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Meditative movement for breathlessness in advanced COPD or cancer: a systematic review and meta-analysis

Claire M. Nolan, Lisa Jane Brighton, Yihan Mo, Joanne Bayly, Irene J. Higginson, William D-C. Man, Matthew Maddocks
European Respiratory Review 2023 32: 220243; DOI: 10.1183/16000617.0243-2022
Claire M. Nolan
1Brunel University London, College of Medicine, Health and Life Sciences, Department of Health Sciences, London, UK
2Harefield Respiratory Research Group, Royal Brompton and Harefield Hospitals, Guy's and St. Thomas’ NHS Foundation Trust, London, UK
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  • For correspondence: claire.nolan@brunel.ac.uk
Lisa Jane Brighton
3Kings College London, Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, London, UK
4King's College London, Department of Psychology, Institute of Psychiatry, Psychology and Neuroscience, London, UK
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Yihan Mo
3Kings College London, Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, London, UK
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Joanne Bayly
3Kings College London, Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, London, UK
5St. Barnabas Hospices, Worthing, UK
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Irene J. Higginson
3Kings College London, Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, London, UK
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William D-C. Man
2Harefield Respiratory Research Group, Royal Brompton and Harefield Hospitals, Guy's and St. Thomas’ NHS Foundation Trust, London, UK
6King's College London, Faculty of Life Sciences and Medicine, London, UK
7National Heart and Lung Institute, Imperial College London, London, UK
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Matthew Maddocks
3Kings College London, Cicely Saunders Institute of Palliative Care, Policy and Rehabilitation, London, UK
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Abstract

The effect of meditative movement, which includes yoga, tai chi and qi gong, on breathlessness in advanced disease is unknown. This systematic review aims to comprehensively assess the evidence on the effect of meditative movement on breathlessness (primary outcome), health-related quality of life, exercise capacity, functional performance and psychological symptoms (secondary outcomes) in advanced disease. 11 English and Chinese language databases were searched for relevant trials. Risk of bias was assessed using the Cochrane tool. Standardised mean differences (SMDs) with 95% confidence intervals were computed. 17 trials with 1125 participants (n=815 COPD, n=310 cancer), all with unclear or high risk of bias, were included. Pooled estimates (14 studies, n=671) showed no statistically significant difference in breathlessness between meditative movement and control interventions (SMD (95% CI) 0.10 (−0.15–0.34); Chi2=30.11; I2=57%; p=0.45), irrespective of comparator, intervention or disease category. Similar results were observed for health-related quality of life and exercise capacity. It was not possible to perform a meta-analysis for functional performance and psychological symptoms. In conclusion, in people with advanced COPD or cancer, meditative movement does not improve breathlessness, health-related quality of life or exercise capacity. Methodological limitations lead to low levels of certainty in the results.

Abstract

Meditative movement is safe but does not improve breathlessness in people with advanced COPD or advanced cancer. Methodological limitations provide uncertainty in the results which future research should address. #PalliPulm #RespiratoryCare https://bit.ly/3ZI9MZH

Introduction

Breathlessness is a common and burdensome symptom in advanced stages of malignant and nonmalignant disease. Prevalence estimates among people living with advanced cancer, COPD and chronic heart failure range from 16 to 77% [1, 2], 56 to 98% [2] and 18 to 88% [2], respectively. A systematic review of interventions for breathlessness in advanced disease highlighted meditative movement as a potential interventional approach to improve this symptom, with research needed to address the paucity of studies in this area [3].

Meditative movement is a category of exercise defined by “some form of movement or body positioning, a focus on breathing, and a cleared or calm state of mind with a goal of deep states of relaxation” [4]. It includes practices of yoga, tai chi and qi gong [4]. Yoga originated in ancient India and is a relaxation and meditation technique based on postures, exercises and breathing techniques [5]. Tai chi originated in ancient China and involves slow, gentle and flowing movements, upper and lower extremity movements, core strengthening, balance techniques, meditative breathing, and body awareness [6]. Qi gong is also an ancient Chinese practice that includes meditation, slow physical movement and controlled breathing [7].

It is postulated that meditative movement may improve breathlessness in advanced disease based on effects seen in nonadvanced cancer and early-stage chronic disease. The mechanisms of the effects include addressing deconditioning and improving cardiopulmonary function [5, 8–12], improving physical activity [13], reducing anxiety and depression [4], a breathing retraining component leading to a reduced respiratory rate [14, 15], and increased tidal breathing and peripheral oxygen saturation levels [15].

