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The use of meditative movement as a non-pharmacologic approach in hematological cancer patients: A systematic review of the literature

Ryan Eckert

Mays Cancer Center, UT Health San Antonio, San Antonio, TX 78229, USA

E-mail : bhuvaneswari.bibleraaj@uhsm.nhs.uk

Jennifer Huberty

Exercise Science and Health Promotion, Arizona State University, Phoenix, AZ 85004, USA

Linda Larkey

College of Nursing and Health Innovation, Arizona State University, Phoenix, AZ 85004, USA

Lisa Marks

Division of Education, Library Services, Mayo Clinic, Scottsdale, AZ 85259, USA

Ruben Mesa

Mays Cancer Center, UT Health San Antonio, San Antonio, TX 78229, USA

DOI: 10.15761/HMO.1000168

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Abstract

Introduction: Hematological cancer patients suffer from long-term physical and psychological comorbidities associated with treatment and disease course, including anxiety, depression, fatigue, and reduced quality of life. Meditative movement (i.e., yoga, qigong tai chi) is a form of complementary and integrative medicine that has received growing interest in recent decades. Meditative movement is efficacious for improving a variety of outcomes in other cancers, including mood, fatigue and quality of life. There is much less research examining the effects of meditative movement on hematological cancer patients. The purpose of this study was to systematically review the literature related to the effects of meditative movement specifically in hematological cancers. The findings of this review will help in making recommendations for future research.

Methods: Search strategies were developed by a medical librarian to scan the literature for published studies examining the effects of meditative movement (i.e., yoga, tai chi, or qigong) on hematological cancer patients. Results: Four studies met our eligibility criteria.

Conclusions: There is preliminary evidence to support the effects of meditative movement on fatigue and sleep quality among hematological cancer patients, but particularly regarding yoga and qigong. No research has been done investigating tai chi on hematological cancer patients. We suggest the need for future research to continue to examine the effects of meditative movement on hematological cancer patients and to determine the minimal dose at which the effects of meditative movement begin to occur.

Key words

mind-body, complementary, quality of life, cancer

Introduction

Hematological cancers are a group of blood- and lymph-related disorders, of which the most common sub-types include leukemia, lymphoma (i.e., Hodgkin and non-Hodgkin), and myeloma [1]. Although less prevalent than some of the more common cancer types (i.e., breast, prostate, lung, colorectal), hematological cancers accounted for ~10% of all new cancer diagnoses and cancer deaths in 2017 [2]. Symptom profiles vary by hematological cancer sub-type, with certain symptoms similar to those experienced by other types of cancer patients (i.e., fatigue, weight loss, pain) and others being somewhat unique to hematological cancers (i.e., anemia, pruritis, bleeding or bruising easily) [3,4]. In general, hematological treatments include chemotherapy and/or other drug therapy, radiation, immunotherapy, blood transfusions, or stem-cell transplantation [1].

The five-year relative survival rate of hematological cancer patients in the United States has seen a significant increase over the past half century. Among the most common hematological cancer sub-types (i.e., leukemia, lymphoma, myeloma) five-year relative survival rates have increased from between 12-40% to between 50-89% depending on diagnosis [2]. Although promising, this also means that there is an increased need to provide long-term care to both hematological cancer patients currently undergoing treatment as well as survivors. It has been shown that hematological cancer patients and survivors often suffer from psychological comorbidities, including anxiety, depressive symptoms, and fatigue [5-7]. Furthermore, each of the aforementioned comorbidities have been found to interfere with quality of life (QoL) and activities of daily living [5].

There has been a growing interest in and use of complementary and integrative medicine (CIM) among cancer patients, with the prevalence of CIM use in cancer patients increasing over the past 30 years from ~25% to ~50% of patients [8]. Additionally, cancer patients have been reported to be more likely to use CIM when compared to non-cancer populations [9]. Meditative movement is defined as practices that include some sort of postural movement, a focus on the breath, and incorporation of a meditative state to achieve deep states of relaxation (i.e., yoga, tai chi, qigong) [10]. Meditative movements are some of most commonly practiced CIM approaches, with ~6.5% of cancer survivors in the U.S. reporting that they practice a form of meditative movement [11]. Additionally, meditative movement has been studied as a means of addressing some of the long-term side effects of cancer and its associated treatment. Given that meditative movement practices tend to have more in common (i.e., promoting similar body, breath and mind states) than differences, albeit different movement types and intensities within and across modalities, we are treating these as a category for exploring effects on symptoms of hematological cancer patients and survivors.

