Virtual Reality for Pain Management in Pediatric Cancer Care
Use of Virtual Reality in Pain Management in Pediatric Oncology
Recruiting
N/AInterventional Study
Pediatric Tumor
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
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At a Glance
Age
6 – 18
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
74 (estimated)
Sponsor
Centre Hospitalier Universitaire de la Réunion · Other
Who this trial is looking for
This trial is looking for children with cancer or benign tumors who are going to have painful medical procedures. Participants will wear a virtual reality headset during the procedure to help manage pain.
Are You a Good Fit for This Trial?
You may be able to join if
I can wear a virtual reality headset.
I am being treated in pediatric oncology.
I have a diagnosis of a benign tumor or cancer.
I need to have a painful medical procedure.
My parents have given permission for me to participate.
I am covered by social security or similar.
You may not be able to join if
I have visual or hearing impairment.
I have epilepsy or another neurological disease.
I have a psychiatric disease.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
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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, l…
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.
Trial Locations
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Eligibility Criteria
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…
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
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