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Clinical Trials/NCT03203772
NCT03203772
Completed
Not Applicable

Management of Pain in Limb Neuropathic Conditions Through Immersive Virtual Reality

Loma Linda University1 site in 1 country14 target enrollmentAugust 14, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neuropathy
Sponsor
Loma Linda University
Enrollment
14
Locations
1
Primary Endpoint
Pain Relief with Virtual Reality Therapy: Visual Analog Scale
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Investigating how neuropathic limb pain, including phantom limb pain or complex regional pain syndrome, is affected by virtual reality. While several studies have looked into virtual reality for treating this type of pain, few have used the latest immersive virtual reality hardware combined with motion control for an engaging virtual mirror therapy experience. The investigators are interested in studying the use of virtual reality as an alternative treatment option for these conditions.

Registry
clinicaltrials.gov
Start Date
August 14, 2016
End Date
December 31, 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of complex regional pain syndrome or phantom limb pain in an upper or lower limb

Exclusion Criteria

  • Cognitive impairment leading to inability to make own medical decisions
  • Complete inability to utilize leg or arm muscles that are needed for motion controller tracking
  • History of seizures within the last year

Outcomes

Primary Outcomes

Pain Relief with Virtual Reality Therapy: Visual Analog Scale

Time Frame: Change from initial scores prior to virtual reality exposure to immediately prior to and following virtual reality sessions, and up to 8 weeks following last sessions

Change in Visual Analog Pain Scale will be measured. This will be done by obtaining pain scale scores immediately prior to therapy session, immediately following therapy, and several weeks post last therapy session.

Pain Relief with Virtual Reality Therapy: Short-Form McGill Pain Scale

Time Frame: Change from initial scores prior to virtual reality exposure to immediately prior to and following virtual reality sessions, and up to 8 weeks following last sessions

Change in Short-Form McGill Pain Questionnaire will be measured. This will be done by obtaining pain scale scores immediately prior to therapy session, immediately following therapy, and several weeks post last therapy session.

Feasibility of Virtual Reality Environment Use Questionnaire

Time Frame: Immediately following final virtual reality session

Using a questionnaire, feedback over participant self-reported tolerance of the virtual reality environment, participant likelihood of recommending this therapy to others with similar conditions, reported sense of presence in presented scenario(s), comfort of virtual reality devices, impact on self-reported functional ability outside of clinic, and overall impression of virtual reality therapy will be recorded.

Pain Relief with Virtual Reality Therapy: Wong-Baker Scale

Time Frame: Change from initial scores prior to virtual reality exposure to immediately prior to and following virtual reality sessions, and up to 8 weeks following last sessions

Change in Wong-Baker Faces pain scale will be measured. This will be done by obtaining pain scale scores immediately prior to therapy session, immediately following therapy, and several weeks post last therapy session.

Study Sites (1)

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