To date, systematic reviews of meditative movement or a single practice, e.g. yoga, have been undertaken in people living with cancer [16–25], COPD [8, 10, 11, 12, 18, 22] and chronic heart failure [5, 9, 18, 22]. Although they demonstrated that meditative movement interventions are safe, none of them investigated breathlessness as a primary outcome and of those that did investigate the effect on breathlessness, the results are conflicting [11, 12, 16, 18, 25]. Furthermore, none of the reviews included people with advanced disease as the population of interest. Therefore, the aim of this review is to provide a comprehensive synthesis of the evidence base regarding the effect of meditative movement on breathlessness in advanced disease. The objectives were to determine the effect of meditative movement on 1) breathlessness, 2) secondary outcomes of exercise capacity, functional performance, psychological symptoms and health-related quality of life, and 3) to determine the safety profile of studies involving meditative movement in people with advanced disease.

Methods

The protocol for this systematic review was pre-specified and registered on the PROSPERO international prospective register of systematic reviews (CRD42021271421) on 23 September 2021 and is reported according to the PRISMA 2020 statement [26].

Information sources

We searched the following databases from their inception to the present, without date or language restrictions: Cochrane Database of Systematic Reviews, the Cochrane Library; Cochrane Central Register of Controlled Trials; Medline (Ovid); Embase (Ovid); PsycINFO (Ovid); CINAHL (EBSCO); the Wanfang database; Chinese National Knowledge Infrastructure; and SinoMed. The searches were conducted on 4 January 2022 and repeated on 4 February 2023. The full strategies are shown in the online supplement. In addition, we checked reference lists of reviews and retrieved articles for relevant studies and performed citation searches on key articles. We included randomised controlled trials (RCTs) or randomised crossover trials if separate data for both time periods was presented (we only used the data of the first period for analysis to avoid any potential for carry-over effects). We required full journal publication; where this was not available or where there was insufficient information or data for extraction, we tried to obtain data by contacting the authors.

Eligibility criteria

Articles were eligible for inclusion if they included adult patients (aged ≥18 years) diagnosed with advanced disease(s) with a high prevalence of breathlessness, undergoing yoga, tai chi and/or qi gong in any setting (comparator arm: treatment, standard care or a comparator intervention). We included articles if the majority (≥50%) of participants met the following criteria for advanced disease: 1) patients with advanced local or metastatic cancer (e.g. T (tumour site and size) N (lymph node involvement) M (metastatic spread) classification of malignant tumours state ≥T3 or N≥1 or M≥1) [27]; patients with severe COPD defined as a forced expiratory volume in 1 s predicted of ≤50% according to Global Initiative for Chronic Obstructive Lung Disease criteria [28]; and patients with chronic heart failure and New York Heart Association stage III or IV [29]. If study participants were stratified for these inclusion criteria, we only included the subgroups of interest.

Studies were excluded if they included paediatric populations. Reviews, editorials, case reports and case series were also excluded.

Selection process

Following the database search, conducted by two reviewers (C.M.N. and Y.M./L.J.B.), all identified records were uploaded Endnote™ 20 (Clarivate®, London, UK) then transferred into Covidence (Melbourne, Australia), where duplicates were identified and removed. At the screening and full-text review stage, the title and abstract and full text were respectively translated from Chinese to English by a native Chinese speaker who is undertaking a PhD (in English) at Kings College London (Y.M.). Two reviewers independently screened the records to identify potentially eligible papers by an initial title and abstract screening (C.M.N. and M.M./L.J.B./J.B./Y.M.). Two reviewers (C.M.N. and M.M./L.J.B./J.B./Y.M.) then independently assessed each article in its entirety for eligibility using standardised eligibility criteria. Disagreements and unclear decision were resolved with a third author. We did not anonymise the studies in any way before assessment. Screening and selection of articles was reported according to the PRISMA criteria and flow chart.

Outcome measures

The primary outcome measure was breathlessness measured by self-reported instruments, including but not limited to the Medical Research Council Dyspnoea Scale (MRC), the modified MRC, the Baseline Dyspnoea Index, the Borg Dyspnoea Scale, the Chronic Respiratory Questionnaire – Dyspnoea domain, the Breathlessness Numerical Rating Scale and the Breathlessness Visual Analogue Scale. Other terms for breathlessness such as dyspnoea, shortness of breath and difficulty breathing were accepted.

Secondary outcome measures included health-related quality of life (e.g. European Organisation for Research and Treatment of Cancer (EORTC) quality of life questionnaires C30 and LC13 (EORTC QLQ-C30; EORTC QLQ-LC13), the Chronic Respiratory Questionnaire (CRQ) and the Kansas City Cardiomyopathy Questionnaire), functional exercise capacity (e.g. 6-min walk test (6MWT) and the incremental shuttle walk test), functional performance measures (e.g. short physical performance battery, 1-min sit-to stand-test, the timed up and go test (TUG) and walking speed tests, e.g. 4-m gait speed), psychological symptoms, i.e. anxiety and depression symptoms (e.g. Hospital Anxiety and Depression Scale (HADS), Generalised Anxiety Disorder Assessment-7 and Public Health Questionnaire-9), and safety (e.g. adverse events and serious adverse events).

