Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
ID06189352

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

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Screening and enrollment visit

Treatment

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

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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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