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Review

Effectiveness of Virtual Reality-Based Interventions for Managing Chronic Pain on Pain Reduction, Anxiety, Depression and Mood: A Systematic Review

by
Ka Po Wong
1,*,
Mimi Mun Yee Tse
2 and
Jing Qin
1
1
Centre for Smart Health, School of Nursing, The Hong Kong Polytechnic University, 11 Yuk Choi Road, Hong Kong
2
School of Nursing and Health Studies, Hong Kong Metropolitan University, 1 Sheung Shing Street, Ho Man Tin, Hong Kong
*
Author to whom correspondence should be addressed.
Healthcare 2022, 10(10), 2047; https://doi.org/10.3390/healthcare10102047
Original submission received: 20 September 2022 / Revised: 9 October 2022 / Accepted: 12 October 2022 / Published: 17 October 2022
(This article belongs to the Special Issue Problems for Managing Chronic Pain)
Browse Figure
Versions Notes

Abstract

:
(1) Background: Patients diagnosed with chronic pain suffer from long-term pain, which negatively affects their daily lives and mental health. Virtual reality (VR) technologies are considered a therapeutic tool to manage pain perception and mental health conditions. This systematic review aimed to appraise the efficacy of VR in improving pain intensity, anxiety, depression and mood among patients with chronic pain; (2) Methods: Five electronic databases were systematically searched using the terms representing VR and chronic pain. Quality assessment was conducted using Cochrane Collaboration’s tool and Newcastle-Ottawa scale; (3) Results: Seventeen peer-reviewed articles were included in this review. It was found that VR was able to reduce pain intensity in patients with phantom limb pain, chronic headache, chronic neck pain and chronic low-back pain. The effects of VR on the improvement of anxiety, depression and mood were not determined due to the inadequate amount of clinical evidence; (4) Conclusions: VR, especially immersive VR, improves pain outcomes and its effects may vary depending on the approach and study design. More research is still needed to investigate the clinical use of VR in patients with chronic pain.

1. Introduction

Chronic pain, one of the most common human experiences, is a complicated and troubling problem. According to the International Association for the Study of Pain’s definition, chronic pain is ‘pain that lasts or recurs for more than three to six months’ [1]. Up to 20% of people worldwide are affected by chronic pain at any given time field [2,3,4]. Common chronic pain types include headache, postsurgical pain, post-trauma pain, lower back pain, cancer pain, arthritis pain, neurogenic pain and psychogenic pain [5]. Chronic pain is a ubiquitous medical complaint that accounts for 15–20% of physician visits [6]. Acute pain typically resolves after tissue healing, but in certain individuals, it persists beyond normal healing time (i.e., between three to six months), contributing to chronic pain.
The situation of acute pain is entirely different from chronic pain [7,8,9]. Acute pain serves a protective purpose; it is evoked by stimuli, such as trauma, surgery, extreme temperature, pressure or illness, which injure or threaten to destroy tissues [10,11]. By contrast, chronic pain is not necessarily associated with physical traumatic events and lacks physiological warning function. The painful sensation cannot be simply explained based on nerve impulse processing in the somatosensory system. Similar to phantom limb pain (PLP), the patient experiences intense pain of the complete absence of neuronal input from an entire field of nociceptors [10]. Pain is always a subjective sense because the experience of chronic pain varies widely between people and even within an individual depending on the context and meaning of pain and the psychological state of the person [12].
Chronic pain is the leading cause of why patients seek medical care [2]. Inappropriate chronic pain management often results in reduced quality of life, alcohol and drug usage, physical dysfunction and mental disorders [13,14]. The relationship between depression and chronic pain exhibits bidirectional characteristics. Patients with a long history of pain disorders have an increased risk of depression and anxiety symptoms [15]. The significant relationship between suicidal thoughts and pain symptoms has also been well demonstrated. Suicidal ideation and attempts were more prevalent in people with chronic pain than in those without [16]. Individuals with chronic pain are two to three times more likely to commit suicide [17]. The World Health Organisation (WHO) has acknowledged chronic pain as an individual key risk factor for suicide [18]. Furthermore, recent evidence shows that chronic pain can lead to anatomical and functional alterations in the brain [19]. Chronic pain poses a huge financial burden to society in addition to physical and emotional burdens [20]. The yearly cost of chronic pain is about $635 billion in the United States, which is higher than the annual costs for cancer and heart diseases [21].
A range of medication options is available for the treatment of chronic pain, including the use of nonsteroidal anti-inflammatory drugs (NSAIDs), opioids, antidepressants and anticonvulsants [22]. However, two-thirds of patients with chronic pain living in the Grampian region of Scotland, UK reported dissatisfaction with pharmacological treatments [14]. Moreover, people using pain medication can develop an addiction and have physical dependence [23,24]. Given the limitations of conventional rehabilitation, developing new rehabilitation strategies for patients with chronic pain is imperative. The purposes of chronic pain rehabilitation include reducing pain levels, overcoming negative mental problems and reducing reliance on the use of pain medication. Continuing neurobiological discoveries have generated new ideas for the development of non-pharmacological rehabilitation, such as physiotherapy, psychological therapy and surgery, to treat pain. Simple psychological manipulation, such as attention distraction, can significantly reduce pain intensity because cognitive and emotional states have an enormous influence on pain perception.
Virtual reality (VR) is a potentially powerful tool for relieving pain by enhancing psychological well-being. VR can provide three-dimensional (3D) environments and multi-sensory stimulation to users. VR can produce therapeutically useful scenarios and allow its appropriate use [25]. VR draws much attention to the computer-generated world, leaving less cognitive capacity available to process pain singles. Recent research demonstrated that VR is a promising tool to help reduce pain among individuals undergoing medical procedures [26], urological endoscopies [27], physical therapy [28] and dental procedures [29]. A review conducted by Malloy and Milling [30] in 2010 evaluated the effects of VR distraction on relieving different types of pain. Kenney et al. [31] conducted a meta-analysis to examine the effectiveness of VR distraction in managing acute and chronic pain. A study by Scapin et al. [32] investigated the effects of VR in the treatment of burn patients. The review of Mallari et al. [33] in 2019 compared the effects of VR and non-VR treatments on acute and chronic pain reduction among adults. Another study conducted by Indovina et al. [34] assessed the use of VR for managing pain and distress during medical procedures. A review by Pittara [35] evaluated the effects of VR on pain management in cancer. A systematic review conducted by Wittkopf [36] examined the effectiveness of interactive VR in managing acute and chronic pain perception. Previous studies evaluating VR intervention for pain were limited by combining overall results of acute and chronic pain, investigation of certain types of pain only, lack of assessment of the effects of VR intervention on anxiety, depression and mood and short of covering patients in different age groups. To fill these research gaps, a systematic review on the efficacy of VR in dealing with different types of chronic pain for patients in different age groups and their anxiety, depression and mood is needed to determine the effect of VR-based pain management intervention on different types of chronic pain, anxiety, depression and mood.
An increasing number of studies have assessed the use of VR as an analgesic for patients with chronic pain. Considering the accumulating evidence, a comprehensive systematic review on the effectiveness of VR in managing pain perception and mental health conditions among patients diagnosed with chronic pain is needed. This review aimed to: (1) widely characterise empirical studies to date on the effectiveness of VR distraction in relieving different types of chronic pain, reducing anxiety and depression, and improving mood (2) identify the primary shortcomings of these studies, (3) provide clinical implications on adopting VR distraction in reducing chronic pain and (4) highlight research gaps and suggest avenues for future research directions. The findings of this review can assist therapists in VR design and selection for patients with different types of chronic pain and mental health conditions.

