Transcranial Magnetic Stimulation (TMS) to Treat Depression in Autism Spectrum Disorder

Recruiting now · Not applicable · Has a placebo group

Conditions studied: Autism Spectrum Disorder

In brief

This study will assess clinical and behavioral measures along with electroencephalogram (EEG), event-related potentials (ERPS), and eye-tracking (ET) prior to and following a single intermittent Theta Burst Stimulation (iTBS) session to provide preliminary insight into the potential of TMS as an intervention for depression in individuals with Autism Spectrum Disorder (ASD).

Key facts

Study ID

NCT06142955

Run by

Yale University

People needed

60

Starts

2024-04-30

Expected to finish

2027-02-01

Last updated by the study team

2026-07-16

Who can join

Age: 18 and older, up to 40. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Individuals from Yale University and the surrounding community who are between the ages of 18 and 40 years old with or without a diagnosis of depression. Or individuals between the ages of 18 and 40 years old with a diagnosis of autism spectrum disorder, autistic disorder, PDD NOS, or Asperger syndrome with or without a diagnosis of depression.
• A depression score on the HDRS-17 of at least 20 will be used as a cut-off for depression.
• Participants are unmedicated or on stable medication treatment for at least two weeks.
• Willingness and ability to participate in an EEG and eye-tracking procedure.
• Provision of signed and dated informed consent.

You may not qualify if…

• Participants reporting significant head trauma or serious brain illness.
• Participants unable to provide signed informed consent.
• Participants with major psychiatric illness that would preclude completion of study measures. Participants with diagnosis of a psychotic or bipolar illness with be excluded.
• Participants with a history of serious medical illness, stroke, seizures, epileptiform EEG abnormalities, or family history of epilepsy.
• Participants taking prescription medications that may affect cognitive processes under study.
• Participants taking any medication that may increase their risk of seizures.
• Participants who have taken alcohol or recreational drugs within the preceding 24 hours prior to the scheduled study visit as determined by the urine toxicology test.
• Participants with a history of substance or alcohol abuse or dependence in the past 6 months.
• Participants with a significant risk of suicide or a h/o suicide attempt in the last 6 months. Participants with active suicidal ideation will be excluded from the study.
• Females of known/suspected pregnancy or who test positive on a pregnancy test.
• Participants with a history of metalworking or injury by shrapnel or metallic objects.
• Participants with a history of prior TMS therapy or use of an investigational drug within 12 weeks of visit
• Participants with an IQ below 80 (as confirmed by the WASI, Wechsler Abbreviated Scale of Intelligence)

Where it is running

• Yale Psychiatric Hospital — New Haven, Connecticut, United States (enrolling)

Full record on ClinicalTrials.gov

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