Data extraction and management

For data extraction, two reviewers (C.M.N. and L.J.B./Y.M./J.B.) used a pre-piloted, standardised data extraction form and checked for agreement. Differences in data extraction were resolved by reference to original articles, discussion to establish consensus or consultation of a third reviewer (M.M.).

The following data were extracted from included studies: basic study information (first author, year of publication, journal, publication language, country study conducted in, study design); participants (number, disease, disease severity, age, sex, ethnicity); intervention and control (setting, type of intervention(s), type of control, prescription and progression of intervention and/or control, level of supervision, duration and frequency); process outcomes (adherence and completion of allocated intervention); primary and secondary outcome(s) (instrument name, measurement domain, time point of assessment; n at each timepoint; statistical description); and adverse and serious adverse events (total number, number and type in intervention and/or control arm).

Assessment of risk of bias

Two reviewers (C.M.N. and L.J.B./Y.M./J.B.) independently assessed each study for risk of bias using the criteria outlined in the Cochrane Handbook for Systematic Reviews of Interventions [30]. The reviewers obtained information to aid this assessment from study reports and protocols. Thereafter, they made a judgement as to the level of risk of bias for a specific domain and rated it as low risk, high risk or level of risk unclear and summarised the results in a risk of bias table. The reviewers assessed the following for each study: random sequence generation; allocation concealment; blinding of participants and personnel; incomplete outcome data; selective reporting; and study size. Discrepancies between the reviewers was resolved by discussion involving a third reviewer (M.M.).

Measurement of treatment effect

The mean change from baseline or mean post-intervention values and standard deviation (sd) for each group were recorded. Means were calculated when medians were reported and sds when 95% confidence interval, standard errors or ranges were reported using the guidance in the Cochrane Handbook for Systematic Reviews of Interventions [30]. Using Review Manager 5.4, mean differences (MDs) for outcomes measured using the same instrument and SMDs for outcomes measured using different instruments with 95% CIs were calculated and these data were plotted using forest plots.

Dealing with missing data

Corresponding study authors were contacted if data were missing on study characteristics or outcome measures which would preclude study inclusion or limit the use of a study at further stages of the review. If studies did not report outcomes based on intention-to-treat analyses this was considered as a source of bias during methodological assessment.

Assessment of reporting bias

Publication bias was minimised by searching trials registers for projected and registered studies that had never been published. Authors were contacted for unpublished information if there were such studies registered or some relevant information was missing and could therefore narrow the risk of reporting bias. We planned to assess publication bias using funnel plots when at least 10 studies are available for meta-analysis.

Assessment of heterogeneity and data synthesis

Statistical heterogeneity in each meta-analysis was assessed using the Chi2 test and I2 statistic and used to assess clinical heterogeneity [30]. Where trials demonstrated statistical homogeneity (I2<50% or p>0.10), a meta-analysis was performed using an inverse variable fixed-effect model to estimate the overall direction, size and consistency of the effect of meditative movement on the outcome. Where included trials demonstrated clinical heterogeneity (I2>50% or p<0.10), the random effects model was used. For outcomes where meta-analysis was considered not appropriate, the findings from individual studies were described. A pooled quantitative analysis was performed when trials were clinically homogenous. We extracted group data according to intervention, comparator and outcome. For multi-arm studies with multiple interventions, we considered each intervention separately.

Subgroup analysis and investigation of heterogeneity

Three subgroup analyses were conducted to explore possible sources of heterogeneity: 1) different types of comparator intervention – active comparator interventions (defined as those that included supervised intervention, e.g. pulmonary rehabilitation, education/counselling sessions) may be more effective in improving breathlessness than passive comparator interventions (which was sub-divided into two groups: usual care, e.g. usual pharmacological care, and usual care plus educational information, e.g. usual pharmacological care supplemented with a leaflet on physical activity); 2) diagnosis, as meditative movement may be influenced by disease category; 3) intervention type, as there may be variation in the effect on breathlessness according to meditative movement discipline, e.g. tai chi, yoga or qi gong.

Results

Article selection

A total of 7019 citations were identified and 3123 duplicates were removed, as depicted in the PRISMA flow diagram (figure 1). In total, 3896 titles and abstracts were screened and 3397 articles were excluded. A total of 499 articles were sought for retrieval, of which 43 were unable to be retrieved. A total of 456 articles underwent full-text review for eligibility. From these, 439 were excluded, leaving 17 unique studies [13, 31–46] The most common reasons for exclusion were failing to meet the review criteria for the proportion of participants with advanced disease (≥50%) and no measure of breathlessness.

