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NCT00153465 Clinical Trial

University of Oklahoma Parenting Program Attrition

Child Abuse Clinical Trial

Official title:
University of Oklahoma Health Sciences Center Parenting Program Attrition and Compliance Efficacy Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00153465
Other study ID # CDC-NCIPC-3899
Secondary ID R49/CCR622338-04
Status Completed
Phase Phase 1
First received September 8, 2005
Last updated September 6, 2007
Start date January 2004
Est. completion date September 2006

Study information
Verified date September 2007
Source Centers for Disease Control and Prevention
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial 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.

Description:

The field of child abuse prevention faces not only the challenge of developing and disseminating effective treatments, but the problem of high attrition rates and treatment noncompliance. This study will compare the effects of a motivational intervention with a "services as usual" orientation group on program retention, treatment compliance, and long-term outcomes in families with histories of child maltreatment.

Recruitment information / eligibility
Status Completed
Enrollment 450
Est. completion date September 2006
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Families referred to service agency for child maltreatment prevention services

- Families with children between 2-1/2 and 12 years of age

Exclusion Criteria:

- 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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Motivational intervention, parent training

Locations
Country Name City State
United States University of Oklahoma Health Sciences Center Oklahoma City Oklahoma

Sponsors (1)
Lead Sponsor Collaborator
Centers for Disease Control and Prevention

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Incidents of child maltreatment 1-3 years post-treatment
Secondary Parenting behaviors, attitudes, and functioning assessed during and post-intervention
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