ClinicalTrials.gg
CompletedNCT05807061Updated Jun 12, 2026

Reducing Children's Racial Biases Via a Parent-Led Intervention

An interventional study of EmBARK and Popular guidance in Racial Bias, sponsored by University of Wisconsin, Madison. Completed at 1 site in United States. Open to participants aged 5 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-12.

Sponsored by University of Wisconsin, Madison · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
704
Allocation
Randomized
Ages
5 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to test a parent-led program for reducing children's racial biases in White families. The main question it aims to answer is: With training, can parents effectively address their children's racial biases? Parent will receive training and tools for addressing their children's racial biases. Researchers will study effects on both parents' and children's racial biases.

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Conditions studied

  • Racial Bias

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03

In context

Racism

47 studies on the registry are indexed under Racism; 8 are open to participants now.

This study's enrollment of 704 is above the median of 106 across 34 interventional studies indexed under Racism.

Browse Racism studies →

Lead sponsor

University of Wisconsin, Madison is the lead sponsor of 1,188 studies on the registry; 181 are open to participants now.

Of its 157 completed or terminated interventional studies of FDA-regulated products, 118 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
5 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • The child is 5.00 to 7.99 years of age
  • The child participant and their parent are both non-Hispanic White

Exclusion criteria

Exclusion criteria are:

  • Non-proficiency in English on the part of the parent or the child
  • The parent is \<18 years old
  • The child or parent identifies with another racial/ethnic identity in addition to White
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
704 participants (actual)

Study arms

  • Experimental
    EmBARK

    Parents receive a narrated training program about children's racial biases and read books that are focused on race with their children.

    Behavioral: EmBARK

  • Experimental
    Popular guidance

    Parents receive interesting popular press articles about children's racial biases and read books that are focused on race with their children.

    Behavioral: Popular guidance

  • Experimental
    Practice first

    Parents practice discussing books about animals with their children first, and then receive a narrated training program about children's racial biases and read books that are focused on race with their children.

    Behavioral: Practice first

Interventions

  • BehavioralEmBARK

    The narrated training teaches parents about children's biases and introduces multiple strategies for addressing children's biases. Families receive children's books to help practice the strategies.

  • BehavioralPopular guidance

    The popular press articles teach parents about children's biases and guide parents about how to talk to children about race. Families receive children's books focused on race to help practice talking about race.

  • BehavioralPractice first

    Animal books are provided to parents to help them practice talking to their children when reading books. Then, families receive a training program about race as well as children's books about race.

06

What researchers measure

Primary outcomes

  1. Change in Likelihood of Child's Racial Bias

    Total possible range of scores from 1-5. Higher scores mean higher likelihood of bias.

    Time frame: Baseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

  2. Change in Concern about Children's Racial Bias

    Total possible range of scores from 1-10. Higher scores indicate more concern.

    Time frame: Baseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

  3. Change in Concern about Own Child's Bias

    Total possible range of scores from 1-10. Higher scores indicate more concern.

    Time frame: Baseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

  4. Change in Motivation to Regulate Children's Bias

    Total possible range of scores from 1-10. Higher scores mean greater motivation.

    Time frame: Baseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

  5. Change in Self-Efficacy for Addressing Children's Bias

    Total possible range of scores from 1-7. Higher scores mean greater self-efficacy.

    Time frame: Baseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

  6. Change in Intergroup Liking

    Total possible range of scores is -12 to +12. Higher scores reflect more ingroup liking.

    Time frame: Baseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

  7. Change in Diversity Preference

    Total possible range of scores is 0 to 4. Higher scores mean a greater preference for homogeneous groups.

    Time frame: Baseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

  8. Change in Reactions to Discrimination: Evaluation

    Total possible range of scores is -6 to +6.

    Time frame: Baseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

  9. Change in Reactions to Discrimination: Confrontation

    Participants can score 0 or 1, with the higher score reflecting confrontation.

    Time frame: Baseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

  10. Change in Predicting Parents' Attitudes

    Total possible range of scores is -6 to +6.

    Time frame: Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

07

Study locations

1 site
  • Waisman Center at UW-Madison
    Madison, Wisconsin 53705, United States
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: Yes — Individual participant data collected during the trial, after de-identification, will be shared. Additionally, the study protocol, statistical analysis plan, informed consent form, and analytic code will be shared. The materials will be shared upon publication of primary outcomes, and will be available indefinitely. They will be shared via an open science platform, namely the Open Science Framework (OSF). Anyone may access the data to verify study outcomes or make additional data discoveries.

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Analytic code

Time frame: The materials will be shared upon publication of primary outcomes, and will be available indefinitely.

Access criteria: The data will be shared via an open science platform, namely the Open Science Framework (OSF). Anyone may access the data to verify study outcomes or make additional data discoveries.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05807061
Responsible party
Sponsor
First posted
Apr 10, 2023
Start date
Apr 25, 2023
Primary completion
Jan 15, 2026
Completion
Jan 15, 2026
Last update
Jun 12, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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