Actively Recruiting

Phase Not Applicable
Age: 8Years +
All Genders
Healthy Volunteers
NCT07191782

Examining the Efficacy of the PRAISE With Coaching Program

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

1008

Participants Needed

1

Research Sites

148 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

The PReventing Aggression In Schools Everyday (PRAISE) Program has evidence of impact when run by research staff. PRAISE was adapted using community-based participatory research to a coaching model whereby school-staff are trained to facilitate the program and receive ongoing coaching from research staff. The overall objective is to demonstrate the efficacy of the adapted PRAISE program when facilitated by in-school staff.

CONDITIONS

Official 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...

  • Students enrolled in one of the participating school sites
  • Students in grades 3 through 5 in classrooms participating in the study
  • Staff employed by one of the participating school sites
  • Staff who teach or provide services to students in grades 3 through 5
Not Eligible

You will not qualify if you...

  • Students who do not speak English
  • Special education students not integrated in regular education classrooms
  • Students not in grades 3 through 5 at the participating school sites
  • Staff who do not speak English
  • Staff who do not teach or provide services to 3rd through 5th grade students at the participating school sites

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States, 19146-2305

Actively Recruiting

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Research Team

T

Tracy E Waasdorp, PhD MSed

CONTACT

B

Brooke Paskewich, PsyD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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