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Background:
Systematic Review

The Effects of Martial Arts on Cancer-Related Fatigue and Quality of Life in Cancer Patients: An Up-to-Date Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials

1
11th Department of Medical Oncology, University of Medicine and Pharmacy “Iuliu Hatieganu”, 400015 Cluj-Napoca, Romania
2
Department of Medical Oncology, Oncology Institute “Prof. Dr. Ion Chiricuta”, 400015 Cluj-Napoca, Romania
3
School of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Western Australia, Nedlands, WA 6009, Australia
4
Terasaki Institute of Biomedical Innovation, Los Angeles, CA 90024, USA
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2021, 18(11), 6116; https://doi.org/10.3390/ijerph18116116
Submission received: 19 March 2021 / Revised: 2 June 2021 / Accepted: 2 June 2021 / Published: 6 June 2021

Abstract

:
Background: To evaluate and synthesize the existing evidence of the effects of practicing martial arts by cancer patients and cancer survivors in relation to overall quality of life (QoL) and cancer-related fatigue (CRF). Methods: Randomized controlled trials (RCTs) from 1 January 2000 to 5 November 2020 investigating the impact of martial arts were compared with any control intervention for overall QoL and CRF among cancer patients and survivors. Publication quality and risk of bias were assessed using the Cochrane handbook of systematic reviews. Results: According to the electronic search, 17 RCTs were retrieved including 1103 cancer patients. Martial arts significantly improved social function, compared to that in the control group (SMD = −0.88, 95% CI: −1.36, −0.39; p = 0.0004). Moreover, martial arts significantly improved functioning, compared to the control group (SMD = 0.68, 95% CI: 0.39–0.96; p < 0.00001). Martial arts significantly reduced CRF, compared to that in the control group (SMD = −0.51, 95% CI: −0.80, −0.22; p = 0.0005, I2 > 95%). Conclusions: The results of our systematic review and meta-analysis reveal that the effects of practicing martial arts on CRF and QoL in cancer patients and survivors are inconclusive. Some potential effects were seen for social function and CRF, although the results were inconsistent across different measurement methods. There is a need for larger and more homogeneous clinical trials encompassing different cancer types and specific martial arts disciplines to make more extensive and definitive cancer- and symptom-specific recommendations.

1. Introduction

In 2020, 19.3 million new cancer cases were diagnosed globally, where breast, lung, and prostate were the most frequent type of malignancies [1]. Cancer is the second cause of mortality worldwide after ischemic heart disease, with 8.97 million deaths, and it is predicted to become the leading cause of death by 2060 with approximately 18.63 million deaths [2]. Improvements in diagnostics and treatments have increased the survival rate of the most prevalent cancers in developed countries [3]. As of January 2019, there were an estimated 16.9 million cancer survivors in the United States. The number of cancer survivors is projected to increase to 22.2 million by 2030 [4]. Furthermore, the burden of cancer incidence and survivors continues to increase in low- and middle-income countries as well [5].
The physical, emotional, and financial impacts of cancer diagnosis and its management, along with the side effects of treatments, normally have long-term consequences on the patient’s overall quality of life (QoL) that can interfere in their activities of daily living [6,7]. The World Health Organization (WHO) defines QoL as an individual’s perception of their position in life in the context of the culture, as well as the value systems in which they live and in relation to their goals, expectations, standards, and concerns [8]. Cancer-specific QoL encompasses all stages of the disease [9].
Cancer standard treatment (surgery, radiation, chemotherapy, hormone therapy, targeted therapy, and immunotherapy) can cause a series of side effects, including nausea, vomiting, diarrhea, constipation, fatigue, depression, and weight loss, which affects physical and psychological functioning, as well as overall QoL [10,11,12]. Fatigue remains one of the most important components of QoL that can vary in intensity and impact based on the stage of disease, treatment received, and patients’ functional status [13]. Cancer-related fatigue (CRF) seems to be due mainly to alterations promoted by cancer in patient homeostasis, such as proinflammatory cytokine upregulations, hydroxytryptophan dysregulation, hypothalamic–pituitary–adrenal axis dysfunction, circadian rhythm disturbances, and increased vagal tone. It is also shown that CRF can vary based on the cancer type [14]. The CRF is defined as a distressing, persistent, and subjective sense of physical, emotional, and/or cognitive tiredness or exhaustion related to cancer or cancer treatment that is not proportional to recent activity and interferes with usual functioning [15]. Moreover, it can lead to a decrease in the participation of activities of daily living and impairment of the patient mood; moreover, it is an important predictor of reduced overall QoL [16,17]. The CRF has been estimated to affect between 25% and 99% of cancer patients and depends on several factors, including patient population, type of treatment received, and assessment method, which can persist for five or more years after cancer diagnosis [18].
Several interventions, such as exercise, heat, cryotherapy, or manual therapy, can be followed to ameliorate some of the above-mentioned side effects and improve QoL [19]. Different exercise programs offer benefits and are safe in cancer patients during and after cancer treatment [20], improving health and functional outcomes in these patients [21]. National guidelines recommend the prescription of exercise to cancer patients; however, it should be tailored to their needs and capabilities [22]. This physical activity has to be done 3–5 times/week and for at least 20 min to be effective and should involve aerobic, resistance exercises, or a combination of both [23].
Martial arts present several benefits to those who practice them. The benefits include physical and psychological aspects, including lessening negative emotional reactions, enhancing balance, and improving cardiovascular and musculoskeletal fitness [24]. Although there is limited evidence of studies with limited number of participants assessing the effects of practicing martial arts in cancer patients [25,26,27], there is a need to clarify their effects on CRF and QoL. This systematic review and meta-analysis aimed to comprehensively review the use of martial arts among cancer survivors and its impact on QoL and CRF. Furthermore, it was attempted to determine the benefits of these types of programs, identify the strengths and gaps in the evidence, and suggest directions to overcome the highlighted limitations.

2. Materials and Methods

Cochrane’s handbook of systematic reviews of interventions and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement were utilized in this study to develop and perform this systematic review and meta-analysis [28].

2.1. Literature Search

Online databases, including PubMed (Medline), Cochrane Web, Web of Science, and Scopus, were searched from 1 January 2000 to 5 November 2020 using the keywords: (Martial Arts OR Hap Ki Do OR Judo OR Karate OR Jujitsu OR Tae Kwon Do OR Aikido OR Wushu OR Kung Fu OR Gong Fu OR Gongfu) AND (Cancer* OR Neoplasm* OR Tumor* OR Malignancy*). Furthermore, the search was continued for PubMed (Medline), which was then formatted to perform the search in other databases.

2.2. Eligibility Criteria

Following the PICO principles (patient, intervention, control, and outcomes) [29], the inclusion criteria were: (a) randomized controlled trials (RCTs) that investigated cancer patients with the primary intervention of martial arts and compared with any comparator for QoL and fatigue; (b) original articles in peer reviewed journals; and (c) eligible studies in English. Non-randomized or any other trials rather than RCTs, non-English RCTs, trials that did not assess the QoL or CRF, non-human studies, studies with no full text, single arm studies, and reviews and secondary works were excluded from this study.

