- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05140460
Cultural Pride Reinforcement for Early School Readiness
Cultural Pride Reinforcement for Early School Readiness: A Quasi-Experimental Trial
Study Overview
Status
Detailed Description
In order to evaluate parental delivery of cultural pride messages, child development, and health services outcomes, 106 parents of children ages 6 months to 5 years old were recruited from two child-serving health institutions in Southern California. This study utilized both an intervention group (n=67) and a control group (n=39). Recruitment and baseline intervention for this study took place on the same day, with one 3-month follow-up conducted over the telephone, and a 1-year post-enrollment review of the child's medical chart. Only a subset (n=14) participated in the medical chart review. Details of the study methodology are provided below.
Recruitment Parents were recruited from two child-serving community health clinics in Southern California. Participants were at least 18 years of age, had a child who was between 6 months and 5 years of age, was of African American, Asian, Latino race/ethnicity or diverse cultural perspective, and reported a primary language that was English or Spanish. Potential participants were identified by the health clinics' coordinating research staff and the clinical pediatrics team. Research assistants (RAs) from the study conferred with the medical staff for each pediatric team to review participant eligibility. The pediatric team distributed the study flyer to those parents who met study eligibility at their scheduled well-child or sick-child visit. Additionally, study flyers were posted at the clinic. Recruitment script and informed consent took approximately 10 minutes.
Intervention Treatment Assignment Participants comprising the intervention group and the control group were determined by designating all participating parents with office visits on even days of the month to the intervention group and all participating parents with office visits on odd days of the month to the control group.
Intervention Group The intervention entails distribution of a children's book with a cultural pride theme, the cultural pride parent book-sharing guide, and the study survey. Consented intervention participants selected and received a developmentally appropriate (baby, toddler, or preschool) book from the RA that featured African American, Latino, Asian, or diverse cultural pride perspectives. All books selected for distribution in the intervention group were vetted through a community advisory board. The cultural pride books differ from the standard ROR books distributed at office visits in that the ROR books address age-related developmental and interactive content, but do not focus on or require specific images and narratives reflective of racial, ethnic, or cultural perspectives in their content. Participating parents were asked to complete the study survey. The survey collected information on demographics, racial socialization (including cultural pride reinforcement), child development, and family-provider communication. Portions of the survey used a 5-point Likert scale to rate the extent to which parents agreed or disagreed with each item. The survey was administered via paper and pencil during the initial intervention in the clinic-designated research room. The RA remained in the room with the participants to address any questions participants may have had when completing the survey. The survey was translated into Spanish. The intervention took approximately 30 minutes: 10 minutes for recruitment/study information and consent, and 20 minutes for book material distribution and review, and survey. Confidentiality of data collected for the survey was maintained through the use of codes.
Control Group The control condition involves distribution of standard ROR book and book-sharing advice, and the study survey. Consented participants received the standard ROR reading advice and a ROR book. Some books from the standard ROR book list may include images reflective of study participants, but without a direct cultural pride message; therefore, books selected from the ROR children's book list for this study were reviewed and selected by the study PI in order to exclude any ROR books for distribution that may resemble cultural pride books. The comparison group was asked to complete the same study survey as the intervention group using the protocol described above.
Three Month Follow-Up Survey Three months following the initial intervention date at clinics with the intervention and control group participants, RAs conducted follow-up telephone calls to participants. Participants were asked, via phone, to complete the same survey as before with 1 additional question to assess feedback on the study experience. For the follow-up survey, participants were read the questions over the phone (in English or Spanish) and their responses documented on a paper survey by RAs. Confidentiality of data collected for the survey was maintained through the use of codes. The follow-up survey took approximately 10 minutes to complete.
One-Year Chart Review In the year following enrollment, clinic personnel reviewed the medical charts of the children whose parents participated in the study and agreed to the optional chart review. Chart reviews identified subsequent records for: number and type of well-child and sick-child visits, dates of office visits, vaccines status at the 1-year mark, and if documented, follow-up visits and diagnosis from emergency room care. During the initial recruitment and intervention at the office visit those participating consented parents were asked if they gave their permission for the clinic to access their child's medical charts for use in the study. Parents were provided with HIPAA information sheets and an authorization form for release of their child's protected health information.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
California
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Los Angeles, California, United States, 90027
- Children's Hospital Los Angeles
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age 18 years or older
- Parent of at least 1 child 6 months to 5 years old
- English-speaking or Spanish-speaking
Exclusion Criteria:
• N/A
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Intervention
|
The intervention entails distribution of a children's book with a cultural pride theme and the cultural pride parent book-sharing guide.
Intervention participants select and receive a developmentally appropriate (baby, toddler, or preschool) book that features African American, Latino, Asian or diverse cultural pride perspectives.
|
Active Comparator: Control
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The control condition involves distribution of a standard ROR book and book-sharing advice.
Distributed books are developmentally appropriate (baby, toddler, or preschool).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
3-Month Change in Language Development
Time Frame: Baseline at enrollment to 3 months after enrollment
|
3-month change in the percentage of child participants who achieved all age-appropriate language development milestones
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Baseline at enrollment to 3 months after enrollment
|
3-Month Change in Social Development
Time Frame: Baseline at enrollment to 3 months after enrollment
|
3-month change in the percentage of child participants who achieved all age-appropriate social development milestones
|
Baseline at enrollment to 3 months after enrollment
|
3-Month Change in Fine Motor Development
Time Frame: Baseline at enrollment to 3 months after enrollment
|
3-month change in the percentage of child participants who achieved all age-appropriate fine motor development milestones
|
Baseline at enrollment to 3 months after enrollment
|
3-Month Change in Gross Motor Development
Time Frame: Baseline at enrollment to 3 months after enrollment
|
3-month change in the percentage of child participants who achieved all age-appropriate gross motor development milestones
|
Baseline at enrollment to 3 months after enrollment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
3-Month Change in Family-Provider Communication
Time Frame: Baseline at enrollment to 3 months after enrollment
|
3-month change in perception of the quality of communication between the family and provider
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Baseline at enrollment to 3 months after enrollment
|
3-Month Change in Family-Provider Cultural Understanding
Time Frame: Baseline at enrollment to 3 months after enrollment
|
3-month change in perception of the level of cultural understanding between the family and provider
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Baseline at enrollment to 3 months after enrollment
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3-Month Change in Family-Provider Cultural Concordance
Time Frame: Baseline at enrollment to 3 months after enrollment
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3-month change in perception of the importance of cultural concordance between the family and provider
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Baseline at enrollment to 3 months after enrollment
|
Up-to-date Status of Well Child Visits
Time Frame: 12 months after study enrollment
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Up-to-date status of well child visits at 12 months
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12 months after study enrollment
|
Up-to-date Status of Vaccination
Time Frame: 12 months after study enrollment
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Up-to-date status of vaccination at 12 months
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12 months after study enrollment
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Emergency Department Visits for Ambulatory-Sensitive Conditions
Time Frame: 12-month time period from study enrollment to 12 months after enrollment
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Number of emergency department visits for ambulatory-sensitive conditions from study enrollment to 12 months after enrollment
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12-month time period from study enrollment to 12 months after enrollment
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ashaunta T Anderson, MD, MPH, Children's Hospital Los Angeles
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- HS-17-139
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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