Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05005026

Virtual Walking Intervention for Neuropathic Pain in Spinal Cord Injury

Led by Texas A&M University · Updated on 2025-12-17

250

Participants Needed

3

Research Sites

249 weeks

Total Duration

On this page

Sponsors

T

Texas A&M University

Lead Sponsor

U

United States Department of Defense

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to determine if playing a virtual reality walking game can help improve neuropathic pain in adults with chronic spinal cord injury.

CONDITIONS

Official Title

Virtual Walking Intervention for Neuropathic Pain in Spinal Cord Injury

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Complete spinal cord injury classified as ASIA A with lumbar, paraplegic, or low tetraplegic (C5-C7) injury
  • Persistent neuropathic pain symptoms with daily severity of at least 4/10 for 3 or more months
  • More than 2 items endorsed on the 7-item Spinal Cord Injury Pain Instrument (SCIPI)
  • Age 18 years or older
  • More than one year post-injury at study start
  • Mobile connectivity with usable service
  • Stable on pain medication for 1 or more months
  • Cleared on the VRWalk physical activity clearance scale
  • No motion sickness interfering with daily life
Not Eligible

You will not qualify if you...

  • Injury levels between C1 and C4
  • Under 18 years of age
  • Injury within the past year
  • Inability to comprehend spoken English
  • Currently in prison
  • Blindness
  • Severe motion sickness

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

University of Alabama at Birmingham

Birmingham, Alabama, United States, 35294

Actively Recruiting

2

Texas A&M University

College Station, Texas, United States, 77843

Actively Recruiting

3

University of New South Wales

Sydney, New South Wales, Australia

Completed

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Research Team

A

Amanda Sainz-Higgins, M.E.d

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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