- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02780557
How Parents Can Help Babies Learn to Talk With Picture Books.
May 1, 2018 updated by: Danielle Matthews, University of Sheffield
A Randomised Control Trial to Test the Effect of Parent Contingent Talk During Shared Book Reading on Infant Language Learning.
The aim of this project is to test whether giving parents advice about book reading is effective in promoting language learning for infants from a range of socio-economic backgrounds.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Children from disadvantaged families tend to have limited language skills compared to their advantaged peers.
While many factors contribute to language ability, two aspects of the early caregiving environment are known to be correlated with child language outcomes 1) caregiver-child book reading and 2) caregiver contingent talk.
Contingent talk refers to a style of communication whereby the caregiver talks about what is in their infant's current focus of attention.
This style of talking can be facilitated when parents read books with their babies.
The aim of this research is to establish whether asking parents to engage in contingent talk in the context of book reading promotes vocabulary learning.
This study will compare the effects of an intervention to promote contingent talk against a control where parents are given books but not given any training in how to read them in a contingent manner.
The study will include children from socio-economically advantaged and disadvantaged families.
Study Type
Interventional
Enrollment (Actual)
156
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
-
-
South Yorkshire
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Sheffield, South Yorkshire, United Kingdom, S10 2TN
- University of Sheffield
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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
11 months to 11 months (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
Infants must be:
- first born and singletons
- full term (i.e. born no more than 3 weeks prematurely)
- with birth weight over 2.5 kg.
Primary caregivers must:
- work less than 24 hours per week (i.e., be the caregiver the child spends most time with)
- be raising their child as monolingual English speakers.
Exclusion criteria:
Neither caregivers nor infants must have any significant known physical, mental or learning disability.
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: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Contingent Reading Intervention
|
Caregivers will be provided with 6 picture books.
They will be trained to use contingent talk when looking at picture books with their infants.
They will be asked to spend 10 mintues each day engaging in contingent talk while looking at picture books.
The intervention will run for 4 months.
Parents will be asked to keep a daily reading diary.
|
Other: Book Provision Control
|
Caregivers will be provided with 6 picture books.
They will not be trained to read with their child.
They will receive information from other sources (e.g.
health visitors and Book Start schemes) as normal.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in infant expressive vocabulary
Time Frame: Baseline: 11 months, outcome: 15 months
|
Parents will complete a standardised assessment of vocabulary, the MacArthur-Bates Communicative Development Inventory (CDI).
|
Baseline: 11 months, outcome: 15 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in caregiver reported frequency of reading
Time Frame: Baseline: 11 months, outcome: 15 months
|
Parents will complete a questionnaire about how frequently they read with their child.
|
Baseline: 11 months, outcome: 15 months
|
Infant Real Time Language Understanding: Accuracy
Time Frame: 15 months
|
Infants' real-time comprehension of familiar words will be assessed at 15 months using the looking-while-listening (LWL) procedure (Fernald et al., 2008).
Infants will sit in front of a computer screen with a picture on either side of it (e.g., a bottle and a shoe).
We will measure the accuracy with which they look to the correct picture upon hearing a word that describes it.
|
15 months
|
Infant Real Time Language Understanding: Reaction Time
Time Frame: 15 months
|
Infants' real-time comprehension of familiar words will be assessed at 15 months using the looking-while-listening (LWL) procedure (Fernald et al., 2008).
We will measure the time it takes the child to look from a distractor to the target.
|
15 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in caregiver contingent talk while book reading
Time Frame: Baseline: 11 months, outcome: 15 months
|
Video recordings of dyads reading books will be analysed for quantity of caregiver contingent talk.
|
Baseline: 11 months, outcome: 15 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Danielle E Matthews, PhD, University of Sheffield
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)
August 24, 2016
Primary Completion (Actual)
January 30, 2018
Study Completion (Actual)
March 22, 2018
Study Registration Dates
First Submitted
May 19, 2016
First Submitted That Met QC Criteria
May 19, 2016
First Posted (Estimate)
May 23, 2016
Study Record Updates
Last Update Posted (Actual)
May 4, 2018
Last Update Submitted That Met QC Criteria
May 1, 2018
Last Verified
May 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- R/139470-11-1-INFANCY
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
With participants' permission, IPD will be archived in accordance with the guidelines of the University of Sheffield, the UK Data Archive and the ESRC's Research Data Policy.
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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