Actively Recruiting
Positive Feeding of the Preterm Infant - a Feasibility Study of a Developmental Supportive Feeding Strategy in the NICU
Led by Oslo Metropolitan University · Updated on 2025-08-11
15
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the feasibility of implementing a feeding strategy called the Positive Feeding of the Preterm Infant (PoP) intervention in a level 3a Neonatal Intensive Care Unit (NICU). It focuses on whether this approach can be practically applied and accepted by both parents of preterm infants and healthcare personnel during the NICU stay. The study is designed as a feasibility trial to understand how this feeding strategy works in a real-world clinical setting. The intervention involves following a detailed feeding protocol tailored to the nutritional needs and developmental cues of each preterm infant. Parents receive counseling sessions to support this feeding strategy, which continues until the infant is discharged from the NICU. This approach is developed according to the Medical Research Council framework for complex interventions, ensuring ongoing refinement and evaluation based on feedback. Participants, including parents and healthcare staff, will follow the protocol during the infant's NICU stay. Researchers will collect data over one year to assess recruitment rates, data collection processes, acceptability of the intervention, and resource use. Infant outcomes will also be monitored. The study emphasizes developmental supportive care and feeding practices based on the infant's cues, with continuous counseling for parents throughout the study period.
CONDITIONS
Brief Title
Positive Feeding of the Preterm Infant
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Infant born at gestational age of 28 weeks
- Infant has a post menstrual age of 28 weeks after transfer from a regional hospital
- Parents able to give written consent for themselves and their infant
You will not qualify if you...
- Diagnoses or malformations that make eating difficult
- Triplets or higher multiple births
- Parents do not speak or understand Norwegian or English
- Parents have challenges or special needs for follow-up
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Screening and enrollment visit
Duration - Until discharge from the NICU
Participants follow a feeding protocol tailored to the infant's developmental needs with parental counseling to support feeding development until discharge from the NICU.
Visits as part of routine NICU care
Trial Site Locations
Total: 1 location
1
Vestre Viken Hospital Trust
Drammen, Norway, 3028
Actively Recruiting
Research Team
N
Nina M Kyno, PhD
L
Linn J Gustavsen, MSc
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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