- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05004766
Effects of Virtual Reality Application on Pain Reduction and Cerebral Blood Flow in Robot Training in Burn Patients
August 9, 2021 updated by: Hangang Sacred Heart Hospital
Effects of Virtual Reality Application on Pain Reduction and Cerebral Blood Flow in Robot-Assisted Gait Training in Burn Patients : Pilot Study
The purpose of this study is to determine whether the application of virtual reality (VR) is effective in reducing training pain in robot-assisted gait training (RAGT) in patients with lower extremity burn.
The investigators investigated through an analysis of the activation status over time in the prefrontal cortex using functional near-infrared spectroscopy (NIRS).
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Burn injuries and their treatment are considered to be among the most painful a person can endure.
Therefore, new modalities that prove effective with burn patients are expected to improve clinical outcomes when applied to painful therapies.
The purpose of this study is to determine whether the application of virtual reality (VR) is effective in reducing training pain in robot-assisted gait training (RAGT) in patients with lower extremity burn.
The investigators investigated through an analysis of the activation status over time in the prefrontal cortex using functional near-infrared spectroscopy (NIRS).
RAGT was performed 10 times for 2 weeks from Monday to Friday, and the cerebral blood flow measurement using NIRS was measured 3 times each while applying or not applying VR for 30 minutes as long as the RAGT is in progress.
The VR program provided non-immersive VR walking along a forest path or a coastal path according to the walking speed while the RAGT was in progress.
For each physical therapy session, each patient spent equal amounts of time in VR and in the control condition (without VR).
The average of oxy-Hb and deoxy-Hb of each session was measured for 10 days.
In the prefrontal cortex, the levels of hemoglobin (Hb) were measured using the fNIRS measurement system.
Average values of both oxy-Hb and deoxy-Hb were calculated at four stages : temporal delay time with RAGT, RAGT without VR, temporal delay time with VR, RAGT with VR.
Before training, all patients verbally rated their most severe pain during physical training as a score of 5 or higher on a visual analog scale (VAS) of 0 to 10, where 0 presents " no pain at all" and 10 presents " worst pain".
Pain, the primary dependent variable, was measured immediately after each experimental treatment.
Patient rated (1) their worst pain (no pain to worst pain), and (2) their average pain ( no pain or worst pain).
Study Type
Interventional
Enrollment (Anticipated)
10
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 55 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- partial-to-full-thickness burns that had spontaneously healed or required skin grafting
- all patients rated their most severe pain during robot assisted gati training (RAGT) as a score 5 or higher on a visual analog scale of 0 to 10, where 0 represents no pain at all, and 10 represents worst pain.
- 1 ≤ functional ambulation category (FAC) score ≤ 3
Exclusion Criteria:
- patients with history of brain injury
- cognitive disorders, intellectual impairment before burn injury
- problems with weight bearing due to unstable fractures
- body weight ≥100 kg
- severe fixed contracture
- skin disorders that could be worsened by RAGT and conventional rehabilitation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: virtual reality apply
Using the VR system during robot training, the auditory stimulation of VR was applied along with the image of walking of a forest road or coastal road at the same speed as the robot walking speed.
The VR programs are a composition of scenic beaty with sounds of nature.
Each program is a blend of scenes such as the ocean, desert, forest, flowers, waterfalls, and wildlife.
|
Using the VR system during robot training, the auditory stimulation of VR was applied along with the image of walking of a forest road or coastal road at the same speed as the robot walking speed.
The VR programs are a composition of scenic beaty with sounds of nature.
Each program is a blend of scenes such as the ocean, desert, forest, flowers, waterfalls, and wildlife.
|
|
No Intervention: control condition
Each patient participated in the control condition, during which he or she performed RAGT with no distraction for the same amount of time spent doing therapy in VR.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
worst pain score
Time Frame: baseline
|
0 presents " no pain at all" and 10 presents "worst pain".
|
baseline
|
|
worst pain score
Time Frame: after 10 days training
|
0 presents " no pain at all" and 10 presents "worst pain".
|
after 10 days training
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
average pain
Time Frame: baseline
|
0 presents " no pain at all" and 10 presents "worst pain".
|
baseline
|
|
average pain
Time Frame: after 10 days training
|
0 presents " no pain at all" and 10 presents "worst pain".
|
after 10 days training
|
|
cerebral blood flow of prefrontal cortex
Time Frame: baseline
|
oxygenated hemoglobin (HbO2) and deoxygenated hemoglobin (HbR) concentration will be measured using an fNIRS device (NIRSIT®; OBELAB Inc., Seoul, Korea) while the participants is training with exoskeleton robot.
|
baseline
|
|
cerebral blood flow of prefrontal cortex
Time Frame: after 10 days training
|
oxygenated hemoglobin (HbO2) and deoxygenated hemoglobin (HbR) concentration will be measured using an fNIRS device (NIRSIT®; OBELAB Inc., Seoul, Korea) while the participants is training with exoskeleton robot.
|
after 10 days training
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Joo SY, Cho YS, Lee SY, Seok H, Seo CH. Effects of Virtual Reality-Based Rehabilitation on Burned Hands: A Prospective, Randomized, Single-Blind Study. J Clin Med. 2020 Mar 9;9(3):731. doi: 10.3390/jcm9030731.
- Yucel MA, Aasted CM, Petkov MP, Borsook D, Boas DA, Becerra L. Specificity of hemodynamic brain responses to painful stimuli: a functional near-infrared spectroscopy study. Sci Rep. 2015 Mar 30;5:9469. doi: 10.1038/srep09469.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
August 20, 2021
Primary Completion (Anticipated)
December 31, 2021
Study Completion (Anticipated)
March 31, 2022
Study Registration Dates
First Submitted
July 29, 2021
First Submitted That Met QC Criteria
August 9, 2021
First Posted (Actual)
August 13, 2021
Study Record Updates
Last Update Posted (Actual)
August 13, 2021
Last Update Submitted That Met QC Criteria
August 9, 2021
Last Verified
July 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HangangSHH-12
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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