MedPath

Immersive Virtual Reality for Neuropathic Pain

Not Applicable
Completed
Conditions
Neuropathic Pain
Neuropathy
Complex Regional Pain Syndromes
Phantom Limb Pain
Interventions
Other: Immersive Virtual Reality
Registration Number
NCT03203772
Lead Sponsor
Loma Linda University
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
14
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Limb neuropathic conditionsImmersive Virtual RealityIncludes phantom limb pain, complex regional pain syndrome
Primary Outcome Measures
NameTimeMethod
Pain Relief with Virtual Reality Therapy: Visual Analog ScaleChange 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 ScaleChange 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 QuestionnaireImmediately 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 ScaleChange 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.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Loma Linda University Health, East Campus Outpatient Rehabilitation Center

🇺🇸

Loma Linda, California, United States

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