Clinical Trials Directory

Trials / Completed

CompletedNCT06773325

Buzzy Application During Heel Blood Collection in the Newborn

The Effect of Buzzy Application on Pain and Comfort Level During Heel Blood Collection in Newborns: A Randomized Controlled Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Yuzuncu Yil University · Academic / Other
Sex
All
Age
0 Days – 28 Days
Healthy volunteers
Accepted

Summary

Objective The aim of this study was to evaluate the effects of Buzzy device application during heel prick blood collection on pain level and comfort in newborns. Method. The study was conducted in a Family Health Center affiliated to the Public Health Directorate of a province in eastern Turkey between September and November 2024 using a randomized controlled experimental design. The study sample consisted of 80 newborn infants born at 37-42 weeks gestational age and within the first 28 days of birth (Buzzy group: n = 40, control group: n = 40). The Buzzy group was treated by placing the Buzzy device approximately 30 seconds before heel prick blood collection. In the control group, routine heel prick was performed without any application. Neonatal introduction form, Neonatal Infant Pain Scale and Neonatal Comfort Behavior Scale were used for data collection.

Conditions

Interventions

TypeNameDescription
BEHAVIORALBuzzy applicationBuzzy application during heel prick blood collection

Timeline

Start date
2024-09-01
Primary completion
2024-11-20
Completion
2024-11-30
First posted
2025-01-14
Last updated
2025-01-14

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT06773325. Inclusion in this directory is not an endorsement.