Participant Database for Autism Research Studies

NCT ID: NCT00549731

Last Updated: 2020-09-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

120 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-06-30

Study Completion Date

2023-06-30

Brief Summary

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The purpose of this study is to create a subject database to recruit for current and future studies in research on autism and other neurodevelopmental disabilities.

Detailed Description

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Aim 1: to recruit people interested in research on autism and other neurodevelopmental disabilities

Aim 2: to complete a diagnostic assessment, to confirm the diagnosis of autism spectrum disorder or other developmental disability (e.g., developmental language delay) in our patient population and rule out a diagnosis of autism spectrum disorder and other comorbid conditions in our control group

Aim 3: to maintain subject information in a database, from which we can recruit for our studies

Conditions

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Autism Spectrum Disorder

Study Design

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Observational Model Type

OTHER

Study Time Perspective

OTHER

Study Groups

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Healthy individuals

No intervention

Healthy participants ages 14-32 for a neuroimaging study.

No interventions assigned to this group

Individuals with Autism Spectrum Disorder

No intervention

ASD participants ages 14-32 for a neuroimaging study.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Typically-developing, healthy adolescents and adults (ages 14-32)
* Adolescents and adults with autism spectrum disorder (ages 14-32)

Exclusion Criteria

* Extreme premature birth (\<34 weeks)
* Known genetic disorders related to autism (e.g. Fragile X)
* Recent diagnosis of psychosis (within 6 months)
* Some other psychiatric diagnoses may be excluded following screening (e.g. Tourette's syndrome).
* Metal implants / permanent retainers / hair dyes with metallic components
Minimum Eligible Age

14 Years

Maximum Eligible Age

32 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute of Mental Health (NIMH)

NIH

Sponsor Role collaborator

National Institutes of Health (NIH)

NIH

Sponsor Role collaborator

Massachusetts General Hospital

OTHER

Sponsor Role lead

Responsible Party

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Tal Kenet

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Tal Kenet, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Massachusetts General Hospital

Locations

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Martinos Center of Biomedical Imaging

Charlestown, Massachusetts, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Nicole McGuiggan, Rsch Coord

Role: CONTACT

617-966-9766

Other Identifiers

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5R01MH117998

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2007-P-000062

Identifier Type: -

Identifier Source: org_study_id

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