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N/A N=10 Randomized Single-blind Prevention

Literacy Promotion Using Automated Hovering

Parent-Child Relations · Parenting · Literacy

Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Nov 2024
Primary outcome: Primary: Acceptability Survey — 4; 3.3; 3.8 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Texting (Behavioral); Regret (Behavioral); Lottery (Behavioral)
Age
Pediatric · 0+ yrs
Sex
All
Sponsor
Children's Hospital of Philadelphia
Primary completion
Feb 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Acceptability Survey
4; 3.3; 3.8
PRIMARY
Feasibility of Study
14; 13; 15; 10
SECONDARY
Change in Score of Cognitive Stimulation Provided in the Home Measure - (StimQ-Read)
1.8; 3.2; 1.3 0.32
SECONDARY
Change in Score for The Parenting Stress Index - Short Form (PSI-SF)
2.2; 5.3; 9 0.78
SECONDARY
Change in Weekly Parent-Child Shared Reading Frequency
4.1; 4.0; 4.8; 3.9; 4.2; 4.9 0.19
SECONDARY
Measure of Child Socio-Emotional Development Using Devereux Early Childhood Assessment (DECA)
77.6; 64.3; 72.1; 79.4; 66.6; 75.6 0.46
SECONDARY
Measure of Child Language Development Using MacArthur Communicative Development Inventory (CDI) - Percentiles
84.6; 78.5; 63.1 0.30

Summary

The purpose of this study is to incorporate behavioral economics (BE) approaches to determine whether 3 novel interventions of varying intensity improve the frequency of parent-child reading behaviors among low-income families. In the first phase, 10 parents will be recruited to participate in rapid cycle interviews to determine the appropriateness of text messages. In the second phase, 45 participants will be randomized to comparative groups to test the effects of automated hovering and other BE approaches on frequency of parent-child shared reading. Investigators long-term goal is to test the effects of these approaches to promote child language and socio-emotional development.

Eligibility Criteria

Inclusion Criteria

  • Parents who:
  • Have an infant aged 6-24 months
  • Have access to a smart phone with text messaging capabilities
  • Have completed an informed consent
  • Children who:
  • Are aged 6-24 months old

Exclusion Criteria

  • Parents who:
  • Non-English speaking
  • Children who:
  • Were born premature (estimated gestational age < 35 weeks)
  • Have been diagnosed with congenital malformations or genetic syndromes which place them at risk for developmental delays
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04576481). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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