MedPath

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

Not Applicable
Conditions
Racial Bias
Registration Number
NCT05807061
Lead Sponsor
University of Wisconsin, Madison
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
ENROLLING_BY_INVITATION
Sex
All
Target Recruitment
648
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 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
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change in Likelihood of Child's Racial BiasBaseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

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

Change in Self-Efficacy for Addressing Children's BiasBaseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

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

Change in Reactions to Discrimination: EvaluationBaseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

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

Change in Concern about Children's Racial BiasBaseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

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

Change in Concern about Own Child's BiasBaseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

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

Change in Motivation to Regulate Children's BiasBaseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

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

Change in Intergroup LikingBaseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

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

Change in Diversity PreferenceBaseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

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

Change in Reactions to Discrimination: ConfrontationBaseline, Post-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

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

Change in Predicting Parents' AttitudesPost-Test 1 (up to 4 weeks on study), Post-Test 2 (up to 16 weeks on study)

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

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Waisman Center at UW-Madison

🇺🇸

Madison, Wisconsin, United States

Waisman Center at UW-Madison
🇺🇸Madison, Wisconsin, United States

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.