- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02625584
Reading Together: How to Promote Children's Language Development Using Family-based Shared Book Reading
September 13, 2018 updated by: Caroline Rowland
The aim of this project is to determine how shared reading promotes child language development, and to use this knowledge to make it an effective language-boosting tool for children from all social and economic backgrounds.
Study Overview
Status
Completed
Conditions
Detailed Description
Two interventions will be created which are intended to boost children's vocabulary and grammar abilities, and will be assessed on how they are implemented by caregivers across different socio economic groups, and how they affect children's development of these language skills.
Previous research has found dialogic reading interventions to be less effective for children from low socio-economic backgrounds.
This project will investigate whether a shared reading intervention, designed to require less of a behaviour change from caregivers than dialogic reading, can be used to effectively boost vocabulary and grammar development in children across the whole socio-economic spectrum.
Study Type
Interventional
Enrollment (Actual)
150
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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Merseyside
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Liverpool, Merseyside, United Kingdom, L69 7ZA
- Liverpool Language Lab at the University of Liverpool
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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
2 years to 3 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- All families will be included unless they fit the exclusion criteria.
Exclusion Criteria:
- Children born before 37 weeks gestation (premature)
- Children who weighed less than 5lb 9oz at birth (low birth weight)
- Children who have had an ear infection/glue ear for longer than 3 months, 4-6 ear infections within a 6 month period or another identified hearing problem (e.g. at newborn hearing screening)
- Children with an identified developmental disability (e.g. Cerebral Palsy, Autism Spectrum Disorder, Fragile X syndrome, Muscular dystrophy, Di George syndrome, Down's syndrome, Williams syndrome)
- Children with a hearing or visual impairment
- Children who hear another language (not English) for 1 day or more in a typical week (please note that this also excludes children of parents who do not speak English)
- Children whose parents have a learning disability which puts their children at risk of language delay and excludes the parents from giving informed consent on their own and on their children's behalf.
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: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Shared Reading Control
Reading Together - Shared Reading Control.
The intervention will run for six weeks and the caregivers will be provided with books to read with their children.
Caregivers will not be trained to read with their child.
The caregivers will be asked to read two books to their child five times a week.
Caregivers will keep a reading diary and audio record all shared book reading sessions with their child.
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|
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Experimental: Dialogic Reading
Reading Together - Dialogic Reading.
The intervention will run for six weeks and the caregivers will be provided with books to read with their children.
Caregivers will be trained to read with their child using a dialogic reading style.
The caregivers will be asked to read two books to their child five times a week.
Caregivers will keep a reading diary and audio record all shared book reading sessions with their child.
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|
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Experimental: Pausing for Reading
Reading Together - Pausing for Reading.
The intervention will run for six weeks and the caregivers will be provided with books to read with their children.
Caregivers will be trained to read with their child using a style which involves pausing, recasting and open questioning.
The caregivers will be asked to read two books to their child five times a week.
Caregivers will keep a reading diary and audio record all shared book reading sessions with their child.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in baseline language skills (PLS-5)
Time Frame: Baseline and 6 weeks
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The Preschool Language Scale Fifth Edition (PLS-5) Will be administered.
This is a published standardized measure of the language knowledge of individual children.
The investigators will use both the Auditory Comprehension and Expressive Communication scales to measure vocabulary and grammar knowledge.
The PLS-5 standard scores are based on a mean of 100 with a standard deviation of 15.
Scores between 85 and 115 are considered to be within the normal range.
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Baseline and 6 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in baseline syntax comprehension (CELF Preschool-2 UK)
Time Frame: Baseline and 6 weeks
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The Clinical Evaluation of Language Fundamentals - Preschool 2 UK (CELF Preschool-2) will be administered.
This is a published standardized measure of the language knowledge of individual children.
The investigators will use the 'Sentence Structure' subtest.
This will allow measurement of the children's understanding of a range of simple and complex sentence structures.
A sentence is read to the child and the child chooses, from a set of pictures, which picture ''goes with'' that sentence.
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Baseline and 6 weeks
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Change in baseline caregiver dialogic reading behaviour
Time Frame: Baseline and 6 weeks
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10 minute video recordings of the dyads reading books at baseline and 6 weeks will be analysed for the number of target dialogic reading behaviours.
This will allow measurement of the caregiver's dialogic reading behaviour pre- and post-intervention.
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Baseline and 6 weeks
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Change in baseline caregiver pause reading behaviour
Time Frame: Baseline and 6 weeks
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10 minute video recordings of the dyads reading books at baseline and 6 weeks will be analysed for the number of target pause reading behaviours.
This will allow measurement of the caregiver's pause reading behaviour pre- and post-intervention.
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Baseline and 6 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Caroline F Rowland, PhD, The University of Liverpool
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.
General Publications
- Manz PH , Hughes C , Barnabas E , Bracaliello C , Ginsburg-Block M. A descriptive review and meta-analysis of family-based emergent literacy interventions: To what extent is the research applicable to low-income, ethnic-minority or linguistically-diverse young children? Early Childhood Research Quarterly 25(4): 409-431, 2010.
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
January 1, 2016
Primary Completion (Actual)
April 1, 2018
Study Completion (Actual)
April 1, 2018
Study Registration Dates
First Submitted
November 24, 2015
First Submitted That Met QC Criteria
December 4, 2015
First Posted (Estimate)
December 9, 2015
Study Record Updates
Last Update Posted (Actual)
September 14, 2018
Last Update Submitted That Met QC Criteria
September 13, 2018
Last Verified
September 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- RETH000849
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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