Multiple systematic reviews and meta-analyses have found that meditative movement practices are efficacious for improving a range of outcomes in cancer patients. Yoga has been shown to improve functional well-being, distress, anxiety, depression, fatigue, emotional function, social function, sleep quality, and QoL in cancer patients [12-15]. Furthermore, Tai chi and qigong have evidence to support improvements in fatigue, mood, QoL, immune function, cortisol levels, and inflammation in cancer patients [16,17]. Much of the aforementioned work, however, has been conducted in solid tumor cancer patients (e.g., breast, liver, lung, prostate, etc.). There has been far less research examining the benefits of meditative movement on hematological cancer patients despite the benefits of this type of complementary treatment for other cancer types.

A review summarizing the effects of meditative movement in hematological cancer patients is needed. Therefore, the purpose of this study was to systematically review the literature on the effects of meditative movement in hematological patients and to provide direction for future research. To examine the effects of meditative movement on hematological cancer patient outcomes, we reviewed published randomized controlled trials and/or single-arm experimental trials that assessed the effects of yoga, tai chi, or qigong interventions specifically in hematological cancer sub-types. The findings of this review will help in 1) advancing our knowledge of the effects of various forms of meditative movement in hematological cancer patients and 2) making recommendations for future research.

Methods

Search Strategy

A medical librarian (LM) developed search strategies for Ovid MEDLINE, Ovid Embase, and PubMed to identify articles. The search strategies were peer-reviewed by another experienced medical librarian. Search strategies included the MeSH terms and key words in Table 1.

Table 1. Keyword Search Terms

MeSH Terms (PubMed)

Keywords (PubMed)

yoga

yoga

Qigong

Qigong

Tai Ji

Tai Chi

Mind-Body Therapies

Mindful movement

 

Meditative movement

 

MBSR

 

Mindfulness based stress reduction

hematologic neoplasms

Blood cancers

multiple myeloma

Multiple myeloma

leukemia

leukemia

lymphoma

Lymphoma

myeloproliferative disorders

Myeloproliferative disorders

Inclusion/Exclusion Criteria

Studies were included if they: (a) were published between 1995 and 2018, (b) were published in English, (c) examined the effects of meditative movement (to include yoga, qigong, or tai chi [10] on patient outcomes (d) had an experimental (i.e., randomized controlled trial [RCT]), quasi-experimental (i.e., single-arm interventions) or epidemiological (e.g., longitudinal, cross-sectional) study design, and (e) were conducted in specific hematological cancer sub-types (i.e., leukemia, lymphoma, myeloma, and/or myeloproliferative neoplasm patients/survivors). Systematic reviews, meta-analyses, studies that examined meditative movement in relation to hematological cancer risk, and conference abstracts were excluded.

Selection Process

Titles and abstracts of articles that were found in the search results were reviewed to exclude articles that were not relevant. Potentially relevant full-text articles were then scanned for eligibility by one reviewer (RE) and were then confirmed and agreed upon by a second reviewer (JH). Only articles that met all inclusion criteria and were agreed upon to be included by both reviewers (RE & JH) were included in this review. The references/bibliographies of included articles were also scanned for additional relevant articles that could be included in the review.

Data Extraction

The following data were extracted: (a) study design, (b) study population/sample, (c) type of meditative movement, (d) prescription (i.e., intervention duration, intensity, length of each session, type/style of meditative movement), (e) effects of meditative movement on patient-reported outcomes, and (f) study limitations.

Quality Assessment

Quality assessment of individual studies was conducted for all studies included in the systematic review. Quality assessment was conducted using the 27-item checklist by Downs and Black [18], which can be used to assess both randomized and non-randomized trials. In the present version of the checklist, the checklist scoring was modified for item 27 that refers to the power of the study. Instead of rating according to an available range of study powers, it was rated by whether the study performed a power calculation or not. Accordingly, the maximum score for item 27 was one (a power analysis was conducted) instead of five and thus the highest possible score for the checklist was 28 (instead of 32). Downs and Black score ranges were given corresponding quality levels as previously reported: excellent (26-28); good (20-25); fair (15-19); and poor (≤ 14) [19]. Two individuals (RE & LM) performed the quality assessment independently. Each assessor then met, reviewed their quality assessment scores, and resolved any discrepancies until quality assessment scores for each item were agreed upon.

