NIH R01 Friend to Friend With Coaching

December 21, 2023 updated by: Children's Hospital of Philadelphia

The Friend to Friend Program: Effectiveness When Conducted by School Staff

This study examines the effectiveness of the Friend to Friend (F2F) program when conducted by teachers and counselors with active coaching from the research team. The project involves 14 small group sessions for relationally aggressive girls and 8 classroom sessions. Students, teachers, counselors and parents at intervention and control schools fill out pre- and post- program questionnaires.

Study Overview

Status

Recruiting

Conditions

Detailed Description

This study takes a proven effective program (Friend to Friend) that was initially run by the research team in a clinical trial and examines for the first time its effectiveness when conducted by teachers and counselors with active coaching from the research team. The primary target population for this study will be 4th-5th grade relationally aggressive girls. In intervention schools, these girls will participate in Friend to Friend with Coaching (14 small group sessions, 8 classroom sessions and additional pre- and post- program questionnaires).

In both intervention and control schools all 4th-5th grade students (boys and girls) will participate in a screening measure to identify the relational aggressors and pre- and post-program questionnaires. Counselors and 4th-5th grade teachers in both conditions will participate in pre/post questionnaires and will also participate in training, coaching, the small group intervention and classroom sessions in intervention schools.

These procedures will be repeated with new students in 5 of the F2F with Coaching schools the following school year, except that the research team will provide minimal coaching to staff running the intervention in year 2.

Study Type

Interventional

Enrollment (Estimated)

5250

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 Contact

  • Name: Stephen Leff, PhD
  • Phone Number: 215-590-7067
  • Email: leff@chop.edu

Study Contact Backup

Study Locations

    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19146
        • Recruiting
        • Children's Hospital of Philadelphia
        • Contact:
          • Stephen Leff, PhD
          • Phone Number: 215-590-7067
          • Email: leff@chop.edu
        • Contact:

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

7 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Aim 1 Inclusion/Exclusion Criteria:

  • Inclusion Criteria for Schools

    40 schools will be selected on the basis of the following inclusion criteria:

    1. Urban school from the School District of Philadelphia
    2. Predominately minority student body (> 80%)
    3. Relatively large school with at least 2 classrooms per grade
    4. School is not currently involved in a systematic anti-aggression or bullying prevention program
    5. School must have at least 1 school counselor who is interested in participating
  • Inclusion Criteria for Students

    1. All boys and girls in regular education 4th-5th grade classrooms will be eligible to participate in screening and outcome assessment activities.
    2. Screening will include a peer-rating procedure that will be utilized to identify girls with relational aggression (GRAs).
    3. GRAs will be based on if they score > .50 of a Standard Deviation above mean on relational aggression on the peer-rating measure. These identified girls will be recruited (with written parent consent and student assent) to participate in the F2F with Coaching or control condition.
  • Inclusion Criteria for Parents

    1) All parents of students in regular education 4th-5th grade classrooms will be eligible to participate in outcome assessment activities.

  • Inclusion Criteria for Teachers/Counselors

    1. Teachers/counselors employed by the participating school sites who provide their verbal consent for participation.
    2. Teachers/counselors who currently teach and/or provide services to students in 4th-5th grade.

Exclusion Criteria:

  • Exclusion Criteria for Students

    1) Students who do not speak English. 2) Students whose parents do not speak English or one of the foreign languages into which the Parent Information Sheet for Child Participation has been translated (who therefore cannot opt their child in or out of the study in an informed manner).

    3) Special education students who are not integrated within the regular education classroom.

    4) In intervention schools, boys are excluded from the F2F small group intervention, however, as noted above, all boys will participate in the class portion of the program. Boys in both conditions will complete screening and outcome assessment activities.

  • Exclusion Criteria for Parents

    1) Parents who do not speak English or one of the foreign languages into which the Parent Information Sheet for Parent Participation and parent questionnaires have been translated.

    2) Parents of students in special education who are not integrated within the regular education classroom.

  • Exclusion Criteria for Teachers/Counselors

    1. Teachers/counselors who do not speak English.
    2. Teachers/counselors who are not working with 4th-5th grade students at the participating school sites.

Aim 2: Inclusion/Exclusion Criteria

  • Aim 2 Inclusion Criteria - Schools 1) 10 of Friend to Friend with Coaching schools in Aim 1 will participate in Aim 2.
  • Aim 2 Inclusion Criteria - Students

    1. 4th grade boys and girls who meet the same criteria as described in Aim 1.
    2. Similar to Aim 1, a peer rating procedure will be used to identify girls with relational aggression (GRAs) and prosocial role models.
  • Aim 2 Inclusion Criteria - Parents 1) Same as Aim 1.

Aim 2 Inclusion Criteria - Teachers/Counselors 1) Counselors and 4th grade teachers who participated in F2F with Coaching in Aim 1.

Aim 2 Exclusion Criteria - Students, Parents, Teacher/Counselors

1) Same as Aim 1.

