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Clinical Trials/NCT00051714
NCT00051714CompletedPhase 4

Early Primary Prevention of Conduct Problems

NYU Langone Health2 sites in 1 country1,050 target enrollmentStarted: March 1997Last updated:
Conditions

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
1,050
Locations
2
Primary Endpoint
behavior problems

Study Overview

Brief Summary

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.

Detailed Description

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
33 Months to 63 Months (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Sibling of youth adjudicated in Family Court

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

behavior problems

Time Frame: March 1997 - December 2012

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Laurie Brotman

Professor Science Professor of Child & Adolescent Psychiatry

NYU Langone Health

Study Sites (2)

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