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University of Oklahoma Parenting Program Attrition

Primary Purpose

Child Abuse

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Motivational intervention, parent training
Sponsored by
Centers for Disease Control and Prevention
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Child Abuse focused on measuring Parent training, Child maltreatment, Motivation, Program attrition

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • University of Oklahoma Health Sciences Center

Outcomes

Primary Outcome Measures

Incidents of child maltreatment 1-3 years post-treatment

Secondary Outcome Measures

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

Full Information

First Posted
September 8, 2005
Last Updated
September 6, 2007
Sponsor
Centers for Disease Control and Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT00153465
Brief Title
University of Oklahoma Parenting Program Attrition
Official Title
University of Oklahoma Health Sciences Center Parenting Program Attrition and Compliance Efficacy Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2007
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Centers for Disease Control and Prevention

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Child Abuse
Keywords
Parent training, Child maltreatment, Motivation, Program attrition

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
Single
Allocation
Randomized
Enrollment
450 (false)

8. Arms, Groups, and Interventions

Intervention Type
Behavioral
Intervention Name(s)
Motivational intervention, parent training
Primary Outcome Measure Information:
Title
Incidents of child maltreatment 1-3 years post-treatment
Secondary Outcome Measure Information:
Title
Parenting behaviors, attitudes, and functioning assessed during and post-intervention

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark J Chaffin, Ph.D.
Organizational Affiliation
University of Oklahoma
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Oklahoma Health Sciences Center
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73190
Country
United States

12. IPD Sharing Statement

Learn more about this trial

University of Oklahoma Parenting Program Attrition

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