FIGURE 1
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FIGURE 1

PRISMA diagram showing literature search and selection of articles. CDSR: Cochrane Database of Systematic Reviews; CENTRAL: Cochrane Central Register of Controlled Trials; CINAHL: Cumulative Index to Nursing and Allied Health Literature; CNKI: Chinese National Knowledge Infrastructure; RCT: randomised controlled trial.

Characteristics of the included studies

A summary of the study characteristics is shown in table 1. The 17 studies were published between 2009 and 2022, 13 in English [13, 34–44, 46] and four in Chinese languages [31–33, 45]. The trials (of which three were three-arm RCTs [39, 43, 45] and one a randomised crossover trial [36]) were conducted in China (n=7) [13, 31–33, 35, 44, 45], USA (n=4) [34, 39, 40, 42], Hong Kong (n=2) [38, 43], India (n=2) [37, 46], Canada (n=1) [36] and Vietnam (n=1) [41].

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TABLE 1

Characteristics of included trials

The studies included 1125 participants with COPD (studies: n=13; combined sample size: n=815) or cancer (studies: n=4; sample size: n=310; cancer type: lung [41, 43], nonsmall cell lung or gastro-intestinal [36] and breast cancer [37]). No study included participants with chronic heart failure. The mean age of participants ranged from 57 to 75 years. 14 [13, 31–33, 35–38, 40, 41, 43–46] and three studies [13, 31, 32] did not report ethnicity and sex, respectively. Across those that did, the majority of participants were male (70%) and white (74%).

Figure 2 provides an overview of the types of meditative movement, supplemental and control interventions. Briefly, meditative movement interventions included yoga [37, 40, 42, 46], tai chi [13, 32, 34, 39, 43, 44] and qi gong [31, 33, 35, 36, 38, 41, 45]). In five studies, meditative movement was supplemented by an additional intervention [13, 31, 35, 38, 40]. The control interventions included eight active (supervised intervention) [13, 35–40, 46] and nine passive comparator interventions, which were sub-divided into five usual care [31–33, 41, 45] and four usual care supplemented with educational information [34, 42–44]. For the three-arm RCTs, the concomitant interventions were supervised walking (n=1) [39], supervised exercise programme (n=1) [43] and supervised breathing sessions (n=1) [45].

FIGURE 2
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FIGURE 2

Number of studies according to a) the type of meditative movement (number on top of bar indicates the number of participants), b) supplemental interventions and c) control interventions. LTOT: long-term oxygen therapy.

Regarding the meditative movement interventions, in 15 studies [31–45] it was delivered in person and in two, in person and via videoconference [13, 46]. 12 studies involved a combination of supervised and unsupervised instruction [13, 35–45] and five involved supervision only [31–33, 45, 46]. 11 [13, 32–36, 38–41, 44] were group-based interventions, one was delivered one-to-one [37] and it was unclear how five were delivered [31, 42, 43, 45, 46]. The median (range) in duration of intervention was 14 (6–24) weeks. The content of the meditative movement interventions was heterogenous: yoga (Iygengar and Visama Vritti pranayama (n=1) [42], Dirgha breath (n=1) [40], intervention type not described (n=2) [37, 46]); tai chi (Master Cheng Man-Ch'ing's Yang-style short form (n=1) [34], simplified tai chi quan (n=1) [32], tai chi modified for older people (n=1) [39], 24-form Yang style (n=1) [43], not described (n=2) [13, 44]); and qi gong (seven-posture (n=1) [41], Guolin qi gong (n=1) [36], Baduanjin qi gong (n=2) [38, 45], Liuzijue qi gong (n=3) [31, 33, 35]). The mean (range) intervention adherence rate was 82 (22–100) %. The mean (range) completion rates for the intervention and control groups were 79 (58–100) % and 89 (71–100) %, respectively.

Risk of bias assessment

A total of 13 studies [13, 32, 33, 36–38, 40–46] were at overall unclear risk of bias and four [31, 34, 35, 39] were at high risk of bias (supplementary figures S1 and S2). No studies were at low risk of bias. Random sequence generation was used in 10 studies [34, 36–41, 43, 44] and allocation concealment described in seven [34, 36, 38, 39, 41, 43, 46]. Blinding of participants was not possible due to the nature of the intervention but blinding of outcome assessors was only reported in nine studies [34–36, 38–41, 43, 46]. There were incomplete outcome data reported in 11 studies [13, 31–35, 39, 40, 44–46] and selective reporting in three [33, 34, 45]. None of the studies met the criteria for low risk of bias for study size.