2. Materials and Methods

2.1. Search Procedure

This review was conducted using the Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) guideline [37]. This review was registered in the PROSPERO International Prospective Register of systematic reviews (registration number: CRD42022325706). Publications were searched in Medline, Embase, PsycInfo, CINAHL complete and Wanfang in December 2021. A search strategy that combined medical subject headings (MeSH) terms and keywords was developed to generate sets for the themes ‘chronic pain’ and ‘virtual reality’. Table 1 demonstrates our search strategy. Data within the 12-year range from January 2010 to December 2021 were retrieved, and collection was ended in December 2021. The reference lists of the selected studies were examined to identify those that may have been missed due to the limitation of the above-mentioned search terms.

2.2. Eligibility Criteria and Selection Process

Studies included in this review should meet the PICO principle (population/patients, intervention, comparison and outcomes) and the following criteria. The research design should be empirical studies, for instance, randomised control trials (RCTs), cross-sectional studies, case series, etc. This criterion was to ensure the comprehensiveness of the review. Studies should contain an investigation of patients with chronic pain diagnoses. The forms of VR interventions for managing chronic pain could be immersive and non-immersive. All comparators (e.g., treatment-as-usual, waitlist control, placebo group and no treatment group) were included. Studies should report the primary outcome obtained from any indication of pain intensity, and secondary outcome indicators responding to anxiety, depression and mood. There was no limit on the change in symptoms lasted for. Each session should be a minimum of 10 min which was applied in other pain reduction-related reviews (e.g., [38]). Other inclusion criteria were written in English, peer-reviewed and published after 2010. A systematic review was conducted by Malloy and Milling [30] in 2010 about the effects of VR distraction on chronic pain and afterwards, no summary work was conducted on the same topic. Therefore, to update the development of VR on chronic pain management in the recent decade, a systematic review including studies related to this issue after 2010 is necessary. The exclusion criteria were as follows: papers without empirical results, those focusing purely on theory and ethical issues and/or those with regulatory issues concerning the use of VR. Articles were screened in two stages. In the first stage, the title and abstract of all studies were screened and any study that appeared to measure the association between VR and chronic pain was held for further analysis. In the second stage, the full text was examined and accepted if the above-mentioned inclusion and exclusion criteria were met.

2.3. Data Extraction and Quality Assessment

The data items extracted from each selected study were evaluated using a modified Cochrane Collaboration’s tool for assessing the risk of bias for randomised controlled trials (RCTs) [39] and the Newcastle-Ottawa scale for nonrandomised studies (NRSs) [40]. The corresponding authors or the co-author of the studies with missing data were contacted for requesting the data. If the author had no response or the data were unavailable, then the studies were excluded from the analysis. The methodological quality and risk of bias of the included articles were assessed based on the established guidelines and quality-assessment tools [37]. Quality probes included research questions, recruitment strategies, randomisation, outcome evaluation and statistical analysis. Two reviewers evaluated all the articles independently. Discrepancies were discussed by three reviewers. Thirteen studies were further excluded from the systematic review due to non-pertinent outcomes. Two studies using duplicate data and two studies that were not available in English were also excluded, resulting in 17 studies included for data synthesis. The overall quality of the studies was assessed according to the criteria in Table 2.