2.3. Screening of Results

Initially, two authors (D.S. and S.S.) screened all titles and abstracts using the inclusion criteria. Subsequently, they coded the abstracts as “yes” for inclusion in full text-review and “no” for excluding the abstract. If both authors coded an abstract as “yes”, they were considered for full text review. If both were coded as no, they were excluded. For abstracts where there were discrepancies, the decision was made through either mutual discussion or with the help of a third reviewer (S.A). In the next stage, a full text review of all articles was performed against the inclusion criteria. Following that, the full text was read carefully for eligibility criteria.

2.4. Data Extraction

The extracted data were divided into three categories. The first one was baseline characteristics, including author name, country, sample size, age, gender, marital status, and cancer treatment (surgery, chemotherapy, and radiation, as well as author name). The second contained the key characteristics of the included studies, such as country, cancer type, the timing of intervention, duration of the intervention (sessions, frequency, and period), and outcomes. The last one was outcome measures, including: (I) quality of life by European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) [30], Functional Assessment of Cancer Therapy—General (FACT-G) [31], and The Short-Form 36 (SF-36) [32]; and (II) fatigue by The Brief Fatigue Inventory (BFI) [33], Functional Assessment of Chronic Illness Therapy—Fatigue (FACIT-F) [34], and the Multidimensional Fatigue Symptom Inventory—Short Form (MFSI-SF) [35,36].

2.5. Quality Assessment

The quality of this meta-analysis was judged based on the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) guideline [37]. GRADE is a transparent and reproducible system that allows the researcher to grade the quality and certainty of the evidence. Based on the quality of the evidence, the level of confidence was assessed that an estimate of the effect could be correct. Following that, two researchers (D.S. and S.S.) evaluated each study. An overall quality score was assigned to each study, ranging from high, moderate, low, to very low grade of evidence. These grades mean the grade certainty/quality of the evidence of the studies. If there was any uncertainty between the two independent researchers, a third researcher (S.A.) evaluated the evidence to obtain the conclusion. The risk of bias of the included studies was also evaluated using the Cochrane’s risk of bias tool [38]. This tool was used to evaluate the RCTs regarding randomization tools; concealment of allocation; blinding of assessors, participants, and personnel; and selective reporting, attrition, and other biases. No paper evaluated was excluded from the results because of low quality or high risk of bias.

2.6. Statistical Analysis

The data were analyzed as a standardized mean difference (SMD) and 95% confidence interval (CI) under a random-effects model using the inverse-variance method in the Review Manager Software (version 5.3, The Nordic Cochrane Centre, Copenhagen, Denmark) package. The heterogeneity was considered when I-square test (I2) and Chi-Square P were more and less than 50% and 0.1, respectively [38,39,40].

3. Results

3.1. Search Results and Summary of Included Studies

Our electronic search retrieved 801 records, 744 of which underwent title and abstract screening after removal of duplicates. Out of these, 38 records progressed for full-text screening, and 21 of them were excluded from the study. Finally, 17 RCTs were included for further analysis [41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57]. Figure 1 illustrates the study selection process. These studies included a total of 1103 cancer patients who were divided into control groups (n = 546) and treatment groups with martial arts (n = 557). The mean age of the included cancer patients was 58 ± 3.1 years. The baseline characteristics and summary of the included studies are shown in Table 1 and Table 2.

3.2. Description of Intervention

Most of the studies analyzed martial arts, such as Tai Chi and Qigong, in one of the comparator arms. They compared the effect of martial arts with standard care, control, psychosocial support, strength training, and even dance. Tai Chi is a traditional Chinese martial art used for defense as well as for its health benefits [58]. Tai Chi and its derivates (Tai Chi Chih, Tai Chi Chuan, Tai Chi Qi Qong, and Tai Chi Easy) are efficient complementary approaches used in improving wellbeing and fatigue [59]. Qigong is considered a form of Chinese martial arts with benefits in immune regulation, balancing the “qi”, and strengthening muscles and tendons [60]. These traditional martial arts forms involved meditation, breathing techniques, coordinating the movements, and relaxation exercises [61]. Another martial art used in the clinical trials was Kyoshu Jitsu. This martial art focuses on pressure points for self-defense as well as its benefits for healing [53]. The majority of the studies analyzed for this meta-analysis focused on breast cancer. Only a small number of studies considered other tumor types, such as lymphoma, ovary, colon, lung, prostate, and nasopharyngeal cancer (Table 1 and Table 2).

3.3. Outcomes

In total, three studies [43,50,53] assessed QoL using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30). A pooled analysis compared the impact of martial arts vs. no intervention among cancer patients and showed no significant improvement in global health, (SMD = 1.30, 95% CI:−1.18, 3.78; p = 0.30, I2 > 95%), physical function (SMD = 0.84, 95% CI: −1.42–3.10; p = 0.47, I2 > 95%), role function (SMD = 1.03, 95% CI: −1.01–3.08]; p = 0.32, I2 > 95%), emotional function (SMD = 1.37, 95% CI: −1.12–3.85; p = 0.28, I2 > 95%), cognitive function (SMD = 1.37, 95% CI: −0.82–3.55]; p = 0.22, I2 > 95%), and social function (SMD = 1.17, 95% CI: −0.99–3.34; p = 0.29, I2 > 95%) (Figure 2). It should be noted that the heterogeneity was solved after excluding the study by Chuang (2017) [43] (p > 0.1), and the results remained non-significant (Figure A1).

3.4. Functional Assessment of Cancer Therapy-General

In total, five studies [42,46,51,54,55] reported the effect of martial arts on QoL by FACT-G. Pooled data show non-significant improvement between the groups in terms of the Functional Assessment of Cancer Therapy—General (SMD = 0.34, 95% CI: −0.02–0.70]; p = 0.06) (Figure 3). The analysis was heterogeneous (p = 0.04, I2 = 61%), and the heterogeneity was solved when removing the study by Oh (2009) [51] (p = 0.70, I2 = 0%). The results remained non-significant (SMD = 0.16, 95% CI: −0.11–0.43; p = 0.25) (Figure A2).

3.5. The Short-Form 36 (SF-36)

The Short-Form 36 (SF-36) was reported in three studies [41,45,52]. The combined SMD between martial art and control groups showed non-significant results regarding physical function (SMD = 0.16, 95% CI: −0.18–0.50; p = 0.36), mental health (SMD = 0.05, 95% CI: −0.27–0.36; p = 0.77), and social function (SMD = 0.07, 95% CI: −1.87–2.01; p = 0.94). It is worth noting that the results of physical function and mental health were homogeneous (p = 0.33, I2 = 10% and p = 0.95, I2 = 0%, respectively) (Figure 4). However, the social function was heterogeneous (p < 0.00001, I2 = 97%), and the heterogeneity was solved by excluding the study by Larkey (2016) [45] (p = 0.47, I2 = 0%). The results after sensitivity analysis show that martial arts significantly reduced social function compared to the control group (SMD = −0.88, 95% CI: −1.36, −0.39]; p = 0.0004) (Figure A3).

