Virtual Reality Walking for Neuropathic Pain in Spinal Cord Injury

Spinal Cord Injuries Clinical Trial

Official title:

Immersive Virtual Walking Treatment for Neuropathic Pain in Spinal Cord Injury

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03735017
• Other study ID #: 383546
• Status: Completed
• Phase: N/A
• Start date: June 16, 2018
• Est. completion date: July 30, 2019

Study information

• Verified date: November 2021
• Source: University of Alabama at Birmingham
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will examine the effectiveness of one of two virtual reality treatments on neuropathic pain in individuals with spinal cord injury.

Description:

The investigators are investigating the effectiveness of one of two possible investigational virtual reality treatments on neuropathic pain in individuals with spinal cord injury. Participants will be randomized to one of these two treatments.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 27
• Est. completion date: July 30, 2019
• Est. primary completion date: July 30, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 64 Years

Eligibility

Inclusion Criteria:

• Individuals with complete paraplegic spinal cord injury who report chronic neuropathic pain

• Individuals with persistent spinal cord injury neuropathic pain

• More than one - year post injury

• Stable medication regimen for the past month

Exclusion Criteria:

• Conditions that impair movement of the arms

• Significant cognitive impairment as suggested by apparent incomprehension of screening questions as judged by the evaluator

• For those for whom voluntary arm movement would cause sufficient discomfort (>4/10) that could prevent trial completion will be excluded from participation

Related Conditions & MeSH terms

• Neuralgia
• Neuropathic Pain
• Spinal Cord Injuries
• Wounds and Injuries

Intervention

Other:
• Non-Interactive Virtual Reality Walking
Individuals will wear a head-mounted display to allow them to visualize virtual legs in the virtual environment. When wearing the display, individuals will see the legs and arms of their virtual avatar from a first-person perspective. Individuals will engage in virtual reality sessions in their home twice daily over the course of 10 days in a two-week period. Each daily session will take approximately 30 minutes, with 5-10 minutes dedicated to the virtual walking experience. Additionally, each daily session will be scheduled a minimum of 4 hours apart.
• Interactive Virtual Reality Walking
Individuals will wear a head-mounted display to allow them to visualize virtual legs in the virtual environment. When wearing the display, individuals will see the legs and arms of their virtual avatar from a first-person perspective. Individuals will engage in virtual reality sessions in their home twice daily over the course of 10 days in a two-week period. Each daily session will take approximately 30 minutes, with 5-10 minutes dedicated to the virtual walking experience. Additionally, each daily session will be scheduled a minimum of 4 hours apart.

Locations

Country	Name	City	State
United States	University of Alabama at Birmingham	Birmingham	Alabama

Sponsors (1)

