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Impact of Virtual Reality on Pediatric Patients with ESRD on Regular Hemodialysis Through Arteriovenous Fistula.

RECRUITINGN/ASponsored by Tanta University
Actively Recruiting
PhaseN/A
SponsorTanta University
Started2024-04-01
Est. completion2024-11-01
Eligibility
Age8 Years – 18 Years
Healthy vol.Accepted
View on ClinicalTrials.gov →

NCT06675877

Summary

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.

Eligibility

Age: 8 Years – 18 YearsHealthy volunteers accepted
Inclusion Criteria:

* Pediatric patients with end stage renal disease aged from 8 to 18 years on regular hemodialysis through functioning arteriovenous fistula and are fully oriented with time, persons and place at time of data collection. All participants either cases or controls suffer from anxiety, depression or both.

Exclusion Criteria:

* Children with temporary or permanent catheter for dialysis.
* Children with mental illness, visual and auditory defects.
* Children took any pharmacological pain reliever or antipsychotic drugs.
* Non anxious or depressed Children.

Conditions3

AnxietyDepressionPain

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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