NCT00956579

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
85

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2013

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 23, 2007

Completed
1.8 years until next milestone

First Posted

Study publicly available on registry

August 11, 2009

Completed
3.8 years until next milestone

Study Start

First participant enrolled

June 1, 2013

Completed
12 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2025

Completed
Last Updated

April 24, 2026

Status Verified

April 1, 2026

Enrollment Period

12 years

First QC Date

October 23, 2007

Last Update Submit

April 21, 2026

Conditions

Keywords

autismautisticsensoryMEGconnectivitybrainMRIlanguagedevelopmentalneurodevelopmentalaspergersasperger'scoherence

Outcome Measures

Primary Outcomes (1)

  • Saliency of Sensory Stimuli in Developmental Disorders

    up to 2 years

Study Arms (2)

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.

Eligibility Criteria

Age14 Years - 32 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Adult/Pediatric

You may qualify if:

  • 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 Informed Consent 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.

You may not qualify if:

  • Any volunteer for whom informed consent 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Martinos Center or Biomedical Imaging

Charlestown, Massachusetts, 02129, United States

Location

MeSH Terms

Conditions

Autism Spectrum DisorderAutistic DisorderLanguage

Condition Hierarchy (Ancestors)

Child Development Disorders, PervasiveNeurodevelopmental DisordersMental DisordersCommunicationBehavior

Study Officials

  • Tal Kenet, Ph.D

    Massachusetts General Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

October 23, 2007

First Posted

August 11, 2009

Study Start

June 1, 2013

Primary Completion

June 1, 2025

Study Completion

June 1, 2025

Last Updated

April 24, 2026

Record last verified: 2026-04

Locations