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Mathieu Lai-King

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	<?xml version="1.0"?>
	<!DOCTYPE pmc-articleset PUBLIC "-//NLM//DTD ARTICLE SET 2.0//EN" "https://dtd.nlm.nih.gov/ncbi/pmc/articleset/nlm-articleset-2.0.dtd">
	<pmc-articleset>
	<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"
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	<front>
	<journal-meta>
	<journal-id journal-id-type="nlm-ta">Integr Cancer Ther</journal-id>
	<journal-id journal-id-type="iso-abbrev">Integr Cancer Ther</journal-id>
	<journal-id journal-id-type="publisher-id">ICT</journal-id>
	<journal-id journal-id-type="hwp">spict</journal-id>
	<journal-title-group>
	<journal-title>Integrative Cancer Therapies</journal-title>
	</journal-title-group>
	<issn pub-type="ppub">1534-7354</issn>
	<issn pub-type="epub">1552-695X</issn>
	<publisher>
	<publisher-name>SAGE Publications</publisher-name>
	<publisher-loc>Sage CA: Los Angeles, CA</publisher-loc>
	</publisher>
	</journal-meta>
	<article-meta>
	<article-id pub-id-type="pmid">38757745</article-id>
	<article-id pub-id-type="pmc">11102686</article-id>
	<article-id pub-id-type="doi">10.1177/15347354241252698</article-id>
	<article-id pub-id-type="publisher-id">10.1177_15347354241252698</article-id>
	<article-categories>
	<subj-group subj-group-type="heading">
	<subject>Study Protocol</subject>
	</subj-group>
	</article-categories>
	<title-group>
	<article-title>Exploring Guolin Qigong (Mind-Body Exercise) for Improving Cancer Related
	Fatigue in Cancer Survivors: A Mixed Method Randomized Controlled Trial Protocol</article-title>
	</title-group>
	<contrib-group>
	<contrib contrib-type="author">
	<contrib-id contrib-id-type="orcid" authenticated="false">
	https://orcid.org/0000-0001-6296-6052</contrib-id>
	<name>
	<surname>Low</surname>
	<given-names>Sara L. K.</given-names>
	</name>
	<degrees>MRes</degrees>
	<xref rid="aff1-15347354241252698" ref-type="aff">1</xref>
	</contrib>
	<contrib contrib-type="author">
	<name>
	<surname>Ho</surname>
	<given-names>Gwo Fuang</given-names>
	</name>
	<degrees>FRANZCR</degrees>
	<xref rid="aff2-15347354241252698" ref-type="aff">2</xref>
	</contrib>
	<contrib contrib-type="author">
	<name>
	<surname>Liu</surname>
	<given-names>Bingkai</given-names>
	</name>
	<degrees>PhD</degrees>
	<xref rid="aff3-15347354241252698" ref-type="aff">3</xref>
	</contrib>
	<contrib contrib-type="author">
	<name>
	<surname>Koh</surname>
	<given-names>Eng-Siew</given-names>
	</name>
	<degrees>FRANZCR</degrees>
	<xref rid="aff4-15347354241252698" ref-type="aff">4</xref>
	</contrib>
	<contrib contrib-type="author">
	<name>
	<surname>Fei</surname>
	<given-names>Yutong</given-names>
	</name>
	<degrees>PhD</degrees>
	<xref rid="aff5-15347354241252698" ref-type="aff">5</xref>
	</contrib>
	<contrib contrib-type="author">
	<contrib-id contrib-id-type="orcid" authenticated="false">
	https://orcid.org/0000-0003-1071-443X</contrib-id>
	<name>
	<surname>Teo</surname>
	<given-names>Chiah Shean</given-names>
	</name>
	<degrees>MD</degrees>
	<xref rid="aff6-15347354241252698" ref-type="aff">6</xref>
	</contrib>
	<contrib contrib-type="author">
	<contrib-id contrib-id-type="orcid" authenticated="false">
	https://orcid.org/0000-0002-2909-5926</contrib-id>
	<name>
	<surname>Zhu</surname>
	<given-names>Xiaoshu</given-names>
	</name>
	<degrees>PhD</degrees>
	<xref rid="aff1-15347354241252698" ref-type="aff">1</xref>
	<xref rid="corresp1-15347354241252698" ref-type="corresp" />
	</contrib>
	</contrib-group>
	<aff id="aff1-15347354241252698"><label>1</label>Western Sydney University, Penrith South,
