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NCT00153439 Clinical Trial

Purdue University Parenting Program Attrition

Child Abuse Clinical Trial

Official title:
Purdue University Parenting Program Attrition and Compliance Efficacy Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00153439
Other study ID # CDC-NCIPC-3928
Secondary ID R49/CCR522339-03
Status Completed
Phase Phase 1
First received September 8, 2005
Last updated September 6, 2007
Start date July 2003
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 purpose of this study is to examine the efficacy of techniques to enhance participation in parenting programs.

Description:

This project addresses the problem of involving parents in interventions that promote parenting effectiveness and child coping-competence in preschoolers as a means of reducing risk of child maltreatment (and related adverse developmental outcomes). Purdue University will examine the impact of partnership (organizational involvement in recruitment and retention), cash incentives, and a motivational goal setting component on participation and engagement in the Parenting Our Children to Excellence program, a group intervention for parents and caregivers of preschool children.

Recruitment information / eligibility
Status Completed
Enrollment 560
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:

- Parents with children 3-5 years old who attend centers in which interventions are offered

Exclusion Criteria:

- See above. No other exclusion criteria will be used.

Study Design

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

Related Conditions & MeSH terms

Intervention

Behavioral:
• Motivational enhancements, parent training

Locations
Country Name City State
United States Purdue University West Lafayette Indiana

Sponsors (2)
Lead Sponsor Collaborator
Centers for Disease Control and Prevention Purdue University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Engagement and participation in an 8-week parenting program
Secondary Measures of parenting behavior and attitudes, incidents of child maltreatment, measures of child adjustment and functioning
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