- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05197998
Promoting ColorBRAVE Conversations in Families
May 22, 2026 updated by: Tulane University
Promoting ColorBRAVE Conversations in Families: A Public Health Strategy to Advance Racial Equity
The objective of this research is to evaluate a mobile app-based intervention for parents of children in K-2nd grade designed that guides them in how to have productive conversations about race with their children.
This study will recruit a national sample of parents and their K-2nd grade children.
The impact of the intervention is tested using a wait-list controlled trial design.
Outcomes include prosocial behaviors and indicators of emotional well-being.
Study Overview
Status
Suspended
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
1200
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
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Louisiana
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New Orleans, Louisiana, United States, 70112
- Tulane University
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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
5 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Residence in the US; caregiver age 18 years or older and child age 5-8 years old; ability to read and understand English
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: ColorBRAVE
The experimental group will be asked to download a multi-module mobile app designed to guide parents and caregivers in having conversations about race with their K-2nd grade children
|
The intervention is a multi-module program delivered via a mobile app for parents of children in K-2nd grade.
Each module in the program will take approximately 30 minutes to complete, with lessons facilitated through interactive storytelling, videos, and games.
|
|
Other: Wait-list Control
The wait-list control group will be placed on the wait-list for the first 6-weeks, the period in which the experimental group will complete the intervention program.
Following the 6-week wait-list period they will receive the ColorBRAVE program.
|
The intervention is a multi-module program delivered via a mobile app for parents of children in K-2nd grade.
Each module in the program will take approximately 30 minutes to complete, with lessons facilitated through interactive storytelling, videos, and games.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Racial Socialization Frequency Scale
Time Frame: 0-12 months
|
Parents will report the frequency with which they engage in racial socialization practices with their K-2nd grade child.
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0-12 months
|
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Racial Socialization Competency Scale
Time Frame: 0-12 months
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Parents will report the degree of comfort, skills, and stress in engaging in different processes related to racial socialization with their K-2nd grade child.
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0-12 months
|
|
Cross-race Friendships
Time Frame: 0-12 months
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Parents will report the race of their K-2nd grade child's 5 closest friends - the number of cross-race friendships will consist of the number of friends that are race discordant to their child.
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0-12 months
|
|
Colorblind Racial Attitudes (CoBRAS) Scale
Time Frame: 0-12 months
|
Color-blind racial attitudes among parents will be assessed using the COBRAS Scale.
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0-12 months
|
|
Child Prosocial Behavior Questionnaire (CPBQ)
Time Frame: 0-12 months
|
Parents will report on the degree to which their K-2nd grade child engages in various prosocial behaviors, including those surrounding helping, sharing, and comforting.
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0-12 months
|
|
Child Bystander Response Questionnaire
Time Frame: 0-12 months
|
Children will report the frequency with which they engage in different bystander behaviors when they see someone being treated poorly or unfairly due to their race, ethnicity, or cultural background.
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0-12 months
|
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Patient-Reported Outcomes Measurement Information System (PROMIS) Parent Proxy Measures
Time Frame: 0-12 months
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Parent reports of child socio-emotional well being (e.g., positive peer relationships, depression, anxiety).
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0-12 months
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Prosocial Children Measure
Time Frame: 0-12 months
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Children (ages 5-8 years old) will be introduced to a child and told scenarios in which that child must choose other children to engage in various activities with, among a group of diverse children.
Children will be asked (1) whether they liked or disliked how that child chose the children to participate in the activity with and (2) if there is anything they would like to say to that child about their choice in children.
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0-12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: David H. Chae, ScD, MA, Tulane University
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 (Estimated)
August 1, 2026
Primary Completion (Estimated)
May 31, 2027
Study Completion (Estimated)
May 31, 2027
Study Registration Dates
First Submitted
November 22, 2021
First Submitted That Met QC Criteria
January 5, 2022
First Posted (Actual)
January 20, 2022
Study Record Updates
Last Update Posted (Actual)
May 27, 2026
Last Update Submitted That Met QC Criteria
May 22, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- 1U01OD033242-01 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Upon completion of key analyses, study documentation and de-identified data will be made available to the research community upon request.
Data requests may be submitted to the Project Coordinator and reviewed by the study PI to determine whether there is significant scientific overlap in the research questions and analyses proposed by the outside investigator.
Those who submit qualified proposals will be provided with a dataset containing only the variables requested and the associated documentation (e.g., codebooks, description of study protocols, data dictionaries) under a data sharing agreement.
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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