Results of synthesis

Primary outcome: breathlessness

All 17 studies assessed at least one measure of breathlessness. The outcome measures included mMRC (n=7) [13, 32, 33, 40, 44–46], CRQ-D (n=5) [34, 35, 38, 39, 42], EORTC QLQ-LC13 (n=1) [43], EORTC QLQ-C30 Dyspnoea (n=1) [37], Borg scale (n=1) [31], 11-point Likert scale – dyspnoea (n=1) [36] and the Cancer Dyspnoea Scale (n=1) [41]. In two studies, data were presented in a format that could not be retrieved for meta-analysis: one study did not report the number of participants who attended the post-intervention assessment [44] and one did not report the standard deviation of the mean [33]. When we performed the meta-analysis, data from one study was a major outlier [35]. We contacted the authors to confirm whether the data reported in the study was accurate but did not receive a response. We therefore excluded this study from the meta-analysis but report the data in the supplementary file (figures S3, S4 and S5). Thus, we included 14 studies (n=671) in the meta-analysis. The pooled estimate showed no statistically significant difference in the mean difference in breathlessness for meditative movement compared with the control intervention (SMD (95% CI) 0.10 (−0.15–0.34); Chi2=30.11; I2=57%; p=0.45) (figures 3, 4, 5). Sub-group analysis according to comparator arm (supervised intervention, usual care plus information, usual care) (figure 3), disease category (COPD, cancer) (figure 4) and intervention (tai chi, yoga, qi gong) (figure 5) demonstrated similar results. The funnel plots, which are symmetrical, are in the supplementary file (figures S6, S7 and S8).

FIGURE 3
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FIGURE 3

Forest plot comparing meditative movement and control intervention for the primary outcome – breathlessness – for all participants, active comparator and passive comparator. Std: standardised; IV: inverse variance; df: degree of freedom.

FIGURE 4
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FIGURE 4

Forest plot comparing meditative movement and control intervention for the primary outcome – breathlessness – for all participants, people with COPD and people with cancer. Std: standardised; IV: inverse variance; df: degree of freedom.

FIGURE 5
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FIGURE 5

Forest plot comparing meditative movement and control intervention for the primary outcome – breathlessness – for all participants and according to intervention type (tai chi, yoga, qi gong). Std: standardised; IV: inverse variance; df: degree of freedom.

Secondary outcome: health-related quality of life

A total of 13 studies [13, 34–44, 46] assessed at least one measure of health-related quality of life. The outcome measures included Short-Form 36 (n=3) [35, 38, 42], St George's Respiratory Questionnaire (n=3) [13, 40, 46], CRQ (n=2) [34, 39], EORTC QLQ-C30 Functional (n=2) [41, 43], EORTC QLQ-C30 Psychological (n=1) [37], COPD Assessment Test (n=1) [44], Functional Assessment of Cancer Therapy–General (n=1) [36]. In two studies, data were presented in a format that could not be retrieved for meta-analysis, as the number of participants who attended the post-intervention assessment were not reported [13, 44]. As described in the previous section, the study with outlier data was excluded but reported in supplementary figure S9. Thus, we included 10 studies (n=454) in the meta-analysis. The pooled estimate did not show a statistically significant difference in the mean difference in health-related quality of life in meditative movement compared with the control intervention (SMD (95% CI) 0.16 (−0.03–0.35); Chi2=15.35; I2=41%; p=0.08) (supplementary figures S10 and S11).

Secondary outcome: exercise capacity

A total of 14 studies [13, 31, 32, 34–36, 38–40, 42–46] assessed exercise capacity using 6MWT. As described in the previous section, two studies [13, 44] were excluded as data were presented in a format that count not be retrieved for meta-analysis and one excluded because of outlier data [35] (data are presented in supplementary figure S12). Thus, we included 11 studies (n=407) in the meta-analysis. The pooled estimate did not show a statistically significant difference in the mean difference in exercise capacity in meditative movement compared with the control intervention (MD (95% CI) 17.250 (−6.06–41.06); Chi2=35.09; I2=72%; p=0.15) (supplementary figures S13 and S14).

Secondary outcome: functional performance

Only three studies [34, 36, 43] assessed functional performance using a variety of outcome measures, therefore a meta-analysis was not performed. The outcome measures included TUG (n=2) [34, 43] 30-s sit-to-stand test (n=1) [43], walking speed over 50 feet (n=1) [36] and two-repetition sit-to-stand test (n=1) [36]. There was no significant within- or between-group difference in TUG [34, 43] 30-s sit-to-stand test [43] or walking speed over 50 feet [36]. Although there was a significant within-group improvement in two-repetition sit-to-stand test in the meditative movement group, the between-group difference was not significant [36].

