| Literature DB >> 31167435 |
Hui-Ting Lin1, Yen-I Li2, Wen-Pin Hu3, Chun-Cheng Huang4, Yi-Chun Du5.
Abstract
To assess the effects of virtual reality on patients with musculoskeletal disorders by means of a scoping review of randomized controlled trials (RCTs). The databases included PubMed, IEEE, and the MEDLINE database. Articles involving RCTs with higher than five points on the Physiotherapy Evidence Database (PEDro) scale were reviewed for suitability and inclusion. The methodological quality of the included RCT was evaluated using the PEDro scale. The three reviewers extracted relevant information from the included studies. Fourteen RCT articles were included. When compared with simple usual care or other forms of treatment, there was significant pain relief, increased functional capacity, reduced symptoms of the disorder, and increased joint angles for the virtual reality treatment of chronic musculoskeletal disorders. Furthermore, burn patients with acute pain were able to experience a significant therapeutic effect on pain relief. However, virtual reality treatment of patients with non-chronic pain such as total knee replacement, ankle sprains, as well as those who went through very short virtual reality treatments, did not show a significant difference in parameters, as compared with simple usual care and other forms of treatment. Current evidence supports VR treatment as having a significant effect on pain relief, increased joint mobility, or motor function of patients with chronic musculoskeletal disorders. VR seems quite effective in relieving the pain of patients with acute burns as well.Entities:
Keywords: musculoskeletal disorders; randomized controlled tria; virtual reality
Year: 2019 PMID: 31167435 PMCID: PMC6616618 DOI: 10.3390/jcm8060791
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241
Figure 1Flow chart displaying the screening process for studies included in this systematic review.
Physiotherapy Evidence Database (PEDro) Score for Included Studies (n = 14).
| Huang et al. 2014 [ | Pekyavas et al. 2017 [ | Bahat et al. 2015 [ | Bahat et al. 2017 [ | Kim et al. 2014 [ | Thomas et al. 2016 [ | Yilmaz Yelvar et al. 2017 [ | Martinho et al. 2016 [ | Kipping et al. 2012 [ | Jeffs et al. 2014 [ | Fung et al. 2012 [ | Koo et al. 2018 [ | Jin et al. 2018 [ | Punt et al. 2016 [ | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2014 | 2017 | 2015 | 2017 | 2014 | 2016 | 2017 | 2016 | 2012 | 2014 | 2012 | 2018 | 2018 | 2016 | |
| Taiwan | Turkey | Australia | Australia | Korea | America | Turkey | Brazil | Australia | America | Canada | Korea | China | Switzerland | |
| Eligibility criteria | Y | N | Y | N | N | Y | Y | Y | Y | Y | Y | Y | Y | Y |
| Random allocation | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y |
| Concealed allocation | N | N | Y | Y | N | Y | N | Y | Y | Y | N | Y | N | Y |
| Baseline comparability | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y |
| Blind subjects | N | N | N | N | N | N | N | N | N | Y | N | N | N | N |
| Blind therapists | N | N | N | N | N | N | N | N | N | N | N | N | N | N |
| Blind assessors | Y | N | Y | Y | N | N | Y | N | N | N | Y | Y | N | Y |
| Adequate follow-up | Y | Y | Y | N | Y | Y | Y | N | Y | Y | Y | N | Y | N |
| Intention-to-treat analysis | Y | N | N | Y | N | N | N | Y | Y | N | N | N | N | Y |
| Between-group comparisons | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y |
| Point estimates and variability | Y | Y | Y | Y | Y | Y | Y | Y | Y | Y | N | Y | Y | Y |
| Total score (0~10) | 7/10 | 5/10 | 7/10 | 7/10 | 5/10 | 6/10 | 6/10 | 6/10 | 7/10 | 7/10 | 5/10 | 6/10 | 5/10 | 7/10 |
Abbreviations: PEDro, Physiotherapy Evidence Database; Y: yes; N: no.