3.6. The Brief Fatigue Inventory

Pooled data of three studies [42,43,47] report that the BFI showed no significant reduction of fatigue between the two groups (SMD = −1.04, 95% CI: −2.96–0.87; p = 0.29). According to the results, the analysis was heterogeneous (p < 0.00001, I2 = 98%) (Figure 5). Furthermore, the heterogeneity was solved after removing the study by Chuang (2017) [43] (p = 0.24, I2 = 26%), and the results remained non-significant (SMD = 0.01, 95% CI: −0.39–0.41; p = 0.96) (Figure A4).

3.7. Functional Assessment of Chronic Illness Therapy-Fatigue

Totally, three studies [48,49,51] reported the use of Functional Assessment of Chronic Illness Therapy—Fatigue (FACIT-F). The results show martial arts significantly improved fatigue, compared to the control group (SMD = 0.68, 95% CI: 0.39–0.96; p < 0.00001). According to the results, the data are homogeneous (p = 0.73, I2 = 0%) (Figure 6).

3.8. The Multidimensional Fatigue Symptom Inventory-Short Form

The multidimensional Fatigue Symptom Inventory—Short Form was used in three studies [44,56,57]. The results reveal that the SMD between martial art and control groups was non-significant (SMD = −0.31, 95% CI: −0.71–0.10; p = 0.14), and the data are heterogeneous (p = 0.06, I2 = 64%) (Figure 7). Furthermore, the heterogeneity was solved after excluding the study by Irwin (2017) [44] (p = 0.92, I2 = 0%), and the results show that martial arts significantly reduced fatigue, compared to the control group (SMD = −0.51, 95% CI: −0.80, −0.22]; p = 0.0005) (Figure A5).

3.9. Quality Assessment of the Included Studies

An overall moderate risk of bias was found in selection, reporting, and other bias. Furthermore, performance, detection, and attribution biases were judged as having a high risk of bias. Detailed risk of bias summary and graph are shown in Figure 8 and Figure 9.

4. Discussion

Cancer patients are encouraged to participate in an exercise program during and following treatment [15]; however, there are still gaps related to regimes and forms of exercise appropriate for each individual. Improvement of QoL in cancer patients and management of their CRF have gained importance in recent years to enhance the general wellbeing of cancer patients and ameliorate the side effects of cancer therapies [62]. Multiple studies have covered the role of physical activity and exercise studying their effects on QoL and CRF of cancer patients during and after standard cancer treatment [63]. In this regard, martial arts have gained popularity in western countries as a new form of physical activity. In addition, martial arts combine musculoskeletal conditioning and training in cognitive skills, together with breathing exercises, which are typically delivered in group training sessions that also provide social support for cancer patients [24]. The results of the benefits of martial arts on QoL and CRF have been reported in several studies with a limited number of participants covering limited martial arts disciplines and cancer types [41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57].
This is the first systematic review and meta-analysis grouping martial arts and their effects on QoL and CRF as a primary intervention in cancer patients during and after treatment, regardless of the cancer type and treatment received. The data extracted from different studies of cancer patients practicing martial arts show a significant improvement of social function measured through SF-36 and a significant reduction of CRF measured using FACIT-F and MFSI-SF. The effects reported on social function by Campo et al. [41] and Sprod et al. [52] were positive but modest in their studied population. Social function is an important dimension for cancer patients since the disease and its treatment can affect diverse aspects, such as marital relationships, parental responsibilities, work environment, and social activities [64]. Regarding the significant reduction of CRF using the FACIT-F assessment scale, Oh et al. found a significant difference in their study of breast cancer survivors practicing Tai Chi Chuan for 60 min, 3 times per week, for 12 weeks [51]. Mustian et al. found a non-significant positive effect on fatigue measured by the same tool in breast cancer survivors practicing Tai Chi, possibly due to the small number of participants in their studies [48,49]. Considering the CRF measured through the MFSI-SF scale, Zhou et al. found a significant reduction of CRF in nasopharyngeal patients undergoing radiotherapy after practicing Tai chi for 60 min, 5 times per week, for 8 months [57]. In line with these results, another study found that lung cancer patients who followed a Tai Chi program of 60 min every other day for 12 weeks and underwent chemotherapy had a significant reduction of CRF, compared to those who were in a low-impact exercise program. This reduction was observed after 6 and 12 weeks of the program initiation [56]. Other outcomes analyzed in this meta-analysis did not reach a significant difference, even after heterogeneity was solved.
In the articles analyzed by our team, most of the patients in the trials were breast cancer patients who finished their treatment and started a program for physical activity or are undergoing chemotherapy or radiotherapy. The trials analyzed had small batches of patients enrolled and the population was too heterogeneous for us to be able to conclude about the optimal load and specifics of exercises. Furthermore, most of the martial arts sessions presented ranged from a period of 3 weeks to 24 weeks of practice, with a normal session being 40–60 min. The schedule of the sessions was from 2 weekly classes to 12 weekly classes depending on the type of martial arts. Taking into account the results of the analyzed trials, we consider that practicing martial arts is safe and recommended for patients undergoing treatment as well as for cancer survivors at the completion of their oncological therapy
Other meta-analyses have reviewed the effects of martial arts in QoL and/or CRF [64,65]. Tao et al. in a study analyzed the effects of acupuncture, Tuina, Tai Chi, Qigong, and traditional Chinese music therapy on symptom management and QoL in cancer patients. According to the results, Tai Chi and Qigong had no effect on QoL or CRF in breast cancer survivors [65]. Wayne et al. also analyzed the effects of Tai Chi and Qigong in cancer survivors, finding a significant improvement in CRF, sleep difficulty, depression, and overall QoL, as well as a non-significant trend in pain control [66].
Albeit all the evidence points to the benefits of physical activity in cancer patients, these changes to increase their physical activity seem harder to implement by cancer patients [67]. Martial arts have been demonstrated in several studies to be a feasible option for cancer patients [41,53]. Moreover, they may reduce some of the negative effects of cancer and improve physical as well as psychological health [68]. This study may help healthcare professionals involved in cancer management and patients decide to choose an activity to improve QoL and reduce CRF. Martial arts offer a wide variety of disciplines with different levels of intensity that would allow cancer patients the possibility of deciding the activity that fits better with their needs.
Different guidelines covering CRF, such as NCCN (National Comprehensive Cancer Network) guidelines, focused on CRF [15], and the guidelines from the Oncology Nursing Society “Putting Evidence into Practice” [69] proposed exercise and physical activity as a first-line intervention for CRF. Other interventions, in addition to erythropoiesis-stimulating agents and low-dose dexamethasone, do not offer effectiveness reducing CRF in patients with cancer [69]. The beneficial effects of martial arts in QoL of cancer patients can be due to the relaxation response and the immunomodulatory [50,70] and hormonal effects [71]. A recent meta-analysis has shown that Tai Chi has an impact on reducing cortisol levels in breast cancer survivors. The same study showed an impact on physical and mental health, improving limb-muscular function and promoted sleep [72].
There is some evidence showing that CRF and QoL are not improved only by physical exercises [73,74], supporting the concept that a more holistic approach should be considered in order to benefit these outcomes in cancer patients. Adverse effects due to martial arts practice did not exist in several studies [42,49,51].
Meta-analyses allow overcoming several limitations. First, pooling the data from different studies allows correcting the statistical limitation of the small sample data of some of the analyzed studies. Another strength is that meta-analyses allow detecting the heterogeneity existing in different studies that used martial arts as a primary intervention in cancer patients. It also helps settle the effect from conflicting results coming from different studies.
Regarding the limitations of this study, one can refer to the analysis of only studies that were published in English. This fact excludes the articles written in other languages that could represent the evidence better and make more general conclusions. Second, the diversity of the outcomes measured in the studies analyzed in this meta-analysis made the task of comparison arduous. Future studies should report outcomes in a more homogeneous way in order to be able to pool all available data. Another limitation is that the majority of the studies analyzed were performed on breast cancer survivors, limiting the conclusions drawn in this study to this group of patients. Accordingly, future studies involving the investigation of the effects on QoL and CRF of martial arts in cancer patients should cover other cancer types. In that way, it would be possible to stratify the results by cancer types and other variables, such as age or other interesting conditions, including gender or grade of disability, which could help tailor the interventions to the patients’ needs. In addition, the control groups analyzed were very heterogeneous, and this could be a source of heterogeneity of this study. Another limitation comes from the fact that the analyzed studies covered broad inclusion criteria related to how fatigue was evaluated in those patients enrolled. Finally, some limitations are due to the sample size of the studies and the fact that the patients in some cases were not homogenously under cancer treatment, limitations that are intrinsic to the scarce available data in this regard.
Future studies should address the limitations existing in previous trials. Sample size was an issue in several trials, not providing enough statistical power to draw significant observations. Furthermore, martial arts should be studied in more cancer types, and patients should be stratified in order to be able to extract cancer- and population-specific conclusions. Moreover, trials should try to overcome a common issue where neither the participants nor the instructors or investigators were blinded to the condition against drug trial recommendations. Another limitation was related to the selection bias found in several of the analyzed studies. Longer intervention periods should be followed in order to see if the interventions have effects on cancer survivors.

