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Purdue University Parenting Program Attrition

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00153439
First Posted: September 12, 2005
Last Update Posted: September 10, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Purdue University
Information provided by:
Centers for Disease Control and Prevention
  Purpose
The purpose of this study is to examine the efficacy of techniques to enhance participation in parenting programs.

Condition Intervention Phase
Child Abuse Behavioral: Motivational enhancements, parent training Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Factorial Assignment
Masking: Single
Primary Purpose: Prevention
Official Title: Purdue University Parenting Program Attrition and Compliance Efficacy Trial

Resource links provided by NLM:


Further study details as provided by Centers for Disease Control and Prevention:

Primary Outcome Measures:
  • Engagement and participation in an 8-week parenting program

Secondary Outcome Measures:
  • Measures of parenting behavior and attitudes, incidents of child maltreatment, measures of child adjustment and functioning

Estimated Enrollment: 560
Study Start Date: July 2003
Study Completion Date: September 2006
Detailed 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.
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

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.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00153439


Locations
United States, Indiana
Purdue University
West Lafayette, Indiana, United States, 47907
Sponsors and Collaborators
Centers for Disease Control and Prevention
Purdue University
Investigators
Principal Investigator: Jean E Dumas, Ph.D. Purdue University
  More Information

ClinicalTrials.gov Identifier: NCT00153439     History of Changes
Other Study ID Numbers: CDC-NCIPC-3928
R49/CCR522339-03
First Submitted: September 8, 2005
First Posted: September 12, 2005
Last Update Posted: September 10, 2007
Last Verified: September 2007

Keywords provided by Centers for Disease Control and Prevention:
parenting
motivation
child maltreatment
program attrition

Additional relevant MeSH terms:
Tooth Attrition
Tooth Wear
Tooth Diseases
Stomatognathic Diseases