Description of Included studies.
| Title | Author | Part | Design | Participant (number) | Intervention | Exercise Mode (Frequency or Intensity) | Outcome Measures | |
|---|---|---|---|---|---|---|---|---|
| Age (years) = mean (SD) | ||||||||
| Intelligent Frozen Shoulder Rehabilitation | Huang et al. 2014 [ | Frozen shoulder | RCT | frozen shoulder syndrome > 3 months | 20 min/time, 2 times/week (Total 4 weeks) | ROM, CMS assessment | ||
| E | Hot pack + ultrasonic + VR | |||||||
| C | Hot pack + ultrasonic + traditional exercise training | |||||||
| Comparison of virtual reality exergaming and home exercise programs in patients with subacromial impingement syndrome and scapular dyskinesis: Short term effect | Pekyavas et al. 2017 [ | subacromial impingement syndrome(SAIS) & scapular dyskinesis | RCT | 18–60 years old; Type II SAIS | VAS(rest, activity, night), SPADI, Neer, Hawkins, SRT, SAT, LSST1-3 | |||
| None rotator cuff problem | ||||||||
| E | VR + control period (after 6 weeks) | VR: 45 min/day, twice a week, for 6 weeks; Control: 1 month for home exercise | ||||||
| C | Exercise + control period (after 6 weeks) | Exercise: 45 min/day, twice a week, for 6 weeks; Control: 1 month for home exercise | ||||||
| Cervical Kinematic Training with and without Interactive VR Training for Chronic Neck Pain—a Randomized Clinical Trial | Bahat et al. 2015 [ | Chronic neck pain | RCT | Neck pain > 3 months, NDI > 10% | VAS, Neck Disability Index, TSK, ROM, Peak velocity, mean velocity, TIP%, Sway SD, Accuracy, Eyes closed balance, singer leg stance, step test | |||
| E | VR + kinematic training | Total 30 min, at least 3 times a week, for 5 weeks | ||||||
| C | kinematic training (using laser point) | |||||||
| Remote kinematic training for patients with chronic neck pain: a randomized controlled trial | Bahat et al. 2017 [ | Chronic neck pain | RCT | Neck pain > 3 months, NDI > 12% | Neck Disability Index, Peak velocity, mean velocity, VAS, EQ5D, TSK, NVP, TTP%, Accuracy, ROM, GPE | |||
| VR | VR | 1 set 5 min, 20 min/day, 4 times/week, for 4 weeks | ||||||
| Laser | Laser point training | |||||||
| C | Not receive any treatment | |||||||
| The Effects of VR-Based Wii Fit Yoga on Physical Function in Middle-Aged Female LBP Patients | Kim et al. 2014 [ | LBP | RCT | LBP > 2 months | VAS, pressure algometer, ODI, RMDQ, FBQ | |||
| E | VR | 30 min/session, 3 session/week, for 4 weeks (1 session had 7 exercise program. 3 min of exercise and 1 min of rest) | ||||||
| C | Trunk stabilizing exercise + physical therapy | 2 sets (30 min), 1set included 10 repetitions, physical therapy 30 min | ||||||
| Feasibility and Safety of a Virtual Reality Dodgeball Intervention for Chronic Low Back Pain: A Randomized Clinical Trial | Thomas et al. 2016 [ | LBP | RCT | 18–50 years old with LBP > 3 months | pain and harm, lumbar spine flexion ROM | |||
| kinesiophobia ≥35 | ||||||||
| E | VR | 3 days (<48 h) | ||||||
| C | Not receive any treatment | |||||||
| Is physiotherapy integrated virtual walking effective on pain, function, and kinesiophobia in patients with non-specific low-back pain? Randomised controlled trial | Yilmaz Yelvar et al. 2017 [ | LBP | RCT | non-specific LBP for longer than 2 months | VAS, ODI, TKS, TUG, and 6MWT scores | |||
| E | VR + Traditional physical therapy | 5 times/week, for 2 weeks | ||||||
| C | Traditional physical therapy | 5 times/week, for 2 weeks | ||||||
| The effects of training by virtual reality or gym ball on pelvic floor muscle strength in postmenopausal women: a randomized controlled trial | Martinho et al. 2016 [ | Pelvic floor muscle | RCT | >50 years old women | Maximum strength, average strength, endurance | |||
| >1 year postmenopausal phase | ||||||||
| APT-VR | Abdominopelvic training by VR | 1 session 5 min with 90 s resting, for 10 session. Twice a week, for 5 weeks | ||||||
| PFMT-GB | Pelvic floor muscle training using a gym ball | 4 series of 10 fast & sustained (8 s maintain with 16 s resting), each exercise 5 times, twice a week, for 5 weeks | ||||||
