Actively Recruiting
Impact of Virtual Reality on Pediatric Patients with ESRD on Regular Hemodialysis Through Arteriovenous Fistula.
Led by Tanta University · Updated on 2024-11-05
60
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This case control study will be conducted to study the effectiveness of Virtual Reality technique on pain during arteriovenous cannulation and on reduction of anxiety and depression in Pediatric Patients with ESRD undergoing regular hemodialysis through arteriovenous fistula.
CONDITIONS
Official Title
Impact of Virtual Reality on Pediatric Patients with ESRD on Regular Hemodialysis Through Arteriovenous Fistula.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pediatric patients aged 8 to 18 years with end stage renal disease
- Receiving regular hemodialysis through a functioning arteriovenous fistula
- Fully oriented with time, persons, and place at data collection
- Suffering from anxiety, depression, or both
You will not qualify if you...
- Children with temporary or permanent catheter for dialysis
- Children with mental illness, visual, or auditory defects
- Children who took any pharmacological pain reliever or antipsychotic drugs
- Children who are not anxious or depressed
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tanta University Hospital
Tanta, Egypt, 31527
Actively Recruiting
Research Team
S
Sara Ma ElGhoul, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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