2.4. Data Synthesis

A narrative synthesis approach was adopted to describe the research designs, participant characteristics, VR interventions, outcomes and findings in this systematic review. This is due to the heterogeneity of major data items (e.g., study designs, comparators, measures and outcomes).

3. Results

3.1. Study Selection

The initial number of articles identified from databases was 404. After discarding duplicates and ineligible records, 181 papers remained. The full texts of the resulting 34 studies were retrieved and examined. After the full-text screening, 17 studies were excluded. The details of these excluded studies are shown in Supplementary Table S1 [41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57]. A total of 17 studies assessed VR-based interventions in chronic pain management. Further information on the selection process of the extracted studies is demonstrated in Figure 1.

3.2. Study Characteristics

Three studies were conducted in Canada, two each from the United States and Spain and one each in Australia, Belgium, Demark, Israel, Italy, Japan, Jorden, Slovenia, Sweden, Switzerland and Turkey. This systematic review included seven RCTs, seven quasi-experimental studies, one controlled study, one case series study and one before and after study. For the studies using RCT designs (n = 8), control groups consisted of treatment-as-usual, pain-relieving medication, virtual wheeling, laser training, traditional physical therapy, audio group, mindfulness-based stress reduction treatment and watching videos. Pretest and post-test assessments were used in all studies, with five studies having follow-up assessments ranging from 1 month to 6 months and one study having an assessment during the treatment. Ten studies were considered to have moderate quality, and nine studies were considered to have low quality. Detailed study characteristics are demonstrated in Table 3.

3.3. Participant Characteristics

A total of 605 participants were evaluated, and sample sizes ranged from 9 to 97 individuals. The participants were aged between 18 and 75. The participants were mainly female with a sample proportion of 58.5% (range from 26.3% to 100%). According to the categorisation of chronic pain types in the 11th version of the International Classification of Diseases (ICD-11) [72], five types of chronic pain were identified among the participants; these types include chronic primary pain, chronic cancer pain, chronic neuropathic pain, chronic headache and chronic musculoskeletal pain. Four studies did not indicate the types of chronic pain. The details of chronic pain categorisation are listed in Table 3. The participants were diagnosed by different approaches including the American College of Rheumatology, Numeric Rating Scale, Quantitative Sensory Testing, Neuropathic Pain Symptom Inventory, Short-Form McGill Pain Questionnaire, International Classification of Headache Disorders, Neck Disability Index, Defence and Veterans Pain Rating Scale and clinical evidence. Two studies [60,68] did not report the diagnosis method. Detailed participant characteristics are provided in Table 3.

3.4. Risk of Bias

Of the 17 included studies, eight of them were RCTs in which Cochrane Collaboration’s tool was used to assess the risk of bias of these RCTs. Five trials had low risk of random sequence generation. Four studies reported low risk of allocation concealment. The interventions in the trials may have unavoidable broken blinding. However, only three studies reported it and thus these three studies were judged to have low risk bias of blinding of participants and personnel. Only three trials, which mentioned blinding of outcome assessors, were judged to have low risk of bias of blinding of outcomes assessment. All trials had low risk of incomplete outcome data. Three studies had low risk of bias in selective reporting as the protocol, primary outcomes and secondary outcomes were reported in the studies. Only one study was judged to have low risk of other bias as the potential bias were reported in the study. The remaining nine studies were NRS, the methodological quality of which was assessed by the Newcastle-Ottawa scale. This scale had three main criteria, namely, the selection of the study groups, the comparability of the study groups, and the ascertainment of the outcome. The total scores of the studies ranged from 6 to 8. The scores of risk of bias of all studies are demonstrated in Table 3 and the details of risk of bias assessment are demonstrated in Supplementary Table S2.

3.5. VR Interventions

All studies examined a unique VR treatment and natural environment (Table 4). Ten studies adopted immersive VR technologies, and seven studies adopted non-immersive VR studies. The treatment purposes included rehabilitation (n = 7), pain reduction (n = 5), pain distraction (n = 3), activity management (n = 1) and relaxation (n = 1). The treatment ranged from 1 to 20 sessions, and the length of each session ranged from 1 min to 120 min. Two studies were designed with a home-based VR program and the remaining studies conducted the intervention in universities and hospitals. Different types of head-mounted displays (HMD) and motion sensors were used to facilitate the treatments for the participants.

3.6. User Engagement with the VR Interventions

The average attrition rate in the VR treatments across all studies was 11.7%, with a range of 0% to 53.3% (Table 4). The user engagement with the VR interventions was measured by Test of Playfulness, Global Perceived Effect, numeric rating scale and nonstandardised questions to indicate satisfaction, acceptability, enjoyment, motivation, attention and involvement. Eight studies did not report user engagement.

