Condition: Newborn · Sponsor: Tarsus University
Aim: The study was designed to determine the effect of Buzzy® and Shotbloker® application on pain and comfort levels in newborns during heel pricking. Method:The study was a randomised controlled trial. The study sample consisted of 159 newborns (Buzzy: 53, Shotbloker: 53, control: 53) who had heel pricks between March 2025 and December 2025 at the Samandağ State Hospital Neonatal Care Unit. The data collection tools used will be the Newborn Information Form, the Newborn Pain Scale, the Newborn Comfort Behaviour Scale, and the Buzzy® and Shotbloker® devices. In the intervention group, the Buzzy® and Shotbloker® devices will be applied before and after heel pricking, while the control group will receive routine care. The infants' pain and comfort levels will be assessed by the nurse before and after the procedure.
This description comes directly from the study's public registry record.
Duygu Sönmez Düzkaya, PhD · +903246000033 · duygusduzkaya@tarsus.edu.tr
Gözde Özkan, BSC
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| Tarsus University | Mersin, Turkey (Türkiye) | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07081048