N/A
N=514
Neonatal Intensive Care Unit Virtual Family-Centered Rounds
Pediatric Disorder · Neonatal Disease
Bottom Line
View on ClinicalTrials.gov: NCT05762835 ↗Enrolled (actual)
514
Serious AEs
0.0%
Results posted
Aug 2025
Primary outcome: Primary: Parent FCR Attendance — 0.56; 0.12 proportion of encounters
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Virtual family-centered rounds (FCR) (Behavioral)
- Age
- Pediatric, Adult, Older Adult
- Sex
- All
- Sponsor
- University of California, Davis
- Primary completion
- Apr 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Parent FCR Attendance |
0.56; 0.12 | — |
| SECONDARY Parent Experience |
— | — |
| SECONDARY Family-Centered Care |
— | — |
| SECONDARY Parent Activation |
— | — |
| SECONDARY Parent Health-related Quality of Life |
— | — |
| SECONDARY NICU Length of Stay |
— | — |
| SECONDARY Breastmilk Feeding |
— | — |
| SECONDARY Postnatal Growth Failure (Dichotomous) |
— | — |
| SECONDARY Postnatal Growth Failure (Categorical) |
— | — |
Summary
The aim of this study is to evaluate the impact of virtual family-centered rounds in the neonatal intensive care unit on parental and neonatal outcomes.
Eligibility Criteria
Enrolling family units (which consists of INFANTS and PARENTS [SURVEYS]):
INFANT Inclusion
- Infants aged less than 365 days who are admitted to the NICU
- Have at least one adult parent or guardian with English proficiency
INFANT Exclusion
- Have restrictions placed by child protective services, including visitation restrictions or restricted access to patient information
- Infants with a previous NICU admission (and enrollment) during the trial period
PARENTS [SURVEYS] Inclusion
- Parents/guardians of the eligible infants (described above)
- Age 18 years and older
PARENTS [SURVEYS] Exclusion
- Age less than 18 years
- Non-English speaking
Data sourced from ClinicalTrials.gov (NCT05762835). 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.