Positive Feeding of the Preterm Infant

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorOslo Metropolitan University

About this trial

The goal of this feasibility study is to assess the feasibility to implement a feeding strategy for preterm infants.

The main questions it aims to answer are:

* Is it feasible to implement the PoP-intervention in a level 3a category Neonatal intensive care unit? * Is the PoP-intervention acceptable for parents of preterm infants and health care personnel working in Neonatal intensive care unit?

Parents of preterm infants and health care personnel will be asked to follow a protocol of a feeding strategy based on the preterm infants development and cues throughout the NICU-stay.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

gestational age of 28 weeks

post menstrual age of 28 weeks after transition from regional hospital

Disqualifiers

diagnoses or malformations that makes eating difficult

triplets or more

parents not speaking/understanding Norwegian or English

parents with challenges or special needs for follow up

Trial design

Design model

Single group

Treatments tested in this trial

  • Positive feeding of the preterm infant

    Other intervention

    Feeding strategy for the preterm infant with description of nutritional needs and based on the infants development and cues.

Treatment groups

15 Participants
are divided into 1 treatment group
Group A: Intervention groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Recruitment rates and sample criteria

Variables to evaluate if we can recruit appropriate participants, the time frame it takes, the eligibility criterias, the recruitment routines.

Time frame
Prospective over a period of 1 year
2

Data collection and outcome variables

How appropriate are the data collection procedures, the participants ability to complete the quiestionnaires, appropriatness of the amount of data collection, completion of datasets,

Time frame
Prospective over a period of 1 year
3

Acceptability

Evaluation of acceptability of the intervention for the participants, adherence to the study procedures, the burden for participants and the health care personnell conducting the intervention, safety and adverse events

Time frame
Prospective over a period of 1 year
4

Resources and organisation

Evaluation of the resources needed to conduct the study procedures, resources needed for training health care personnel or other costs related to the study

Time frame
Prospective over a period of 1 year

Secondary outcomes

1

Infant outcome variables

A pilotstudy of the intervention with focus on the infants outcomes, such as weight gain, feeding milestones, nutrition, feeding methods,

Time frame
Prospective over a period of 1 year

Other outcomes

Sponsors and contacts

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