Secondary outcome: psychological symptoms

Only seven studies [34, 36, 39, 41–43, 46] assessed psychological symptoms using a variety of outcome measures, therefore a meta-analysis was not performed. Of these studies, one assessed anxiety symptoms only Depression Anxiety Stress Scale21 – Anxiety [41]), two assessed depression symptoms only (Centre for Epidemiological Studies – Depression scale (CES-D) [34, 39]) and four assessed both (HADS (n=2) [36, 43], State Anxiety Inventory – Anxiety and CES-D (n=1) [42], PHQ-9 and GAD-7 (n=1) [46]). All of the studies, except one [46] reported no significant within- or between-group differences in psychological symptoms.

Secondary outcome: safety

Adverse and serious adverse events are reported in supplementary table S1. A total of 10 (63%) [13, 32, 34, 35, 39, 40, 42, 43, 45, 46] and 11 (69%) [13, 32, 34–36, 38, 40–43, 46] studies collected data on adverse and serious adverse events, respectively, in both the intervention and control groups. The overall number (% of study population) of adverse and serious adverse events were 81 (14%) and 32 (5%), respectively. Two studies that reported 11 adverse [40, 42] and two serious adverse events [36, 40] in total, did not report the number of events according to study arm. Excluding these studies, there were (number (% of intervention/control arm population)) 44 (19%) and 26 (11%) adverse events and 16 (6%) and 15 (5%) serious adverse events in the meditative movement and control arms, respectively. However, none appeared to be related to the intervention.

Discussion

Summary of findings

This systematic review identified 17 studies involving 1125 people with advanced COPD or cancer from six countries. The meditative movement interventions included tai chi, yoga and qi gong and their component parts were heterogenous. All studies were determined to have a high or unclear risk of bias. The effect of meditative movement on breathlessness in people with advanced disease was compared to a control intervention, with additional sub-group analysis according to control intervention, disease category and intervention type. The effect of meditative movement on secondary outcome measures (health-related quality of life, exercise capacity, functional performance, mood and safety) was explored, but there were only sufficient data to conduct a meta-analysis of health-related quality of life and exercise capacity. Overall, no statistically significant improvement in breathlessness, health-related quality of life, exercise capacity, functional performance or mood was found. There was incomplete reporting of safety outcomes. The overall number (% of study population) of adverse and serious adverse events were 81 (14%) and 32 (5%), respectively. Although there were a higher proportion of adverse events in the intervention arm, none appeared to be related to a meditative movement intervention.

Strengths and limitations

This is the largest systematic review to investigate the effect of meditative movement in people with advanced disease. Strengths of this review include the comprehensive literature search, encompassing Chinese language databases and the inclusion of studies published in languages other than English, namely Chinese. We employed a rigorous methodology following a protocol published on PROSPERO (CRD42021271421). Reviewers worked independently in pairs and ensured that all titles and abstracts were duplicate-screened, and disagreements resolved in discussion with separate reviewer. Although we searched for a number of advanced diseases, the included studies only recruited people with COPD or cancer and there was a preponderance for the former, so the findings are not generalisable to other advanced diseases. All of the included studies were categorised as unclear or high risk of bias and despite using a random effects model when I2>50% for the meta-analysis, statistical heterogeneity was high for breathlessness (including all sub-group analyses) and exercise capacity, therefore the results should be interpreted with caution. We were unable to include all 17 retrieved studies in the meta-analysis because of missing outcome data. In addition, we excluded one study from the meta-analysis because the data was a major outlier and the authors did not clarify whether the data was accurate. This provides confidence in our results. Nonetheless, the meta-analysis of breathlessness included 14 studies involving 671 participants. The mMRC scale was the most common outcome measure used to assess breathlessness. Although it is valid and widely used in advanced COPD and advanced cancer, it is a blunt outcome measure that may not be sufficiently sensitive to changes in breathlessness experience. We were unable to perform a meta-analysis on functional performance or psychological symptoms due to the paucity of studies measuring these outcomes.

Interpretation of findings in the context of published literature

This meta-analysis demonstrates that meditative movement does not improve breathlessness in advanced COPD or cancer. As this is the first meta-analysis to evaluate meditative movement in advanced disease, it is not possible to compare the results to previous literature in this population. A systematic review of nonpharmacological interventions for breathlessness outcomes in advanced disease did not synthesise data on meditative movement due to lack of study homogeneity [3]. Of note, systematic reviews that investigated meditative movement in nonadvanced diseases only included breathlessness as a secondary outcome measure and the number of included studies is small. However, similar to this review, there was heterogeneity in both the meditative movement and control interventions. Cramer et al. [11] (three studies, n=140) and Chen et al. (three studies, n=367) [18] reported that yoga and tai chi, respectively, did not improve breathlessness in people with COPD, and Van Vu et al. [25] (two studies, n=82) reported that qi gong did not improve breathlessness in people with lung cancer. In contrast, Wu et al. [12] (two studies, n=48) reported a significant improvement in breathlessness favouring the control group, not meditative movement, in people with COPD, and Buffart et al. [16] reported that there were insufficient data to investigate the effect of yoga on breathlessness in people with cancer or cancer survivors. Our large and comprehensive meta-analysis confirms that meditative movement does not improve breathlessness outcomes in people advanced COPD and cancer.

