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

T

Tanta University

Status

Enrolling

Conditions

Anxiety
Pain

Treatments

Other: virtual reality camera

Study type

Interventional

Funder types

Other

Identifiers

NCT06675877
VR on HD children

Details and patient eligibility

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.

Full description

This case control study will be conducted at nephrology and dialysis Unit Pediatric Department Tanta University Hospital (TUH) for a period of 6 months starting from April 2024.This study will be conducted on convenient sample of 60 participants. they will be classified as follow group A (cases) Group B (controls)each group will contain 30 children and adolescents with end stage renal disease on regular hemodialysis for three times weekly at our nephrology Unit at TUH during the period of the study

Enrollment

60 estimated patients

Sex

All

Ages

8 to 18 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

group A
Active Comparator group
Description:
Group A Cases only will receive in each dialysis session standard care together with VR camera.
Treatment:
Other: virtual reality camera
group B
No Intervention group
Description:
Group B control group undergo three to four dialysis sessions weekly; they will receive the standard care only in their dialysis sessions without VR camera

Trial contacts and locations

1

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Central trial contact

Sara Ma ElGhoul, MD

Data sourced from clinicaltrials.gov

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