Waisman Center at UW-Madison
Madison, Wisconsin, 53705, United States
NCT Number: NCT05807061
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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Notify Me5 year and older
All sexes
Interventional
Not applicable
Madison, Wisconsin, 53705, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
are:
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.
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.
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.
Time frame: Baseline, 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.
Time frame: Baseline, 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.
Time frame: Baseline, 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.
Time frame: Baseline, 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.
Time frame: Baseline, 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.
Time frame: Baseline, 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.
Time frame: Baseline, 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.
Time frame: Baseline, 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.
Time frame: Baseline, 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.
Time frame: 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.
University of Wisconsin, Madison
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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