The reasons why meditative movement does not improve breathlessness in advanced disease may be multifactorial. As noted in the limitation section, the most common measurement of breathlessness, the mMRC, may not be sufficiently sensitive to detect changes in breathlessness.

The meditative movement interventions were heterogenous, even within single practices, e.g. different types of yoga, variation in breathing and physically active components, and in many studies were offered alongside other interventions, e.g. education; therefore, it is challenging to evaluate the effect on breathlessness. Of the 17 studies included in this review, one involved breathing exercises only [40] whereas the remaining studies included both breathing and exercise components. Owing to limitations in the intervention description and lack of objective measurement to quantify intervention energy expenditure, it is not possible to understand the extent balance the of breathing and/or exercise the interventions involved. Nonetheless, meditative movement interventions are hypothesised to influence breathing through a number of mechanisms including addressing deconditioning and breathing retraining, i.e. both breathing and exercise mechanisms. Furthermore, sub-group analysis according to intervention type demonstrated no statistically significant difference in breathlessness compared to control intervention.

In addition, the comparator interventions were heterogenous and ranged from usual care to supervised exercise interventions, which renders investigation of the specific effect of meditative movement on breathlessness difficult. However, sub-group analysis according to control intervention demonstrated no statistically significant difference on the effect of meditative movement on breathlessness. Of note, there was a trend for improvement in breathlessness favouring meditative movement compared to supervised control interventions. This trend was not evident in the usual care plus information or usual care control interventions. This may be because of the small number of studies and sample sizes in these groups compared to the supervised control intervention group (supervised intervention: eight studies, n=551; usual care plus information: three studies, n=54; usual care: four studies, n=184).

Meditative movement did not improve health-related quality of life, exercise capacity or psychological symptoms. Published literature on the effect of meditative movement on health-related quality of life is conflicting. Seven systematic reviews involving people with nonadvanced diseases (study range: n=2–9; sample size range: n=59–708) [5, 8, 12, 16, 17, 19, 47] report that meditative movement, or individual interventions (e.g. tai chi, yoga, qi gong), improve health-related quality of life in people with cancer (active cancer, cancer survivors), heart failure and COPD. In contrast, three reviews (study range: n=3–11; sample size range: n=91–788) report that meditative movement [8], tai chi [18] and yoga [11] did not improve this outcome. Irrespective of the outcome of the review, there was heterogeneity in the meditative movement and control interventions.

Exercise capacity and psychological symptoms are known to influence breathlessness; therefore, it follows that there was no effect on this outcome. The results of qualitative interviews [24] of one of the studies included in the review [39] stated that participants with COPD who underwent tai chi reported experiencing changes in their breathing including increased awareness of and capacity for regulating breathing. This may suggest that the outcome measures used to assess breathlessness in this review did not capture these experiences, e.g. breathlessness when performing activities of daily living, and/or that there was no carry-over of these changes outside meditative movement practice.

Regarding exercise capacity, previous systematic reviews in populations including nonadvanced COPD, heart failure and cancer (active cancer, cancer survivors) provide conflicting results. Four reviews, involving heterogenous meditative movement and control interventions (study range: n=2–14; sample range: n=59–1054) reported that meditative movement and yoga improve exercise capacity [5, 8, 10, 11] whereas two involving meditative movement and tai chi (study range: n=2–8; sample size range: n=348–644) reported no improvement [12, 18]. Meditative movement may not improve exercise capacity in advanced disease because the interventions may not have been sufficiently challenging to result in physiological adaptations to exercise.

It was not possible to perform meta-analysis of the effect of meditative movement on functional performance and psychological symptoms, but the reviewed literature suggests that there may not be an effect on these measures in advanced COPD or cancer. Only one systematic review has evaluated functional performance measure in nonadvanced disease and reported that tai chi did not improve this outcome in people with osteoarthritis or heart failure [18]. The literature on psychological outcomes is contradictory and predominantly relates to cancer. Three reviews report that qi gong [19], yoga [16] and tai chi [23] improve depression in cancer (active cancer, cancer survivors) whereas one reports that tai chi does not improve this outcome in people with chronic conditions [18]. Only one review investigated anxiety as an individual domain in people with cancer and reported that qi gong did not improve this outcome [19]. The conflicting results may be explained by the disease state, meditative movement and control intervention heterogeneity, as well as measurement heterogeneity. For example, one review reported that tai chi improves the mental health domains of quality of life in cancer survivors [17], whereas another reported that meditative movement does not improve psychosocial outcomes in men with cancer [19].

