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

Yale University · with American Academy of Child Adolescent Psychiatry. · NCT06142955

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18–40 · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
60
US sites recruiting
1
Study start
April 30, 2024
Record last updated
July 16, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

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).

Being studied: MAGSTIM Rapid2 TMS system

Conditions: Autism Spectrum Disorder

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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)

Recruiting US locations

Study contacts (from the official record)

  • Sherab Tsheringla, MD · 2032158046 · sherab.tsheringla@yale.edu
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Transcranial Magnetic Stimulation (TMS) to Treat Depression in… (NCT06142955) | Bored Studies