NCT00444197

Brief Summary

Study Aims: 1) Assess the receptiveness of youth and families to injury prevention interventions initiated from the emergency department; 2) In a sample of high risk youth presenting to the ED with interpersonal assault injuries, determine the effectiveness of a home-based family intervention with community linkage compared to a control group.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
198

participants targeted

Target at P75+ for phase_2

Timeline
Completed

Started Aug 2001

Typical duration for phase_2

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2001

Completed
4.4 years until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2006

Completed
1.2 years until next milestone

First Submitted

Initial submission to the registry

March 5, 2007

Completed
2 days until next milestone

First Posted

Study publicly available on registry

March 7, 2007

Completed
Last Updated

March 7, 2007

Status Verified

March 1, 2007

First QC Date

March 5, 2007

Last Update Submit

March 5, 2007

Conditions

Outcome Measures

Primary Outcomes (4)

  • Fighting behavior

  • Weapon carrying

  • Aggression

  • Misdemeanors

Secondary Outcomes (2)

  • Attitudes About Violence

  • Self Efficacy

Interventions

Eligibility Criteria

Age9 Years - 15 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • adolescents age 9-15 presenting to a large urban children's hospital or university hospital
  • residence in the metropolitan area
  • emergency department presentation with an interpersonal assault injuries (E960, 961-966, 968-969) excluding sexual assault, child abuse, sibling fights, or legal intervention
  • mental and physical ability of parent and child to participate in the intervention and assessments.

You may not qualify if:

  • sexual assault, child abuse, sibling fights, or legal intervention
  • non English speaking

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Children's National Medical Center

Washington D.C., District of Columbia, 20010, United States

Location

Johns Hopkins University

Baltimore, Maryland, 21287, United States

Location

Related Publications (1)

  • Cheng TL, Haynie D, Brenner R, Wright JL, Chung SE, Simons-Morton B. Effectiveness of a mentor-implemented, violence prevention intervention for assault-injured youths presenting to the emergency department: results of a randomized trial. Pediatrics. 2008 Nov;122(5):938-46. doi: 10.1542/peds.2007-2096.

MeSH Terms

Conditions

Aggression

Condition Hierarchy (Ancestors)

Aberrant Motor Behavior in DementiaBehavioral SymptomsBehaviorSocial Behavior

Study Officials

  • Tina L Cheng, MD, MPH

    Johns Hopkins University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
SINGLE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

March 5, 2007

First Posted

March 7, 2007

Study Start

August 1, 2001

Study Completion

January 1, 2006

Last Updated

March 7, 2007

Record last verified: 2007-03

Locations