- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05508282
Testing an App-Based Approach to Reading and Screen Time Guidance for Parents of Infants
Reading Bees: Randomized Trial of an App-Based Approach to Reading (SHARE/STEP) and Screen Time Guidance for Parents of Infants During Pediatric Clinic Visits
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Ohio
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Cincinnati, Ohio, United States, 45229
- Cincinnati Children's Hospital Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- child age at enrollment less than 2.5 months old,
- no documented history of neurologic insult, extreme prematurity (<32-weeks), or neurodevelopmental condition conveying risk of language delays,
- custodial parent present is at least 18-years old,
- custodial parent present is fluent in English without need of an interpreter, 5) child has no acute illness,
- parent has an Android or iOS-compatible smartphone.
The subset of parent-child dyads recruited for video observation will be on a first-come, first-served basis from those enrolled in the parent study.
Exclusion Criteria:
Violating the above inclusion criteria.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Intervention
These parents will have a new mobile app (Reading Bees) installed onto their smartphone during a baseline clinic visit between 0 and 2-months old. They will also receive a specially designed children's book modeling the SHARE/STEP approach to reading with infants. At 6-months, these parents will also receive guidance regarding limiting digital media use (screen time) using content in the app and a specially designed children's book. They will also receive usual guidance during clinic visits via the Reach Out and Read program |
The reading intervention will be provided at the baseline clinic well-visit (0-2 months), and is based on the SHARE/STEP approach.
The digital media (screen time) intervention will be provided at the 6-month clinic well-visit and is based on Baby Unplugged materials (book and app content).
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No Intervention: Control
These parents will receive usual reading and screen time guidance during pediatric clinic visits, including via the Reach Out and Read program.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility of intervention
Time Frame: Baseline visit (0-2 months)
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Feasibility of Reading Bees app for reading and screen time guidance; includes time of presentation and barriers encountered
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Baseline visit (0-2 months)
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Usability - reading and screen time materials
Time Frame: Baseline visit (0-2 months) for reading, 6-month visit for screen time. Higher scores suggest greater usability.
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Brief survey adapted from prior work involving anticipated usefulness and parental plans to use the infant reading book (SHARE This Book) and related content provided in the Reading Bees app.
Items are categorical, Likert scale.
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Baseline visit (0-2 months) for reading, 6-month visit for screen time. Higher scores suggest greater usability.
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Efficacy - language
Time Frame: 12-month visit
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MacArthur-Bates Communicative Development Inventories, a validated parent-report measure of child language.
Given time and possible literacy constraints, the Words & Gestures Short Form will be used.
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12-month visit
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Efficacy - change in quantitative home reading behaviors
Time Frame: Change between 6- and 12-month visits compared between groups.
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Books in the home, reading frequency and routines (StimQ Reading subscale).
Higher score suggests more stimulating reading environment.
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Change between 6- and 12-month visits compared between groups.
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Efficacy - digital media use (screen time)
Time Frame: 12-month visit
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ScreenQ-I/T report measure/survey reflecting AAP screen time guidelines involving access to screens, frequency, content and co-viewing.
Higher score reflects greater non-adherence with guidelines.
Higher score suggests greater non-adherence with AAP guidelines and subsequently higher risk of adverse impacts.
Range is 0-20 points.
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12-month visit
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Efficacy - change in qualitative home reading behaviors
Time Frame: Change between 6- and 12-month visits compared between groups.
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Shared reading quality/interactivity (SharePR report measure).
Higher score suggests higher quality of shared reading.
Range is 0-30 points.
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Change between 6- and 12-month visits compared between groups.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Video Observation of Shared Reading - Reading Quality
Time Frame: Change between 6- and 12-month visits compared between groups.
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A subset of parents (goal 40 per group) will be recruited for video observation of shared reading.
Videos will be scored using a structured checklist of SHARE/STEP behaviors, with higher scores reflecting greater interactivity and reading quality.
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Change between 6- and 12-month visits compared between groups.
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Video Observation of Shared Reading - Change in Parent-Child Bonding
Time Frame: Change Between 6- and 12-month visits compared between groups.
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A subset of parents (goal 40 per group) will be recruited for video observation of shared reading.
Videos will be scored using an established, observation-based measure of parent-child bonding (WECS), with higher scores reflecting greater connection.
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Change Between 6- and 12-month visits compared between groups.
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Collaborators and Investigators
Investigators
- Principal Investigator: John Hutton, MD, Assistant Professor
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
- 2021-0635
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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