Tactile/kinesthetic Stimulus Program

Recruiting now · Not applicable

Conditions studied: Breast Feeding, Exclusive, Enteral Feeding, Hospital Stay

In brief

The study will be carried out as a prospective randomized controlled clinical study to determine the effect of tactile/kinesthetic stimulus program on preterm infants on transition time to full sucking, sucking success and hospital stay.

Key facts

Study ID

NCT05486663

Run by

Gonca Karatas Baran

People needed

80

Starts

2022-08-01

Expected to finish

2025-08-01

Last updated by the study team

2024-11-22

Who can join

Age: 1 and older, up to 1. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Born between 28-32 weeks of gestation,
• Stable vital signs,
• 1st and 5th minute APGAR score between 6-10,
• Babies who have received mechanical ventilator or continuous positive air pressure (CPAP) or both support after 48 hours have passed after stabilization,
• Does not have an anomaly that will prevent feeding,
• Oral feeding decision has been made,
• Babies of mothers who are willing to breastfeed their babies,
• Babies of parents who volunteered to participate in the study will be taken.

You may not qualify if…

• IUGG,
• Infants with severe asphyxia,
• Babies born with low birth weight according to their gestational week,
• Having an anomaly that will prevent her from feeding,
• Babies with unstable vital signs,
• Babies with congenital anomalies or serious complications
• Infants with intraventricular bleeding.
• Dismissal Criteria
• Babies whose oral feeding process is interrupted for more than 1 day due to neonatal problems.

Where it is running

• Etlık Zubeyde Hanım Kadın Hastalıkları Eğitim Ve Araştırma Hastanesi — Ankara, Eyalet/Yerleşke, Turkey (Türkiye) (enrolling)

Full record on ClinicalTrials.gov

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