Results

A total of 256 articles were found with the literature search conducted on July 23, 2018. A total of 90 duplicates were removed, leaving 166 articles that were screened for eligibility. A total of 151 were excluded after examining the titles of each as they did not meet our pre-defined inclusion criteria, leaving 15 potentially relevant articles left for review. After examining the full-texts of each of the 15 articles, four articles met our inclusion criteria and were included for review. Table 2 describes the study selection process and reasons for excluding articles (Figure 1). A detailed description of the included articles is included in the next section below (Table 2).

Table 2. Summary of Included Articles

Reference

Study Design

Study Sample

Type of Meditative Movement

Prescription

Results & Significant Findings

Limitations

Cohen, et al. [21]

RCT (wait-list control group)

Lymphoma patients (n=38; 19 in intervention)

Yoga

7 weeks; 1x/week; light-intensity; unknown session duration; Tibetan yoga

89% completed 2-3 sessions; 57% completed ≥
5 sessions; ↓sleep disturbance; ↑sleep
quality; faster sleep latency; ↓use of sleep meds

Low overall exercise dose; small sample
size in intervention group (n=20);
yoga session duration not specified

Huberty et al. [23]

Quasi-Experimental (single-arm feasibility design)

Myeloproliferative neoplasm patients (n=38)

Yoga

12 weeks; 60 min/week; mild/moderate-intensity; 20-30 min sessions; style of yoga varied

Average yoga participation of ~50 min/week; 37%
averaged ≥ 60 min/week; ↓total symptom burden; ↓fatigue; ↓
anxiety; ↓depression; ↓sleep disturbance

Small sample size (n=38); no control group to test for
effectiveness; potential bias due to study being advertised
as yoga intervention; biased proportion of females in study

Yeh, et al. [24]

RCT (usual care control group)

Non-Hodgkin’s lymphoma patients (n=102; 51 in intervention)

Qigong

21 days; 20-60 min/session (including a 5-min warm-up); 2-5x daily; Chan-Chuang qigong

Qigong participation averaged ~47 min/day; ↓average
fatigue; ↓worst fatigue; ↑overall sleep quality

 

 

Significant differences at baseline between groups for primary
outcome measures; short duration of study (i.e., 21 days);
lack of placebo control group; self-report qigong participation

Chuang, et al. [22]

RCT (usual care control group)

Non-Hodgkin’s lymphoma patients (n=96; 48 in intervention)

Qigong

21 days; 25 min/session (including a 5-min warm-up and 5-min cool-down); 2-3x/day; Chan-Chuang qigong

A total of 96% of patients practiced qigong on 21 days and
average daily qigong participation averaged ~48 min/day; ↓fatigue
intensity & interference; ↑WBC count, hemoglobin, and platelets; ↑sleep quality; ↑QoL

significant differences at baseline between groups in fatigue,
sleep quality, and QoL sub-domains; short duration of study (i.e., 21 days)

Quality Assessment

Results of the quality assessment are presented in Table 3. The four studies included were rated as “good” [20,21] and “fair” [22,23] quality according to the Downs and Black [18] checklist (Table 3).

Table 3. Downs and Black Quality Assessment Checklist

 

Study Reference

Item

Scale

Cohen, et al.[l21]

Huberty, et al.[23]

Yeh, et al.[24]

Chuang et al.[22]

Reporting

1. Is the hypothesis/aim/objective of the study clearly described?

Yes=1; no=0

yes

yes

yes

yes

2. Are the main outcomes to be measured clearly described in the 

Introduction or Methods section? 

Yes=1; no=0

yes

yes

yes

yes

3. Are the characteristics of the patients included 

in the study clearly described? 

Yes=1; no=0

yes

yes

yes

yes

4. Are the interventions of interest clearly described? 

Yes=1; no=0

yes

yes

yes

yes

5. Are the distributions of principal confounders in each group of   subjects to be compared clearly described? 

Yes=2; partially=1; no=0

no

no

no

no

6. Are the main findings of the study clearly described? 

Yes=1; no=0

yes

yes

yes

yes

7. Does the study provide estimates of the random variability in the data or the main outcomes? 

Yes=1; no=0

yes

yes

yes

yes

8. Have all important adverse events that may be a consequence of the intervention been reported? 

Yes=1; no=0

no

yes

yes

yes

9. Have the characteristics of patients lost to follow‐up been described? 

Yes=1; no=0

yes

yes

no

yes

10. Have actual probability values been reported (e.g. 0.035 rather than <0.05) for the main outcomes except where the probability value is less than 0.001?

