- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04166591
Study 1 Replication and Extension of Prior Work
Learning New Words From Overhearing in Children With ASD
The goal of this research is to explore abilities to learn word meanings from overheard conversations in children with ASD (and, as a control, typically developing children).
Specific Aim 1 (Experiment 1): Subaim 1a: Identify child characteristics associated with learning from overhearing. In a prior study, the investigators found that 13 children with ASD were able to learn the meanings of novel words that they heard used in a conversation involving two adults. In the current study, the investigators aim to study a larger sample to identify what child characteristics are associated with good learning in an overhearing situation as compared to a situation in which the child is directly taught the new word. Subaim 1b: Assess retention and generalization of words learned from overhearing. The investigators will re-test children on their knowledge of the word meanings after a 10-minute delay to see if they both retain the word meanings and can generalize the new words to new situations.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Massachusetts
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Boston, Massachusetts, United States, 02116
- Emerson College
-
-
New York
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New York, New York, United States, 10012
- New York University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- children with or without a diagnosis of ASD between 18 to 71 months of age
Exclusion Criteria:
- native language is not English
- born premature (< 36 weeks)
- has uncorrected hearing or vision impairments
- has developmental disorders or medical conditions other than ASD that affect language or cognition (excepting psychiatric conditions often comorbid with ASD such as ADHD)
- has a history of photosensitive epileptic seizures
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Addressed
Children participate in an interaction with an experimenter who uses the word to be learned.
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New words are introduced directly to the child by an experimenter.
|
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Experimental: Overheard
Children observe while an experimenter uses the word to be learned in an interaction with another experimenter.
|
New words are introduced with the child as an observer rather directly taught.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Children Who Select the Target Object as Measured by Gaze Preference.
Time Frame: immediately after viewing 3-minute interaction
|
Children are prompted to identify the object that is associated with the target word.
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immediately after viewing 3-minute interaction
|
|
Number of Children Who Select the Target Object as Measured by Gaze Preference.
Time Frame: 5 minutes after viewing interaction
|
Children are prompted to identify the object that is associated with the target word.
|
5 minutes after viewing interaction
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 280521
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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