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Clinical Trial

Buzzy® and Cognitive Behavioral Intervention Package During Blood Draw in Children

NCT: NCT07689370 · COMPLETED

NCT IDNCT07689370
StatusCOMPLETED
Start Date2025-01-10
Completion2026-04-24
SponsorKocaeli University (OTHER)
First posted
Last updated

Brief Summary

This study evaluated the effects of Buzzy® and a Cognitive Behavioral Intervention Package on pain and fear/anxiety during blood draw in children aged 7-12 years. Blood draw is a common procedure in children, but it may cause pain, fear, and anxiety. Non-pharmacological methods may help children cope better with this procedure. Children were randomly assigned to one of three groups: a control group, a Cognitive Behavioral Intervention Package group, or a Buzzy® group. Children in the control group received routine blood draw care. Children in the Cognitive Behavioral Intervention Package group received preparation, age-appropriate information, distraction, supportive guidance, parent support, and positive reinforcement. Children in the Buzzy® group received cold and vibration application before and during the blood draw procedure. Pain and fear/anxiety levels were assessed by child self-report before and immediately after the blood draw. The study aimed to determine whether Buzzy® and the Cognitive Behavioral Intervention Package reduce pain and fear/anxiety compared with routine care.

Frequently Asked Questions

What is Buzzy® and Cognitive Behavioral Intervention Package During Blood Draw in Children?

Buzzy® and Cognitive Behavioral Intervention Package During Blood Draw in Children is a clinical trial registered under NCT07689370. Current status: COMPLETED.

What is the status of NCT07689370?

The current status of NCT07689370 (Buzzy® and Cognitive Behavioral Intervention Package During Blood Draw in Children) is: COMPLETED.

When did Buzzy® and Cognitive Behavioral Intervention Package During Blood Draw in Children start?

Buzzy® and Cognitive Behavioral Intervention Package During Blood Draw in Children started on 2025-01-10.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.