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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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05592132
Acronym
DOREVI
Enrollment
74
Registered
2022-10-24
Start date
2023-01-17
Completion date
2026-12-01
Last updated
2026-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric Tumor

Brief summary

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.

Interventions

OTHERVirtual reality headset

Each patient in this treatment group will use a virtual reality headset during 3 procedures. During each procedure, the pain level will be assessed and compared with the assessed group.

Sponsors

Centre Hospitalier Universitaire de la Réunion
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

intervention plus standard care versus standard care

Eligibility

Sex/Gender
ALL
Age
6 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* patient with visual or hearing impairement * patient with epilepsy or other neurological disease * patient with psychiatric disease

Design outcomes

Primary

MeasureTime frameDescription
Self pain evaluationbefore blood sampling on catheter with implantable chamberPain will be assessed by the analogic visual scale (minimal score = 0 (no pain) , maximal score = 10 (maximal pain))

Countries

Reunion

Contacts

CONTACTYves REGUERRE
yves.reguerre@chu-reunion.fr+262262905676
CONTACTEmilie TECHER
emilie.techer@chu-reunion.fr+262262906289
PRINCIPAL_INVESTIGATORYves REGUERRE

CHU de La Réunion

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 12, 2026