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Double blinded Randomized control study Immersive virtual reality to reduce neuropathic pain in spinal cord injury persons

Immersive virtual reality to reduce neuropathic pain in persons with Spinal cord injury: A double blind Randomized controlled trial - VR-NEUPASCI

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036990
Enrollment
50
Registered
2021-09-30
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: S241- Other and unspecified injuries ofthoracic spinal cord

Interventions

Intervention1: INTERVENTION GROUP: The participants in the intervention group in addition to standard care will receive immersive virtual reality illusion environment exposure for two 15 minutes sessi

Sponsors

Christian Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Persons with SCI between 16 and 60 years of age, both genders and who are able to follow therapy instructions and capable of participating in daily therapy sessions. Persons with SCI thoracic level lesion with Complete (ASIA â?? A) and sensory incomplete (ASIA - B) and motor incomplete (ASIA - C) lesions based on â??The International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI)â?? Presence of neuropathic pain with LANSS score of 12 or more Persons with ongoing stable pharmacological treatment for at least 2 weeks prior to the study and throughout the trial

Exclusion criteria

Exclusion criteria: SCI persons with associated traumatic brain injury and comorbidities such as neurological and psychiatric disorders, visual impairment and who are not willing to give consent to participate in the study will be excluded.

Design outcomes

Primary

MeasureTime frame
Neuropathic pain Timepoint: At baseline At two weeks

Secondary

MeasureTime frame
DepersonalizationTimepoint: At baseline At two weeks

Countries

India

Contacts

Public ContactSAMSON SELVARAJ J

Christian Medical College

henry.cmcv@gmail.com9789249812

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026