RECRUITING

Evaluating the Feasibility of VR for Pediatric Renal Biopsies

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Conditions

Pain, ProceduralProcedural AnxietySedation Complication

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to assess the use of virtual reality (VR) as an adjunct or alternative to pharmacologic sedation in pediatric patients undergoing renal biopsy.

Official Title

Evaluating the Feasibility of Virtual Reality for Procedural Sedation in Pediatric Renal Biopsy Patients

Quick Facts

Study Start:2022-10-11
Study Completion:2024-08-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05267704

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:5 Years to 17 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. * Patients who cannot lie supine for their renal biopsy will be excluded from the study
  2. * Patients with injuries to the head/face that would prohibit wearing a headset
  3. * Patients with loss of consciousness, altered mental status, life-threatening injuries/illness or multi-trauma
  4. * Patients with open skin, lice, scabies, or other infectious skin conditions on the head/face
  5. * Patients with a history of or current symptoms of vertigo
  6. * Patients who are blind
  7. * Patients with significant developmental or cognitive delays who may not be able to engage with or tolerate the virtual reality environment, as determined by their parent/caregiver
  8. * Patients on whom the VR headset does not fit appropriately

Contacts and Locations

Study Contact

Justin Libaw, MD, MPH
CONTACT
415-443-1366
justin.libaw@ucsf.edu
Omar Salman, MD
CONTACT
415-514-1815
omar.salman@ucsf.edu

Principal Investigator

Justin Libaw, MD, MPH
PRINCIPAL_INVESTIGATOR
University of California, San Francisco

Study Locations (Sites)

UCSF Benioff Children's Hospital
San Francisco, California, 94143
United States

Collaborators and Investigators

Sponsor: University of California, San Francisco

  • Justin Libaw, MD, MPH, PRINCIPAL_INVESTIGATOR, University of California, San Francisco

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-10-11
Study Completion Date2024-08-01

Study Record Updates

Study Start Date2022-10-11
Study Completion Date2024-08-01

Terms related to this study

Additional Relevant MeSH Terms

  • Pain, Procedural
  • Procedural Anxiety
  • Sedation Complication