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Virtual Reality for Chronic Neuropathic Pain

Unknown statusPhase 3NCT03592394
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The investigators hypothesize that SCI patients using immersive IVR training will show improved reduction of neuropathic pain that will outlast the training sessions and transfers into daily life.

Study details

Official title
Immersive Virtual Reality for Chronic Neuropathic Pain After Spinal Cord Injury: A Feasibility Trial
Interventions
  • Device: Immersive Virtual Reality (Gear VR)
Sponsor
Kathleen Friel
Organization
Burke Medical Research Institute
Start date
2016-07
Primary completion
2017-12
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Presence of chronic neuropathic pain at or below SCI level for at least 6 months following trauma or disease of the spinal cord; * A pain intensity of at least 4 out of 10 in the numerical rating scale (NRS) in the Neuropathic Pain Scale (NPS) test at both screening (baseline) and randomization (pre-evaluation); * Stable pharmacological treatment for at least 2 weeks prior to the study and throughout the trial; * Incomplete lesion (American Spinal Injury Association Impairment Scale, AIS B, C or D; B= motor complete, sensory incomplete; C= sensorimotor incomplete with an average strength of the muscles below the level of the lesion \<3, D= sensorimotor incomplete with average muscle strength \>3); * Cervical level of lesion (C2 to T1) with presence of pain in the upper extremities Exclusion Criteria: * Presence of severe pain of other origin, such as musculoskeletal pain * Psychiatric or other neurological disorders * Head injuries causing cognitive or visual impairment * Severe vertigo * Presence of potential risk factors for brain stimulation (TMS): history of seizures, presence of surgically implanted foreign bodies such as a pacemaker, metal plate in the skull, and metal inside the skull; * Medically unstable

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03592394