rTMS for Executive Function Deficits in Autism Spectrum Disorder
Study Details
Study Description
Brief Summary
In this study, the investigators will be examining the effects of repetitive transcranial magnetic stimulation (rTMS) on executive function deficits in individuals with autism spectrum disorder. Half of the participants will be chosen by chance to receive active rTMS stimulation while half will be chosen by chance to receive sham rTMS. Sham rTMS will feel the same as active rTMS only there will be no direct brain stimulation. This is necessary to ensure that active rTMS is efficacious in the enhancement of executive function in individuals with autism spectrum disorder. Based on results from a recently published pilot study, the investigators propose that active rTMS treatment will result in a significant improvement in working memory performance compared to sham rTMS treatment.
Condition or Disease | Intervention/Treatment | Phase |
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N/A |
Detailed Description
This study is a randomized, double blind, sham controlled study to evaluate the efficacy of repetitive transcranial magnetic stimulation (rTMS) as a treatment for executive function deficits in individuals with autism spectrum disorder between 16 and 25 years of age. The study duration is approximately 3 months, with the rTMS sessions lasting for 4 weeks, 5 times a week, for about 1 hour each. Several scales will be used to assess for symptom severity and adaptive functioning. Cognition will be assessed using a validated battery.
This study also involves a type of brain imaging known as magnetic resonance imaging (MRI) at the beginning and at the end of the 4 weeks of daily rTMS to better understand the effects of rTMS on brain structure and function. Investigators will measure the size and connections of different parts of the brain to assess brain structure and blood flow while participants are completing some basic tasks to asses brain function.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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Active Comparator: Active rTMS Active treatment will be delivered at an intensity that is 90% of the resting motor threshold (RMT). Stimulation will be delivered at 20 Hz with 25 simulation trains of 30 stimuli each (i.e., 750 stimuli) and an intertrain interval of 30 sec. Treatment will be applied in sequential order bilaterally to the left and right dorsolateral prefrontal cortex (DLPFC). The order of bilateral stimulation (i.e. right then left or left than right) will be held constant for all 20 treatments. Intervention: Device: Repetitive Transcranial Magnetic Stimulation |
Device: Repetitive Transcranial Magnetic Stimulation
rTMS is a non-invasive procedure involving the use of magnetic fields to stimulate nerve cells.
Other Names:
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Sham Comparator: Sham rTMS Sham stimulation will be delivered using the same stimulation parameters and at the site of active treatment, but with only the side-edge resting on the scalp. The coil will be angled 45 degrees way from the skull in a single-wing tilt position. This method produces sound and some somatic sensation (e.g. contraction of scalp muscles) similar to those of active stimulation, but with minimal direct brain effects. Intervention: Device: Repetitive Transcranial Magnetic Stimulation |
Device: Repetitive Transcranial Magnetic Stimulation
rTMS is a non-invasive procedure involving the use of magnetic fields to stimulate nerve cells.
Other Names:
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Outcome Measures
Primary Outcome Measures
- Change in accuracy on the Cambridge Neuropsychological Test Automated Battery (CANTAB) Spatial Working Memory Task [Baseline; Post rTMS (4 weeks after baseline); One month follow up ( 4 weeks after post rTMS); 6 month follow up (post rTMS); One year follow up (post rTMS)]
Specifically the investigators will evaluate the changes in spatial working memory scores before and after rTMS treatment.
Secondary Outcome Measures
- Change in scores on Behaviour Rating Inventory of Executive Functioning (A) (BRIEF) (A) [Baseline; Post rTMS (4 weeks after baseline); One month follow up ( 4 weeks after post rTMS); 6 month follow up (post rTMS); One year follow up (post rTMS)]
Specifically the investigators will evaluate the changes in executive function (EF) scores before and after rTMS treatment.
Eligibility Criteria
Criteria
Inclusion Criteria Autism Spectrum Disorder (ASD):
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Are fluent in the English language
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Have a diagnosis of high functioning ASD (HF-ASD) (i.e., are verbal with an Intelligence Quotient (IQ) ≥ 70)
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Are competent to consent based on the subjects' ability to provide a spontaneous narrative description of the key elements of the study
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Are clinically stable as determined by their treating physician, with no medication changes over the past 4 weeks
Exclusion Criteria (ASD):
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Have a history of substance abuse or dependence in the last 6 months or have a positive urine toxicology screen
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Have a concomitant major medical or neurologic illness
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Have had a seizure in the past, or have a first-degree relative with epilepsy
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Have an abnormal clinical EEG
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Are pregnant or likely to get pregnant during the next 4 weeks
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Are clinically unstable
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Are on benzodiazepines or anticonvulsant medication
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Have a history of rTMS treatment.
Inclusion Criteria (Healthy Controls):
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Are fluent in the English language
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Competent to consent
Exclusion Criteria (Healthy Controls):
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Have a history of substance abuse or dependence in the last 6 months or have a positive urine toxicology screen
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Have a major medical or neurologic illness
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Have a diagnosed learning disorder or impaired academic or adaptive functioning on history
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Are pregnant
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Have an IQ < 80
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Have a psychiatric diagnosis on diagnostic interview assessments.
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | Centre for Addictions and Mental Health | Toronto | Ontario | Canada | M6J 1H4 |
Sponsors and Collaborators
- Centre for Addiction and Mental Health
- Academic Health Science Centres
Investigators
- Principal Investigator: Stephanie H Ameis, M.D., M.S.C, Centre for Addiction and Mental Health
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- 119/2013