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Neonatal Intensive Care Unit Virtual Family-Centered Rounds

University of California (UC) Davis logo

University of California (UC) Davis

Status

Completed

Conditions

Pediatric Disorder
Neonatal Disease

Treatments

Behavioral: Virtual family-centered rounds (FCR)

Study type

Interventional

Funder types

Other

Identifiers

NCT05762835
1764454

Details and patient eligibility

About

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.

Enrollment

514 patients

Sex

All

Ages

Under 365 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

514 participants in 2 patient groups

Intervention (Virtual Family-Centered Rounds [FCR])
Experimental group
Description:
Virtual FCR-arm parents/guardians (referred to as "parents" hereafter) will have the option use have the option to use telehealth for virtual rounds. Parents can participate in virtual FCR as much, or as little, as they choose. Parents also will have the option to attend FCR in person or to not attend FCR.
Treatment:
Behavioral: Virtual family-centered rounds (FCR)
Control (Usual Care)
No Intervention group
Description:
Usual care-arm parents will receive usual care. Usual care-arm parents will have the option to attend FCR in person or to not attend FCR.

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Jennifer L Rosenthal, MD, MAS; Elva Horath

Data sourced from clinicaltrials.gov

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