The Effect of the Finger Feeding Method Premature Babies

N/AUnknownNCT06204263

Ataturk University64 enrolled

Overview

This study aimed to determine the effect of the finger feeding method applied by fathers on the transition time to oral feeding and sucking success in premature babies.

Premature babies followed in the Neonatal Intensive Care Unit will be randomly divided into two groups: control group and finger-feeding group. Babies in the experimental group will be breastfed by their father three times a day. Before nasogastric feeding, the baby will be allowed to suck his finger by putting his finger in his mouth for five minutes three times a day. This procedure will be applied three times a day (morning, noon and evening) for a full 7 days. Babies in the control group will be given only routine ward care (breast milk or formula via tube without stimulation of the pacifier or mother's finger). Preterm Baby Monitoring Form and LATCH Breastfeeding Diagnostic Measurement Tool will be used to determine the transition time to oral feeding and breastfeeding success.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

DOUBLE

Enrollment

Conditions

Premature

Interventions

finger feedingOTHER

The fathers of premature babies in intensive care will be interviewed and an educational booklet will be prepared about finger feeding, cleaning, hygiene, hand washing, the importance of sucking, and the rules to be followed to prevent infection in the newborn, and how to apply it will be explained by the researcher. Babies will be breastfed three times a day for seven days.

Eligibility

Sex: MALEMin age: 18 YearsMax age: 45 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Premature babies at 29-31 weeks * Birth weight of 1300 g or more * Those whose 1st and 5th minute Apgar scores are over 6 * Those whose vital signs and health status are stable * In babies who have received mechanical ventilation and continuous positive air pressure support, those who have passed 48 hours after stability has been achieved * No facial or oral anomalies * Premature babies without swallowing difficulties * Those fed via nasogastric tube * Fathers who can read, write and speak Turkish * Fathers of preterm babies who agreed to participate in the research. Exclusion Criteria: * Those whose vital and health conditions are unstable * Those whose father has a skin condition or those who developed it later * Any upper respiratory tract infection in the father * Premature babies without swallowing difficulties * Fathers who cannot read, write or speak Turkish * Fathers with preterm babies who do not consent to this study will not be included in the scope of the research.

Locations (1)

Zülbiye DEMİR BARBAK

Erzurum, Center, Turkey (Türkiye)

Outcomes

Primary Outcomes

Patient Identification Form

This form contains information such as the age of the mother and father, the baby's weight, time to independent oral feeding, discharge weight, length of hospital stay, fetal age at birth, Apgar score, gender of the baby, etc.

Time frame: Baseline

Secondary Outcomes

Preterm Baby Monitoring Form

During the study process, it will be used to record the preterm baby's "first finger feeding, transition to oral feeding, first latch on the mother's breast, transition to full mother's breast, discharge dates and body weight at these stages, as well as the finger feeding chart" information.

Time frame: Baseline

Central Contacts

Zülbiye DEMİR BARBAK

CONTACT

+904422314066 zulbiye.demir@atauni.edu.tr

FATMA KURUDİREK

CONTACT

+905435164229 fatmasaban25@hotmail.com

Data from ClinicalTrials.gov

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