- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03147547
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
Status
Completed
Conditions
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
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Arizona
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Tempe, Arizona, United States, 85287-6005
- Arizona State University
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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.
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Promotional brochure with information about the Triple P Positive Parenting Program and an enrollment form.
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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.
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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.
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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
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Number of sessions a caregiver from a student's family attended the parenting intervention, the Triple P Positive Parenting Program
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Attendance was recorded by Triple P providers at each session, once per week for 8 weeks
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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
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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
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from the date engagement strategies commenced until the date the Triple P Positive Parenting Program began, up to 7 weeks
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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
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Caregiver report of completion of Triple P Positive Parenting Program assignments between sessions
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collected once per week for 7 weeks, at the beginning of each Triple P Positive Parenting Program sessions 2 through 8
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Parenting Intervention Session Involvement
Time Frame: collected once per week for 8 weeks, after each Triple P Positive Parenting Program session
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Provider reports of the extent to which a caregiver actively participated in each Triple P Positive Parenting Program session attended
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collected once per week for 8 weeks, after each Triple P Positive Parenting Program session
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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
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Teacher report of child behavior in the classroom
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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
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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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