5. Conclusions

The results of this systematic review and meta-analysis reveal that the effects of practicing martial arts on CRF and QoL in cancer patients and survivors are inconclusive. Although some potential effects were seen for social function and CRF, the results are inconsistent across different measurement methods. Therefore, larger and more homogeneous clinical trials encompassing different cancer types and specific martial arts disciplines are needed before definitive cancer- and symptom-specific recommendations can be made.

Author Contributions

Formal analysis, S.S.; Investigation, D.S., S.S. and S.A.; Resources, S.A.; Data curation, D.S., S.S. and S.A.; writing—original draft preparation, D.S.; and writing—review and editing, D.S., S.S. and S.A. All authors have read and agreed to the published version of the manuscript.

Funding

There is no financial support for this study.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data that support the findings of this study are available on request from the corresponding author.

Acknowledgments

The authors would like to thank all people who participated in this study and Antoni Torres for professional medical writing and editing services.

Conflicts of Interest

The authors have no conflict of interests regarding the publication of this study.

Appendix A

Figure A1. Results of EORTC QLQ-C30 after sensitivity analysis.
Figure A1. Results of EORTC QLQ-C30 after sensitivity analysis.
Ijerph 18 06116 g0a1
Figure A2. Results of FACT-G change after sensitivity analysis.
Figure A2. Results of FACT-G change after sensitivity analysis.
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Figure A3. Results of SF-36 after sensitivity analysis.
Figure A3. Results of SF-36 after sensitivity analysis.
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Figure A4. Results of BFI after sensitivity analysis.
Figure A4. Results of BFI after sensitivity analysis.
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Figure A5. Results of MFSI-SF after sensitivity analysis.
Figure A5. Results of MFSI-SF after sensitivity analysis.
Ijerph 18 06116 g0a5