	NSW, Australia</aff>
	<aff id="aff2-15347354241252698"><label>2</label>University Malaya Medical Centre, Kuala
	Lumpur, Wilayah Persekutuan, Malaysia</aff>
	<aff id="aff3-15347354241252698"><label>3</label>Pitié-Salpêtrière Hospital,
	Paris, France</aff>
	<aff id="aff4-15347354241252698"><label>4</label>University of New South Wales, Liverpool,
	NSW, Australia</aff>
	<aff id="aff5-15347354241252698"><label>5</label>Beijing University of Chinese Medicine,
	Beijing, China</aff>
	<aff id="aff6-15347354241252698"><label>6</label>UCSI University, Malaysia</aff>
	<author-notes>
	<corresp id="corresp1-15347354241252698">Xiaoshu Zhu, Chinese Medicine Centre (an
	international collaboration between Western Sydney University and Beijing University of
	Chinese Medicine), Western Sydney University, Locked Bag 1797, Penrith, NSW 2751,
	Australia. Email: <email>[email protected]</email></corresp>
	</author-notes>
	<pub-date pub-type="epub">
	<day>17</day>
	<month>5</month>
	<year>2024</year>
	</pub-date>
	<pub-date pub-type="collection">
	<year>2024</year>
	</pub-date>
	<volume>23</volume>
	<elocation-id>15347354241252698</elocation-id>
	<history>
	<date date-type="received">
	<day>5</day>
	<month>8</month>
	<year>2023</year>
	</date>
	<date date-type="rev-recd">
	<day>5</day>
	<month>4</month>
	<year>2024</year>
	</date>
	<date date-type="accepted">
	<day>18</day>
	<month>4</month>
	<year>2024</year>
	</date>
	</history>
	<permissions>
	<copyright-statement>© The Author(s) 2024</copyright-statement>
	<copyright-year>2024</copyright-year>
	<copyright-holder content-type="sage">SAGE Publications Inc unless otherwise noted.
	Manuscript content on this site is licensed under Creative Commons Licenses</copyright-holder>
	<license>
	<ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/"
	specific-use="textmining" content-type="ccbylicense">
	https://creativecommons.org/licenses/by/4.0/</ali:license_ref>
	<license-p>This article is distributed under the terms of the Creative Commons
	Attribution 4.0 License (<ext-link ext-link-type="uri"
	xlink:href="https://creativecommons.org/licenses/by/4.0/">
	https://creativecommons.org/licenses/by/4.0/</ext-link>) which permits any use,
	reproduction and distribution of the work without further permission provided the
	original work is attributed as specified on the SAGE and Open Access page (<ext-link
	ext-link-type="uri"
	xlink:href="https://us.sagepub.com/en-us/nam/open-access-at-sage">
	https://us.sagepub.com/en-us/nam/open-access-at-sage</ext-link>).</license-p>
	</license>
	</permissions>
	<abstract>
	<sec id="section1-15347354241252698">
	<title>Background:</title>
	<p>Cancer-related fatigue and its associated symptoms of sleep disorder and depression
	are prevalent in cancer survivors especially among breast, lung, and colorectal cancer
	survivors. While there is no gold standard for treating cancer-related fatigue
	currently, studies of mind-body exercises such as Qigong have reported promise in
	reducing symptoms. This study was designed to evaluate the feasibility and effect of
	Guolin Qigong on cancer-related fatigue and other symptoms in breast, lung and
	colorectal cancer survivors while exploring their perceptions and experiences of
	Guolin Qigong intervention.</p>
	</sec>
	<sec id="section2-15347354241252698">
	<title>Methods:</title>
	<p>This is an open-label randomized controlled trial with 60 participants divided into 2
	study groups in a 1:1 ratio. The intervention group will receive 12 weeks of
	Guolin Qigong intervention with a 4-week follow-up while control will receive usual
