N/A, no intervention, participation in survey: N/A, no intervention, participation in survey
Study summary
This study aims to explore parents' experiences and emotional burdens related to their newborn's hospital stay using an online survey. Our target population consists of parents of newborns born preterm, with low birthweight, or critically ill. Particularly the presence of infant- and family-centred developmental care (IFCDC) principles as well as support through political framework conditions will be investigated.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
Parent or caregiver of a newborn infant born on January 1, 2023, or thereafter, who received/is receiving special/intensive care starting within the first week of life such as oxygen therapy or other respiratory support, incubator treatment, intravenous infusions, treatment of (suspected) sepsis, pneumonia, necrotising enterocolitis, malformations, jaundice, nutritional/feeding problems, hypoglycemia, etc.
Exclusion Criteria:
* Other family members than parents/(primary) caregivers
* Parents of newborns that did not receive special/intensive care starting within the first week of life
* Parents or caregivers of infants born before 1 January 2023
* Persons with insufficient proficiency of one of the languages of the questionnaire
Primary outcome measure(s)
Infant Family-Centered Developmental Care principles — 01/09/2025 - 31/12/2027 The implementation of IFCDC principles will be measured as the percentage of infants receiving specific care, such as skin-to-skin contact, receiving breastfeeding support, access of parents/caregivers to the neonate, involvement in daily care procedures etc.
Trial sites (1)
Facility
City
Region
Status
Global Foundation for the Care of Newborn Infants (GFCNI)
Munich
Bavaria
More Global Foundation for the Care of Newborn Infants trials in Germany
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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