References

  1. Sung, H.; Ferlay, J.; Siegel, R.L.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 2018, 68, 394–424. [Google Scholar] [CrossRef]
  2. Mattiuzzi, C.; Lippi, G. Current cancer epidemiology. J. Epidemiol. Glob. Health 2019, 9, 217–222. [Google Scholar] [CrossRef] [Green Version]
  3. Allemani, C.; Matsuda, T.; Di Carlo, V.; Harewood, R.; Matz, M.; Niksic, M.; Bonaventure, A.; Valkov, M.; Johnson, C.J.; Estève, J.; et al. Global surveillance of trends in cancer survival: Analysis of individual records for 37,513,025 patients diagnosed with one of 18 cancers during 2000–2014 from 322 population-based registries in 71 countries (CONCORD-3). Lancet 2018, 391, 1023–1075. [Google Scholar] [CrossRef] [Green Version]
  4. Siegel, R.L.; Miller, K.D.; Jemal, A. Cancer statistics, 2020. CA Cancer J. Clin. 2020, 70, 7–30. [Google Scholar] [CrossRef]
  5. Shah, S.C.; Kayamba, V.; Peek, R.M., Jr.; Heimburger, D. Cancer control in low- and middle-income countries: Is it time to consider screening? J. Glob. Oncol. 2019, 5, 1–8. [Google Scholar] [CrossRef]
  6. Pearman, T. Quality of life and psychosocial adjustment in gynecologic cancer survivors. Health Qual. Life Outcomes 2003, 1, 1–6. [Google Scholar] [CrossRef] [Green Version]
  7. Trask, P.C. Quality of life and emotional distress in advanced prostate cancer survivors undergoing chemotherapy. Health Qual. Life Outcomes 2004, 2, 1–5. [Google Scholar] [CrossRef] [Green Version]
  8. WHO WHOQOL: Measuring Quality of Life 2020. Available online: https://www.who.int/toolkits/whoqol (accessed on 14 December 2020).
  9. Hornquist, J.O. Quality of life: Concept and assessment. Scand. J. Public Health 1990, 18, 69–79. [Google Scholar] [CrossRef]
  10. Schirrmacher, V. From chemotherapy to biological therapy: A review of novel concepts to reduce the side effects of systemic cancer treatment (review). Int. J. Oncol. 2019, 54, 407–419. [Google Scholar] [CrossRef]
  11. Byar, K.L.; Berger, A.M.; Bakken, S.L.; Cetak, M.A. Impact of adjuvant breast cancer chemotherapy on fatigue, other symptoms, and quality of life. Oncol. Nurs. Forum 2006, 33, 18–26. [Google Scholar] [CrossRef]
  12. Hickok, J.T.; Roscoe, J.A.; Morrow, G.R.; Mustian, K.; Okunieff, P.; Bole, C.W. Frequency, severity, clinical course, and correlates of fatigue in 372 patients during 5 weeks of radiotherapy for cancer. Cancer 2005, 104, 1772–1778. [Google Scholar] [CrossRef]
  13. Meneses, K.; Benz, R. Quality of life in cancer survivorship: 20 years later. Semin. Oncol. Nurs. 2010, 26, 36–46. [Google Scholar] [CrossRef]
  14. Berger, A.M.; Mitchell, S.A.; Jacobsen, P.B.; Pirl, W.F. Screening, evaluation, and management of cancer-related fatigue: Ready for implementation to practice? CA Cancer J. Clin. 2015, 65, 190–211. [Google Scholar] [CrossRef]
  15. Berger, A.M.; Mooney, K.; Alvarez-Perez, A.; Breitbart, W.S.; Carpenter, K.M.; Cella, D.; Cleeland, C.; Dotan, E.; Eisenberger, M.A.; Escalante, C.P.; et al. Cancer-related fatigue, version 2. 2015. J. Natl. Compr. Cancer Netw. 2015, 13, 1012–1039. [Google Scholar] [CrossRef]
  16. Siefert, M.L. Fatigue, pain, and functional status during outpatient chemotherapy. Oncol. Nurs. Forum 2010, 37, E114–E123. [Google Scholar] [CrossRef]
  17. Lis, C.G.; Rodeghier, M.; Gupta, D. Distribution and determinants of patient satisfaction in oncology: A review of the literature. Patient Prefer. Adherence 2009, 3, 287–304. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  18. Bower, J.E. Cancer-related fatigue--mechanisms, risk factors, and treatments. Nat. Rev. Clin. Oncol. 2014, 11, 597–609. [Google Scholar] [CrossRef] [PubMed]
  19. Maltser, S.; Cristian, A.; Silver, J.K.; Morris, G.S.; Stout, N.L. A focused review of safety considerations in cancer rehabilitation. PM R 2017, 9, S415–S428. [Google Scholar] [CrossRef] [PubMed]
  20. Campbell, K.L.; Winters-Stone, K.M.; Wiskemann, J.; May, A.M.; Schwartz, A.L.; Courneya, K.S.; Zucker, D.S.; Matthews, C.E.; Ligibel, J.A.; Gerber, L.H.; et al. Exercise guidelines for cancer survivors: Consensus statement from international multidisciplinary roundtable. Med. Sci. Sports Exerc. 2019, 51, 2375–2390. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  21. Silver, J.K.; Gilchrist, L.S. Cancer rehabilitation with a focus on evidence-based outpatient physical and occupational therapy interventions. Am. J. Phys. Med. Rehabil. 2011, 90, 5–15. [Google Scholar] [CrossRef] [PubMed]
  22. Demark-Wahnefried, W.; Rogers, L.Q.; Alfano, C.M.; Thomson, C.A.; Courneya, K.S.; Meyerhardt, J.A.; Stout, N.L.; Kvale, E.; Ganzer, H.; Ligibel, J.A. Practical clinical interventions for diet, physical activity, and weight control in cancer survivors. CA Cancer J. Clin. 2015, 65, 167–189. [Google Scholar] [CrossRef] [PubMed]
  23. Hayes, S.C.; Newton, R.U.; Spence, R.R.; Galvão, D.A. The exercise and sports science australia position statement: Exercise medicine in cancer management. J. Sci. Med. Sport 2019, 22, 1175–1199. [Google Scholar] [CrossRef] [Green Version]
  24. Burke, D.T.; Al-Adawi, S.; Lee, Y.T.; Audette, J. Martial arts as sport and therapy. J. Sports Med. Phys. Fit. 2007, 47, 96–102. [Google Scholar]
  25. Pons van Dijk, G.; Leffers, P.; Lodder, J. The effectiveness of hard martial arts in people over forty: An attempted systematic review. Societies 2014, 4, 161–179. [Google Scholar] [CrossRef] [Green Version]
  26. Lomas-Vega, R.; Obrero-Gaitán, E.; Molina-Ortega, F.J.; Del-Pino-Casado, R. Tai chi for risk of falls. A meta-analysis. J. Am. Geriatr. Soc. 2017, 65, 2037–2043. [Google Scholar] [CrossRef]
  27. Witte, K.; Kropf, S.; Darius, S.; Emmermacher, P.; Böckelmann, I. Comparing the effectiveness of karate and fitness training on cognitive functioning in older adults—A randomized controlled trial. J. Sport Health Sci. 2016, 5, 484–490. [Google Scholar] [CrossRef] [Green Version]
  28. Shamseer, L.; Moher, D.; Clarke, M.; Ghersi, D.; Liberati, A.; Petticrew, M.; Shekelle, P.; Stewart, L.A.; Altman, D.G.; Booth, A.; et al. Preferred reporting items for systematic review and meta-analysis protocols (prisma-p) 2015: Elaboration and explanation. BMJ 2015, 349, 1–25. [Google Scholar] [CrossRef] [Green Version]
  29. Aslam, S.; Emmanuel, P. Formulating a researchable question: A critical step for facilitating good clinical research. Indian J. Sex. Transm. Dis. AIDS 2010, 31, 47–50. [Google Scholar] [CrossRef] [Green Version]