3.7. Pain Intensity, Anxiety, Depression and Mood Measurements and Outcomes

The details of the pain intensity measurements and the VR intervention outcomes in the included studies are summarised in Table 5. The measurements included Brief Pain Inventory (n = 3), Visual Analogue Scale (n = 5), numerical rating scale (n = 6), McGill Pain Questionnaire (n = 3), nonstandardised questions (n = 2), Short Leeds Assessment of Neuropathic Symptoms and Signs (n = 1) and Retroactive Pain Intensity (n = 1). Out of 17 studies, 13 studies reported a significant reduction in pain intensity after VR-based treatment.
Among the 17 studies, only seven studies assessed the mental health condition of the participants. The mental health condition consisted of depression, anxiety and relaxation. The measurements included Beck Depression Inventory (n = 2), patient health questionnaire (n = 1), State Anxiety Inventory (n = 1), numerical rating scale (n = 1) and nonstandardised questions (n = 3). Five studies reported a significant reduction in anxiety and depression and improvement in mood.
About 10 studies utilised immersive VR technologies, and eight of them reported a significant effect on pain reduction and three of them reported a significant effect on managing anxiety, depression and mood. Among the seven studies that adopted non-immersive VR, only four showed effectiveness in chronic pain reduction and two demonstrated effectiveness in mental health management. VR primary works through distraction to reduce the pain intensity. The details of the pain intensity, anxiety, depression and mood measurements and outcomes in the included studies are summarised in Table 5.

4. Discussion

This systematic review aimed to characterise empirical studies, describe the shortcomings of the selected studies, provide clinical implications of using VR distraction to manage chronic pain and mental health conditions, and highlight research gaps for future research directions. Despite particular methodological concerns that emerged across the studies, the review provides clinical evidence supporting the efficacy of VR distraction in chronic pain reduction, particularly in PLP, chronic headache, chronic neck pain and chronic low-back pain. The use of VR in pain reduction appears to be unpromising for patients suffering from chronic primary pain. The assessments of anxiety, depression and mood for patients with chronic pain were neglected in most studies, and thus the effectiveness of VR intervention for managing the mental health of patients with chronic pain was not concluded in this review. The study also suggested immersive VR potentially provided a way of exposing patients to a more attractive computer-generated environment that is more likely to exert an influence on pain reduction compared with non-immersive VR. Humans have a finite attentional capacity, and a distraction task consumes more portion of the capacities believed to leave less cognitive resources available for processing pain [12]. An immersive VR provides more sensory information that helps the person absent from the perception of pain.

4.1. Shortcomings of Included Studies

A significant problem is apparent with regard to the study methods used for estimating treatment effects. Firstly, most studies adopted a quasi-experimental design and RCT. The major concern of quasi-experimental studies is that randomisation is not applied, limiting the capability to draw a causal relationship between the intervention and the outcome. Meanwhile, conducting RCT can reduce confounding and bias. Secondly, the assessment of the mental health conditions of chronic pain after VR treatment was not conducted in most studies, confining our understanding of the feasibility of VR treatment in anxiety and depression reduction and mood management among patients with chronic pain. Thirdly, the hardware and software used in some studies were not clearly described. The commonly used tools for VR systems in these studies were HMD and digital computers. Several studies provided the content of the virtual environment without using software for developing the VR treatment. Fourthly, the arrangement of the duration of each session and the time interval between each session should be the significant factors of concern. According to the study of Strickland et al. [73], a 20 min duration is a threshold that normal adults tend to be discomforted with while using VR technologies. More than half of the selected studies conducted immersive VR and non-immersive VR sessions for more than 20 min. This effect possibly affects the results of the experiments and the physical health of the participants. Furthermore, a long-term interval may influence the actual effect of the VR treatment because treatments other than VR intervention on non-intervention days may generate effects that may enhance or weaken the effect of VR distraction. For example, Alemanno et al. [66] conducted the intervention twice per week in six weeks. During the non-intervention days, the patient may take other pharmacological or psychological treatments that may ultimately affect the outcome measures. Therefore, addressing the loophole on the influences in the non-intervention days is vital. Fifthly, some studies had a small sample size, for instance, the study of Garrett et al. [70] had nine subjects. Lastly, the quality of the included studies was moderate and low, implying that high-quality research and RCTs on this topic are still needed.

4.2. Clinical Implications

VR is needed to be applied more in daily clinical practice. Nonetheless, some clinical implications can be drawn at this stage. Five out of seven categories of chronic pain were included in this review. VR is used as a pain management tool in this clinical situation. VR technologies efficaciously reduce pain for patients with different types of chronic pain, particularly for adult patients. Immersive VR used as an adjuvant intervention is effective in relieving pain and anxiety for female patients with breast cancer and patients with chronic low-back pain. Non-immersive VR can improve motor function and neuropathic pain in patients with spinal cord injury-related pain, but the positive findings are limited to quasi-experimental studies. Immersive and non-immersive VR can restore phantom limb movement and alleviate PLP; however, an RCT is lacking to validate this significant finding. Non-immersive VR can reduce pain intensity and improve the quality of life among paediatric patients with chronic headache; these findings were limited to quasi-experimental studies. The pain intensity of patients with chronic low-back pain can be reduced under the VR intervention.
Each study initiated a cutting-edge VR treatment by using different hardware setups mainly including HMD and display screen and unique virtual environments created by VR software development tools. The hardware used in the studies are reasonably priced and commercially available in public markets. Active (e.g., walking in natural environments), passive (e.g., watching a video and movies) and interactive (e.g., playing interactive games) VR experiences were therapeutic for managing chronic pain among the patients. Rapid relief from pain perception and anxiety seem to be provided by the VR intervention. Out of two studies, one or two sessions varying from 10 to 20 min were adequate to prompt the relaxation of pain intensity and anxiety.
Adult patients with chronic pain reported high satisfaction and engagement with the VR treatment. This finding suggests that adults may find VR technologies as supportive and feasible in managing chronic pain; as such, adults may positively respond to digital technologies. Only one study examined the satisfaction of adolescent patients with the VR treatment and reported high satisfaction. This finding implies that experiments involving paediatric patients with chronic pain are scarce, and RCT is limited; thus, more RCTs are needed to be conducted for this group.