Yes=1; no=0

yes

yes

yes

yes

External Validity

11. Were the subjects asked to participate in the study representative of the entire population from which they were 

recruited? 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

12. Were those subjects who were prepared to participate representative of the entire population from which they were recruited? 

 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

13. Were the staff, places, and facilities where the patients were 

treated, representative of the treatment the majority of patients 

receive?  

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

Internal Validity – Bias

14. Was an attempt made to blind study subjects to the interventionthey have received? 

 

Yes=1; no=0; unable to determine=0

Unable to determine

no

no

no

15. Was an attempt made to blind those measuring the main outcomes of the intervention?

Yes=1; no=0; unable to determine=0

Unable to determine

Unable to determine

no

yes

16. If any of the results of the study were based on 

“data dredging”, was this made clear? 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

17. In trials and cohort studies, do the analyses adjust for different 

lengths of follow‐up of patients, or in case-control studies, is the 

time period between the intervention and outcome the same for 

cases and controls? 

Yes=1; no=0; unable to determine=0

yes

yes

no

yes

18. Were the statistical tests used to assess the main outcomes appropriate? 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

19. Was compliance with the intervention/s reliable? 

 

Yes=1; no=0; unable to determine=0

no

no

no

no

20. Were the main outcome measures used accurate (valid and 

reliable)? 

 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

Internal Validity – Confounding (Selection Bias)

21. Were the patients in different intervention groups (trials and 

cohort studies) or were the cases and controls (case-control 

studies) recruited from the same population? 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

22. Were study subjects in different intervention groups (trials and cohort studies) or were the cases and controls (case‐control 

studies) recruited over the same period of time? 

Yes=1; no=0; unable to determine=0

yes

no

yes

yes

23. Were study subjects randomized to intervention groups? 

 

Yes=1; no=0; unable to determine=0

yes

no

yes

yes

24. Was the randomised intervention assignment concealed from 

both patients and health care staff until recruitment was complete 

and irrevocable? 

Yes=1; no=0; unable to determine=0

yes

no

no

no

25. Was there adequate adjustment for confounding in the analyses from which the main findings were drawn? 

 

Yes=1; no=0; unable to determine=0

no

no

no

no

26. Were losses of patients to follow‐up taken into account? 

 

Yes=1; no=0; unable to determine=0

Unable to determine

yes

yes

yes

Power

27. Did the study conduct a power calculation?

Yes=1; no=0; unable to determine=0

yes

no

yes

yes

 

Total Score

(total possible score of 28)

20 (good)

18 (fair)

19 (fair)

22 (good)

Effects of Meditative Movement in Hematological Cancers

A study conducted in 2004 by Cohen, et al. [21] examined the effects of yoga on lymphoma patients. Patients (n=39) were randomized to participate in a yoga intervention group (n=20) or a wait-list control group (n=19). Only one participant dropped out in the yoga intervention group, leaving a total of 38 patients that completed the study (n=19 in each group). The intervention group performed in-person Tibetan yoga (e.g., breathing, visualization, mindfulness, and low-impact postures) at the University of Texas MD Anderson Cancer Center 1x/week for seven weeks (duration of each session was not specified). Each yoga session was led by an experienced Tibetan Yoga instructor. The primary outcomes for this study included sleep quality measures (i.e., overall quality, latency, duration, sleep medication use), state anxiety, depression, and fatigue. Although significant improvements in subjective sleep quality, shorter sleep latency, longer sleep duration, and less reported use of sleep medications were found, there were no significant differences between groups for state anxiety, depression or fatigue. However, this may be due, in part, to both the adherence rate as only 58% of patients in the intervention group completed at least five of the seven prescribed yoga sessions.

