- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00611832
Evaluation of a Video-Based Media Series to Promote Effective Parenting (ParentMedia)
March 27, 2014 updated by: Oregon Research Institute
Researchers are developing and experimentally evaluating two variants of a 10-episode, brief (12 minutes per episode), infotainment-style television series targeted at parenting practices, to determine the potential value of television for bringing evidence-based parenting practices to parents.
The study compares an "information-only" version of the television series against an "enhanced" version that is designed to actively promote parents' adoption of the targeted strategies.
Both versions of the series are compared against a waitlist control group.
The media series is derived from the Triple P Positive Parenting Program.
Study Overview
Status
Completed
Conditions
Detailed Description
The mass media, and television in particular, hold significant potential as part of a population-wide strategy for bringing evidence-based parenting practices to a broad range of parents experiencing challenges raising their children.
The potential of television for affecting parenting has received very little research attention, however; thus, little is known about how media messages to affect parenting practices might be optimally designed.
This study will develop and experimentally evaluate two variants of a 10-episode, brief (12 minutes per episode), infotainment-style television series targeted at parenting practices, derived from the Triple P-Positive Parenting Program (Sanders, 1999).
A sample of 300 families of children ages 3-6 years with somewhat elevated disruptive behavior problems will be randomized to (a) receive a standard "information-only" version of the series that includes only modeling and demonstration of target parenting skills, (b) receive an enhanced "behavior activation" version of the series designed to actively promote parental behavior change, through elements addressing attributions, self-efficacy and expectancies, social support, and emotional reactivity, or (c) a waitlist control group.
Measures of parents' parenting practices, cognitions, affect, and social support, and children's disruptive behavior problems, will be obtained at baseline, post-intervention, and 6-month follow-up.
The relative efficacy of the standard and enhanced versions of the Triple P Media Series in improving these outcomes will be examined, as well as moderators of these effects, such as baseline level of behavior problems and parental stress.
This study will further our understanding of the potential value of television programming for improving parenting practices.
Study Type
Interventional
Enrollment (Actual)
318
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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Oregon
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Eugene, Oregon, United States, 97403
- Oregon Research Institute
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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
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- parent(s) living with a child 3 to 6 years old
- child scores 1 or more standard deviations above the mean on the Eyberg Child Behavior Inventory
- English speaking
- parent at least 20 years old
Exclusion Criteria:
- currently receiving any other structured parenting intervention (home visits, parenting classes, individual parent training, family therapy)
- father-only households
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 |
---|---|
No Intervention: Control
Waitlist control
|
|
Active Comparator: Standard
Standard "information-only" version of the television series that includes only modeling and demonstration of the targeted parenting skills
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10 episodes, 12 minutes per episode, 2 episodes viewed per week for a total of 5 weeks.
Demonstrates parenting practices for effectively handling a range of difficult child behaviors.
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Experimental: Enhanced
Enhanced "behavior activation" version of the television series that includes all of the content of the standard "information-only" version, but is also designed to actively promote parental behavior change, through additional content elements addressing attributions, self-efficacy and expectancies, social support, and emotional reactivity.
|
10 episodes, 12 minutes per episode, 2 episodes viewed per week for a total of 5 weeks.
Demonstrates parenting practices for effectively handling a range of difficult child behaviors; includes specific content elements designed to promote parents' adoption of the targeted parenting skills
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Child problem behavior: measured by the Eyberg Child Behavior Inventory (Eyberg & Ross, 1978), phone interview, and observation coding from a structured lab task procedure
Time Frame: baseline, immediate post, 6-month follow-up
|
baseline, immediate post, 6-month follow-up
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Problematic parenting practices: measured by the Parenting Scale (Arnold et al., 1993), phone interview, and observation coding from a structured lab task procedure
Time Frame: baseline, immediate post, 6-month follow-up
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baseline, immediate post, 6-month follow-up
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Parent knowledge: Triple P Parenting Quiz
Time Frame: baseline, immediate post, 6-month follow-up
|
baseline, immediate post, 6-month follow-up
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Parental attributions for child misbehavior: Parent's Attributions for Child's Behavior Measure (Pidgeon & Sanders, 2004)
Time Frame: baseline, immediate post, 6-month follow-up
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baseline, immediate post, 6-month follow-up
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Parental self-efficacy: Problem Behavior and Setting Checklist (Sanders & Wooley, 2005)
Time Frame: baseline, immediate post, 6-month follow-up
|
baseline, immediate post, 6-month follow-up
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Parental stress: Depression Anxiety Stress Scale, Short Form (Lovibond & Lovibond, 1995)
Time Frame: baseline, immediate post, 6-month follow-up
|
baseline, immediate post, 6-month follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Carol W Metzler, PhD, Oregon Research Institute
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
May 1, 2008
Primary Completion (Actual)
December 1, 2011
Study Completion (Actual)
March 1, 2014
Study Registration Dates
First Submitted
February 6, 2008
First Submitted That Met QC Criteria
February 6, 2008
First Posted (Estimate)
February 11, 2008
Study Record Updates
Last Update Posted (Estimate)
March 31, 2014
Last Update Submitted That Met QC Criteria
March 27, 2014
Last Verified
March 1, 2014
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DA021307
- R01DA021307 (U.S. NIH Grant/Contract)
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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