| Virtual reality for acute pain reduction in adolescents undergoing burn wound care: A prospective randomized controlled trial | Kipping et al. 2012 [ | Burn wound | RCT | 11–18 years old | VAS, FLACC scale | |||
| burn wound Total Body Surface Area (TBSA) > 1% | ||||||||
| E | VR | Dressing period (3–58 min), only 1 time | ||||||
| C | Another distraction way or no distraction | |||||||
| Effect of Virtual Reality on Adolescent Pain During Burn Wound Care | Jeffs et al. 2014 [ | Burn wound | RCT | 10–17 years old | Adolescent Pediatric Pain Tool, Spielberger State-Trait Anxiety InventoryFor Children, Pre-Procedure Questionnaire, Post-Procedure Questionnaire | |||
| standard care | standard care | Dressing period only 1 time | ||||||
| passive distraction | passive distraction watching a movie | |||||||
| virtual reality | virtual reality | |||||||
| Use of Nintendo Wii Fit™ in the Rehabilitation of Outpatients Following Total Knee Replacement: a Preliminary Randomized Controlled Trial | Fung et al. 2012 [ | TKR | RCT | requiring twice-weekly physiotherapy treatment for TKR rehabilitation | active knee flexion/extension ROM, 2 min walk test, NPRS, ABCS, LEFS | |||
| Full lower extremity weight bearing | ||||||||
| E | physiotherapy + VR | physiotherapy (45 min), 15 min VR until discharge | ||||||
| C | physiotherapy + lower extremity exercise | physiotherapy (45 min), 15 min lower extremity exercise until discharge | ||||||
| Enhanced Reality Showing Long-Lasting Analgesia after Total Knee Arthroplasty: Prospective, Randomized Clinical Trial | Koo et al. 2018 [ | TKR | RCT | Full term | VR + physiotherapy for 2 weeks | VR + PT: 5 days/week, for 2 weeks | VAS, WOMAC, 6 min walk test, Timed-stands test | |
| Half term | VR + physiotherapy for 1 week before physiotherapy for 1 week | VR + PT for 1 week | ||||||
| Virtual reality intervention in postoperative rehabilitation after total knee arthroplasty: a prospective and randomized controlled clinical trial | Jin et al. 2018 [ | TKR | RCT | E | VR(begin 2nd days for TKA) + conventional rehabilitation | three sets of 30 repetitions | WOMAC, HSS, VAS, ROM. | |
| C | conventional rehabilitation | three sets of 30 repetitions | ||||||
| Wii Fit™ Exercise Therapy for the Rehabilitation of Ankle Sprains: Its Effect Compared with Physical Therapy or No Functional Exercises at All | Punt et al. 2016 [ | Ankle sprain | RCT | 18–64 years old | FAAM-ADL, FAAM-sport, VAS-rest, VAS-walk | |||
| Grade I or II lateral ankle sprain | ||||||||
| requiring 4 weeks RICE and can pain free movement | ||||||||
| VR | VR | 30 min/time, 2 times/week, for 6 weeks | ||||||
| Physiotherapy | modalities, joint mobilization, muscle strengthening, proprioceptive exercise | 30 min/time, 9 times/6 weeks | ||||||
| C | Not receive any treatment | - | ||||||
Abbreviations: n (number); E (experimental group); C (control group); VR (Virtual reality); min (minute); ROM (range of motion); CMS (Constant-Murley score); VAS (Visual Analog Scale); SPADI (Shoulder Pain and Disability Index); SRT (Scapular Retraction Test); SAT (Scapular Assistance Test); LSST (Lateral Scapular Slide Test); TSK (Tampa scale of kinesiophobia); TIP% (Time to peak velocity percentage); GPE (Global perceived effect); sway SD (standard deviation of the static head sway); EQ-5D(EQ-5D™, http://www.euroqol.org); NVP (Number of velocity peaks); ODI (Oswestry low-back pain disability index); RMDQ (Roland Morris disability questionnaire); FBQ (fear avoidance beliefs questionnaire); NPRS (Numeric Pain Rating Scale); LEFS (Lower Extremity Functional Scale); ABCS (Activity-specific Balance Confidence Scale); WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index); FAAM (Foot and Ankle Ability Measure); ADL (activities of daily living); RICE (rest, ice, compression and elevation); FLACC (Faces, legs, activity, cry, consolability scale); Hospital for Special Surgery knee score (HSS); TKS (TAMPA Kinesiophobia Scale), TUG (timed-up and go test); 6MWT (6-Minute Walk Test); RCT (randomized controlled trial); LBP (low back pain); TKR (Total Knee Replacement).