4.3. Recommendations for Future Research Directions

VR technology is a non-invasive tool used to treat pain. This review demonstrates the efficiency of this therapy in chronic pain management, anxiety and depression reduction and mood improvement. Further research regarding PLP and chronic headaches is still needed because current studies are mostly limited to quasi-experimental design. An RCT is also required to provide high-reliability findings. Among the 17 studies, the VR distraction programs in 15 studies were guided by therapists or instructors. Two studies were designed with a home-based VR program (i.e., [67,70]). Home-based VR programs can benefit patients with limited mobility and the elderly. However, without the guidance of therapists, the patients might not be able to attain the ideal effects of the rehabilitation program or injuries may incur. The advantages or disadvantages of home-based or self-administered VR intervention have rarely been discussed, and no comparison has been conducted on the effectiveness between guided and self-administrated VR treatment. These issues still need further research. Furthermore, participants in these studies were mainly adults and elderly but fewer children and adolescents. However, 20% to 35% of children and adolescents are affected by chronic pain [74]. Despite the significance of considering the paediatric population, few quantitative studies have investigated the efficacy of VR distraction in chronic pain reduction as well as mental health management. However, the use of VR also exerts side effects. The possible side effects and safety issues of VR treatment, which may vary from different forms of VR, have seldom been raised in discussion. This concern can be resolved using measurement tools, such as the Virtual Reality Sickness Questionnaire (VRSQ) [75], to evaluate the feelings of the users after conducting VR treatment. One of the significant issues that needed to be addressed is the duration of the treatment and the time interval of each session. As mentioned, a 20 min duration is an appropriate time for VR intervention, so researchers should design it with 20 min or less for each session. To avoid the effects of VR treatment interfered by other non-VR treatments, researchers can design an intensive program to evaluate the influence of the activities carried out on the non-intervention days during the period of the experiment or propose one session of VR treatment. These mentioned concerns are necessary to be resolved before VR becomes a normal daily clinical treatment for chronic pain reduction.

4.4. Limitations

This systematic review has several limitations. One of the purposes of this review is to identify studies on the use of VR for patients with chronic pain. The keywords related to VR in searching through electronic databases were not adequate to locate all relevant studies. To address this issue, the keywords used in the article-searching process were common naming. The second limitation of this review is that several study designs (i.e., RCT, quasi-experiment study and case study) were included. Although this approach can provide a comprehensive overview, the clinical evidence may be weakened. Furthermore, this systematic review only included the studies published after 2010 and thus a meta-analysis consisting of studies not limited to those published after 2010 is recommended to be conducted in the future. The last limitation is that only studies published in English language were included. Thus, non-English written studies related to this issue were neglected.

5. Conclusions

This review provides moderate evidence of the positive effect of VR treatment on reducing chronic pain and low evidence of the encouraging impact of VR intervention on anxiety and depression reduction and mood improvement. Most adult participants rated their VR experiment with high satisfaction; the attrition rates, however, were reported to have a large discrepancy. The effects may vary depending on the VR-intervention approach and study design. The promising results of VR, especially immersive VR, encourage its application as an adjunct therapy in clinical practices. Given the harmful effect of pharmacological treatment, many studies have proposed the use of VR distraction instead of the traditional method or as an adjunct analgesic technique. The main shortcomings observed in the studies include the inadequate number of RCT studies, a lack of evidence on moderate and long-term application, an inappropriate setting for the duration of treatment and time interval between each session and small sample size. Additionally, new areas can be explored, such as a comparison of the effects between self-administrated and guided VR treatment, an investigation of the paediatric population and an evaluation of the side effects of the VR approach. Due to the increasing application and continuous development of VR technologies among healthcare practitioners, more RCTs should be conducted to provide highly credible clinical evidence on the efficacy of VR distraction in patients with chronic pain.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/healthcare10102047/s1, Table S1: Exclusion of full-text article (n = 17); Table S2: Risk of bias assessment.

Author Contributions

Conceptualization, K.P.W., M.M.Y.T. and J.Q.; methodology, K.P.W., M.M.Y.T. and J.Q.; validation, K.P.W. and M.M.Y.T.; formal analysis, K.P.W.; investigation, K.P.W., M.M.Y.T. and J.Q.; resources, K.P.W.; data curation, K.P.W., M.M.Y.T. and J.Q.; writing—original draft preparation, K.P.W.; writing—review and editing, K.P.W., M.M.Y.T. and J.Q.; visualization, K.P.W.; supervision, M.M.Y.T. and J.Q.; project administration, K.P.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data utilized for the purpose of this study are available publicly and online.

