Elsevier

Brain Stimulation

Volume 4, Issue 4, October 2011, Pages 275-280
Brain Stimulation

Original Article
Tolerability of transcranial direct current stimulation in childhood-onset schizophrenia

https://doi.org/10.1016/j.brs.2011.01.001Get rights and content

Background

In recent years, transcranial direct current stimulation (tDCS) has been used to study and treat many neuropsychiatric conditions. However, information regarding its tolerability in the pediatric population is lacking.

Objective

This study aims to investigate the tolerability aspects of tDCS in the childhood-onset schizophrenia (COS) population.

Methods

Twelve participants with COS completed this inpatient study. Participants were assigned to one of two groups: bilateral anodal dorsolateral prefrontal cortex (DLPFC) stimulation (n = 8) or bilateral cathodal superior temporal gyrus (STG) stimulation (n = 5). Patients received either 2 mA of active treatment or sham treatment (with possibility of open active treatment) for 20 minutes, for a total of 10 sessions (2 weeks).

Results

tDCS was well tolerated in the COS population with no serious adverse events occurring during the study.

Conclusions

This is the first study to demonstrate that a 20-minute duration of 2 mA of bilateral anodal and bilateral cathodal DC polarization to the DLPFC and STG was well tolerated in a pediatric population.

Section snippets

Participants

Twelve children/adolescents with COS completed the inpatient study; the sample included five boys and seven girls, ages (10-17 years). Participants had no history of significant neurologic illness. The guardians of participants provided written informed consent and COS subjects provided written assent before entering the study. This study was approved by the National Institutes of Health Neuroscience Institutional Review Board (IRB).

Study design

Participants were eligible for one of two study options.

Results

Of the 15 patients initially enrolled, two withdrew before randomization. One subject was randomly assigned to active temporal treatment but withdrew after 1 week of treatment because of a family issue that required her to return home. The remaining participants (five males, seven females) completed the entire study. Table 1 shows subject demographic and central nervous system (CNS) medication data. No subject asked to stop the study, required a change in CNS medications, or needed medical

Discussion

This pilot study, based on analyses of 125 tDCS sessions, is the first to demonstrate that tDCS is easily tolerated in adolescents. The most frequent side effect during active treatment was tingling (n = 6, 46.1%) or itching (n = 7, 53.8%) at the electrode sites. Several patients complained of fatigue (n = 4, 30.7%). However, this could be related to medication regimens that frequently include the atypical antipsychotic clozapine. As noted previously, no subjects asked to stop the study because

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