-go
stimulus during go/no-go tasks compared to anodal and sham conditions in adolescents with
ADHD. It was postulated that the inter-hemispheric inhibition (IHI) between two regions (left
and right DLPFC) might play a role in this finding. Based on the possibility that cathodal
stimulation decreases excitability and thus IHI drive from the left DLPFC is decreased,
facilitating activity of the right DLPFC where is involved in inhibition of motor response as
demonstrated by neuroimaging studies. Using a single session of oscillatory tDCS during early
sleep, memory consolidation and reaction times in a go/no-go task were improved on the next
day in children with ADHD. This is an argument to explore its possible therapeutic effect in
long-term use. Five tDCS sessions for five consecutive days was reported to be safe and
improves aspect of attention in children and adolescents with ADHD, however, its after-effect
in this population is unknown. In patients with depressive disorder, multiple sessions of
tDCS over the left DLPFC for five or ten days has been demonstrated to decrease depressive
symptoms and lasted for a month. It was reported in patient with depressive disorder that
after five days of tDCS sessions on alternative day did not show an improvement, positive
results was observed after 10 days. This suggests that a longer observation period is
probably required to detect a true tDCS effect.
The use of electrophysiological techniques, especially of event-related potentials (ERP)
measured by means of electroencephalography (EEG) allows for analysis of neural change
accompanying inhibitory process in the brain. Two ERP components, the no-go N2 and P3 that
are the most commonly studied in go/no-go tasks have been linked to response conflict and
response inhibition. Studies have reported lower N2 and P3 amplitudes during go/no-go tasks
in children and adolescents with ADHD.
To expand current information on tDCS as an emerging treatment for ADHD patients, in this
study, investigators will investigate the effectiveness of multiple sessions of cathodal tDCS
over the left DLPFC on inhibitory control in children and adolescents with ADHD. tDCS
(cathodal/sham) will be applied every day for five consecutive days. Behavioral and
neurophysiological parameters using an inhibitory task (go/no-go tasks) and the no-go N2 and
P3 ERP components will be measured before tDCS, immediately after 5 sessions of tDCS, one
week later, and one month after treatment onset.
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