Acknowledgments

The work described in this paper is partly supported by a grant under Project of Strategic Importance scheme of The Hong Kong Polytechnic University (project no. 1-ZE2Q) and a grant of Innovation and Technology Fund—Guangdong-Hong Kong Technology Cooperation Funding Scheme (ITF-TCFS) (project no. GHP/051/20GD).

Conflicts of Interest

The authors declare no conflict of interest.

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Healthcare 10 02047 g001 550
Figure 1. PRISMA flow chart of the article selection process.
Figure 1. PRISMA flow chart of the article selection process.
Healthcare 10 02047 g001
Table
Table 1. Medical subject headings (MeSH) terms and keywords.
Table 1. Medical subject headings (MeSH) terms and keywords.
ThemeMeSH TermsKeywords
Chronic pain Chronic pain
Arthralgia
Back pain
Cancer pain
Metatarsalgia
Musculoskeletal pain
Neck pain
Neuralgia
Nociceptive pain		Persistent pain
Chronic primary pain
Chronic cancer pain
Chronic posttraumatic and postsurgical pain
Chronic neuropathic pain
Chronic headache and orofacial pain
Chronic visceral pain
Chronic musculoskeletal pain
Virtual realityVirtual realityVirtual reality
Virtual realities
VR
VR exposure
Virtual environment
Table
Table 2. Overall quality assessment using Cochrane’s tool for assessing risk of bias and Newcastle-Ottawa scale.
Table 2. Overall quality assessment using Cochrane’s tool for assessing risk of bias and Newcastle-Ottawa scale.
Quality RatingDefinition
HighRCTs with low risk of bias in all domains
ModerateRCTs with high or unclear risk of bias in one or two domains
NRSs with six to nine stars
LowRCTs with high or unclear risk of bias in three or more domains
NRSs with three to five stars
Very lowNRSs with three to five stars
NRS: nonrandomised study; RCT: randomised control trial.
Table
Table 3. Description of study and participants characteristics.
Table 3. Description of study and participants characteristics.
StudyCountryType of PainDiagnosisNFemales, n (%)Mean AgeAge RangeStudy DesignTrial ArmsMeasurementsQuality Score
Garcia-Palacios (2015) [55]SpainChronic primary pain: FibromyalgiaACR6161 (100)No mention23–70RCTVRAM (31); TAU (30)Pre, Post4/7 (Low)
Mortensen (2015) [58]DenmarkChronic primary pain: FibromyalgiaACR157 (100)49.344–55Quasi-experimental studyMCVG (15)Pre, Post6/9 (Moderate)
House (2016) [59]The United StatesChronic cancer pain: Chronic pain post-cancer surgeryNRS126 (100)57.822–78Quasi-experimental studyBrightArm Duo therapy (12)Pre, Post, 8-week FU7/9 (Moderate)
Mohammad (2018) [60]JordanChronic cancer pain: Breast cancerNo mention8080 (100)5230–70RCTVR (40); Morphine (40)Pre, Post3/7 (Low)
Jordan (2016) [61]SpainChronic neuropathic pain: Spinal cord injury-related painQST358 (29.1)47.530–70RCTVWT (8); VW (7)Pre, Post3/7 (Low)
Villiger (2013) [62]SwitzerlandChronic neuropathic pain: Spinal cord injury-related painClinical evidence145 (35.7)52.728–71Quasi-experimental studyVRAT (14)Pre-pre, Pre, Post, FU at 12-16 weeks8/9 (Moderate)
Ortiz-Catalan (2016) [63]Sweden, SloveniaChronic neuropathic pain: PLPClinical evidence14No mention50.328–74Quasi-experimental studyVR (14)Pre, Post, FU at 1, 3 and 6 months7/9 (Moderate)
Osumi (2018) [28]JapanChronic neuropathic pain: PLPNPSI, SF-MPQ195 (26.3)49.123–71Quasi-experimental studyVRR (19)Pre, Post6/9 (Moderate)
Shiri (2013) [64]IsraelChronic headacheICHD103 (30)13.410.5–17.5Quasi-experimental studyVR (10)Pre, Post, FU at 1 and 3 months7/9 (Moderate)
Sarig Bahat (2018) [51]AustraliaChronic musculoskeletal pain: Chronic neck painNDI9063 (70)48 (median)18 or aboveRCTVR (30); Laser (30); Control (30)Pre, Post, FU at 3 months6/7 (Moderate)
Yelvar (2016) [65]TurkeyChronic musculoskeletal pain: Chronic low-back painDiagnosed by physicians4629 (63.0)49.54LessRCTVWT (23); Traditional Physiotherapy (23)Pre, Post4/7 (Low)
Alemanno (2019) [66]ItalyChronic musculoskeletal pain: Chronic low-back painClinical evidence2011 (55)47.519–72Before-after studiesVRR (20)Pre, Post6/9 (Moderate)
Darnall (2020) [67]The United StatesChronic musculoskeletal pain: Chronic nonmalignant low back pain or fibromyalgiaDVPRS9722 (29.7)No mention18–75RCTVR (47); Audio (50)Pre, Mid, Post4/7 (Low)
Wiederhold (2014) [68]BelgiumNon-specific chronic pain: Average daily painNo mention40No mentionNo mention22–68Quasi-experimental studyVR (40)Pre, Post7/9 (Moderate)
