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CompletedNCT00956579Updated Apr 24, 2026

Sensory and Connectivity Abnormalities in Autism Spectrum Disorders

An observational study in Autism Spectrum Disorder, sponsored by Massachusetts General Hospital. Completed at 1 site in United States. Open to participants aged 14 Years to 32 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-24.

Primary conditionAutistic DisorderRegistry: Autism Spectrum DisorderReclassifiedWhy we changed it
Registry
Autism Spectrum Disorder — the first condition term the registry derived for this study.
ClinicalTrials.gg
Autistic Disorder
Why
  1. The study's listed conditions name Autistic Disorder, a narrower term within Autism Spectrum Disorder.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Massachusetts General Hospital · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
85
Ages
14 Years to 32 Years
Sex
All
01

Study summary

Study the neural substrates of autism spectrum disorders using neuroimaging methods such as MEG/EEG/MRI.

Read the detailed description

(NOTE: we are currently recruiting individuals between the ages of 14 and 32, either typically developing or with an autism spectrum disorder.)

To study how sensory information is processed by the brain, we primarily use an instrument called MEG (MagnetoEncephaloGraphy), which measures the magnetic brainwaves emitted by our brains. The device does not have any output (i.e., there is no magnetic field); it only measures the waves produced in the brain.

We measure those waves as the participants in the study listen to, view, or otherwise experience simple, non painful, stimuli. For instance, participants may listen to words while sitting in the MEG room, and watching a movie with the sound turned off.

We then combine this information with pictures of the brain from MRI (Magnetic Resonance Imaging - when available), to get an idea about both the anatomy and the function of the brain, so that we can study how the brains of populations with autism spectrum disorders or language disorders may be different from those of typically developing populations.

02

Conditions studied

  • Autism Spectrum Disorder

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Keywords

  • autism
  • autistic
  • sensory
  • MEG
  • connectivity
  • brain
  • MRI
  • language
  • developmental
  • neurodevelopmental
  • aspergers
  • asperger's
  • coherence
03

In context

Autistic Disorder Reclassified

1,030 studies on the registry are indexed under Autistic Disorder; 266 are open to participants now.

This study's enrollment of 85 is below the median of 101 across 189 observational studies indexed under Autistic Disorder.

Browse Autistic Disorder studies →

Lead sponsor

Massachusetts General Hospital is the lead sponsor of 2,586 studies on the registry; 447 are open to participants now.

Of its 222 completed or terminated interventional studies of FDA-regulated products, 168 (76%) have results posted.

Compared within Autistic Disorder, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Autism Spectrum Disorder. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
14 Years to 32 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Adult/Pediatric

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • All of the following criteria must be met by all participants:

    • The participant or the participant's legal guardian is able to understand and is willing to comply with the requirements of the study
    • The participant meets the age requirements (14-32 years old)
    • The participant or legal guardian has signed an Form specific to this study, and is able to understand the consent form.
    • The participant must have English as their first language.
    • The participant must have a non-verbal IQ > 70
  • For the ASD/language disorder group only:

    • Autism Spectrum Disorder: Participants must meet criteria for Autism Spectrum Disorder on the ADOS.

Exclusion criteria

Exclusion Criteria:

  • The following exclusion criteria apply to both control and autism groups:

    • Any volunteer for whom cannot be obtained
    • Volunteers with metal braces, extensive dental work involving metals, implanted electromagnetically activated medical equipment (cardiac pacemakers, neurostimulators, functioning infusion pumps), all of which would interfere with the MEG signal, will be excluded from the MEG portion of the study
    • Volunteers with any medically diagnosed sensory loss
    • Volunteers with a known genetic disorder (e.g. Tourette's syndrome, etc), or other medical condition affecting the brain, such as progressive encephalopathy as well as those who are on high doses of multiple anti-seizure medications and have frequent, uncontrolled seizures
    • Asphyxia at birth or any other time, premature birth (Fewer than 34 weeks gestation)
  • For the control group only:

    • Volunteers diagnosed with a mental condition such as depression, anxiety, aggression, hyperactivity, attention deficit disorder (with or without hyperactivity).
    • Volunteers who score below the autism spectrum cut-off (in the normal range) on the ADOS and SCQ
    • Volunteers on any sort of neuro-psychopharmacological treatment (including antidepressants, stimulants, antipsychotics, anticonvulsants, benzodiazepines).
  • For the autism group only:

    • Children or adults not meeting criteria for autism spectrum disorder
    • Volunteers with co-morbid disorders such as tuberous sclerosis or fragile X.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Other
Time perspective
Other
Enrollment
85 participants (actual)

Groups and cohorts

  • Healthy individuals

    No intervention Healthy participants ages 14-32 for a neuroimaging study

  • Individuals with Autism Spectrum Disorder

    No intervention ASD participants ages 14-32 for a neuroimaging study.

06

What researchers measure

Primary outcomes

  1. Saliency of Sensory Stimuli in Developmental Disorders

    Time frame: up to 2 years

07

Study locations

1 site
  • Martinos Center or Biomedical Imaging
    Charlestown, Massachusetts 02129, United States
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References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00956579
Responsible party
Tal Kenet (Associate Professor, Massachusetts General Hospital) — Principal investigator
First posted
Aug 11, 2009
Start date
Jun 2013
Primary completion
Jun 2025
Completion
Jun 2025
Last update
Apr 24, 2026

Study contacts

Tal Kenet, Ph.D
principal investigator · Massachusetts General Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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