Lead Sponsor	Collaborator
University of Alabama at Birmingham

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pain Intensity as assessed by Numeric Rating Scale	The Numeric Rating Scale (NRS) measures pain intensity measured via 0-10 numeric rating scale.; Range of scores: 0-10	Baseline - Final assessment (average 1 week post treatment)
Primary	Neuropathic Pain Qualities as assessed by Neuropathic Pain Scale	The Neuropathic Pain Scale (NPS) was designed to assess the distinct pain qualities associated with neuropathic pain.The NPS consists of 10 items. Seven of the 10 items contain the words intense, sharp, hot, dull, cold, and itchy to characterize the patient's pain and the word sensitive to describe the patient's pain reaction to light touch or clothing.One item describes the time quality of the pain (all the time or some of the time). The ninth item describes the overall unpleasantness of the pain, whereas the last item indicates the intensity of the deep and surface pain. In the NPS each item is rated separately. All the items are rated 0-10 scale, with higher score indicative of more neuropathic pain for each type of respective pain.; Range of scores: 0-10 for each item.	Baseline - Final assessment (average 1 week post treatment)
Primary	Neuropathic Pain Diagnosis as assessed by Doleur Neuropatique 4	Doleur Neuropatique 4 is a 10 item survey that evaluates neuropathic pain following central and neurological lesions. It has components of how the pain feels to the patient (e.g. burning, cold, electrical shocks, tingling, hypoaesthesia). Responses to each item is yes or no, with each yes response equaling one point.; Range of scores: 0-10. 4/10 and greater indicate neuropathic pain.	Baseline - Final assessment (average 1 week post treatment)
Primary	Pain Interference specific to spinal cord injury as assessed by International Spinal Cord Injury Pain Basic Data Set version 2.0	Pain interference measured International Spinal Cord Injury Pain Basic Data Set version 2.0 interference items. There are 3 pain interference items using a 0-10 numeric rating scale for each item. Items can be assessed by summing the score or by individual assessment of items.; Summed range of scores: 0-30. Individual item range of scores: 0-10	Baseline - Final assessment (average 1 week post treatment)
Primary	Pain Interference as assessed by Brief Pain Inventory	Pain interference measured by Brief Pain Inventory interference items. 7 items each use a 0-10 scale. Item scores may be assessed individually, or by taking the average score of all items.; Range of Scores: 0-10. Increased scores indicate higher levels of interference due to pain.	Baseline - Final assessment (average 1 week post treatment)
Secondary	Patient Treatment Evaluation as assessed by the Ease of Usefulness, Satisfaction, and Ease of Use Questionnaire	Ease of Usefulness, Satisfaction, and Ease of use Questionnaire is a 30 item survey. Subscales include: treatment's usefulness, ease of use, ease of learning, and satisfaction. Each item is presented on a 7-point Likert scale. Each subscale is calculated by averaging all items in subscale.; Range of scores for each subscale: 1-7	Final assessment (average 1 week post treatment)
Secondary	Patient Treatment Evaluation as assessed by the Patient Global Impression of Change Scale	Patient treatment evaluation is assessed by the Patient Global Impression of Change. This is a one item 7 point Likert item assessing improvement of the participants overall status.; Range of scores: 1-7	Final assessment (average 1 week post treatment)
Secondary	Patient Treatment Evaluation as assessed by the Modified Treatment Evaluation Inventory	Patient treatment evaluation is assessed by Treatment Evaluation Inventory. This is a 9 item scale with a 5-point Likert responses for each question. The items are scored by summing all items.; Range of scores: 9-45. A higher score indicates greater acceptance of treatment.	Final assessment (average 1 week post treatment)
Secondary	Patient Treatment Evaluation as assessed by Semi-structured Qualitative Interviewing	Patient treatment evaluation is assessed by semi-structured interviewing. Qualitative feedback from participant experience will be assessed by thematic analyses.	Final assessment (average 1 week post treatment)
Secondary	Quality of Life and Participation are assessed by the SF-36 Walk-Wheel	Quality of life and participation are assessed by the SF-Walk Wheel. This is a 36 item assess health concepts which represent basic human values and were relevant to a person's functional status and well-being. The responses are based on a Likert scale. There are the following subscales: Physical functioning, role limitations due to physical health, role limitations due to emotional problems, energy/fatigue, emotional well-being, social functioning, pain, and general health.; Each item is recoded to a preset value between 0-100 per the scoring key.; Range of scores: 0-100 for each sub-scale. A higher score defines a more favorable health state.	Baseline - Final assessment (average 1 week post treatment)
Secondary	Quality of Life is assessed by Satisfaction with Life Scale	Quality of life is assessed by the Satisfaction with Life Scale. This is a 5 item survey. Response options are a 7-point Likert scale. Items may be assessed individually or by summing items.; Range of scores: 5-35. Higher scores indicate more satisfaction in life	Baseline - Final assessment (average 1 week post treatment)
Secondary	Depression and mood are assessed by the Patient Health Questionnaire -9	Depression and mood are measured by Patient Health Questionnaire-9. This is a 10 item tool. The first 9 items are a 4-point Likert scale assessing depressive symptoms. The first 9 items are summed to determine depressive symptom severity. Item 10 assesses difficulty dealing with items 1-9. Item 10 is not used in scoring severity.; Range of scores: 0-27. Higher scores indicate more depressive symptom severity.	Baseline - Final assessment (average 1 week post treatment)
Secondary	Perceived Disability is assessed by the Pain Disability Index	Perceived Disability measured by a modified Pain Disability Index. The rating scales are designed to measure the degree to which aspects of life are disrupted by chronic pain. This is a 7 item survey with response options of 0-10. Each item may be assessed individually, or by summing all items.; Individual item range of scores: 0-10 Total range of scores: 0-70. The higher the index, the greater the person's disability due to pain.	Baseline - Final assessment (average 1 week post treatment)
Secondary	Absorption is assessed by the Tellegen Absorption Scale	Tellegen Absorption Scale is a 34-item multi-dimensional measure that assesses imaginative involvement and the tendency to become mentally absorbed in everyday activities. Item responses are on a 5-point Likert scale. Items are summed to score.; Range of scores: 0-136. Higher scores indicate greater levels of absorption.	Baseline
Secondary	Immersive Tendencies are assessed by the Immersive Tendencies Questionnaire	Immersive Tendencies are assessed by the Immersive Tendencies Questionnaire (ITQ). This is an 18-item survey. Item responses use a 7 point Likert scale. Subscales include: focus, involvement, emotions, and play. Each subscale is scored by summing items. A total score is scored by summing all items.; Range of total score: 18-126 Focus range of scores: 5-35 Involvement range of scores: 5-35 Emotions range of scores: 4-28 Play range of scores: 3-21 Higher scores indicate higher immersive tendencies overall and in each sub-scale.	Baseline
Secondary	fMRI Imaging	We are studying pain by functional Magnetic Resonance Imaging (fMRI) which allows us to identify certain parts of the brain that show how the brain works in controlling pain perception and cognitions.	Baseline - Final assessment (average 1 week post treatment)