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FamilyLink Family-Centered Rounds

FamilyLink Family-Centered Rounds Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04265677
Enrollment
110
Registered
2020-02-11
Start date
2020-04-01
Completion date
2021-02-02
Last updated
2021-03-05

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

Conditions

Family Centered Rounds

Brief summary

This study will be a pilot test of using FamilyLink software to bring parents of patients in the neonatal intensive care unit (NICU) virtually to the bedside during Family Centered Rounds.

Interventions

OTHERTelemedicine FCR

Parents/guardians will be able to join family centered rounds using telemedicine (audio and visual)

OTHERStandard of care

Parents/guardians will not be able to join family centered rounds using telemedicine (audio and visual)

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients admitted to the Blue Team in the NICU aged 0-365 days * Parents/guardians of patients admitted to the Blue Team in the NICU aged ≥ 18 years * Medical team members (physicians, nurse practitioners, fellows, residents, medical students, nurses) of patients admitted to the Blue Team in the NICU aged ≥ 18 years

Exclusion criteria

* Patients who are not discharged home from the NICU (e.g., transferred to another inpatient unit or another hospital) * Parents/guardians of patients admitted to the Blue Team in the NICU who do not speak English, as a translator will not reliability be available to participate in rounds when the parent/guardian is not physically present * Patients who have more than one admission to the Blue Team during our study period will only be included on their first admission

Design outcomes

Primary

MeasureTime frameDescription
CAHPS Communication with Parent SubscaleThrough study completion, approximately 3 months19 questions from the Communication with Parent Subscale of the Consumer Assessment of Healthcare Providers and Systems Child Hospital Survey; specifically, we will report the following measures: Communication between you and your child's nurses (composite measure); Communication between you and your child's doctors (composite measure); Communication about your child's medicines (composite measure); Keeping you informed about your child's care (composite measure) Privacy when talking with doctors, nurses, and other providers (single-item measure); Preparing you and your child to leave the hospital (composite measure); Keeping you informed about your child's care in the Emergency Room (single-item measure). Higher scores are better; 0 (minimum) - 100 (maximum)

Secondary

MeasureTime frameDescription
Rates of adverse eventsUp to 6 monthsRates of adverse events reported by parents, providers, or nurses
Hospital Length of StayThrough study completion, approximately 3 monthsHospital length of stay of the patient measured in days
Breastmilk at dischargeThrough study completion, approximately 3 monthsIf the patient was receiving all, some or no breastmilk

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026