NCT00153465

Brief Summary

The study will examine the extent to which a group motivational intervention (ME) impacts retention, treatment compliance, and long-term outcomes in families with a history of, or high risk for, child maltreatment.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
450

participants targeted

Target at P75+ for phase_1

Timeline
Completed

Started Jan 2004

Typical duration for phase_1

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2004

Completed
1.7 years until next milestone

First Submitted

Initial submission to the registry

September 8, 2005

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 12, 2005

Completed
12 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2006

Completed
Last Updated

September 10, 2007

Status Verified

September 1, 2007

First QC Date

September 8, 2005

Last Update Submit

September 6, 2007

Conditions

Child Abuse

Keywords

Parent trainingChild maltreatmentMotivationProgram attrition

Outcome Measures

Primary Outcomes (1)

  • Incidents of child maltreatment 1-3 years post-treatment

Secondary Outcomes (1)

  • Parenting behaviors, attitudes, and functioning assessed during and post-intervention

Interventions

Motivational intervention, parent trainingBEHAVIORAL

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Families referred to service agency for child maltreatment prevention services
  • Families with children between 2-1/2 and 12 years of age

You may not qualify if:

  • Parents with cognitive, psychiatric, or social conditions that would limit their ability to provide voluntary consent or benefit from the intervention
  • Parents who have sexually abused their children

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Oklahoma Health Sciences Center

Oklahoma City, Oklahoma, 73190, United States

Location

Study Officials

  • Mark J Chaffin, Ph.D.

    University of Oklahoma

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
SINGLE
Purpose
TREATMENT
Intervention Model
CROSSOVER
Sponsor Type
FED

Study Record Dates

First Submitted

September 8, 2005

First Posted

September 12, 2005

Study Start

January 1, 2004

Study Completion

September 1, 2006

Last Updated

September 10, 2007

Record last verified: 2007-09

Locations

US(1)