- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06550245
Babies' Brain Responses to Strangers
March 3, 2025 updated by: University of California Santa Cruz
The Malleability of Social Group Understanding in Infancy and Early Childhood
Researchers at the Diversity in Development Lab at UC Santa Cruz are investigating how babies' brain activities respond to people from familiar and unfamiliar racial backgrounds.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The goal of this observational study is to learn how infants' brain activities, as captured by EEG, differ for familiar or unfamiliar racial group in typically developing infants. The main questions of the study are:
- Will infants show greater event-related desynchronization (i.e., more motor system activation), frontal theta synchronization (i.e., more attention), and more positive frontal alpha asymmetry (i.e., more approach motivation) to familiar than unfamiliar racial group?
- How does infants' exposure to racial diversity in their social network and neighborhoods relate to these EEG activities? Participants will visit a laboratory at the UC Santa Cruz campus for this study. Infants will put an EEG cap on and watch about 15 minutes of videos, in which people from different racial backgrounds do different actions (e.g., grabbing an object, saying hi and approaching closer, and playing peek-a-boo). Caregivers will be asked to fill out a demographic form and a social network survey.
Study Type
Observational
Enrollment (Estimated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Seaera Juarez, BA
- Phone Number: (831) 264-8155
- Email: did.lab@ucsc.edu
Study Locations
-
-
California
-
Santa Cruz, California, United States, 95064
- Recruiting
- Social Science 2 Building
-
Contact:
- Seaera Juarez, BA
- Phone Number: (831) 264-8155
- Email: did.lab@ucsc.edu
-
Contact:
- Hyesung Hwang, PhD
-
Contact:
- Samantha Fong, BA
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
community sample from the larger Santa Cruz area
Description
Inclusion Criteria:
- typically developing
- age 7 to 12 months
- at least 37 weeks gestation
Exclusion Criteria:
- any known developmental delays
- less than 37 weeks gestation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mu event related desynchronization
Time Frame: Through study completion, an average of 10 years.
|
EEG oscillation in alpha power over central regions
|
Through study completion, an average of 10 years.
|
|
Frontal theta synchronization
Time Frame: Through study completion, an average of 10 years.
|
EEG oscillation in theta power over frontal regions
|
Through study completion, an average of 10 years.
|
|
Frontal alpha asymmetry
Time Frame: Through study completion, an average of 10 years.
|
left and right hemispheric difference in EEG oscillation in alpha power in the frontal regions
|
Through study completion, an average of 10 years.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Hyesung Hwang, PhD, University of California Santa Cruz
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 23, 2024
Primary Completion (Estimated)
October 1, 2025
Study Completion (Estimated)
October 1, 2025
Study Registration Dates
First Submitted
August 6, 2024
First Submitted That Met QC Criteria
August 9, 2024
First Posted (Actual)
August 13, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 3, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- HS-FY2023-23 Study 2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
All IPD that are anonymized and underlie results in a publication will be shared through open science framework (OSF)
IPD Sharing Time Frame
The data will become available within a period of 10 years.
Anonymized aggregate data will be available indefinitely.
No identifiable data will be shared.
IPD Sharing Access Criteria
All anonymized data will be available once study has been published and will be available indefinitely.
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ANALYTIC_CODE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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