Although the data were incomplete, this review demonstrates that meditative movement interventions are safe in people with advanced disease, which is similar to data reported in nonadvanced populations [9, 11, 17, 20, 22, 23, 24].

Implications for clinical practice and research

The results of this review suggest that meditative movement, although a safe intervention, should not routinely be offered to people with advanced COPD or cancer for the purpose of improving breathlessness, health-related quality of life, exercise capacity, functional performance or psychological symptoms. There is a paucity of studies that have investigated functional performance (and none of these evaluated functional performance of activities of daily living) and psychological symptoms, especially in diseases other than cancer, which should be evaluated in future research.

Future research should explore the synergistic effect of meditative movement and other evidence-based interventions that improve breathlessness on this outcome, the effect on meditative movement on outcomes such as activities of daily living and physical activity, and the role of meditative movement in other advanced diseases, e.g. chronic heart failure.

Points for clinical practice and questions for future research

  • Meditative movement is safe but does not improve breathlessness, exercise capacity or health-related quality of life or in advanced COPD or advanced cancer. Future research should explore the synergistic effect of meditative movement and other evidence-based interventions that improve breathlessness in advanced disease.

  • The interpretation of this research is limited by bias and wide heterogeneity in study populations, interventions, comparator interventions and outcome measures, leading to low levels of certainty in the results.

  • Future research should investigate the broader effects of meditative movement on functional performance, psychological symptoms, physical activity and activities of daily living in advanced diseases.

Conclusion

Our findings suggest that meditative movement does not improve breathlessness in people with advanced COPD or advanced cancer, irrespective of disease category, intervention or comparator group. However, limitations including unclear or high risk of bias and heterogeneity in study populations, interventions, comparators and outcome measures limit the strength of conclusions. Future research should address these limitations.

Supplementary material

Supplementary Material

Please note: supplementary material is not edited by the Editorial Office, and is uploaded as it has been supplied by the author.

Supplementary material ERR-0243-2022.SUPPLEMENT

Acknowledgements

We would like to thank Dr Neil O’Connell (Brunel University London, Co-ordinating editor for the Cochrane Pain, Palliative and Supportive Care group) for his advice on outlier data.

Footnotes

  • Provenance: Submitted article, peer reviewed.

  • Conflict of interest: C.M. Nolan reports personal fees from Novartis, consultancy work (not reimbursed) with Vicore Pharma and grants from the National Institute for Health and Care Research outside the submitted work. W.D-C. Man reports grants from the National Institute for Health and Care Research (NIHR), outside the submitted work. M. Maddocks reports grants from NIHR, outside the submitted work. The remaining authors have nothing to disclose.

  • Support statement: L.J. Brighton is funded by an Economic and Social Research Council Post-Doctoral Fellowship (ES/X005259/1). Y. Mo is funded by King's-China Scholarship Council (K-CSC 202106370016). I.J. Higginson, M. Maddocks, J. Bayly and L.J. Brighton are supported by the NIHR Applied Research Collaboration South London (NIHR ARC South London) at King's College Hospital NHS Foundation Trust. M. Maddocks is supported by a National Institute for Health and Care Research (NIHR) Career Development Fellowship (CDF-2017–10–009) and the NIHR Applied Research Collaboration South London. The views expressed in this publication are those of the author(s) and not necessarily those of the NHS, NIHR or the Department of Health and Social Care.

  • Received December 12, 2022.
  • Accepted March 23, 2023.
  • Copyright ©The authors 2023
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Meditative movement for breathlessness in advanced COPD or cancer: a systematic review and meta-analysis
Claire M. Nolan, Lisa Jane Brighton, Yihan Mo, Joanne Bayly, Irene J. Higginson, William D-C. Man, Matthew Maddocks
European Respiratory Review Jun 2023, 32 (168) 220243; DOI: 10.1183/16000617.0243-2022

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Meditative movement for breathlessness in advanced COPD or cancer: a systematic review and meta-analysis
Claire M. Nolan, Lisa Jane Brighton, Yihan Mo, Joanne Bayly, Irene J. Higginson, William D-C. Man, Matthew Maddocks
European Respiratory Review Jun 2023, 32 (168) 220243; DOI: 10.1183/16000617.0243-2022
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