	care under waitlist. The primary outcome will be feasibility measured based on
	recruitment and retention rates, class attendance, home practice adherence, nature,
	and quantum of missing data as well as safety. The secondary subjective outcomes of
	fatigue, sleep quality and depression will be measured at Week-1 (baseline), Week-6
	(mid-intervention), Week-12 (post-intervention), and Week-16 (4 weeks
	post-intervention) while an objective 24-hour urine cortisol will be measured at
	Week-1 (baseline) and Week-12 (post-intervention). We will conduct a semi-structured
	interview individually with participants within 3 months after Week-16
	(4 weeks post-intervention) to obtain a more comprehensive view of practice
	adherence.</p>
	</sec>
	<sec id="section3-15347354241252698">
	<title>Discussion:</title>
	<p>This is the first mixed-method study to investigate the feasibility and effect of
	Guolin Qigong on breast, lung, and colorectal cancer survivors to provide a
	comprehensive understanding of Guolin Qigong’s intervention impact and
	participants’ perspectives. The interdisciplinary collaboration between Western
	Medicine and Chinese Medicine expertise of this study ensures robust study design,
	enhanced participant care, rigorous data analysis, and meaningful interpretation of
	results. This innovative research contributes to the field of oncology and may guide
	future evidence-based mind-body interventions to improve cancer survivorship.</p>
	</sec>
	<sec id="section4-15347354241252698">
	<title>Trial registration:</title>
	<p>This study has been registered with ANZCTR (ACTRN12622000688785p), was approved by
	Medical Research Ethic Committee of University Malaya Medical Centre (MREC ID NO:
	2022323-11092) and recognized by Western Sydney University Human Research Ethics
	Committee (RH15124).</p>
	</sec>
	</abstract>
	<kwd-group>
	<kwd>Qigong</kwd>
	<kwd>cancer</kwd>
	<kwd>cancer survivors</kwd>
	<kwd>fatigue</kwd>
	<kwd>sleep</kwd>
	<kwd>insomnia</kwd>
	<kwd>depression</kwd>
	<kwd>cortisol</kwd>
	<kwd>mind body exercise</kwd>
	</kwd-group>
	<funding-group specific-use="FundRef">
	<award-group id="award1-15347354241252698">
	<funding-source id="funding1-15347354241252698">
	<institution-wrap>
	<institution>Chinese Medicine Centre</institution>
	<institution-id />
	</institution-wrap>
	</funding-source>
	<award-id rid="funding1-15347354241252698">Research Fund</award-id>
	</award-group>
	<award-group id="award2-15347354241252698">
	<funding-source id="funding2-15347354241252698">
	<institution-wrap>
	<institution>Western Sydney University</institution>
	<institution-id institution-id-type="FundRef">https://doi.org/10.13039/501100018822</institution-id>
	</institution-wrap>
	</funding-source>
	<award-id rid="funding2-15347354241252698">Research Training Program Fund</award-id>
	</award-group>
	</funding-group>
	<custom-meta-group>
	<custom-meta>
	<meta-name>cover-date</meta-name>
	<meta-value>January-December 2024</meta-value>
	</custom-meta>
	<custom-meta>
	<meta-name>typesetter</meta-name>
	<meta-value>ts1</meta-value>
	</custom-meta>
	</custom-meta-group>
	</article-meta>
	</front>
	<body>
	<sec id="section5-15347354241252698">
	<title>Background</title>
	<p>Cancer-related fatigue (CRF) has been increasingly recognized as an important symptom
	during and after treatment of cancer, impacting physical, mental, and emotional functions.<sup>
	<xref rid="bibr1-15347354241252698" ref-type="bibr">1</xref>
	</sup> CRF is a
	prevalent symptom among survivors of the most common types of cancer, including breast,