Gromala (2015) [69]CanadaNon-specific chronic painClinical evidence137 (53.8)4935–55Controlled studyVR (7); Listen to the MBSR training audio track (6)Pre, Post1/7 (Low)
Garrett (2017) [70]CanadaNon-specific chronic painClinical evidence96 (66.7)45.331–71Case seriesVR (9)Pre, Post6/9 (Moderate)
Amin (2017) [71]CanadaNon-specific chronic painClinical evidence3013 (43.3)No mention22–29RCTCardboard VR (10); VR (10); non-VR (10)Pre, Post2/7 (Low)
ACR: American College of Rheumatology; DVPRS: Defense and Veterans Pain Rating Scale; FU: Follow-up; ICHD: International Classification of Headache Disorders; Mid: During the treatment; MBSR: Mindfulness-based stress reduction; MCVG: Motion-Controlled Video Games; NDI: Neck Disability Index; NPSI: Neuropathic Pain Symptom Inventory; NRS: Numeric Pain Rating Scale; Pre: Pretest; Post-test; Pre-pre: Pre-pretest; Post: PLP: phantom limb pain; QST: Quantitative Sensory Testing; RCT: randomised control trial; SF-MPQ: Short-Form McGill Pain Questionnaire; TAU: treatment-as-usual; VR: Virtual reality; VRR: Virtual reality rehabilitation; VRAM: VRAT: Virtual Reality–Augmented Training; VR activity management; VW: Virtual wheeling; VWT: Virtual walking treatment.
Table
Table 4. Details of the VR-based interventions and user engagement measure outcomes.
Table 4. Details of the VR-based interventions and user engagement measure outcomes.
StudyTypes of VRSoftwarePurposeHardwareLengthAttrition (%)Engagement MeasuresEngagement Outcomes
Garcia-Palacios (2015) [55]Non-immersive EMMA, VR environment of a desert, a beach, a forest, a snowy landscape and a meadowActivity managementLarge screen, projector 6 2 h sessions in 3 weeks1/31 (3.2)NSQHigh satisfaction and acceptability
Mortensen (2015) [58]Non-immersive VR environment of 6 to 12 different activities (e.g., bowling, table tennis and volleyball)Rehabilitation Wii, PS3 Move, Xbox Kinect15 30 min sessions8/15 (53.3)ToPHigh enjoyment
House (2016) [59]Non-immersive Unity 3D, VR environment of nine games: Breakout 3D, Card Island, Remember that Card, Musical Drums, Xylophone, Pick & Place, Arm Slalom, Avalanche and Treasure Hunt.Rehabilitation Low-friction robotic rehabilitation table, computerized forearm supports, a display16 20–50 min sessions in 8 weeks6/12 (50)NSQHigh acceptability
Mohammad (2018) [60]ImmersiveVR environment of deep-sea diving “Ocean Rift” and beach with the “Happy Place” trackPain distractionHMD with headphones1 15 min session0/40 (0)No mentionNo mention
Jordan (2016) [61]ImmersiveVR environment of an actor walking along a pathPain reductionNo mention1 20 min session0/8 (0)No mentionNo mention
Villiger (2013) [62]Non-immersive Unity 3-dimensional (3D) game engineRehabilitation 3-degrees of freedom accelerometer sensor nodes, finger bend sensors16–20 sessions in 4 weeks, 45-min/session0/14 (0)NRS High enjoyment, motivation and attention
Ortiz-Catalan (2016) [63]Non-immersive Neuromotus™Rehabilitation Webcam, fiducial markersurface, electrodes over the stump 12 120 min sessions0/14 (0)No mentionNo mention
Osumi (2018) [28]Immersive3D-CG, VR environment of mirror-reversed imageRehabilitation Oculus Rift HMD, Infrared sensor (Kinect for Winds v2)1 20 min session0/19 (0)No mentionNo mention
Shiri (2013) [64]Non-immersive ProComp Infiniti systemRelaxationElectrodes10 sessions1/10 (10)NRSHigh satisfaction
Sarig Bahat (2018) [51]ImmersiveUnity-proRehabilitation Oculus Rift DK1 HMD equipped with 3D motion tracking 16 20 min sessions in 4 weeks5/30 (16.7)GPE satisfactionHigh satisfaction (84.1%)
Yelvar (2016) [65]ImmersiveVR environment of a video clip was taken by a cameraman who was naturally walking down Ireland forestPain reduction, rehabilitationiPod (Apple Inc., Cupertino, CA, USA) with video glasses (Wrap920)10 15 min sessions in 2 weeks1/23 (4.35)NSQ: nonstandardised questionsSatisfied
Alemanno (2019) [66]Non-immersive An avatar reproducing online the performance of the patient who also gets an immediate visual and acoustic feedback on his/her performanceRehabilitation Computer workstation connected to a 6 degrees of freedom motion-tracking system (Polhemus G4), high-resolution LCD12 60 min sessions over 4–6 weeks0/20 (0)No mentionNo mention
Darnall (2020) [67]ImmersiveAppliedVRPain reductionOculus Go headset4–8 sessions in 21 days, 1–15 min/session12/47 (25.5)NRSHigh satisfaction
Wiederhold (2014) [68]ImmersiveVR environment of natural areasPain distractionHMD1 15 min session6/40 (15)No mentionNo mention