A study conducted by Yeh, et al. [20] aimed to evaluate the effects of qigong on non-Hodgkin’s lymphoma patients undergoing chemotherapy. This RCT randomly assigned 108 non-Hodgkin’s lymphoma patients to either a qigong intervention group or a usual care control group. The qigong group was asked to participate in self-directed qigong (i.e., on their own with the help of an instruction manual) for 21 consecutive days, 2-5x/day, and 20-60 min/session during the course of chemotherapy treatment. Qigong participants were provided with a modified version of a Chan-Chuang qigong instruction manual and were taught on a single day how to practice qigong by a research nurse who was trained by two qualified qigong practitioners. The control group received their normal course of chemotherapy treatment and was not asked to participate in qigong. The primary outcomes for this study included fatigue intensity (i.e., average fatigue, worst fatigue) and sleep quality measures (i.e., sleep disturbance, sleep effectiveness, sleep supplementation, overall sleep quality) and were assessed every seven days throughout the study (i.e., day 0, 7, 14, & 21).

A total of 108 patients signed an informed consent. Of these 108 patients, 54 were randomized to each group. Six patients dropped out, leaving a total of 102 patients (n=51 in each group) that completed the study. Overall qigong participation averaged ~47 min/day for the 21-day study duration. There were significant improvements over time in the qigong group compared to the control group for average fatigue (p<0.001), fatigue intensity (p<0.001) and overall sleep quality (p<0.001). There are several limitations of this study, including 1) the short study duration (i.e., 21 days), 2) the lack of placebo control group, 3) self-report qigong participation, and 4) significant differences between the intervention and control groups at baseline for primary outcomes (i.e., fatigue intensity and sleep quality).

Another study conducted by Chuang, et al. [22] evaluated the effectiveness of qigong for fatigue, complete blood counts, sleep quality, and QoL in non-Hodgkin’s lymphoma patients undergoing chemotherapy. This RCT randomly assigned 100 non-Hodgkin’s lymphoma patients to either a qigong intervention group or a usual care control group. The methods for this study were similar to those of the previous study by Yeh, et al. [20,22] and asked participants to complete 25-min qigong sessions on their own 2-5x/day for 21 consecutive days after receiving chemotherapy treatment. The primary outcomes for this study included fatigue intensity, fatigue interference, complete blood cells (i.e., white blood cells, hemoglobin, platelets) sleep quality measures (i.e., sleep disturbance, sleep effectiveness, sleep supplementation, overall sleep quality) and QoL and were assessed every seven days throughout the study (i.e., day 0, 7, 14, & 21).

A total of 100 patients signed an informed consent. Of these 100 patients, 50 were randomized to each group. Four patients dropped out, leaving 96 patients (n=48 in each group) that completed the study. A total of 96% of patients (n=46/48) practiced qigong on 21 days and daily qigong participation across all participants averaged ~48 min/day. There was a significant decrease over time for the qigong group compared to the control group for fatigue intensity and fatigue interference. Additionally, there were significant increases over time in the qigong group compared to the control group for white blood cells, hemoglobin, and platelets as well as sleep quality and QoL. Limitations to note for this study include 1) significant differences at baseline between the groups for fatigue measures, sleep quality, and QoL and 2) the short duration of the study (i.e., 21 days).

A recent study conducted by Huberty, et al. [23] aimed to examine the feasibility and preliminary effectiveness of online-streamed yoga (www.Udaya.com) for myeloproliferative neoplasm (MPN) patients. This was a single-arm feasibility trial that enrolled 38 patients to participate in 60 min/week of home-based, online-streamed yoga for 12 weeks. A 12-week yoga prescription was provided to participants via Udaya.com, which is a consumer-based online-streaming yoga platform. Participants were asked to participate in a minimum of 60 min/week by completing 20-30 min videos, 2-3x/week. The type of yoga sessions included in the 12-week prescription varied slightly but included primarily hatha-style yoga and meditation/mindfulness classes. Each class was led by an experienced, certified yoga instructor. The primary outcome was feasibility (i.e., practicality, acceptability and demand) and secondary outcomes included total symptom burden, fatigue, anxiety, depression, pain intensity, sexual function, and sleep disturbance. Participants completed questionnaires assessing demographics, symptom burden and study satisfaction at baseline, mid-point (week 7, post-intervention (week 12) and follow-up (week 16).

