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Family Integrated Care in the NICU

A Family Integrated Care Model For The Neonatal Intensive Care Unit: A Cluster Randomised Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01852695
Acronym
FICare
Enrollment
720
Registered
2013-05-14
Start date
2013-03-31
Completion date
2017-03-31
Last updated
2016-10-04

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

Conditions

Premature Birth

Keywords

Family integrated Care, Family centered care, NICU family centered care, NICU parent program

Brief summary

In the highly technological environment of the modern neonatal intensive care unit (NICU), the infant is physically, psychologically and emotionally separated from its parents. Recognition that this impedes parent- infant interaction and is detrimental to the infant, led to the development of programs such as family centered care, kangaroo care and skin-to-skin care1-3. However, they are based on the common premise that only NICU professionals with special skills can provide care for the infant. Parents are relegated to a supportive role, and some have described themselves as voyeurs who are allowed to visit and hold their infants4. Many feel anxious and unprepared to care for their infants after discharge5. In 1979, a shortage of NICU nurses in Estonia prompted Levin1,6 to implement a humane care model in which parents provided nursing care for the infant (except for administration of IV fluid and medication), while nurses provided teaching and guidance to parents. This resulted in 30% improvement in weight gain1,30% reduction in infections, 20% reduction in NICU length of stay, 50% reduction in nurse utilization and overall improved satisfaction among parents and staff \[personal communication, Levin,A.\]. Building on the Estonian experience, we have developed a new Family Integrated Care (FIC) model that is adapted for the NICU environment in North America. In a pilot study at Mount Sinai Hospital, Toronto 46 infants and their families were enrolled in the study. Preliminary results and feedback from parents and healthcare providers (HCP) show that the FIC model is both feasible and safe, and may lead to improved outcomes including improved weight gain(paper submitted for publication). This study is a cluster randomized controlled trial in 16 tertiary level NICUs, to evaluate the efficacy of the FIC model in Canada.

Interventions

Parents are integrated into the care of their infants in the NICU. Parents consent to spending up to eight hours a day with their infant, attend special education sessions, participate in daily medical rounds, and do basic infant charting. This will enable parents to provide care for infants with nursing supervision in the areas of feeding, bathing, dressing and holding skin to skin.

Sponsors

Foothills Medical Centre
CollaboratorOTHER
Sunnybrook Health Sciences Centre
CollaboratorOTHER
London Health Sciences Centre
CollaboratorOTHER
St. Boniface Hospital
CollaboratorOTHER
CHU de Quebec-Universite Laval
CollaboratorOTHER
IWK Health Centre
CollaboratorOTHER
Hamilton Health Sciences Corporation
CollaboratorOTHER
The Hospital for Sick Children
CollaboratorOTHER
Horizon Health Network
CollaboratorOTHER
Regina General Hospital
CollaboratorOTHER
Royal University Hospital Foundation
CollaboratorOTHER
Windsor Regional Hospital
CollaboratorOTHER
Centre de recherche du Centre hospitalier universitaire de Sherbrooke
CollaboratorOTHER
The Moncton Hospital
CollaboratorUNKNOWN
Health Sciences Centre, Winnipeg, Manitoba
CollaboratorOTHER
Kingston Health Sciences Centre
CollaboratorOTHER
Victoria General Hospital
CollaboratorUNKNOWN
Janeway Hospital
CollaboratorUNKNOWN
Mount Sinai Hospital, Canada
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 33 Weeks
Healthy volunteers
No

Inclusion criteria

* \< 33 weeks gestational age at birth; * On no respiratory support or low level respiratory support (i.e., oxygen by cannula or mask, or continuous positive airway pressure (CPAP); * A primary caregiver parent who is willing and able to commit to spending at least 8 hours per day with her/his infant between the hours of 0700 and 2000; * Parental consent.

Exclusion criteria

* Palliative care; * Major life threatening congenital anomaly; * Critical illness (unlikely to survive); * On high level of respiratory support (mechanical ventilator, high frequency oscillatory or jet ventilation, extra-corporeal membrane oxygenation) * Parental request for early transfer to another hospital; * Parental inability to participate (e.g., health, social or language issues that might inhibit their ability to communicate with the healthcare team).

Design outcomes

Primary

MeasureTime frameDescription
Weight GainDay 0-21Change in weight from enrollment to day 21 following commencement of the intervention

Secondary

MeasureTime frameDescription
Breastfeeding rateup to 16 weeksParticipants will be followed until first discharge home from hospital, an expected average 13 weeks
Clinical outcomes (mortality and Nosocomial infection (NI), Necrotizing Enterocolitis (NEC), Bronchopulmonary Dysplasia(BPD), Retinopathy of prematurity(ROP) & Intraventricular haemorrhage(IVH)up to 16 weeksPatients will be followed for the duration of their hospital stay for an expected average of 13 weeks. Mortality and five major morbidities: (a) Nosocomial infection will be defined using the Center for Disease Control criteria; (b) Necrotizing enterocolitis is defined using Bell's criteria;(c) Bronchopulmonary dysplasia is defined according to Shennan et al; (d) Intraventricular hemorrhage will be classified using the Canadian Pediatric Society classification, from cranial ultrasound performed during the first 28 days of life; (e) Retinopathy of prematurity will be staged according to the International Classification of Retinopathy of Prematurity.
Weight gain velocityDay 0-21Weight gain velocity at 21 days post-intervention commencement;
Parental stress and anxietyDay 0 and when the infant reaches 35 weeks corrected gestational ageWe will administer questionnaires to parents in the first week following admission and when their infant reaches 35 weeks corrected gestational age, in both the intervention and control sites
Resource UseDay 0 -week 16Data on health care utilisation will be collected during the patients entire hospital stay until the first discharge home, averaging 13 weeks including length of stay, duration of oxygen therapy. Per diem costs will be used to estimate potential cost savings derived from any reduced length of stay.
Safety1000 patient daysNumber of critical incident reports/1000 patient days

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026