Depression Clinical Trial
Official title:
Transcranial Magnetic Stimulation for Adults With Autism Spectrum Disorder and Depression
The goal of this proposal is to investigate whether a standard rTMS protocol for depression, including multiple sessions applied to left dorsolateral prefrontal cortex (DLPFC) results in reduction of depressive symptoms for adult patients with ASD and MDD (Aim 1). The secondary goal is to investigate and whether there is any beneficial reduction in the core symptoms of autism (Aim 2).
Aim 1. Determine the safety and therapeutic efficacy of left-sided DLPFC high frequency rTMS
on MDD symptoms in patients with ASD: The investigators hypothesize that patients receiving
the rTMS will tolerate the treatment course without difficulty and have clinically
significant reduction of depressive symptoms after receiving all 25 sessions, as compared
with their symptom burden prior to initiating TMS. Depression symptom data will be collected
as pre- and post-TMS scores on Hamilton Depression Rating Scale (HAM-D). Depression scores
will also be monitored periodically during course of TMS with Patient Health Questionnaires
(PHQ-9).
Exploratory sub-aim - Monitoring for durability of response: The investigators hypothesize
that subjects receiving rTMS will demonstrate durability of response in their depression
symptom reduction, as measured by HAM-D scores at 1 month and 3 months post-TMS.
Aim 2. Determine the effect of left DLPFC rTMS on core symptoms of ASD: The investigators
hypothesize that subjects will experience reduction in core symptoms of ASD after completing
all 25 sessions, as compared with their symptom burden prior to initiating treatment. For
social and communication deficits, informant and/or self-report evaluations will be made pre-
and post-TMS with the Social Responsiveness Scale (SRS), the Ritvo Autism Aspergers
Diagnostic Scale-Revised (RAADS-R) and the Aberrant Behavior Checklist (ABC). Repetitive and
restricted behavior will be evaluated using the Repetitive Behavior Scale-Revised (RBS-R),
the ABC, and RAADS.
Exploratory sub-aim: Determine if there are changes to functional brain connectivity during
face and object processing tasks via functional MRI imaging in patients with Autism who
receive rTMS: The study investigators hypothesize that there will be altered brain
connectivity evident in patients' baseline fMRI during cognitive processing tasks prior to
TMS reflected as both hyper- and hypo-connectivity, and that there will be some level of
normalization of these patterns in fMRI after completion of TMS series, particularly in the
prefrontal cortex.
Exploratory sub-aim - Monitoring for durability of response: The study investigators
hypothesize that subjects receiving rTMS will exhibit durability of response in their ASD
symptom reduction, as measured by ABC, SRS, RAADS, AND RBR scores at 1 month and 3 months
post-TMS.
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