Yoga participation averaged ~50 min/week and 37% of participants averaged ≥ 60 min/week of yoga (i.e., demand). A total of 68% (n=21/28) of responding participants felt either satisfied or very satisfied with online yoga, 75% (n=23/31) felt that it was helpful for coping with MPN-related symptoms, and 75% of participants (n=23/31) reported that they felt safe while participating in online yoga (acceptability). A total of 82% (n=31/38) completed the mid-point questionnaire, 79% (n=30/38) completed the post-intervention questionnaire, and 74% (n=28/38) completed the follow-up questionnaire. There were significant pre-post differences in total symptom burden (p=0.04; ES=-0.36), fatigue (p=0.04; ES=-0.33), anxiety (p=0.002; ES=-0.67), depression (p=0.049; ES=-0.41), and sleep disturbance (p<0.0001; ES=-0.58). There were no significant differences in outcomes between those that averaged <60 min/week of yoga and those that averaged >60 min/week of yoga. Although this study was deemed to be feasible and demonstrated significant findings, limitations of this study include 1) the potential for selection bias due to the study being advertised as an online yoga study and 2) the lack of a control group and a small sample size, limiting the ability of the study to determine effectiveness.

Discussion

Research investigating the effects of meditative movement (i.e., yoga, tai chi, qigong) on hematological cancer patients is still in its infancy. Our study highlights the limited amount of research that has been done in the study of meditative movement for hematological cancer patients and the need for future interventions. Based on the findings of this review, there is some preliminary evidence to suggest that meditative movement may improve patient outcomes in hematological cancer patients, particularly fatigue and sleep quality as these outcomes were improved by meditative movement across the majority of studies (n=3/4) included in our review.

Only four studies were included in our review, each of which carries its own limitations. Two studies included small sample sizes (i.e., <40 participants in both trials) [21,23] demonstrating the need for larger sample sizes in future studies. Additionally, the study by Cohen, et al. [21] included a low yoga dose that may partially explain a lack of significant effects of yoga on anxiety, depression, and fatigue. Seven prescribed sessions may not have been a potent enough dose to improve psychosocial outcomes (i.e., anxiety, depression, and fatigue). Previous yoga studies in breast cancer patients have demonstrated significant improvements in anxiety, depression, and fatigue after higher doses of yoga (i.e., 18-24, 60-minute sessions) [24-26] Furthermore, the study by Huberty, et al. [23] was a feasibility study that was not powered for effects and a study sample that was primarily female (89.5%), potentially introducing bias and limiting generalizability.

We found two studies investigating yoga and two studies investigating qigong, whereas we did not find any studies that examined the effects of tai chi on hematological cancer patients. Future studies are warranted that examine the effects of tai chi on hematological cancer patients as tai chi has demonstrated to be beneficial in solid tumor cancer patients [27]. Additionally, further research is needed to better understand the effects of qigong and yoga on hematological cancer patients. There has been a growing body of literature surrounding the effects of yoga, qigong, and tai chi on other cancer patients with little literature in hematological cancers. Due to unique differences in etiology and treatment between solid tumor cancers and hematological cancers, research is needed that examines meditative movement in hematological cancers specifically.

Future research should aim to 1) examine the effects of meditative movement (i.e., yoga, tai chi, qigong) on hematological cancer patient outcomes (i.e., symptoms and QoL) and 2) determine the ideal dose of meditative movement for changes in symptoms and QoL. In the study conducted by Huberty, et al. [23] there were no significant differences in outcomes (i.e., total symptom burden, fatigue, anxiety, depression, sleep disturbance) between those that averaged ≥ 60 min/week of online yoga and those that averaged less. Randomized controlled trials that explore varying doses (i.e., different durations and frequencies) of yoga, or other forms of meditative movement, could determine the minimal dose at which effects of meditative movement begin to occur.

Research that identifies the effectiveness of meditative movement for hematological cancer patients is important in providing justification for implementing meditative movement into clinical practice as an evidence-based CIM strategy. Hematological cancer patients/survivors often suffer from long-term co-morbidities that ultimately end up affecting overall QoL [5-7]. The availability of evidence-based CIM strategies will be beneficial for cancer patients in the maintenance of their long-term health and QoL.

Limitations

Even though this review identified some preliminary evidence demonstrating the potential benefits of meditative movement for hematological cancer patients, there are limitations to note. First, the body of literature from which we draw our conclusions is very small. Our systematic review yielded only four studies. It is always possible that we missed some publications that could have been included in the review and could have changed our findings. We also only included articles published in English, which may have caused us to miss relevant articles published in other languages. Second, inherent with any systematic review is the possibility of publication and location bias [28,29].

