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Improving Preterm Infant Outcomes With Family Integrated Care and Mobile Technology

Not Applicable
Completed
Conditions
Premature Birth of Newborn
Interventions
Behavioral: Family Integrated Care
Registration Number
NCT03418870
Lead Sponsor
University of California, San Francisco
Brief Summary

The purpose of this study is to compare the standard of care in the neonatal intensive care unit (NICU), known as Family Centered Care, to a new model of care, called mobile enhanced Family Integrated Care. This exploratory two-group comparison study will examine the feasibility, acceptability and effectiveness, providing the first United States (US) information about outcomes of a new NICU care model that better integrates parents into all aspects of their baby's care. The use of mobile technology as part of this new model of care could improve access and equity in family integration for the many US families who face barriers to NICU involvement.

Detailed Description

Poor growth during neonatal intensive care unit (NICU) hospitalization is a modifiable risk factor contributing to mortality and serious long-term morbidity for many of the nearly 400,000 preterm infants born each year in the United States (US). Active parent involvement in preterm infant caregiving promotes parent-infant attachment and leads to higher breastfeeding rates, earlier discharge, and improved long-term neurodevelopment. Despite decades of evidence of the positive effects of parental involvement, parents remain for the most part passive bystanders in the NICU setting. Even with many NICUs adopting a Family-Centered Care (FCC) approach, parent-infant contact and parenting skills remain well below desired levels.

Family Integrated Care (FI-Care) is a novel intervention that differs from FCC because it formally teaches and supports parents to be primary caregivers for their infants and restructures the relationship between parents and clinicians so that parents are fully integrated into the care team. There is strong evidence from a large, well-designed cluster randomized trial conducted in Canada and Australia that FI-Care improves infant growth and breastfeeding rates and reduces maternal stress. However, these findings cannot be generalized to US NICUs where parents face many barriers to involvement in their infant's NICU care. The research team has developed a secure, HIPAA-compliant, mobile application to capture high quality data about parent involvement in NICU caregiving and to deliver essential elements of the FI-Care program remotely. This mobile-enhanced FI-Care (mFI-Care) may improve involvement of parents who cannot be present in the NICU during daytime hours due to distance, employment or other responsibilities and family commitments. Increasing access and equity in family-integrated care may improve outcomes for US preterm infants.

This exploratory two-group, multi-site comparison study will compare usual FCC with mFI-Care on growth and clinical outcomes of preterm infants \< 33 weeks gestational age, as well as the stress, competence and self-efficacy of their parents. The feasibility and acceptability of using mobile technology to gather data about parent involvement in the care of preterm infants receiving FCC or mFICare as well as of the mFI-Care intervention will be evaluated (Aim 1). The effect sizes for infant growth (primary outcome) and for secondary infant and parent outcomes at NICU discharge and three months after discharge will be estimated (Aim 2). This study will provide important new information on innovative approaches to increasing parent involvement in NICU infant caregiving, including the use of a novel mobile application. The findings will be used to develop a future US cluster-randomized trial of mFI-Care with the aim of improving outcomes for preterm infants and their parents.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
347
Inclusion Criteria
  • Infant ≤ 33 weeks and their parent or guardian
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Exclusion Criteria
  • Infant has a life-threatening congenital anomaly, is unlikely to survive or is receiving palliative care
  • Parent is not English literate
  • Parent < 18 years of age
  • Parent does not have access to hand-held computer (smartphone or tablet)
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
Family Integrated Care (mFI-Care)Family Integrated CareParents of infants assigned to the Family Integrated Care (mFI-Care) intervention will be treated as primary caregivers for their infants and participate in daily medical rounds, with mFI-Care-trained nurses serving as teachers and coaches. Parent training on the Canadian FI-Care Parent Curriculum will be provided during small group sessions facilitated by the study team. Parents will receive peer support from mFI-Care-trained alumni parents and can interact with other mFI-Care parents through the We3Health App secure online parent forum. mFI-Care parents will be expected to track time spent with their infant; record infant activity, feeds and output; track learning and skills acquisition; and keep a journal of the NICU experience using the We3Health app.
Primary Outcome Measures
NameTimeMethod
Change in infant weight (z-score)21 days of age after enrollment

Z-score will be calculated by obtaining weight in kilograms from medical record and compared between the mFICare and usual FCC groups

Secondary Outcome Measures
NameTimeMethod
Major morbiditiesat NICU discharge, usually 21 days after admission

Nosocomial infection, necrotizing enterocolitis, intraventricular hemorrhage, retinopathy of prematurity, and adverse events.

Parenting competenceat NICU discharge, usually 21 days after admission

self reported survey

Length of stayNumber of days of NICU and hospital stay, usually 21 days after admission

Number of days of NICU and hospital stay

Amount of human milk/formula supplementationAt study enrollment and at hospital discharge, usually 21 days after admission

number of ml for all breast feeding, breast pumping, bottle feeding, and nasal gastric (NG) feeding will be obtained from the medical record

Frequency of breastfeedingAt study enrollment and at hospital discharge, usually 21 days after admission

Number of feedings for breast feeding, breast pumping, bottle feeding, and NG feeding will be obtained from the medical record

Weight gain velocityat NICU discharge, usually 21 days after admission

number of grams gained from enrollment to specified date divided by the number of days = weight gain velocity

Breastfeeding rateAt study enrollment and at hospital discharge, usually 21 days after admission

Breastfeeding rate will be calculated using amount of Number of feedings and ml for breast feeding, breast pumping, bottle feeding, and NG feeding will be obtained from the medical record

Parent perceived stressat NICU discharge, usually 21 days after admission

Self- reported survey

Perceived parenting self-efficacyat NICU discharge, usually 21 days after admission

self-reported survey

Trial Locations

Locations (6)

Community Regional Medical Center

🇺🇸

Fresno, California, United States

UCSF Benioff Children's Hospital Oakland

🇺🇸

Oakland, California, United States

UCSF Benioff Children's Hospital San Francisco

🇺🇸

San Francisco, California, United States

Jacobs Medical Center, UC San Diego Health

🇺🇸

La Jolla, California, United States

Kaiser Permanente - Santa Clara

🇺🇸

Santa Clara, California, United States

UCLA Medical Center, Santa Monica

🇺🇸

Santa Monica, California, United States

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