Actively Recruiting
The Effect of Storigami Method on Pain, Fear and Anxiety Levels Associated With Peripheral Intravenous Catheterisation in Children
Led by Ege University · Updated on 2025-06-06
120
Participants Needed
2
Research Sites
14 weeks
Total Duration
On this page
Sponsors
E
Ege University
Lead Sponsor
T
The Scientific and Technological Research Council of Turkey
Collaborating Sponsor
AI-Summary
What this Trial Is About
The aim of this study was to determine the effect of storigami method on reducing pain, fear and anxiety of children in peripheral intravenous catheter applications in children aged 6-9 years who were hospitalized in the pediatric health and diseases clinic.
CONDITIONS
Official Title
The Effect of Storigami Method on Pain, Fear and Anxiety Levels Associated With Peripheral Intravenous Catheterisation in Children
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Volunteering to participate in the study
- Child is between 6 and 9 years old
- First time peripheral intravenous catheter insertion since admission
- No vision, hearing, or speech problems
- No mental retardation
- Child knows and speaks Turkish
- No pain, nausea, or vomiting affecting fear and anxiety
- No sedative or analgesic given immediately before the catheter procedure
You will not qualify if you...
- Child has a chronic, congenital, metabolic, or neurodegenerative disease
- Failed attempt at peripheral intravenous catheterization
- Incomplete or missing questionnaires
- Different invasive intervention immediately before catheter insertion
- Child does not cooperate during the procedure
- Child wishes to leave the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Ege University
Izmir, Bornova, Turkey (Türkiye), 35030
Actively Recruiting
2
Ege University
Izmir, İzmir, Turkey (Türkiye), 35030
Actively Recruiting
Research Team
E
Emine ÇUBUKCU, MSc
CONTACT
A
Ayşe Kahraman, Assoc Prof
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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