Conclusions

There is preliminary evidence that meditative movement may be beneficial for hematological cancer patient outcomes, particularly fatigue and sleep quality. There has been no research to date investigating the effects of tai chi on hematological cancer patients. Future research is needed to establish the effects of yoga, qigong, and tai chi on symptoms and QoL in hematological cancer patients. Future studies should also aim to determine the minimal dose at which effects begin to occur in hematological cancer patients.

Authorship and Contributorship

RE conceptualized the literature review, performed the literature review after search results had been obtained, interpreted the literature review results, conducted the quality assessment, drafted the manuscript, and edited/revised the manuscript; JH edited/revised the manuscript; AD edited/revised the manuscript; HK edited/revised the manuscript; LL edited/revised the manuscript; LM performed the literature search and conducted the quality assessment; RM edited/revised the manuscript. All authors read and approved the final manuscript.

Acknowledgements

The authors do not report any acknowledgements.

Funding

The authors do not report any sources of funding.

Competing Interests

The authors do not report any competing interests.

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Editorial Information

Editor-in-Chief

Ciro Rinaldi
University Federico II Naples

Article Type

Research Article

Publication history

Received date: October 03, 2018
Accepted date: October 15, 2018
Published date: October 18, 2018

Copyright

© 2018 Eckert R. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Eckert R, Huberty J, Larkey L, Marks L, Mesa R (2018) The use of meditative movement as a non-pharmacologic approach in hematological cancer patients: A systematic review of the literature. Hematol Med Oncol 3: DOI: 10.15761/HMO.1000168

Corresponding author

Ryan Eckert

Mays Cancer Center, UT Health San Antonio, 7979 Wurzbach Road, San Antonio, TX 78229, USA

E-mail : bhuvaneswari.bibleraaj@uhsm.nhs.uk

Figure 1. Study Selection Flow Chart

Table 1. Keyword Search Terms

MeSH Terms (PubMed)

Keywords (PubMed)

yoga

yoga

Qigong

Qigong

Tai Ji

Tai Chi

Mind-Body Therapies

Mindful movement

 

Meditative movement

 

MBSR

 

Mindfulness based stress reduction

hematologic neoplasms

Blood cancers

multiple myeloma

Multiple myeloma

leukemia

leukemia

lymphoma

Lymphoma

myeloproliferative disorders

Myeloproliferative disorders

Table 2. Summary of Included Articles

Reference

Study Design

Study Sample

Type of Meditative Movement

Prescription

Results & Significant Findings

Limitations

Cohen, et al. [21]

RCT (wait-list control group)

Lymphoma patients (n=38; 19 in intervention)

Yoga

7 weeks; 1x/week; light-intensity; unknown session duration; Tibetan yoga

89% completed 2-3 sessions; 57% completed ≥
5 sessions; ↓sleep disturbance; ↑sleep
quality; faster sleep latency; ↓use of sleep meds

Low overall exercise dose; small sample
size in intervention group (n=20);
yoga session duration not specified

Huberty et al. [23]

Quasi-Experimental (single-arm feasibility design)

Myeloproliferative neoplasm patients (n=38)

Yoga

12 weeks; 60 min/week; mild/moderate-intensity; 20-30 min sessions; style of yoga varied

Average yoga participation of ~50 min/week; 37%
averaged ≥ 60 min/week; ↓total symptom burden; ↓fatigue; ↓
anxiety; ↓depression; ↓sleep disturbance

Small sample size (n=38); no control group to test for
effectiveness; potential bias due to study being advertised
as yoga intervention; biased proportion of females in study

Yeh, et al. [24]

RCT (usual care control group)

Non-Hodgkin’s lymphoma patients (n=102; 51 in intervention)

Qigong

21 days; 20-60 min/session (including a 5-min warm-up); 2-5x daily; Chan-Chuang qigong

Qigong participation averaged ~47 min/day; ↓average
fatigue; ↓worst fatigue; ↑overall sleep quality

 

 

Significant differences at baseline between groups for primary
outcome measures; short duration of study (i.e., 21 days);
lack of placebo control group; self-report qigong participation

Chuang, et al. [22]

RCT (usual care control group)

Non-Hodgkin’s lymphoma patients (n=96; 48 in intervention)

Qigong

21 days; 25 min/session (including a 5-min warm-up and 5-min cool-down); 2-3x/day; Chan-Chuang qigong

