Virtual reality offers new hope for chronic back pain sufferers
NCT ID NCT01407653
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a virtual reality device to see if it could reduce pain in adults with chronic low back pain that didn't respond to medication. 122 participants used the VR system, which creates a 3D environment with changing colors. The main goal was to measure pain levels after 4 months of use.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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122 people
The number who actually took part.
- Start date
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Jun 2011
- Finished
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Apr 2015
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * More than 18 and less than 60 years (inclusive) * Chronic low back pain or chronic sciatica (between 3 months and 1 year of the current episode), without neurological deficit (low back pain more important than sciatica), common spinal origin, resistant to medical therapy, and the numerical pain scale \> 30/100 * Written informed consent * Membership or beneficiary of an insurance Exclusion Criteria: * Low back pain related to a spinal infectious disease, inflammatory, neoplasia, osteodystrophic, malformative and traumatic. * Deficit sciatica (motor weakness and / or sensory) * Low back pain secondary to failure of spinal intervention. * Co-existence of pain of another etiology. * Seizures. * Psychiatric disorder, uncontrolled. * Visual disturbances (significant decrease in visual acuity without correction possibility, problems with re-cognition of color, visual field loss). * Inclusion in another trial to evaluate new ways of treating pain * Sick leave over 1 year * Pregnant women * Inability to give informed consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cochin Hospital
Paris, 75014, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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