Parent Engagement Package: Initial Testing of Strategies to Increase Participation in Parenting Interventions

May 8, 2017 updated by: Emily Winslow PhD, Arizona State University

Participation in Preventive Parenting Interventions

This study evaluated the effectiveness of strategies for engaging parents into parenting programs. Engagement strategies included a booklet showing testimonial quotes and photos from prior participants, a recommendation to attend for the child's teacher, and a motivational call from the parenting program provider. It was hypothesized that the combination of engagement strategies would increase attendance at a parenting intervention compared to receiving only a promotional brochure and research interview.

Study Overview

Study Type

Interventional

Enrollment (Actual)

122

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Arizona
      • Tempe, Arizona, United States, 85287-6005
        • Arizona State University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Is the biological or adoptive mother of a child in kindergarten or 3rd grade at the participating school (i.e., "target child");
  • The target child lived with the mother at least half of the time;
  • The mother spoke English or Spanish;

Exclusion Criteria:

  • The target child changed schools;
  • The mother reported the target child would be changing schools during the school year;
  • The target child attended one of the participating schools during a previous cohort of the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Promotional Brochure
Participants in this condition received one of the strategies in the Parent Engagement Package: a promotional brochure with information about the parenting intervention being offered at their child's school, the Triple P Positive Parenting Program. This information included the location of meetings, free childcare, topics covered, choice of English or Spanish groups, meeting day and time, and an enrollment form. Parents who returned the enrollment form received a confirmation letter prior to the first parenting program session.
Promotional brochure with information about the Triple P Positive Parenting Program and an enrollment form.
Experimental: Parent Engagement Package
Participants in this condition received all engagement strategies in the Parent Engagement Package, which included: 1) the promotional brochure; 2) family testimonial flyer that included photos and quotes from prior participants; 3) teacher endorsement of the Triple P program; 4) provider engagement call to motivate parents to attend; and 5) phone reminders prior to each Triple P session.
Promotional brochure with information about the Triple P Positive Parenting Program and an enrollment form.
Flyer that included quotes and photos from parents who had previously participated in the Triple P Positive Parenting Program and/or their children who participated in the free childcare.
Brief conversation between the parent and their child's teacher in which the teacher told the parent about the benefits of participating in the Triple P Positive Parenting Program and recommended the parent attend.
This was a manualized, 20-minute call from the Triple P Positive Parenting Program provider to a parent in which the provider elicited the parent's child-focused goals and showed how the parent's goals could be addressed by Triple P. The provider also helped the parent problem solve barriers to attendance and develop an action plan to handle common barriers (e.g., scheduling conflicts) as well as set session reminders.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Parenting Intervention Attendance
Time Frame: Attendance was recorded by Triple P providers at each session, once per week for 8 weeks
Number of sessions a caregiver from a student's family attended the parenting intervention, the Triple P Positive Parenting Program
Attendance was recorded by Triple P providers at each session, once per week for 8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Parenting Intervention Enrollment
Time Frame: from the date engagement strategies commenced until the date the Triple P Positive Parenting Program began, up to 7 weeks
Whether or not a family enrolled in the Triple P Positive Parenting Program by completing an enrollment form or answering 'yes' to an enrollment question during the provider engagement call or attention-control research interview
from the date engagement strategies commenced until the date the Triple P Positive Parenting Program began, up to 7 weeks
Parenting Intervention Homework Completion
Time Frame: collected once per week for 7 weeks, at the beginning of each Triple P Positive Parenting Program sessions 2 through 8
Caregiver report of completion of Triple P Positive Parenting Program assignments between sessions
collected once per week for 7 weeks, at the beginning of each Triple P Positive Parenting Program sessions 2 through 8
Parenting Intervention Session Involvement
Time Frame: collected once per week for 8 weeks, after each Triple P Positive Parenting Program session
Provider reports of the extent to which a caregiver actively participated in each Triple P Positive Parenting Program session attended
collected once per week for 8 weeks, after each Triple P Positive Parenting Program session
Child Behavior Problems
Time Frame: collected 1 week before Triple P session 1 and at Triple P post-test, which was 9 weeks after the first behavior reports were collected
Teacher report of child behavior in the classroom
collected 1 week before Triple P session 1 and at Triple P post-test, which was 9 weeks after the first behavior reports were collected

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Emily B Winslow, Ph.D., Arizona State University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2009

Primary Completion (Actual)

May 1, 2010

Study Completion (Actual)

May 1, 2010

Study Registration Dates

First Submitted

April 18, 2017

First Submitted That Met QC Criteria

May 8, 2017

First Posted (Actual)

May 10, 2017

Study Record Updates

Last Update Posted (Actual)

May 10, 2017

Last Update Submitted That Met QC Criteria

May 8, 2017

Last Verified

May 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 0812003515

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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