Gromala (2015) [69]ImmersiveVR environment of a peaceful, non-distracting and safe environmentPain reductionDeepStream VR viewer20-minNo mentionNo mentionNo mention
Garrett (2017) [70]ImmersiveVR environment of an Iceland, and a boat ride, 3D mandalas, an underwater, the solar system and a natural environment and active problem-solving experiencesPain reductionOculus Rift DK230 min session in 1 month, 3 times a week 0/8 (0)NSQNo mention
Amin (2017) [71]ImmersiveUnity3D, CryoblastPain distractionGoogle LG Nexus 5 smartphone, Dodocase Virtual Reality Kit 1.2, Cardboard viewer with velcro, Oculus Rift Development Kit 22 10 min sessions in 1 day0/10 (0)NRSHigh involvement
3D-CG: three-dimensional computer graphic; GPE: Global perceived effect; HMD: Head-mounted display; min: minutes; NRS: Numeric Rating Scale; NSQ: nonstandardised questions; ToP: Test of Playfulness.
Table
Table 5. Details on pain intensity, anxiety, depression and mood measures and outcomes.
Table 5. Details on pain intensity, anxiety, depression and mood measures and outcomes.
StudyMeasuresOutcomes
Garcia-Palacios (2015) [55]Pain intensity and interference: BPI
Mood: BDI-II		No significant difference in pain intensity and depression in VRAM compared with TAU
Mortensen (2015) [58]Pain improvement: VASNo significant difference in pain improvement
House (2016) [59]Pain intensity: NRS
Depression: PHQ-9		No significant difference in pain reduction; large reduction in depression (8.3/10)
Mohammad (2018) [60]Pain intensity: VAS
Anxiety: SAI		Significant reduction in pain and anxiety in VR plus morphine compared with morphine alone
Jordan (2016) [61]Pain intensity: NRSNo significant change in pain reduction; VWT is better than VW in pain reduction.
Villiger (2013) [62]Pain intensity: NPSSignificant improvement in neuropathic pain
Ortiz-Catalan (2016) [63]Pain intensity: NRS, MPQSignificant improvement in PLP intensity
Osumi (2018) [28]Pain intensity: NPS, SF-MPQSignificant alleviation in PLP intensity
Shiri (2013) [64]Pain severity: VASSignificant reduction in pain severity
Sarig Bahat (2018) [51]Pain intensity: VASSignificant reduction in pain intensity
Yelvar (2016) [65]Pain intensity: VASSignificant improvement in pain intensity in VWT compared with traditional physiotherapy
Alemanno (2019) [66]Pain intensity: MPQ, BPI; Mood: BDI Significant improvement in pain intensity, mood and depression
Darnall (2020) [67]Pain intensity: NRS
Depression: NRS		Significant improvement in pain intensity and depression
Wiederhold (2014) [68]Pain intensity: NRSSignificant reduction in pain intensity
Gromala (2015) [69]Pain intensity: NRSSignificant reduction in pain intensity
Garrett (2017) [70]Pain intensity: NSQ, BPI, S-LANSS
Anxiety: NSQ, Relaxation:NSQ		Pain reduction during the VR among 62.5% of participants; no overall treatment difference in pain scores postexposure
Amin (2017) [71]Pain intensity: RPI
Anxiety: NSQ		Significant improvement in pain intensity in Cardboard VR (coupled with a smartphone) compared with traditional VR and significant improvement in anxiety
BDI-II: Beck Depression Inventory II; BPI: Brief Pain Inventory; MPQ: McGill Pain Questionnaire; NPS: Neuropathic Pain Scale; NRS: Numerical Rating Scale; NSQ: nonstandardised questions; PHQ: Patient Health Questionnaire; RPI: Retroactive Pain Intensity; SAI: State Anxiety Inventory; S-LANSS: Short Leeds Assessment of Neuropathic Symptoms and Signs; VAS: Visual Analogue Scale.
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MDPI and ACS Style

Wong, K.P.; Tse, M.M.Y.; Qin, J. Effectiveness of Virtual Reality-Based Interventions for Managing Chronic Pain on Pain Reduction, Anxiety, Depression and Mood: A Systematic Review. Healthcare 2022, 10, 2047. https://doi.org/10.3390/healthcare10102047

AMA Style

Wong KP, Tse MMY, Qin J. Effectiveness of Virtual Reality-Based Interventions for Managing Chronic Pain on Pain Reduction, Anxiety, Depression and Mood: A Systematic Review. Healthcare. 2022; 10(10):2047. https://doi.org/10.3390/healthcare10102047

Chicago/Turabian Style

Wong, Ka Po, Mimi Mun Yee Tse, and Jing Qin. 2022. "Effectiveness of Virtual Reality-Based Interventions for Managing Chronic Pain on Pain Reduction, Anxiety, Depression and Mood: A Systematic Review" Healthcare 10, no. 10: 2047. https://doi.org/10.3390/healthcare10102047

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