  30. Fayers, P.; Aaronson, N.; Bjordal, K.; Groenvold, M. EORTC QLQ-C30 Scoring Manual, 3rd ed.; European Organisation for Research and Treatment of Cancer: Brussels, Beigium, 2001. [Google Scholar]
  31. Cella, D.F.; Tulsky, D.S.; Gray, G.; Sarafian, B.; Linn, E.; Bonomi, A.; Silberman, M.; Yellen, S.B.; Winicour, P.; Brannon, J.; et al. The functional assessment of cancer therapy scale: Development and validation of the general measure. J. Clin. Oncol. 1993, 11, 570–579. [Google Scholar] [CrossRef]
  32. Ware, J.E.; Kosinski, M.A.; Keller, S.D. SF-36 Physical and Mental Health Summary Scales—A User’s Manual; Health Assessment Lab.: Boston, MA, USA, 1994; pp. 1–147. [Google Scholar]
  33. Mendoza, T.R.; Wang, X.S.; Cleeland, C.S.; Morrissey, M.; Johnson, B.A.; Wendt, J.K.; Huber, S.L. The rapid assessment of fatigue severity in cancer patients. Cancer 1999, 85, 1186–1196. [Google Scholar] [CrossRef]
  34. Cella, D.; Nowinski, C.J. Measuring quality of life in chronic illness: The functional assessment of chronic illness therapy measurement system. Arch. Phys. Med. Rehabil. 2002, 83, 10–17. [Google Scholar] [CrossRef]
  35. Donovan, K.A.; Stein, K.D.; Lee, M.; Leach, C.R.; Ilozumba, O.; Jacobsen, P.B. Systematic review of the multidimensional fatigue symptom inventory-short form. Support. Care Cancer 2015, 23, 191–212. [Google Scholar] [CrossRef] [PubMed]
  36. Pien, L.C.; Chu, H.; Chen, W.C.; Chang, Y.S.; Liao, Y.M.; Chen, C.H.; Chou, K.R. Reliability and validity of a Chinese version of the multidimensional fatigue symptom inventory-short form (MFSI-SF-C). J. Clin. Nurs. 2011, 20, 2224–2232. [Google Scholar] [CrossRef]
  37. The Grading of Recommendations Assessment, Development and Evaluation (Grade) Guidelines 2020. Available online: https://www.gradeworkinggroup.org/ (accessed on 10 December 2020).
  38. Higgins, J.P.T.; Thomas, J.; Chandler, J.; Cumpston, M.; Li, T.; Page, M.J.; Welch, V.A. Cochrane Handbook for Systematic Reviews of Interventions, version 6.1 (updated September 2020); John Wiley & Sons: Hoboken, NJ, USA, 2020; Available online: www.training.cochrane.org/handbook (accessed on 10 December 2020).
  39. Matthews, J.N.S.; Altman, D.G. Statistics notes: Interaction 3: How to examine heterogeneity. BMJ 1996, 313, 862. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Terrin, N.; Schmid, C.H.; Lau, J.; Olkin, I. Adjusting for publication bias in the presence of heterogeneity. Stat. Med. 2003, 22, 2113–2126. [Google Scholar] [CrossRef]
  41. Campo, R.A.; O’Connor, K.; Light, K.C.; Nakamura, Y.; Lipschitz, D.L.; Lastayo, P.C.; Pappas, L.; Boucher, K.; Irwin, M.R.; Agarwal, N.; et al. Feasibility and acceptability of a Tai Chi Chih randomized controlled trial in senior female cancer survivors. Integr. Cancer Ther. 2013, 12, 464–474. [Google Scholar] [CrossRef] [Green Version]
  42. Chen, Z.; Meng, Z.; Milbury, K.; Bei, W.; Zhang, Y.; Thornton, B.; Liao, Z.; Wei, Q.; Chen, J.; Guo, X.; et al. Qigong improves quality of life in women undergoing radiotherapy for breast cancer: Results of a randomized controlled trial. Cancer 2013, 119, 1690–1698. [Google Scholar] [CrossRef] [PubMed]
  43. Chuang, T.Y.; Yeh, M.L.; Chung, Y.C. A nurse facilitated mind-body interactive exercise (Chan-Chuang Qigong) improves the health status of non-Hodgkin lymphoma patients receiving chemotherapy: Randomised controlled trial. Int. J. Nurs. Stud. 2017, 69, 25–33. [Google Scholar] [CrossRef] [PubMed]
  44. Irwin, M.R.; Olmstead, R.; Carrillo, C.; Sadeghi, N.; Nicassio, P.; Ganz, P.A.; Bower, J.E. Tai Chi Chih compared with cognitive behavioral therapy for the treatment of insomnia in survivors of breast cancer: A randomized, partially blinded, noninferiority trial. J. Clin. Oncol. 2017, 35, 2656–2665. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Larkey, L.K.; Roe, D.J.; Smith, L.; Millstine, D. Exploratory outcome assessment of Qigong/Tai Chi easy on breast cancer survivors. Complement. Ther. Med. 2016, 29, 196–203. [Google Scholar] [CrossRef] [Green Version]
  46. Loh, S.Y.; Lee, S.Y.; Murray, L. The Kuala Lumpur Qigong trial for women in the cancer survivorship phase-efficacy of a three-arm RCT to improve QOL. Asian Pac. J. Cancer Prev. 2014, 15, 8127–8134. [Google Scholar] [CrossRef] [Green Version]
  47. McQuade, J.L.; Prinsloo, S.; Chang, D.Z.; Spelman, A.; Wei, Q.; Basen-Engquist, K.; Harrison, C.; Zhang, Z.; Kuban, D.; Lee, A.; et al. Qigong/Tai Chi for sleep and fatigue in prostate cancer patients undergoing radiotherapy: A randomized controlled trial. Psychooncology. 2017, 26, 1936–1943. [Google Scholar] [CrossRef] [PubMed]
  48. Mustian, K.M.; Katula, J.A.; Gill, D.L.; Roscoe, J.A.; Lang, D.; Murphy, K. Tai Chi Chuan, health-related quality of life and self-esteem: A randomized trial with breast cancer survivors. Support. Care Cancer 2004, 12, 871–876. [Google Scholar] [CrossRef] [PubMed]
  49. Mustian, K.; Palesh, O.; Flecksteiner, S. Tai Chi Chuan for breast cancer survivors. Med. Sport Sci. 2008, 52, 209–217. [Google Scholar] [CrossRef] [Green Version]
  50. Oh, B.; Butow, P.; Mullan, B.; Clarke, S. Medical qigong for cancer patients: Pilot study of impact on quality of life, side effects of treatment and inflammation. Am. J. Chin. Med. 2008, 36, 459–472. [Google Scholar] [CrossRef]
  51. Oh, B.; Butow, P.; Mullan, B.; Clarke, S.; Beale, P.; Pavlakis, N.; Kothe, E.; Lam, L.; Rosenthal, D. Impact of medical qigong on quality of life, fatigue, mood and inflammation in cancer patients: A randomized controlled trial. Ann. Oncol. 2009, 21, 608–614. [Google Scholar] [CrossRef]
  52. Sprod, L.K.; Janelsins, M.C.; Palesh, O.G.; Carroll, J.K.; Heckler, C.E.; Peppone, L.J.; Mohile, S.G.; Morrow, G.R.; Mustian, K.M. Health-related quality of life and biomarkers in breast cancer survivors participating in Tai Chi Chuan. J. Cancer Surviv. 2012, 6, 146–154. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Strunk, M.A.; Zopf, E.M.; Steck, J.; Hamacher, S.; Hallek, M.; Baumann, F.T. Effects of kyusho jitsu on physical activity-levels and quality of life in breast cancer patients. In Vivo 2018, 32, 819–824. [Google Scholar] [CrossRef]
