Actively Recruiting

Phase Not Applicable
Age: 8Years +
All Genders
Healthy Volunteers
ID07191782

Examining the Efficacy of the PRAISE With Coaching Program in Reducing Peer Aggression and Bullying

Led by Children's Hospital of Philadelphia · Updated on 2025-11-19

1008

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

Sponsors

C

Children's Hospital of Philadelphia

Lead Sponsor

T

The School District of Philadelphia

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the PRAISE program, an aggression and bullying prevention curriculum designed for 3rd through 5th graders. This program teaches students skills to understand feelings, use calming techniques, interpret others' intentions, and make thoughtful choices in conflicts. The study aims to test the effectiveness of the adapted PRAISE program, delivered by trained school staff with coaching support, in reducing peer aggression and bullying while improving social problem-solving, positive bystander actions, and confidence in peaceful behavior. The study uses a randomized control trial involving at least 8 elementary schools. Some schools will receive the PRAISE program, which includes about 14 sessions and training plus coaching for school staff who facilitate the program. Other schools will continue their usual practices without the PRAISE intervention, such as community meetings or other existing programs. The research team will measure and compare outcomes in both groups. Participants include students in 3rd to 5th grade and school staff who teach or support these students. Assessments occur at the start and about 8 months later, measuring peer aggression, social understanding, bullying behaviors, empathy, academic engagement, and class environment. The study tracks various types of aggression and bullying, including cyberbullying, and evaluates improvements in social skills and relationships. The total study duration spans this baseline to post-intervention period, with no masking or blinding involved.

CONDITIONS

Brief Title

Examining the Efficacy of the PRAISE With Coaching Program

Who Can Participate

Age: 8Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Enrolled in one of the participating school sites
  • In a 3rd-5th grade classroom participating in the study
  • Employed by one of the participating school sites and teach or provide services to 3rd-5th grade students
Not Eligible

You will not qualify if you...

  • Do not speak English
  • Special education students not integrated in a regular education classroom
  • Students not in Grades 3-5 at the participating school sites
  • Staff who do not teach or provide services to 3rd-5th grade students at the participating school sites
  • Staff who do not speak English

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Approximately 8 months

Participants in intervention schools receive the PRAISE program, a classroom-based bullying and aggression prevention program with about 14 sessions, including training and coaching for school-based facilitators.

Multiple classroom sessions over the school year

Outpatient Treatment

Duration - Approximately 8 months

Participants in comparison schools continue with their standard aggression and bullying practices without receiving the PRAISE program.

No additional visits required beyond routine school attendance

Follow-up

Duration - At post-intervention, approximately 8 months after baseline

Participants complete assessments of peer aggression, bullying, social problem-solving skills, and other outcomes at the end of the intervention period.

1 follow-up assessment visit (in-person)

Trial Site Locations

Total: 1 location

1

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States, 19146-2305

Actively Recruiting

Loading map...

Research Team

T

Tracy E Waasdorp, PhD MSed

B

Brooke Paskewich, PsyD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

Similar Trials

Detour: a Smartphone Game to Help Youth Quit Smoking

Smoking Cessation

Actively Recruiting

1 location

Using Music-Based Interventions to Improve the Quality of Li...

Speech Perception

Actively Recruiting

1 location

Identification of Neural Markers of Aggression and Irritabil...

ADHD - Attention Deficit Disorder With Hyperactivity

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here