Effect of virtual reality (VR) versus another intervention.
| Study | Outcome Measure | Mean Difference between VR Groups and Another Intervention | Significance of Difference between Groups | |
|---|---|---|---|---|
| Huang et al. 2014 [ | ROM | 8% | Between groups | |
| CMS | NA | Between groups | ||
| Pekyavas et al. 2017 [ | Neer | post-intervention/1 month follow-up | NA | |
| SRT | post-intervention/1 month follow-up | NA | ||
| SAT | post-intervention/1 month follow-up | NA | ||
| VAS (rest, activity, night) | post-intervention/1 month follow-up | NA | - | |
| SPADI | post-intervention/1 month follow-up | NA | - | |
| Hawkins | post-intervention/1 month follow-up | NA | - | |
| LSST1-3 | post-intervention/1 month follow-up | NA | - | |
| Bahat et al. 2015 [ | cervical flexion ROM | post-intervention | NA | Between groups |
| 3 months follow-up | NA | - | ||
| Global Perceived change | post-intervention | NA | - | |
| 3 months follow-up | NA | Between groups | ||
| VAS | post-intervention/3 months follow-up | NA | - | |
| NDI | post-intervention/3 months follow-up | NA | - | |
| TSK | post-intervention/3 months follow-up | NA | - | |
| Velocity | post-intervention/3 months follow-up | NA | - | |
| TIP% | post-intervention/3 months follow-up | NA | - | |
| Accuracy | post-intervention/3 months follow-up | NA | - | |
| sway SD | post-intervention/3 months follow-up | NA | - | |
| Eyes closed balance | post-intervention/3 months follow-up | NA | - | |
| singer leg stance | post-intervention/3 months follow-up | NA | - | |
| Bahat et al. 2017 [ | Vmean (F,LR) | Post-pre intervention | NA | Between groups |
| Vpeak (LR) | Post-pre intervention | NA | Between groups | |
| Vmean (F,E,LR) | 3 months follow up-pre intervention | NA | Between groups | |
| Vpeak (E,LR) | 3 months follow up-pre intervention | NA | Between groups | |
| VAS | Post-pre/3 months-pre | NA | Between groups | |
| EQ5D | Post-pre/3 months-pre | NA | Between groups | |
| Accuracy (F,RR,LR) | Post-pre intervention | NA | Between groups | |
| Accuracy (F) | 3 months follow up-pre intervention | NA | Between groups | |
| TTP% | Post-pre/3 months-pre | NA | Between groups | |
| ROM | Post-pre/3 months-pre | NA | - | |
| NDI | Post-pre/3 months-pre | NA | - | |
| TSK | Post-pre/3 months-pre | NA | - | |
| NVP | Post-pre/3 months-pre | NA | - | |
| GPE | Post-pre/3 months-pre | NA | - | |
| Kim et al. 2014 [ | VAS | NA | Between groups | |
| Pressure algometer | NA | |||
| ODI | NA | |||
| FBQ | NA | |||
| RMDQ | NA | - | ||
| Yilmaz Yelvar et al. 2017 [ | VAS | NA | Between groups | |
| TKS | NA | |||
| TUG | NA | |||
| 6 MWT scores | NA | |||
| Martinho et al. 2016 [ | Maximum strength | −0.08 | ||
| average strength | 0.01 | |||
| Endurance | 1.83 | |||
| Jeffs et al. 2014 [ | Pain | 23.7 | ||
| Fung et al. 2012 [ | Active knee flexion ROM | −0.33 | - | |