  54. Thongteratham, N.; Pongthavornkamol, K.; Olson, K.; Ratanawichitrasin, A.; Nityasuddhi, D.; Wattanakitkrilert, D. Effectiveness of Tai Chi Qi Qong program for Thai women with breast cancer: A randomized control trial. Pac. Rim Int. J. Nurs. Res. 2015, 19, 280–294. [Google Scholar]
  55. Vanderbyl, B.L.; Mayer, M.J.; Nash, C.; Tran, A.T.; Windholz, T.; Swanson, T.; Kasymjanova, G.; Jagoe, R.T. A comparison of the effects of medical Qigong and standard exercise therapy on symptoms and quality of life in patients with advanced cancer. Support. Care Cancer 2017, 25, 1749–1758. [Google Scholar] [CrossRef] [PubMed]
  56. Zhang, L.L.; Wang, S.Z.; Chen, H.L.; Yuan, A.Z. Tai Chi exercise for cancer-related fatigue in patients with lung cancer undergoing chemotherapy: A randomized controlled trial. J. Pain Symptom Manag. 2016, 51, 504–511. [Google Scholar] [CrossRef] [Green Version]
  57. Zhou, W.; Wan, Y.H.; Chen, Q.; Qiu, Y.R.; Luo, X.M. Effects of Tai Chi exercise on cancer-related fatigue in patients with nasopharyngeal carcinoma undergoing chemoradiotherapy: A randomized controlled trial. J. Pain Symptom Manag. 2018, 55, 737–744. [Google Scholar] [CrossRef] [Green Version]
  58. Huston, P.; McFarlane, B. Health benefits of Tai Chi. Can. Fam. Physician 2016, 62, 881–890. [Google Scholar]
  59. Chang, P.S.; Knobf, T. Qigong exercise and Tai Chi in cancer care. Asia Pac. J. Oncol. Nurs. 2019, 6, 315–317. [Google Scholar] [CrossRef] [PubMed]
  60. Klein, P. Qigong in cancer care: Theory, evidence-base, and practice. Medicines 2017, 4, 2. [Google Scholar] [CrossRef] [Green Version]
  61. Jahnke, R.; Larkey, L.; Rogers, C.; Etnier, J.; Lin, F. A comprehensive review of health benefits of qigong and tai chi. Am. J. Health Promot. 2010, 24, e1–e25. [Google Scholar] [CrossRef]
  62. Charalambous, A.; Kouta, C. Cancer related fatigue and quality of life in patients with advanced prostate cancer undergoing chemotherapy. Biomed. Res. Int. 2016, 2016. [Google Scholar] [CrossRef] [Green Version]
  63. Velthuis, M.J.; Agasi-Idenburg, S.C.; Aufdemkampe, G.; Wittink, H.M. The effect of physical exercise on cancer-related fatigue during cancer treatment: A meta-analysis of randomised controlled trials. Clin. Oncol. 2010, 22, 208–221. [Google Scholar] [CrossRef]
  64. Hahn, E.A.; Kallen, M.A.; Jensen, R.E.; Potosky, A.L.; Carol, M.; Ramirez, M.; Cella, D.; Teresi, J.A. Measuring social function in diverse cancer populations: Evaluation of measurement equivalence of the Patient Reported Outcomes Measurement Information System® (PROMIS®) ability to participate in social roles and activities short form. Psychol. Test. Assess. Model. 2016, 58, 403–421. [Google Scholar] [PubMed]
  65. Tao, W.W.; Jiang, H.; Tao, X.M.; Jiang, P.; Sha, L.Y.; Sun, X.C. Effects of acupuncture, tuina, tai chi, qigong, and traditional chinese medicine five-element music therapy on symptom management and quality of life for cancer patients: A meta-analysis. J. Pain Symptom Manag. 2016, 51, 728–747. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Wayne, P.; Lee, M.; Novakowski, J.; Osypiuk, K.; Ligibel, J.; Carlson, L.; Rong, S. Tai Chi and Qigong for cancer-related symptoms and quality of life: A systematic review and meta-analysis. J. Cancer Surviv. 2018, 12, 256–267. [Google Scholar] [CrossRef]
  67. Yaw, Y.H.; Shariff, Z.M.; Kandiah, M.; Weay, Y.H.; Saibul, N.; Sariman, S.; Hashim, Z. Diet and physical activity in relation to weight change among breast cancer patients. Asian Pac. J. Cancer Prev. 2014, 15, 39–44. [Google Scholar] [CrossRef] [Green Version]
  68. Abbott, R.; Lavretsky, H. Tai Chi and Qigong for the treatment and prevention of mental disorders. Psychiatr. Clin. North. Am. 2013, 36, 109–119. [Google Scholar] [CrossRef] [Green Version]
  69. Mitchell, S.A.; Hoffman, A.J.; Clark, J.C.; Degennaro, R.M.; Poirier, P.; Robinson, C.B.; Weisbrod, B.L. Putting evidence into practice: An update of evidence-based interventions for cancer-related fatigue during and following treatment. Clin. J. Oncol. Nurs. 2015, 18, 38–58. [Google Scholar] [CrossRef] [PubMed]
  70. Bower, J.E.; Irwin, M.R. Mind-body therapies and control of inflammatory biology: A descriptive review. Brain Behav. Immun. 2016, 51, 1–11. [Google Scholar] [CrossRef] [Green Version]
  71. Rassovsky, Y.; Harwood, A.; Zagoory-Sharon, O.; Feldman, R. Martial arts increase oxytocin production. Sci. Rep. 2019, 9, 1–8. [Google Scholar] [CrossRef]
  72. Ni, X.; Chan, R.J.; Yates, P.; Hu, W.; Huang, X.; Lou, Y. The effects of Tai Chi on quality of life of cancer survivors: A systematic review and meta-analysis. Support. Care Cancer 2019, 27, 3701–3716. [Google Scholar] [CrossRef] [PubMed]
  73. Mutrie, N.; Campbell, A.M.; Whyte, F.; McConnachie, A.; Emslie, C.; Lee, L.; Kearney, N.; Walker, A.; Ritchie, D. Benefits of supervised group exercise programme for women being treated for early stage breast cancer: Pragmatic randomised controlled trial. Br. Med. J. 2007, 334, 517–520. [Google Scholar] [CrossRef] [Green Version]
  74. Courneya, K.S.; Segal, R.J.; Mackey, J.R.; Gelmon, K.; Reid, R.D.; Friedenreich, C.M.; Ladha, A.B.; Proulx, C.; Vallance, J.K.H.; Lane, K.; et al. Effects of aerobic and resistance exercise in breast cancer patients receiving adjuvant chemotherapy: A multicenter randomized controlled trial. J. Clin. Oncol. 2007, 25, 4396–4404. [Google Scholar] [CrossRef] [PubMed]
Figure 1. PRISMA flow diagram.
Figure 1. PRISMA flow diagram.
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Figure 2. Analysis of European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (QLQ-C30).
Figure 2. Analysis of European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (QLQ-C30).
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Figure 3. Analysis of Functional Assessment of Cancer Therapy—General.
Figure 3. Analysis of Functional Assessment of Cancer Therapy—General.
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Figure 4. Analysis of the Short-Form 36.
Figure 4. Analysis of the Short-Form 36.
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Figure 5. Analysis of the Brief Fatigue Inventory.
Figure 5. Analysis of the Brief Fatigue Inventory.
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Figure 6. Analysis of Functional Assessment of Chronic Illness Therapy—Fatigue.
Figure 6. Analysis of Functional Assessment of Chronic Illness Therapy—Fatigue.