A total of 96% of patients practiced qigong on 21 days and
average daily qigong participation averaged ~48 min/day; ↓fatigue
intensity & interference; ↑WBC count, hemoglobin, and platelets; ↑sleep quality; ↑QoL

significant differences at baseline between groups in fatigue,
sleep quality, and QoL sub-domains; short duration of study (i.e., 21 days)

Table 3. Downs and Black Quality Assessment Checklist

 

Study Reference

Item

Scale

Cohen, et al.[l21]

Huberty, et al.[23]

Yeh, et al.[24]

Chuang et al.[22]

Reporting

1. Is the hypothesis/aim/objective of the study clearly described?

Yes=1; no=0

yes

yes

yes

yes

2. Are the main outcomes to be measured clearly described in the 

Introduction or Methods section? 

Yes=1; no=0

yes

yes

yes

yes

3. Are the characteristics of the patients included 

in the study clearly described? 

Yes=1; no=0

yes

yes

yes

yes

4. Are the interventions of interest clearly described? 

Yes=1; no=0

yes

yes

yes

yes

5. Are the distributions of principal confounders in each group of   subjects to be compared clearly described? 

Yes=2; partially=1; no=0

no

no

no

no

6. Are the main findings of the study clearly described? 

Yes=1; no=0

yes

yes

yes

yes

7. Does the study provide estimates of the random variability in the data or the main outcomes? 

Yes=1; no=0

yes

yes

yes

yes

8. Have all important adverse events that may be a consequence of the intervention been reported? 

Yes=1; no=0

no

yes

yes

yes

9. Have the characteristics of patients lost to follow‐up been described? 

Yes=1; no=0

yes

yes

no

yes

10. Have actual probability values been reported (e.g. 0.035 rather than <0.05) for the main outcomes except where the probability value is less than 0.001?

Yes=1; no=0

yes

yes

yes

yes

External Validity

11. Were the subjects asked to participate in the study representative of the entire population from which they were 

recruited? 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

12. Were those subjects who were prepared to participate representative of the entire population from which they were recruited? 

 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

13. Were the staff, places, and facilities where the patients were 

treated, representative of the treatment the majority of patients 

receive?  

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

Internal Validity – Bias

14. Was an attempt made to blind study subjects to the interventionthey have received? 

 

Yes=1; no=0; unable to determine=0

Unable to determine

no

no

no

15. Was an attempt made to blind those measuring the main outcomes of the intervention?

Yes=1; no=0; unable to determine=0

Unable to determine

Unable to determine

no

yes

16. If any of the results of the study were based on 

“data dredging”, was this made clear? 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

17. In trials and cohort studies, do the analyses adjust for different 

lengths of follow‐up of patients, or in case-control studies, is the 

time period between the intervention and outcome the same for 

cases and controls? 

Yes=1; no=0; unable to determine=0

yes

yes

no

yes

18. Were the statistical tests used to assess the main outcomes appropriate? 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

19. Was compliance with the intervention/s reliable? 

 

Yes=1; no=0; unable to determine=0

no

no

no

no

20. Were the main outcome measures used accurate (valid and 

reliable)? 

 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

Internal Validity – Confounding (Selection Bias)

21. Were the patients in different intervention groups (trials and 

cohort studies) or were the cases and controls (case-control 

studies) recruited from the same population? 

Yes=1; no=0; unable to determine=0

yes

yes

yes

yes

22. Were study subjects in different intervention groups (trials and cohort studies) or were the cases and controls (case‐control 

studies) recruited over the same period of time? 

Yes=1; no=0; unable to determine=0

yes

no

yes

yes

23. Were study subjects randomized to intervention groups? 

 

Yes=1; no=0; unable to determine=0

yes

no

yes

yes

24. Was the randomised intervention assignment concealed from 

both patients and health care staff until recruitment was complete 

and irrevocable? 

Yes=1; no=0; unable to determine=0

yes

no

no

no

25. Was there adequate adjustment for confounding in the analyses from which the main findings were drawn? 

 

Yes=1; no=0; unable to determine=0

no

no

no

no

26. Were losses of patients to follow‐up taken into account? 

 

Yes=1; no=0; unable to determine=0

Unable to determine

yes

yes

yes

Power

27. Did the study conduct a power calculation?

Yes=1; no=0; unable to determine=0

yes

no

yes

yes

 

Total Score

(total possible score of 28)

20 (good)

18 (fair)

19 (fair)

22 (good)