- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03040154
Engaging Immigrants in Preventive Parenting Interventions
October 6, 2023 updated by: Joyce Javier, Children's Hospital Los Angeles
The objective of this community-based randomized controlled trial is to evaluate the outcomes of a theory-based parent engagement intervention (i.e., culturally-tailored video) aimed at promoting the participation of Filipino parents and grandparents in an evidence-based preventive parenting intervention.
Study Overview
Status
Completed
Conditions
Detailed Description
Data will be obtained using pre and post surveys with self-report instruments and enrollment logs.
It is hypothesized that 1) Parents and grandparents in the Intervention Arm will demonstrate greater behavioral outcomes (intention to enroll, actual enrollment, and participation in parenting intervention sessions) than those in the Control Arm. 2) Parents and grandparents in the Intervention Arm will show greater improvements from baseline in parent determinants (knowledge, beliefs, attitudes, benefits, and barriers) compared to the Control Arm. 3) Parents' intention to enroll, and actual enrollment in IY will be predicted by the study arm and parent determinants.
This study is expected to have an important impact on the uptake of evidence-based parenting interventions among hard-to-reach populations and holds the promise of eliminating disparities in behavioral health outcomes in this understudied and growing minority population.
Study Type
Interventional
Enrollment (Actual)
217
Phase
- Not Applicable
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
18 years and older (Child)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
The sample will consist of Filipino parents and grandparents of children/grandchildren between ages 6-12 years old. Inclusion criteria include:
- the parent or grandparent has at least one child between 6 to 12 years of age
- the participating parent/grandparent is Filipino
- At least one parent/grandparent is willing to complete pre and post surveys and watch a brief video
- the parent/grandparent is age 18 or older
- English fluency
Exclusion Criteria:
- Younger than 18 years of age
- Does not speak English
- Target child has a developmental disability such as Trisomy 21 or autism
- Parent or grandparent plans to move out of the area within the next nine months
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention Arm
Culturally-tailored video that includes parent testimonials, health and mental health clinicians, community-based providers, and church leaders
|
Other Names:
|
|
Other: Control Arm
Usual care video publicly available describing the evidence-based parenting intervention
|
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Enrollment in Evidence-Based Parenting Program
Time Frame: Up to two years after completing the survey
|
The number of participants from each arm who enrolled in the Incredible Years Parenting Program after completing this study.
Enrollment in the parenting program helped determine if the culturally-tailored video intervention effectively increases program participation among Filipino parents.
|
Up to two years after completing the survey
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Joyce R. Javier, MD, MPH, MS, Children's Hospital Los Angeles, University of Southern California Keck School of Medicine
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
June 1, 2016
Primary Completion (Actual)
December 1, 2016
Study Completion (Actual)
December 1, 2016
Study Registration Dates
First Submitted
January 31, 2017
First Submitted That Met QC Criteria
January 31, 2017
First Posted (Estimated)
February 2, 2017
Study Record Updates
Last Update Posted (Actual)
October 11, 2023
Last Update Submitted That Met QC Criteria
October 6, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CCI-13-00159
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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