- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02713659
Early Literacy Promotion Intervention (ELPI)
August 2, 2019 updated by: Children's Hospital of Philadelphia
Early Literacy Promotion Among Poor Urban Children in Philadelphia
This study is testing the effects of early literacy promotion compared to standard literacy promotion at The Children's Hospital of Philadelphia.
Eligible participants and their families will be consented and randomly assigned into either a standard literacy program or an early literacy program.
Standard literacy will consist of the receipt of books and reading promotion beginning at 6 months of age, while early literacy will consist of the receipt of books and reading promotion beginning in the newborn period.
In both groups, participants will receive weekly text messages until the child is 6 months old (the text messages will either about reading or safety) and have follow-up study visits at 6, 12, 18, and 24 months.
The study will examine the effects of the intervention on language development and reading behaviors.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Poor urban children are at an increased risk for language and cognitive delays.
Such delays can lead to poor school readiness and disparities in educational outcomes when compared to children from middle and upper income strata.
Reach Out and Read (ROR), a national program which promotes parent-child reading activities for children 6 months through 5 years of age at pediatric well child visits, has been shown to improve at-risk children's expressive and receptive language development.
However, poor children who participate in ROR still demonstrate language outcomes that are below national averages.
It isn't clear whether early literacy promotion, i.e. promotion of parent-child reading prior to six months of age, is more effective than standard literacy promotion and can further improve poor children's language and cognitive outcomes.
Therefore, this study will test the effectiveness of early literacy promotion compared to standard literacy promotion among poor at-risk children.
Children with Medicaid insurance who are under 1 month of age, were born at least 35 weeks gestation, whose mothers speak English or Spanish and are 15 years of age and older, and are without any neurodevelopmental disabilities will be eligible to participate.
One to two urban practices affiliated with The Children's Hospital of Philadelphia (CHOP) who have implemented ROR as standard practice will be recruited to participate.
One hundred twenty eligible children attending participating practices will be recruited to participate and consented, stratified by practice site, and randomized to receive early literacy promotion or standard literacy promotion.
Early literacy promotion will consist of the provision of developmentally appropriate books selected specifically for well visits starting from one month of age to six months; discussion of the importance of reading, talking, and singing by pediatric clinicians; and text message reminders to parents concerning early literacy and daily reading.
Standard literacy promotion will consist of the Reach Out and Read Program with provision of developmentally appropriate books at all well visits from six months of age onward and promotion of reading, talking, and singing activities by pediatric clinicians.
Mothers will complete study measures consisting of demographic characteristics, postpartum depression symptoms, health literacy, and adverse childhood experiences at enrollment, and mothers and children will complete measures of reading activity (Stim-Q) at 6, 12, 18, and 24 months of age and child expressive and receptive language development (Preschool Language Scale) at 6 and 24 months of age.
Differences in child language outcomes will be assessed using intention-to-treat.
Results of this study will be disseminated to key stakeholders through peer-reviewed manuscripts, reports, social media, and evidence-to-action briefs prepared by Policylab at the Children's Hospital of Philadelphia.
Study findings will be of importance to the Annie E. Casey Foundation's Read!
By 4th in Philadelphia and other community Grade-Level Reading Campaigns, the Clinton Foundation's Too Small to Fail initiative to advance early brain development, and Great Start Collaborative's Early to Read campaign.
Study Type
Interventional
Enrollment (Actual)
120
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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Pennsylvania
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Philadelphia, Pennsylvania, United States, 19104
- Children's Hospital of Philadelphia
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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
15 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- English or Spanish speaking
- Mothers 15 years of age or older at the start of the study
- Child born ≥ 35 weeks estimated gestational age (EGA)
- Child less than 4 weeks old at enrollment
- Child with Medicaid Insurance
Exclusion Criteria:
- Child born premature < 35 weeks EGA
- Children with neurodevelopmental disabilities or congenital malformation at increased risk of language delays
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Early Literacy Promotion
Parents and children randomized to the Early Literacy Promotion arm.
|
Parents will receive a book with developmentally appropriate advice about reading at each well child visit from one week through 5 months of age, as well as weekly text reminders related to reading.
From 6 months of age, both groups will receive standard literacy promotion and will attend study visits every six months until age 2.
|
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Active Comparator: Standard Literacy Promotion
Parents and children randomized to the Standard Literacy Promotion arm.
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Parents will receive weekly text messages about child safety, and no books before the age of 6 months from their provider.
From 6 months of age, both groups will receive standard literacy promotion and will attend study visits every six months until age 2.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Preschool Language Scale-5th Edition Score
Time Frame: Change in PLS scores from 6 to 24 months of age
|
The Preschool Language Scale-5th Edition (PLS) is a validated measure of expressive and receptive language function among children from birth through 7 years of age and is available in Spanish and English.
PLS-5 provides three norm-referenced standard scores: Auditory Comprehension (AC) standard score, Expressive Communication (EC) standard score, and Total Language (TL) composite score.
The scores are on a normalized standard score scale that has a mean of 100 and a standard deviation of 15 with scores ranging from 0-200.
Higher scores represent better language development..
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Change in PLS scores from 6 to 24 months of age
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in StimQ Score
Time Frame: Change in StimQ score from 6 to 24 months of age
|
Reading activity is measured using the StimQ Read Subscale, a subscale scale of the overall StimQ that measures the home reading environment among young children ages 5 to 36 months, and is available in Spanish and English.
The Read Subscale of the StimQ-I is used for infants 5-12 months old and contains 12 questions, while the Read Subscale of the StimQ-T is used for children aged 12-36 months old and contains 11 questions.
Scores range from 0-19 with higher scores representing better home reading environments.
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Change in StimQ score from 6 to 24 months of age
|
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Health Services Utilization
Time Frame: Birth to 6 months of age
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Immunizations and well child visit data will be collected from electronic health records to measure impact of ELP intervention on health services use.
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Birth to 6 months of age
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: James P Guevara, MD, MPH, Children's Hospital of Philadelphia
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)
March 1, 2016
Primary Completion (Actual)
December 1, 2018
Study Completion (Actual)
December 1, 2018
Study Registration Dates
First Submitted
March 10, 2016
First Submitted That Met QC Criteria
March 15, 2016
First Posted (Estimate)
March 21, 2016
Study Record Updates
Last Update Posted (Actual)
September 9, 2019
Last Update Submitted That Met QC Criteria
August 2, 2019
Last Verified
August 1, 2019
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- IRB 15-012507
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Following completion of all analyses, data will be de-identified and made available for other investigators.
IPD Sharing Time Frame
12 months after publication of all relevant papers
IPD Sharing Access Criteria
De-identified only
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
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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