Actively Recruiting

Phase Not Applicable
Age: 29Weeks - 33Weeks
All Genders
Healthy Volunteers
NCT07306793

The Effect of PIOMI and Chronobiological Nutrition on Readiness for Feeding, Full Transition to Oral Feeding and Body Weight

Led by Aydin Adnan Menderes University · Updated on 2026-01-06

54

Participants Needed

1

Research Sites

82 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a randomized controlled experimental study evaluating the effects of oral motor intervention and chronobiological approach to feeding model applied to preterm infants on feeding readiness, transition to total oral feeding and body weight.

CONDITIONS

Official Title

The Effect of PIOMI and Chronobiological Nutrition on Readiness for Feeding, Full Transition to Oral Feeding and Body Weight

Who Can Participate

Age: 29Weeks - 33Weeks
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Preterm infants aged 29 to 33 weeks postnatal
  • Stable vital signs and clinical condition for at least 24 hours
  • APGAR score of 4 or higher at 1 and 5 minutes after birth
Not Eligible

You will not qualify if you...

  • Infants with major congenital anomalies such as congenital heart disease, cleft palate, or cleft lip
  • Infants with respiratory distress syndrome
  • Infants diagnosed with asphyxia
  • Infants with intraventricular hemorrhage
  • Infants with neonatal withdrawal syndrome
  • Infants with fetal alcohol syndrome
  • Infants who develop complications or whose stable condition worsens during the study
  • Infants with feeding intolerance or feeding interruptions over 48 hours
  • Infants who develop sepsis
  • Infants who develop necrotizing enterocolitis
  • Infants receiving mechanical ventilation
  • Infants receiving narcotic analgesia or sedation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Aydın Adnan Menderes University, Faculty of Nursing, Department of Child Health and Disease Nursing

Aydin, Turkey (Türkiye)

Actively Recruiting

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Research Team

E

Esra Bozkurt, MSc

CONTACT

S

Seher Sarıkaya Karabudak, Associate Professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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