Babies' Expectations About Racial Interactions (BEARI)

April 22, 2024 updated by: Hyesung Grace Hwang, University of Chicago
This study will examine whether infants view race as an inductively useful social cue to predict third-party social relationships.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Based on findings that infants expect more affiliation between same language speakers than different language speakers (i.e., infants will look longer at affiliation between different language speakers than same language speakers), this study will assess whether infants' expectations about intra- and inter-racial interactions will also follow the same pattern as language. After informed consent, participants who meet the eligibility requirements will be randomized into one of the 3 conditions: Watching (1) two White adults affiliating and disengaging, (2) two Black adults affiliating and disengaging, and (3) one White and one Black adults affiliating and disengaging.

Study Type

Interventional

Enrollment (Actual)

128

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Illinois
      • Chicago, Illinois, United States, 60637
        • Infant Learning and Development Laboratory at University of Chicago

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

8 months to 1 year (Child)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • full term (at least 37 weeks at birth)
  • no known developmental delays

Exclusion Criteria:

  • not full term (less than 37 weeks at birth)
  • known developmental delays

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

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: White-White
Infants will first view 4 familiarization trials, in which the two adults each take turns waving and saying a short sentence. Each trial will last 10.5s. Which adult speaks first and which side she appears on will be counterbalanced. These familiarization trials will ensure infants encode each person separately. Then infants will watch 6 test trials (3 affiliation and 3 disengagement). The test trials will alternate, and the order will be counterbalanced across infants. In affiliation trials, the two adults will say "hello" and wave, whereas in the disengagement trials, the two adults will say "hmph", and turn away from each other. Both affiliation and disengagement will have the same length (3s), with actors maintaining the same distance from each other throughout the video. The procedure will be identical for all arms except in "White-White" arm, the two adults infants see will be two White adults.
This is a basic science experiment to test whether infants' looking time to video stimuli differ according to the race of the individuals shown.
Experimental: Black-Black
The procedure is identical to the "White-White" arm except the two adults infants see will be two Black adults.
This is a basic science experiment to test whether infants' looking time to video stimuli differ according to the race of the individuals shown.
Experimental: Black-White
The procedure is identical to the "White-White" arm except the two adults infants see will be one White and one Black adult.
This is a basic science experiment to test whether infants' looking time to video stimuli differ according to the race of the individuals shown.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Participants' Average Time Spent Looking at Stimuli According to Condition
Time Frame: After the infants completed the study (which lasted about 10 minutes), two coders viewed the video recording of the session to measure infants' looking at the affiliation and disengagement stimuli.
Infants' looking time to affiliation vs. disengagement stimuli was measured by two coders blind to the condition that infants were assigned to. Then, the values from each coders were compared and if there was disagreement, after discussion one value was selected. Thus, the reported outcome is the single value that both coders produced or agreed upon values from the two coders.
After the infants completed the study (which lasted about 10 minutes), two coders viewed the video recording of the session to measure infants' looking at the affiliation and disengagement stimuli.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Hyesung G Hwang, PhD, University of Chicago

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)

September 1, 2021

Primary Completion (Actual)

March 27, 2022

Study Completion (Actual)

March 27, 2022

Study Registration Dates

First Submitted

April 1, 2022

First Submitted That Met QC Criteria

April 8, 2022

First Posted (Actual)

April 12, 2022

Study Record Updates

Last Update Posted (Actual)

April 24, 2024

Last Update Submitted That Met QC Criteria

April 22, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • IRB18-1257

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All data that was used in analysis will be shared publicly on Open Science Framework repository.

IPD Sharing Time Frame

Once data has been collected and cleaned it will be available to the public indefinitely.

IPD Sharing Access Criteria

Anonymized individual participant data will be publicly available for anyone to access on Open Science Framework repository.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • 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

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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