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Friend to Friend with Coaching
Program for relationally aggressive girls and their classmates delivered by school personnel who have been coached by study team.
Friend to Friend (F2F) with Coaching has 14 small group sessions and 8 classroom sessions as led by school staff with coaching from the Children's Hospital of Philadelphia (CHOP) research team. The program aims to improve problem solving and prosocial behaviors, and decrease aggressive behaviors.
No Intervention: Control
Referral to school counselor as needed as per standard practice.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Staff Self-Efficacy for Handling Aggression
Time Frame: Given two times throughout the study, first at baseline (early in the school year, October/November) and on up to 8 months later
This 12-item measure called "Staff Self-Efficacy for Handling Aggression" has been designed for this study for school counselors and teachers to rate their own strategies for intervening, comfort in intervening, and perceived effectiveness for intervening with girls who are relationally aggressive on a five point scale from (1 = strongly disagree to 5 = strongly agree). Scores are averaged across items with higher scores indicating a better outcome.
Given two times throughout the study, first at baseline (early in the school year, October/November) and on up to 8 months later
Change in hostile attribution biases
Time Frame: Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later
The self-report Cartoon-Based Hostile Attributional Bias measure will be used to assess hostile attributions with 2 relational vignettes and 2 physical vignettes, with one question asking whether a behavior was intentional or unintentional and a second questions asking whether the behavior was harmful or not harmful. Scores on the 2 items per vignette type (relational, physical) are summed, each vignette has a range of 0 (no bias) to 4 (strong bias) where higher scores reflect a worse outcome (i.e. more relational hostile attributional biases and/or more physical hostile attributional biases).
Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later
Change in Knowledge of Anger Problem-Solving Steps
Time Frame: Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later
Knowledge of Anger Problem Solving (KAPS) is a 9 item abbreviated multiple choice measure (original measure was 15 items) designed to assess students' general knowledge of the steps underlying the social information processing model of aggression and of anger management techniques. Scores are calculated through summing across all 9 items, where a score is given a 1 if a correct answer is selected or 0 if an incorrect answer is selected; with a range of 0 (no correct) to 9 (all correct), higher scores reflect a better outcome.
Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later
Change in Relational Aggression
Time Frame: Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later

Teacher report of relational aggression will be assessed using the Children's Social Behavior Questionnaire with 5 items. Scores are calculated by averaging across all items, with a range of 1 to 5, higher scores reflect a worse outcome (more relational aggression).

Peer reports of relational aggression will be measured using two items. These items are based on Crick and Grotpeter and have strong psychometric properties. Students rate the frequency that each classmate engages in relational aggression on 2 items (leaving out, rumor spreading) on a scale from 1- Not at All to 5- A Whole Lot. Each individual child has a mean score ranging from 1 to 5 (drawn from an average rating across all students/peers in a class). Higher scores reflect a worse outcome (more relational aggression).

Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later
Change in Prosocial Leadership
Time Frame: Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later
This 7-item measure combines items from the leadership and prosocial competence scales from the Behavior Assessment System for Children (BASC) to create a combined scale called Prosocial Leadership that has been found to be reliable and valid in prior studies. Items are rated on a 4-point scale (1-hardly ever to 4-almost always).
Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later
Change in Teacher-Student Relationships
Time Frame: Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later
The STRS has demonstrated strong psychometric properties, and a strong student-teacher relationship has been shown to be predictive of adaptive adjustment in school. Ten items drawn from the Closeness subscale (e.g., "shares information about self") (α = .89) and the Conflict subscale (e.g., "easily becomes angry at me") (α = .93) will be completed by teachers for all assented students (boys and girls) in their class. Teachers respond to each item on a five-point scale (1 = definitely does not apply to 5 = definitely applies), with higher scores indicating higher closeness or higher conflict.
Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Explore peer rejection as mediator/moderator
Time Frame: Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later.
Peer reports of rejection are measured using two items asking how much students like each classmate and how much they dislike each classmate on a scale from 1- Not at All to 5- A Whole Lot. Each individual child has a mean score ranging from 1 to 5 (drawn from an average rating across all students/peers in a class). Level of peer rejection is calculated by subtracting an individual child's likeability mean score from their dislikability mean score. Higher scores represent greater peer rejection. We anticipate using the first time point for this analysis.
Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later.
Explore implementation factors
Time Frame: This will be first administered during the first session/lesson in the school year (approximately October/November) and to be filled out weekly by facilitators for up to 8 months.
Measured by number of sessions attended
This will be first administered during the first session/lesson in the school year (approximately October/November) and to be filled out weekly by facilitators for up to 8 months.
Explore perception of intervention attributes as mediator/moderator
Time Frame: Up to 8 months after the study began.
Given one time in the study, this measure was adapted from the Teacher perceptions of the intervention attributes measure and includes 10 items with a scale of 1- Not at All to 5- A Whole Lot. Scores are averaged across items with higher scores indicating a better outcome (positive perception of the intervention)
Up to 8 months after the study began.
Explore student self-efficacy for non-violence
Time Frame: Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later.
Self-Efficacy for Nonviolence is an 9-item, self-report measure adapted from the Multisite Violence Prevention Project, which used modified items from the Teen Conflict Survey. Questions ask how confident students are on a scale from 1=Not at all confident to 4=very confident. Items are averaged with higher scores indicating a better outcome (more self-efficacy for using non-violent approaches to conflict). We will use the first time point for this analysis.
Given two times throughout the study, first at baseline (early in the school year, October/November) and up to 8 months later.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 (Actual)

November 12, 2019

Primary Completion (Estimated)

December 15, 2024

Study Completion (Estimated)

January 31, 2025

Study Registration Dates

First Submitted

October 23, 2019

First Submitted That Met QC Criteria

November 14, 2019

First Posted (Actual)

November 15, 2019

Study Record Updates

Last Update Posted (Actual)

December 22, 2023

Last Update Submitted That Met QC Criteria

December 21, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 18-015582
  • 1R01HD094833-01A1 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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