| Active knee extension ROM | −0.6 | - | ||
| 2 min walk test | 2.68 | - | ||
| NPPS | 16.84 | - | ||
| ABCS | 14.11 | - | ||
| LEFS | 31.85 | - | ||
| Koo et al. 2018 [ | VAS | NA | - | |
| WOMAC | NA | - | ||
| 6 min walk test | NA | - | ||
| Timed-stands test | NA | - | ||
| Jin et al. 2018 [ | VAS (at 3, 5, 7 days after TKR) | NA | ||
| WOMAC (at 1, 3, 6 months after TKR) | NA | |||
| HSS (at 1, 3, 6 months after TKR) | NA | |||
| Punt et al. 2016 [ | FAAM-ADL | NA | - | |
| FAAM-sport | NA | - | ||
| VAS-rest | NA | - | ||
| VAS-walk | NA | - | ||
Abbreviations: VR (Virtual reality); ROM (range of motion); CMS (Constant-Murley score); VAS (Visual Analog Scale); SPADI (Shoulder Pain and Disability Index); SRT (Scapular Retraction Test); SAT (Scapular Assistance Test); LSST (Lateral Scapular Slide Test); NDI (Neck Disability Index); TSK (Tampa scale of kinesiophobia); TIP% (Time to peak velocity percentage); GPE (Global perceived effect); sway SD (standard deviation of the static head sway); EQ-5D(EQ-5D™, http://www.euroqol.org); NVP (Number of velocity peaks); ODI (Oswestry low-back pain disability index); RMDQ (Roland Morris disability questionnaire); FBQ (fear avoidance beliefs questionnaire); NPRS (Numeric Pain Rating Scale); LEFS (Lower Extremity Functional Scale); ABCS (Activity-specific Balance Confidence Scale); WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index); FAAM (Foot and Ankle Ability Measure); ADL (activities of daily living); vmean (Mean velocity); Vpeak (Peak velocity); F (Flexion), E (Extension), LR (Left rotation), RR (Right rotation); the-marked mean p > 0.05; NA (not available); Hospital for Special Surgery knee score (HSS); TKS (TAMPA Kinesiophobia Scale), TUG (timed-up and go test); 6 MWT (6-Minute Walk Test).
Effect of VR versus no intervention.
| Study | Outcome Measure | Mean Difference between VR Groups and Control Group | Significance of Difference between Groups |
|---|---|---|---|
| Bahat et al. 2017 [ | NDI | NA | Between groups |
| velocity | NA | ||
| TTP% (F,LR) | NA | ||
| Accuracy (F,RR) | NA | ||
| ROM | NA | - | |
| EQ5D | NA | - | |
| TSK | NA | - | |
| NVP | NA | - | |
| Thomas et al. 2016 [ | ROM | NA | - |
| Pain | NA | - | |
| Kipping et al. 2012 [ | VAS | NA | - |
| FLACC (dressing removal) | NA | Between groups | |
| Punt et al. 2016 [ | FAAM-ADL | NA | - |
| FAAM-sport | NA | - | |
| VAS-rest | NA | - | |
| VAS-walk | NA | - |
Abbreviations: VR (Virtual reality); NDI (Neck Disability Index); TIP% (Time to peak velocity percentage); ROM (range of motion); EQ-5D (EQ-5D™, http://www.euroqol.org); TSK (Tampa scale of kinesiophobia); NVP (Number of velocity peaks); VAS (Visual Analog Scale); FLACC (Faces, legs, activity, cry, consolability scale); FAAM (Foot and Ankle Ability Measure); ADL (activities of daily living); the-marked mean p > 0.05; NA (not available).