- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00720486
Effectiveness of Anger Management Treatment in Reducing Anger-Related Behaviors in Female Juvenile Offenders
Anger Management Treatment for Female Juvenile Offenders
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Girls represent a growing segment of the juvenile justice population in the United States, with a large number of them being victims of sexual, physical, and psychological abuse. These girls have special needs in terms of treatment and rehabilitation; however, little research exists on effective mental health treatments for female juvenile offenders in justice facilities. Despite the severity of anger-related behaviors displayed by girls in the juvenile justice system, no anger management treatments have been systematically developed to meet the unique treatment needs of delinquent girls. Treatment programs that provide gender-specific education, counseling, and emotional support are necessary for addressing the aggressive behaviors and psychological distress often displayed among this population. One such treatment program, the Juvenile Justice Anger Management (JJAM) for Girls, is an anger management program adapted from Lochman's Coping Power program, an empirically supported school-based anger management treatment for younger children. This study will evaluate the effectiveness of JJAM for Girls in reducing anger-related behaviors displayed by girls in the juvenile justice system.
Participation in this study will last about 8 months. All participants will first undergo initial assessments that will include a combination of structured interviews, self-report measures, rating scales, and reviews of program behavioral records and incident reports. Participants will then be assigned randomly to receive JJAM for Girls plus treatment as usual or treatment as usual alone. Participants receiving JJAM for Girls will attend two 1.5-hour sessions per week for 8 weeks. Sessions will aim to help youth develop skills in the following areas: identifying different types of physical and relational aggression, recognizing early warning signs of anger, avoiding anger-provoking situations, managing anger to prevent aggression, solving problems, communicating about anger-related events, and repairing relationships damaged by anger-related behaviors. Participants will also complete between-session practice activities that will include practicing skills involved in planning personal goals. Treatment as usual for all participants will include all standard activities in the female juvenile justice program. All participants will repeat the initial assessments at treatment completion and Month 6 of follow-up.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Pennsylvania
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Philadelphia, Pennsylvania, United States, 19102
- Drexel University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Assigned to one of the designated juvenile justice facilities
- Has the ability to speak, read, and understand English sufficiently well to complete the procedures of the study
- Disposition to the juvenile justice program must last the 8 weeks of scheduled treatment plus 1 week before and after treatment
Exclusion Criteria:
- Fails to complete pretreatment assessments
- Current psychotic symptoms, mental retardation, or severe developmental disabilities
- Considered to be a ward of the state (defined as a youth without a parent, either biological or adoptive, as the legal custodian)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 1
Participants will receive Juvenile Justice Anger Management for Girls plus treatment as usual.
|
JJAM will include two 1.5-hour group treatment sessions per week for 8 weeks.
JJAM sessions will be manual based and will be designed to help youth develop skills in the following areas: identifying different types of physical and relational aggression, recognizing early warning signs of anger, avoiding anger-provoking situations, managing anger to prevent aggression, solving problems, communicating about anger-related events, and repairing relationships damaged by anger-related behaviors.
Treatment as usual will include standard activities in the female juvenile justice program.
|
|
Active Comparator: 2
Participants will receive treatment as usual.
|
Treatment as usual will include standard activities in the female juvenile justice program.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Reduction in anger
Time Frame: Measured at pretreatment, post-treatment, and Month 6 follow-up
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Measured at pretreatment, post-treatment, and Month 6 follow-up
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Naomi Goldstein, PhD, Drexel University
Publications and helpful links
General Publications
- Goldstein NE, Kemp KA, Leff SS, Lochman JE. Guidelines for Adapting Manualized Interventions for New Target Populations: A Step-Wise Approach Using Anger Management as a Model. Clin Psychol (New York). 2012 Dec 1;19(4):385-401. doi: 10.1111/cpsp.12011.
- Goldstein NE, Serico JM, Riggs Romaine CL, Zelechoski AD, Kalbeitzer R, Kemp K, Lane C. Development of the Juvenile Justice Anger Management Treatment for Girls. Cogn Behav Pract. 2013 May;20(2):171-188. doi: 10.1016/j.cbpra.2012.06.003.
- Lane C, Goldstein NE, Heilbrun K, Cruise KR, Pennacchia D. Obstacles to research in residential juvenile justice facilities: recommendations for researchers. Behav Sci Law. 2012 Jan-Feb;30(1):49-68. doi: 10.1002/bsl.1991. Epub 2012 Jan 4.
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- K23MH070400 (U.S. NIH Grant/Contract)
- DSIR 82-SEMS (Other Identifier: National Institute of Mental Health)
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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