	lung, and colon cancer.<sup><xref rid="bibr2-15347354241252698" ref-type="bibr">2</xref>,<xref
	rid="bibr3-15347354241252698" ref-type="bibr">3</xref></sup> It is a distressing
	symptom<sup>
	<xref rid="bibr3-15347354241252698" ref-type="bibr">3</xref>
	</sup> and one of
	the main reasons for the interruption of treatment or exacerbation of the disease.<sup>
	<xref rid="bibr2-15347354241252698" ref-type="bibr">2</xref>
	</sup> Between 74%
	and 90% of cancer survivors undergoing chemotherapy or radiotherapy<sup><xref
	rid="bibr4-15347354241252698" ref-type="bibr">4</xref>
	<xref
	rid="bibr5-15347354241252698" ref-type="bibr" />-<xref rid="bibr6-15347354241252698"
	ref-type="bibr">6</xref></sup> experienced fatigue with adverse effect on other
	co-morbidity, quality of life, independent living, and work productivity.<sup><xref
	rid="bibr3-15347354241252698" ref-type="bibr">3</xref>,<xref
	rid="bibr7-15347354241252698" ref-type="bibr">7</xref></sup> While fatigue is more
	prevalent within 6 months of receiving cancer treatment, cancer survivors including
	those who did not receive treatment continue to experience fatigue many years after
	treatment.<sup>
	<xref rid="bibr5-15347354241252698" ref-type="bibr">5</xref>
	</sup></p>
	<p>Cancer diagnosis and its treatment also bring with it a host of physiological changes
	affecting various functions of the body including cortisol dysregulation associated with
	fatigue,<sup><xref rid="bibr8-15347354241252698" ref-type="bibr">8</xref>
	<xref
	rid="bibr9-15347354241252698" ref-type="bibr" /><xref rid="bibr10-15347354241252698"
	ref-type="bibr" /><xref rid="bibr11-15347354241252698" ref-type="bibr" />-<xref
	rid="bibr12-15347354241252698" ref-type="bibr">12</xref></sup> sleep disorders,<sup><xref
	rid="bibr8-15347354241252698" ref-type="bibr">8</xref>,<xref
	rid="bibr13-15347354241252698" ref-type="bibr">13</xref>
	<xref
	rid="bibr14-15347354241252698" ref-type="bibr" />-<xref rid="bibr15-15347354241252698"
	ref-type="bibr">15</xref></sup> depression,<sup><xref rid="bibr12-15347354241252698"
	ref-type="bibr">12</xref>,<xref rid="bibr16-15347354241252698" ref-type="bibr">16</xref></sup>
	anxiety, stress,<sup><xref rid="bibr17-15347354241252698" ref-type="bibr">17</xref>,<xref
	rid="bibr18-15347354241252698" ref-type="bibr">18</xref></sup> functional disability,<sup>
	<xref rid="bibr12-15347354241252698" ref-type="bibr">12</xref>
	</sup> survival
	outcomes, and prognosis<sup><xref rid="bibr13-15347354241252698" ref-type="bibr">13</xref>
	,<xref rid="bibr18-15347354241252698" ref-type="bibr">18</xref>
	<xref
	rid="bibr19-15347354241252698" ref-type="bibr" /><xref rid="bibr20-15347354241252698"
	ref-type="bibr" />-<xref rid="bibr21-15347354241252698" ref-type="bibr">21</xref></sup>
	in cancer survivors.</p>
	<p>The pathogenesis of CRF is still unclear, but might include proinflammatory cytokines,
	growth factors, circadian rhythm modulation, adrenal axis interruption, serotonin
	imbalance, afferent activation of the vagus nerve, and the production or use of abnormal
	adenosine triphosphate.<sup>
	<xref rid="bibr22-15347354241252698" ref-type="bibr">22</xref>
	</sup> Host
	factors not related to cancer and its treatment such as genetic, biological, psychosocial,
	and behavioral factor also play an important role in the development of CRF.<sup>
	<xref rid="bibr23-15347354241252698" ref-type="bibr">23</xref>
	</sup></p>
	<p>CRF is also associated with various risk factors such as low performance status,
	undergoing chemoradiotherapy, insomnia, pain, neuroticism, depression and being female.<sup>