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Figure 7. Analysis of the multidimensional fatigue symptom inventory-short form.
Figure 7. Analysis of the multidimensional fatigue symptom inventory-short form.
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Figure 8. Risk of bias summary.
Figure 8. Risk of bias summary.
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Figure 9. Risk of bias graph.
Figure 9. Risk of bias graph.
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Table 1. Baseline characteristics of the included studies.
Table 1. Baseline characteristics of the included studies.
IDArmsNumberAge (Years)Female n
(% of Total)
Cancer Treatment
SurgeryChemotherapyRadiation
Campo 2013Tai Chi Chih3266.54 (55–89) 132 (100)271921
Health Education Class3165.64 (57–84) 131 (100)281920
Chen 2013Qigong4945.3 (6.3)49 (100)49-49
Usual care4744.7 (9.7)47 (100)46-45
Chuang 2017Qigong4855.85 (16.78)22 (45)-48-
Usual care4864.54 (15.51)19 (40)-48-
Irwin 2017Tai Chi Chih4559.6 (7.9)45 (100)61822
Cognitive behavioral therapy for insomnia4560.0 (9.3)45 (100)42134
Larkey 2016Sham Qigong4559.8 (8.93)45 (100)---
Qigong and Tai Chi Easy4257.7 (8.94)42 (100)---
Loh 2014Qigong3218–6532 (100)322318
Line dance31 31 (100)312318
McQuade 2017Qigong/tai chi2162.2 (7.4)21 (100)--21
Waitlist control2466.0 (8.4)24 (100)--24
Mustian 2004Tai Chi Chuan1152 (9)11 (100)211813
Psychosocial support10 10 (100)
Mustian 2008Tai Chi Chuan1152 (9)11 (100)211813
Psychosocial support10 10
Oh 2008Qigong1554 (9)12 (80)---
Usual care15 12 (80)---
Oh 2009Qigong7960.1 (11.7)48 (61)---
Usual care8359.9 (11.3)45 (54)---
Sprod 2011Tai Chi Chuan954.33 (3.55) 29 (100)968
Standard support therapy1052.70 (2.11) 210 (100)1039
Strunk 2018Kyusho Jitsu3054.2 (7.8)30 (100)291423
Control2151.5 (8.4)21 (100)211517
Thongteratham 2015Tai Chi Qi Qong15-15 (100)151515
Usual care15-15 (100)151515
Vanderbyl 2017Qigong1166.1 (11.7)4 (37)---
standard endurance and strength training1363.7 (7.7)6 (46)---
Zhang 2016Tai Chi Chih4762.810 (21)47--
Control44 13 (30)44--
Zhou 2017Tai Chi Chih5718–7019 (33)-5757
Control57 12 (21)-5757
Values reflect number or mean (standard deviation); 1 median (range); 2 standard error of the mean.
Table 2. Summary of the included studies.
Table 2. Summary of the included studies.
ID.CountryCancer TypeTiming of InterventionType of TreatmentSession, MinutesFrequency, Times/WeekPeriod, WeekOutcomesTime
Questionnaires
Campo 2013USABreast, colorectal, ovarian, cervical/uterine, thyroid, bladder, nasopharyngeal≥3 months after TTT 3Surgery, radiation, chemotherapy, hormone, other60312SF-36 6Baseline and 1 week after
Chen 2013ChinaBreastDuring TTTRadiation6055–6FACT-G, BFI 7Baseline, during and at the end of treatment, and 1 and 3 months later.
Chuang 2017TaiwanLymphomaDuring TTTChemotherapy60210EORTC QLQ-C30, BFI 4Baseline and 21 days after
Irwin 2017USABreast≥ 6 months after TTTSurgery, radiation and/or chemotherapy120 min weekly12MFSI-SF 9Baseline and 2, 3, 6, and 15 months
Larkey 2016USABreast6 months to 5 years after TTTSurgery, radiation, or chemotherapy30512SF-36Baseline and 12 and 24 weeks
Loh 2014MalaysiaBreastTTT completedNM3028FACT-G 5Baseline and 8 weeks
McQuade 2017USAProstateDuring TTTRadiation6036–8BFIBaseline, midway, during the last week of TTT, and 3 months after TTT.
Mustian 2004USABreast1 week to 30 months after TTT NM60312FACIT–F 8Baseline and 12 weeks after
Mustian 2008USABreast1 week to 30 months after TTT NM60312FACIT–FBaseline and 12 weeks after intervention
Oh 2008AustraliaBreast, ovary, lung, lymphoma, colonDuring or completed TTTCancer treatment, chemotherapy601 or 28EORTC QLQ-C30Baseline and 8 weeks
Oh 2009AustraliaBreast, lung, prostate, colorectal, bowelDuring or completed TTTNM90 min weekly10FACIT–F, FACT-GBaseline and 10 weeks after intervention
Sprod 2011USABreast1 month to 30 months after TTTNM60312SF-36Baseline and 6 and 12 weeks
Strunk 2018GermanBreast≥ 6 months after TTTNot hormone treatment90224EORTC QLQ-C30Baseline and 12 and 24 weeks
Thongteratham 2015ThailandBreastTTT completedNM60312FACT-GBaseline and 12 and 24 weeks
Vanderbyl 2017CanadaNSCLC 1 or GI 2 During TTTChemotherapy4526FACT-GBaseline and 6 weeks
Zhang 2016ChinaLungDuring TTTChemotherapy60312MFSI-SFBaseline and 43 and 85 days
Zhou 2017ChinaNasopharyngeal carcinomaDuring TTTChemotherapy6056MFSI-SFBaseline and after treatment
NM, not mentioned; 1 NSCLC, non-small cell lung cancer; 2 GI, gastrointestinal cancer; 3 TTT, treatment; 4 EORTC QLQ-C30, European Organization for Research and Treatment of Cancer Quality of Life Questionnaire; 5 FACT-G, Functional Assessment of Cancer Therapy—General; 6 SF-36, the Short-Form 36; 7 BFI, the Brief Fatigue Inventory; 8 FACIT-F, Functional Assessment of Chronic Illness Therapy—Fatigue; 9 MFSI-SF, the Multidimensional Fatigue Symptom Inventory—Short Form.
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Sur, D.; Sabarimurugan, S.; Advani, S. The Effects of Martial Arts on Cancer-Related Fatigue and Quality of Life in Cancer Patients: An Up-to-Date Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials. Int. J. Environ. Res. Public Health 2021, 18, 6116. https://doi.org/10.3390/ijerph18116116

AMA Style

Sur D, Sabarimurugan S, Advani S. The Effects of Martial Arts on Cancer-Related Fatigue and Quality of Life in Cancer Patients: An Up-to-Date Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials. International Journal of Environmental Research and Public Health. 2021; 18(11):6116. https://doi.org/10.3390/ijerph18116116

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Sur, Daniel, Shanthi Sabarimurugan, and Shailesh Advani. 2021. "The Effects of Martial Arts on Cancer-Related Fatigue and Quality of Life in Cancer Patients: An Up-to-Date Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials" International Journal of Environmental Research and Public Health 18, no. 11: 6116. https://doi.org/10.3390/ijerph18116116

APA Style

Sur, D., Sabarimurugan, S., & Advani, S. (2021). The Effects of Martial Arts on Cancer-Related Fatigue and Quality of Life in Cancer Patients: An Up-to-Date Systematic Review and Meta-Analysis of Randomized Controlled Clinical Trials. International Journal of Environmental Research and Public Health, 18(11), 6116. https://doi.org/10.3390/ijerph18116116

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