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Early Prevention of Conduct Problems

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00051714
First Posted: June 4, 2003
Last Update Posted: July 16, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
National Institute of Mental Health (NIMH)
Information provided by (Responsible Party):
Laurie Brotman, New York University School of Medicine
January 15, 2003
June 4, 2003
July 16, 2013
March 1997
December 2012   (Final data collection date for primary outcome measure)
behavior problems [ Time Frame: March 1997 - December 2012 ]
Not Provided
Complete list of historical versions of study NCT00051714 on ClinicalTrials.gov Archive Site
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Early Prevention of Conduct Problems
Early Primary Prevention of Conduct Problems
The purpose of this study is to examine the immediate and long-term effects of a prevention program in children at risk for developing conduct problems and antisocial behavior.

Participants are randomly assigned to a year-long family-based intervention or to a no contact control group. The intervention focuses on improving parenting practices, parent-child interactions, and child social competence.

Children are assessed at the beginning of the study and again after one year. The development of conduct problems, social competence, and school functioning is assessed from second through fifth grade. Assessments are made through observations, parent and teacher ratings, and diagnostic interviews.

Interventional
Phase 4
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Conduct Disorder
Behavioral: Family-Based Preventive Intervention
Experimental: Early Primary Prevention
Intervention: Behavioral: Family-Based Preventive Intervention
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
1050
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December 2012   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Sibling of youth adjudicated in Family Court
Sexes Eligible for Study: All
33 Months to 63 Months   (Child)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00051714
R01MH055188( U.S. NIH Grant/Contract )
R01MH055188 ( U.S. NIH Grant/Contract )
DSIR 84-CTP
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Laurie Brotman, New York University School of Medicine
New York University School of Medicine
National Institute of Mental Health (NIMH)
Not Provided
New York University School of Medicine
July 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP
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