	<xref rid="bibr24-15347354241252698" ref-type="bibr">24</xref>
	</sup></p>
	<p>It is further suggested that cancer-related fatigue is a composite of interacting
	responses to stress related to diagnosis and treatment, with the relationship of sleep
	disorders, depression, anemia, and inflammation featuring centrally for those under
	treatment as well as into the survivorship phase.<sup>
	<xref rid="bibr25-15347354241252698" ref-type="bibr">25</xref>
	</sup> CRF and a
	number of these factors and symptoms, including sleep disruption and emotional distress
	often co-occur as a symptom cluster,<sup><xref rid="bibr26-15347354241252698"
	ref-type="bibr">26</xref>
	<xref rid="bibr27-15347354241252698" ref-type="bibr" />-<xref
	rid="bibr28-15347354241252698" ref-type="bibr">28</xref></sup> with some of these
	associations potentially linked to the underlying inflammatory biomarker changes such as
	cortisol level<sup>
	<xref rid="bibr29-15347354241252698" ref-type="bibr">29</xref>
	</sup> most
	associated with fatigue.<sup><xref rid="bibr3-15347354241252698" ref-type="bibr">3</xref>,<xref
	rid="bibr24-15347354241252698" ref-type="bibr">24</xref>,<xref
	rid="bibr30-15347354241252698" ref-type="bibr">30</xref></sup></p>
	<p>Exploring symptom clusters is an important gap in symptom research to shed light on the
	common biological mechanisms<sup>
	<xref rid="bibr31-15347354241252698" ref-type="bibr">31</xref>
	</sup> and is
	gaining increased attention in the field of oncology in an attempt to improve the quality
	of life of patients diagnosed with cancer.<sup>
	<xref rid="bibr32-15347354241252698" ref-type="bibr">32</xref>
	</sup></p>
	<p>Hence, there is a need to pay attention to the co-occurrences of fatigue, sleep disorder
	and depression as a symptom cluster in the evaluation and treatment of cancer survivors
	experiencing CRF.<sup><xref rid="bibr3-15347354241252698" ref-type="bibr">3</xref>,<xref
	rid="bibr26-15347354241252698" ref-type="bibr">26</xref>
	<xref
	rid="bibr27-15347354241252698" ref-type="bibr" />-<xref rid="bibr28-15347354241252698"
	ref-type="bibr">28</xref></sup></p>
	<p>In spite of fatigue being the most common symptom reported by patients, they were least
	likely to report getting wanted help for it, perhaps due to the complexity of treating
	this common condition.<sup>
	<xref rid="bibr5-15347354241252698" ref-type="bibr">5</xref>
	</sup> Given the
	multifactorial nature of CRF which is still poorly understood, there is currently no
	“gold standard” treatment for CRF despite some approaches such as exercise,
	psychosocial interventions, and mind-body interventions being reported to yield beneficial
	effects in improving CRF.<sup>
	<xref rid="bibr23-15347354241252698" ref-type="bibr">23</xref>
	</sup></p>
	<p>Emerging studies have shown that mind-body exercise such as Qigong can reduce fatigue,
	improve sleep, depression, anxiety, quality of life and cognitive changes associated with
	cancer as well as biomarkers of stress, cortisol level, inflammation and immune function
	in cancer survivors during and after treatment.<sup><xref rid="bibr29-15347354241252698"
	ref-type="bibr">29</xref>,<xref rid="bibr33-15347354241252698" ref-type="bibr">33</xref>
	<xref
	rid="bibr34-15347354241252698" ref-type="bibr" /><xref rid="bibr35-15347354241252698"
	ref-type="bibr" /><xref rid="bibr36-15347354241252698" ref-type="bibr" /><xref
	rid="bibr37-15347354241252698" ref-type="bibr" /><xref rid="bibr38-15347354241252698"
	ref-type="bibr" /><xref rid="bibr39-15347354241252698" ref-type="bibr" /><xref
	rid="bibr40-15347354241252698" ref-type="bibr" /><xref rid="bibr41-15347354241252698"
