Effectiveness of Treatment for Relational Aggression in Urban African American Girls

June 3, 2015 updated by: Children's Hospital of Philadelphia

Determining the Efficacy of a Relational Aggression Intervention for Urban African American Girls

This study will evaluate the effectiveness of a school-based social cognitive group treatment in reducing aggression (bullying) among relationally aggressive urban African American girls.

Study Overview

Detailed Description

Relational aggression, also known as "female bullying," is a type of psychological aggression in which covert tactics are used to harm other people and their relationships. These tactics include humiliation, intimidation, coercing, shaming, malicious teasing, shunning, and using other forms of emotional abuse in an attempt to harm others. Although aggressive behavior is typically common among younger children, most children become less aggressive as they mature and develop better interpersonal skills. However, consistent aggressive behavior can lead to further problems and increased violence in the aggressor. In this study, a social cognitive anger management group intervention called Friend to Friend (F2F) will be evaluated as a way to develop more productive social and emotional functioning among relationally aggressive urban African American girls.

Participants will be randomly assigned to either the F2F program or a psycho-educational attention control (PAC) group. All participants will attend 40-minute treatment sessions twice a week for a total of 10 weeks. The sessions will occur during the girls' lunch or recess period. Participants assigned to the F2F program will learn how to identify signs of physiological arousal, react to a potential conflict while generating alternatives to the solution, and apply previously discussed social cognitive strategies to different situations. Culturally specific cartoons, videotape illustrations, and role playing will be used to portray these improved strategies and behaviors. Participants assigned to the PAC group will learn different organization and homework strategies as well as how to improve their study skills in an attempt to improve their overall academic performance. Outcomes will be assessed through observation, school reports, and questionnaires for all participants at baseline, immediately after treatment, and 9 months after treatment.

Study Type

Interventional

Enrollment (Actual)

144

Phase

  • Phase 3

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

    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19104
        • The Children's Hospital of Philadelphia

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

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria for Schools :

  • Urban school located in Southwest Philadelphia
  • Student body is more than 80% African American
  • Large school with at least three classrooms per grade
  • Not currently involved with systematic anti-aggression social skills program

Inclusion Criteria for Participants:

  • In the 3rd, 4th, or 5th grade
  • Meets diagnostic criteria for relational aggression

Exclusion Criteria for Participants:

  • Enrolled in special education and not integrated into a regular education classroom

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
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: 1
Participants will receive the Friend to Friend program
Friend to Friend arm is a social information processing group treatment to help aggressive girls learn better social problem solving and decision making choices. Participants will learn how to identify signs of physiological arousal, evaluate others' intentions, react to a potential conflict situation, and generate and evaluate alternatives. Treatment sessions are twice per week (30 to 40 minutes per session) for ten weeks.
Other Names:
  • Relational aggression intervention
ACTIVE_COMPARATOR: 2
Participants will receive the psychoeducational attention control intervention
Psychoeducational attention control group also meets two times per week for 10 weeks to control for nonspecific factors of treatment. Participants learn homework, study skills, and organizational skills.
Other Names:
  • Homework and study skills intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Peer nominations
Time Frame: Measured pre-treatment and immediately post-treatment
Measured pre-treatment and immediately post-treatment
Playground observations
Time Frame: Measured pre-treatment and immediately post-treatment
Measured pre-treatment and immediately post-treatment
Children's Social Behavior Questionnaire
Time Frame: Measured pre-treatment and immediately post-treatment and at 9-month follow-up
Measured pre-treatment and immediately post-treatment and at 9-month follow-up
Social Cognitive Assessment Profile
Time Frame: Measured pre-treatment and immediately post-treatment and at 9-month follow-up
Measured pre-treatment and immediately post-treatment and at 9-month follow-up
Cartoon Based Hostile Attribution Bias Measure
Time Frame: Measured pre-treatment and immediately post-treatment and at 9-month follow-up
Measured pre-treatment and immediately post-treatment and at 9-month follow-up
Knowledge of Anger Problem Solving (KAPS)
Time Frame: Measured pre-treatment, immediately post-treatment, and at 9 month follow-up
Measured pre-treatment, immediately post-treatment, and at 9 month follow-up

Secondary Outcome Measures

Outcome Measure
Time Frame
Discipline referrals and suspensions
Time Frame: Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Academic Performance Rating Scale
Time Frame: Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Homework Performance Questionnaire
Time Frame: Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Asher-Wheeler Loneliness Questionnaire
Time Frame: Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Iowa-Conner Aggression subscale
Time Frame: Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Student-Teacher Relationship Scale
Time Frame: Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Measured pre-treatment, immediately post-treatment and at 9-month follow-up
Peer Ratings of Aggression and Prosocial Behavior
Time Frame: Measured pre-treatment, immediately post-treatment
Measured pre-treatment, immediately post-treatment
Harter, Self-Perception Profile for Children
Time Frame: Measured pre-treatment, immediately post-treatment, and at 9 month follow-up
Measured pre-treatment, immediately post-treatment, and at 9 month follow-up
Peer Sympathy Scale
Time Frame: Measured pre-treatment, immediately post-treatment, and at 9 month follow-up
Measured pre-treatment, immediately post-treatment, and at 9 month follow-up

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Stephen S. Leff, PhD, Children's Hospital of Philadelphia

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

October 1, 2007

Primary Completion (ACTUAL)

May 1, 2014

Study Completion (ACTUAL)

May 1, 2015

Study Registration Dates

First Submitted

July 30, 2007

First Submitted That Met QC Criteria

July 30, 2007

First Posted (ESTIMATE)

August 1, 2007

Study Record Updates

Last Update Posted (ESTIMATE)

June 4, 2015

Last Update Submitted That Met QC Criteria

June 3, 2015

Last Verified

June 1, 2015

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2006-10-5013
  • DSIR 84-CTS (Division of Services and Intervention Research)
  • R01MH075787 (NIH)

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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