Skip to content

Impact of Implementing Reach Out and Read in the Neonatal Intensive Care Unit

Developmental Promotion in the Neonatal Intensive Care Unit; A New Shared Reading Program

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07511075
Enrollment
101
Registered
2026-04-06
Start date
2021-10-18
Completion date
2023-06-05
Last updated
2026-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neonates or Premature Babies, NICU Infants, Parent, Reading

Keywords

shared reading, infant development, relational health, interventional, neonatal intensive care unit, educational intervention

Brief summary

This is a pre/post quasi-interventional study with two arms. First, a baseline cohort of parent-infant dyads admitted to the Neonatal Intensive Care Unit (NICU) were enrolled and surveyed at three timepoints (admission, discharge, and one-month post-discharge) to characterize baseline habits, attitudes, and barriers toward shared reading in the NICU in the absence of a shared reading program. Reach Out and Read (ROR) in the NICU, a shared reading program modified from the national ROR outpatient program to the NICU setting was then implemented. Following program implementation, a subsequent cohort of parent-infant dyads admitted to the NICU were enrolled (the "ROR" cohort) and surveyed at the same three timepoints. Feasibility, acceptability, and preliminary efficacy of ROR NICU to promote shared reading in the NICU were evaluated.

Interventions

OTHERShared reading program

Reach Out and Read in the NICU (ROR NICU) was implemented. All infants admitted to the NICU receive a book paired with education/anticipatory guidance on shared reading every two weeks during their NICU admission.

Sponsors

Catherine Caruso
Lead SponsorOTHER
Academic Pediatric Association
CollaboratorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE

Intervention model description

A baseline cohort not exposed to a shared reading program was recruited and surveyed at three timepoints. After implementing a shared reading program, a second cohort (exposed to the shared reading program) was recruited and surveyed at the same three timepoints. Cohorts were then compared.

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Parent-infant dyads were recruited with the following criteria: Inclusion Criteria: * New neonatal admission to the NICU at less than or equal to 14 days old * Estimated length of stay 2 weeks or longer * English or Spanish speaking

Exclusion criteria

* Nonviable neonates or those with uncertain viability * Families with discontinuous social situations or parent/infant separation

Design outcomes

Primary

MeasureTime frameDescription
Rate of regular readingTime point 1: baseline. Time point 2: average 6 weeks after baseline. Time point 3: 4 weeks after time point 2Parent-reported frequency of shared reading (days/week) in the last week with "regular reading" defined as at least 3 times per week.

Secondary

MeasureTime frameDescription
Proportion of eligible infants who received the interventionAfter infant discharge, average of 6 weeks from baseline.This is a program fidelity measure assessing how many infants admitted to and discharged from the NICU received the intervention (defined as receiving a book paired with education about shared reading)
Program acceptabilityTime point 1: baseline. Time point 2: average 6 weeks after baseline. Time point 3: 4 weeks after time point 2Survey questions exploring parent experience of the program and an "Acceptability of Intervention Measure" 4-item scaled score (likert scale 1-5) from Weiner et al 2017.
Frequency of intervention per patient (fidelity to the model)After infant discharge, average of 6 weeks from baselineThe frequency and timing of when each ROR cohort infant received a book during admission was tracked

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 14, 2026