Supporting and Enhancing NICU Sensory Experiences (SENSE) (SENSE)
Premature Birth of Newborn

About this trial
This is an interventional treatment trial for Premature Birth of Newborn focused on measuring preterm
Eligibility Criteria
Inclusion Criteria:
Preterm Infants:
- A prospective cohort very preterm infants (VPT) born less than or equal to 32 weeks gestation at the St. Louis Children's Hospital in St. Louis, Missouri.
- Infant is less than or equal to 7 days old when approached about the study.
Parents:
-Parents (including emancipated minors age 12-17) of very preterm infants (VPT) born less than or equal to 32 weeks gestation at the St. Louis Children's Hospital in St. Louis, Missouri.
Exclusion Criteria:
Preterm Infants:
- Known or suspected congenital anomaly, congenital infection (e.g., syphilis, HIV, TORCH), or known prenatal brain lesions (e.g., cysts or infarctions)
- Infants that are wards of the state, or become wards of the state after enrolling in the study. Any data collected beginning at the time the state obtains custody onward will not be used in the research study.
- Infants who are in the open ward area/bed spaces of the SLCH NICU (due to the significant variation in sensory exposure among those infants, and also to provide consistency during the hospital's impending transition to strictly private rooms in the very near future).
Parents:
-Parents with limited or no understanding of the English Language
Sites / Locations
- St. Louis Children's Hospital
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Control
Intervention
The control group received standard hospital care.
Parents in the sensory-based intervention group were educated to provide daily sensory-based interventions across the length of hospitalization as outlined in the manualized intervention (the SENSE Program). A sensory support team completed the doses of sensory exposures when parents were unable.