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N/A N=885 Randomized Basic Science

Developing Inclusive Youth: Promoting Intergroup Friendships and Inclusive Classrooms in Childhood

Social Exclusion · Prejudice, Racial · Prejudice · Sexism · Peer Group

Enrolled (actual)
885
Serious AEs
0.0%
Results posted
Sep 2025
Primary outcome: Primary: School Belonging Scale — 4.72; 4.72 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Developing Inclusive Youth (DIY) (Behavioral)
Age
Pediatric · 7+ yrs
Sex
All
Sponsor
University of Maryland, College Park
Primary completion
Dec 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
School Belonging Scale
4.72; 4.72
PRIMARY
Classroom Life Scale: Peer Personal Support Subscale Personal Support Subscale
4.35; 4.40
PRIMARY
Classroom Life Scale: Teacher Personal Support Subscale
5.12; 5.03
PRIMARY
Trait Attributions for Gender, Race, & Ethnicity
4.83; 4.82
PRIMARY
High Status Occupation Expectations
204; 131; 295; 211; 269; 185
PRIMARY
Reported Contact Scale
3.34; 3.31
PRIMARY
Desire for Intergroup Contact
3.99; 3.92
PRIMARY
Personal Experiences With Exclusion
2.02; 1.96
PRIMARY
Evaluations of Exclusion in Intergroup and Same Group Contexts
3.05; 2.96
PRIMARY
Likelihood of Inclusion in Intergroup and Same Group Contexts
4.53; 4.54
PRIMARY
Stereotypes About Inclusivity
3.70; 3.75
PRIMARY
Stereotypes About Math & Science Competence
4.89; 4.89

Summary

The goal of this clinical trial is to test the beneficial impacts of a web based intervention program called Developing Inclusive Youth for children in 3rd, 4th, and 5th grade. The main questions it aims to answer are: * Does the Developing Inclusive Youth (DIY) program, which is a web-based curriculum tool with a teacher-led classroom discussion, reduce prejudicial attitudes and biases as well as increase intergroup friendships for a sample of 8 -11 year old children enrolled in 3rd , 4th, and 5th grade U.S. classrooms? * Does the Developing Inclusive Youth (DIY) program lead to grade-related, gender-related and ethnic-related differences regarding reducing prejudicial attitudes and increasing intergroup friendships? * Does the Developing Inclusive Youth (DIY) program change teacher attitudes regarding the malleability of prejudice, the importance of intergroup friendships, and comfort levels with discussing social inclusion and exclusion experiences in the classroom? Student participants will take 15-20 minutes to use a Chrome notebook and headphones to access the online tool and the teacher will then lead a classroom discussion lasting 25-30 minutes. The intervention program will occur once a week for eight weeks. The student outcome measures, given at pretest and posttest, are also assessed with Chrome notebooks while children are sitting at their desks in the classroom. The outcome measures take 25-30 minutes. Researchers will compare children in the intervention classes to children in other classes of the same grade at their school to see if the tool promotes positive peer relationships and reduces prejudice and bias. Teacher participants will take a 25-minute online pretest and posttest survey in their classroom to assess their theories of prejudice, their awareness of their students' intergroup friendships, comfort with discussing peer social inclusion and exclusion in class, and their awareness of student experiences of exclusion.

Eligibility Criteria

For Child Participants

Inclusion Criteria

  • children with parental consent in grades 3, 4, or 5 at participating schools
  • be between the ages of 7 and 12 years
  • children who need assistance sitting at their desk or reading the text can participate provided that an adult mentor is assigned to them to assist with the protocol

For Teacher Participants:

  • teachers of students in grades 3, 4, and 5 at participating schools and who provide assent
  • no age limits for teacher participation

Exclusion Criteria

  • school has identified the student as unable to participate due to disability status.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05619523). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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