Actively Recruiting
Tactile/kinesthetic Stimulus Program
Led by Gonca Karatas Baran · Updated on 2024-11-22
80
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Tactile/kinesthetic Stimulus Program
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Born between 28-32 weeks of gestation
- Stable vital signs
- APGAR score between 6-10 at 1 and 5 minutes
- Received mechanical ventilator or CPAP support after stabilization for at least 48 hours
- No anomaly preventing feeding
- Oral feeding decision has been made
- Mothers willing to breastfeed their babies
- Parents who volunteer to participate in the study
You will not qualify if you...
- Intrauterine growth restriction (IUGR)
- Severe asphyxia
- Low birth weight for gestational age
- Anomaly preventing feeding
- Unstable vital signs
- Congenital anomalies or serious complications
- Intraventricular bleeding
- Oral feeding interrupted for more than 1 day due to neonatal problems
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Etlık Zubeyde Hanım Kadın Hastalıkları Eğitim Ve Araştırma Hastanesi
Ankara, Eyalet/Yerleşke, Turkey (Türkiye), 06290
Actively Recruiting
Research Team
G
GONCA K KARATAS BARAN, PHD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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