Improving Social Interaction for Adolescents With Autism During the Transition to Adulthood
NCT ID: NCT03785327
Last Updated: 2022-12-23
Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
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TERMINATED
NA
78 participants
INTERVENTIONAL
2019-01-18
2021-09-22
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TD participants were assigned to receive or not receive a training session.
BASIC_SCIENCE
SINGLE
Study Groups
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Active anodal tDCS
Active anodal tDCS followed by behavioral testing Intervention: Device: active anodal tDCS
tDCS
Participants either complete active and sham tDCS sessions one week apart or an autism training program.
Sham tDCS
Sham tDCS followed by behavioral testing Intervention: Device: sham tDCS
tDCS
Participants either complete active and sham tDCS sessions one week apart or an autism training program.
Autism Training Program
Training program designed to increase autism understanding followed by behavioral testing Intervention:Training program
Autism Training
Autism Information Presentation developed by Dr. Grace Iarocci's Autism \& Developmental Disorders Lab at Simon Fraser University
Social interaction without intervention
Control condition: Behavioral testing without an intervention component
No interventions assigned to this group
Interventions
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tDCS
Participants either complete active and sham tDCS sessions one week apart or an autism training program.
Autism Training
Autism Information Presentation developed by Dr. Grace Iarocci's Autism \& Developmental Disorders Lab at Simon Fraser University
Eligibility Criteria
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Inclusion Criteria
* DSM-IV-TR or DSM-5 diagnosis of an Autism Spectrum Disorder
* IQ\>70
Exclusion Criteria
* Presence or history of medical, cardiac, or neurological disorders that may affect brain function (e.g., cardiac disease, endocrine disorders, renal disease, pulmonary disease, history of seizures or head trauma with unconsciousness for a period of 15 minutes or greater or CNS tumors)
* Presence of sensory limitation including visual (e.g., blindness, glaucoma, vision uncorrectable to 20/40) or hearing (e.g. hearing loss) impairments that interfere with assessment
* Not proficient in English
* Presence of substance abuse in the past one month
* Presence of substance dependence not in remission for the past six months
* Contraindications for tDCS (e.g., pregnancy or implanted devices such as pace maker)
18 Years
21 Years
MALE
Yes
Sponsors
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The University of Texas at Dallas
OTHER
Responsible Party
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Noah Sasson
Associate Professor
Locations
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The University of Texas at Dallas
Richardson, Texas, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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1806799
Identifier Type: -
Identifier Source: org_study_id