Sign in

NCT05592132Recruiting

Use of Virtual Reality in Pain Management in Pediatric Oncology

Use of Virtual Reality in Pain Management During Invasive Gestures in Pediatric Oncology: Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 11 Sept 2026

Brief summary (registry, in English)

DOREVI is a monocentric randomized controlled study that will evaluate the efficacy of virtual reality helmets for pain prevention during invasive care on 78 oncologic pediatric patients. Two groups of children (between 6 and 11 and between 12 and 18 years old) will be randomized to use helmet plus standard care or standard care alone during invasive procedures (central venous catheter puncture, lumbar puncture, or bone marrow aspiration). The pain intensity will be evaluated using a visual analogic scale during three invasive procedures, and results will be compared between the patients with or without virtual reality.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
74 (estimated)
First submitted
30 Jun 2022
Start date
17 Jan 2023
Primary completion date
Dec 2026
Lead sponsor
Centre Hospitalier Universitaire de la Réunion
NCT number
NCT05592132

What you commit to

  • Study type: Interventional
  • Planned participants: 74
  • From 17 Jan 2023 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • patient with epilepsy or other neurological disease
  • patient with psychiatric disease

Other

  • patient with visual or hearing impairement

Who the study is looking for

  • patient who tolerates the virtual reality headset
  • patient followed in pediatric oncology
  • patient with a diagnosis of benign tumor or cancer
  • patient who needs to have painful medical procedure during their treatment
  • patient whose parents have signed the informed consent
  • patient affiliated with social security or equivalent

Age in the registry: 6 years to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
CHU de La Réunion
Coordinator of this site? Confirm its status
Saint-DenisRéunionRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.