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The Effect of the Finger Feeding Method Applied by Fathers on the Transition Time to Oral Feeding and Sucking Success in Premature Babies

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What is being tested

finger feeding

Other
Who is being recruted

Urogenital Diseases+3

+ Female Urogenital Diseases and Pregnancy Complications

+ Obstetric Labor Complications

From 18 to 45 Years
+16 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Supportive Care Study

Interventional
Study Start: February 2024
See protocol details

Summary

Principal SponsorAtaturk University
Study ContactZülbiye DEMİR BARBAKMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: February 15, 2024

Actual date on which the first participant was enrolled.

This study focuses on helping premature babies in the Neonatal Intensive Care Unit transition more effectively to oral feeding. It aims to explore whether a method called the "finger feeding method," applied by fathers, can improve the success of babies learning to feed by mouth. It involves fathers gently allowing their babies to suck on their fingers before regular feeding times. The study seeks to improve the speed and success of oral feeding in these vulnerable infants, potentially enhancing their overall development and wellbeing. In this study, premature babies are placed into two groups. One group, the experimental group, receives the finger feeding method, where fathers let their babies suck on their fingers for five minutes before nasogastric feeding, three times daily for seven days. The control group receives standard care without this additional stimulation. Researchers use tools like the Preterm Baby Monitoring Form and LATCH Breastfeeding Diagnostic Measurement Tool to assess how quickly the babies transition to oral feeding and how successful they are at breastfeeding. This method provides a safe way to encourage feeding skills in premature infants, with the potential benefit of faster development. There are no specified risks involved in the study.

Official TitleThe Effect of the Finger Feeding Method Applied by Fathers on the Transition Time to Oral Feeding and Sucking Success in Premature Babies
NCT06204263
Principal SponsorAtaturk University
Study ContactZülbiye DEMİR BARBAKMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

64 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Male

Biological sex of participants that are eligible to enroll.

From 18 to 45 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsObstetric Labor ComplicationsObstetric Labor, PrematurePregnancy ComplicationsPremature Birth

Criteria

10 inclusion criteria required to participate
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

Show More Criteria

6 exclusion criteria prevent from participating
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

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
The baby will be allowed to suck his father's finger for five minutes three times a day before nasogastric feeding.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Zülbiye DEMİR BARBAK

Erzurum, Turkey (Türkiye)Open Zülbiye DEMİR BARBAK in Google Maps
Recruiting soonOne Study Center