NCT06497920Recruiting
rTMS to Improve Motor Function in Autism
Modulating Plasticity in the Motor Cortex Using Repetitive Transcranial Magnetic Stimulation to Improve Motor Function in Autism Spectrum Disorder
Source: ClinicalTrials.gov · Last updated 15 Jun 2026
Brief summary (registry, in English)
In the current project, investigators have two main goals: i) Testing whether an excessive plasticity, i.e. hyperplasticity in the motor cortex underlies motor function difficulties in autistic adults, and ii) Using repetitive Transcranial Magnetic Stimulation (rTMS) with autistic adults to examine whether resulting reduced hyperplasticity in the motor cortex will be associated with clinical improvements in the motor function.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 150 (estimated)
- First submitted
- 13 Jun 2024
- Start date
- 24 Apr 2024
- Primary completion date
- 30 Apr 2029
- Lead sponsor
- Centre for Addiction and Mental Health
- Diseases
- Autism
- NCT number
- NCT06497920
What you commit to
- Study type: Interventional
- Planned participants: 150
- From 24 Apr 2024 to the primary completion date, 30 Apr 2029
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- DSM-5 substance use disorder (other than tobacco) within the past 6 months; however, all participants will be asked to refrain from smoking or taking caffeine four hours prior to the iTBS session;
- Metal implants or a pace-maker;
- Prior rTMS treatment;
- In addition, ASD participants will be excluded if they report taking benzodiazepines or anticonvulsants currently.
- NT controls will be excluded if they have:
Other illness
- Current or past history of co-morbid medical condition that may require urgent medical intervention;
- Significant hearing or visual impairment interfering with the ability to read or hear instructions;
- Significantly debilitating medical or neurologic illness (e.g., encephalitis, aneurysms, tumors, central nervous system infections), or acute or unstable medical illnesses as determined by project physician (e.g., uncontrolled diabetes);
- A known diagnosis of Pervasive Developmental Disorder or ASD among any biologically related family members.
Other
- ASD or control participants will be excluded if they experience/have:
- Current pregnancy;
- Presence of psychopathology other than specific phobia, as screened by Personality Assessment Inventory and;
Who the study is looking for
- ASD or control participants must meet all of the inclusion criteria to eligible for this study:
- Aged between 18 and 40 years old. 40 years is chosen as the cut-off because of the report of high rates of Parkinsonism in autistic adults \> 39years;
- Have IQ\>70;
- Are able to read, write and communicate effectively in English;
- Are able to provide informed consent. We will recruit only intellectually-able autistic adults. The intellectual ability will be determined using WASI-II. The ability to provide consent will be determined using clinical assessment.
- Have no prior history of seizure;
- Must sign and date the informed consent form;
- Stated willingness to comply with all study procedures;
- Agreement to adhere to Lifestyle Considerations, that is: refrain from consumption of alcohol, tobacco, marijuana, or caffeine on the day of study visits.
- All ASD participants:
- Will have DSM-5 diagnosis of ASD without intellectual disability, confirmed by clinical assessment and the Autism Diagnostic Observation Schedule - 2 (ADOS-2);
- Will have significant motor function difficulties defined as a standard composite score \<40 (i.e., \>1 standard deviation below the mean) on either fine or gross motor composite scores of the Bruininks-Oseretsky Test of Motor Proficiency, Second Edition or BOT-2;
- Are clinically stable as determined by clinical assessment, with no medication changes over the past 4 weeks. Given the high variability of handedness in ASD, we will include participants with left, right or mixed handedness.
Age in the registry: 18 years to 40 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Center for addiction and Mental Health (CAMH) Coordinator of this site? Confirm its status | Toronto | Canada | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.