	ref-type="bibr" /><xref rid="bibr42-15347354241252698" ref-type="bibr" /><xref
	rid="bibr43-15347354241252698" ref-type="bibr" />-<xref rid="bibr44-15347354241252698"
	ref-type="bibr">44</xref></sup></p>
	<p>The term “Qigong” is made up of 2 characters: Qi and Gong translated as the
	skill or practice to cultivate Qi. The concept of Qi, an inherent function and energizing
	essence of human being, is found in Traditional Chinese Medicine.<sup>
	<xref rid="bibr45-15347354241252698" ref-type="bibr">45</xref>
	</sup> Qi also
	refers to life force, vitality, or intelligence within a bio-electric body<sup><xref
	rid="bibr46-15347354241252698" ref-type="bibr">46</xref>,<xref
	rid="bibr47-15347354241252698" ref-type="bibr">47</xref></sup> as well as the
	universe.<sup>
	<xref rid="bibr48-15347354241252698" ref-type="bibr">48</xref>
	</sup> There are
	a few thousand different forms of Qigong such as Tai Chi, BaDuanJin, Chan Chuang, Zhineng
	Qigong, and Guolin Qigong, all of which can be broadly classified into Chinese Medical
	Qigong, Daoist Qigong, Buddhist Qigong, Confucian Qigong, and martial arts Qigong. All
	forms of Qigong involve the recognition and cultivation of Qi to promote a balanced Qi and
	smooth flow of Qi in the body<sup>
	<xref rid="bibr49-15347354241252698" ref-type="bibr">49</xref>
	</sup> to
	enhance physical, psychological, and spiritual health through mind-body integration of
	specific movements, breathing techniques, and meditation.<sup>
	<xref rid="bibr50-15347354241252698" ref-type="bibr">50</xref>
	</sup> Mind-body
	integration of Qigong is also believed to promote health through the activation of
	neurohormonal pathways and other physiological mechanisms.<sup>
	<xref rid="bibr51-15347354241252698" ref-type="bibr">51</xref>
	</sup> Qigong
	offers several potential advantages when compared to modern medical therapy as it
	emphasizes a holistic approach with minimal adverse effects<sup><xref
	rid="bibr40-15347354241252698" ref-type="bibr">40</xref>,<xref
	rid="bibr52-15347354241252698" ref-type="bibr">52</xref></sup> when practiced
	correctly after proper guidance. It is also known to improve neuropsychiatric conditions<sup>
	<xref rid="bibr53-15347354241252698" ref-type="bibr">53</xref>
	</sup> without
	the side effects of pharmaceutical drugs. More importantly, it promotes self-empowerment
	as it empowers individuals to take an active role in their health. Lastly, Qigong is more
	cost- effective compared to certain medical treatments as once learned, it can be
	practiced regularly to promote a healthy lifestyle without the need to incur additional
	expenses.</p>
	<p>Among the many styles of Qigong is Guolin Qigong (GQ). This form of Qigong has been
	specifically adapted for cancer survivors by offering a moderate and adaptable exercise
	routine. It is a moderate walking exercise that integrates coordinated arm movements and
	trunk rotations, coupled with controlled breathing techniques. What sets it apart is its
	gentle nature, designed to be accommodating and adjustable. This adaptability is crucial,
	as it allows for modifications in speed, duration, and intensity, ensuring that it caters
	to the unique health conditions and needs of individual cancer survivors. The flexible
	approach of GQ prioritizes the well-being and comfort of each participant, making it a
	safe and beneficial practice for those navigating the complexities of cancer recovery.
	Therefore GQ is suitable for cancer survivors—especially advanced cancer patients
	who may be unable to engage in other forms of physical activity.<sup>
	<xref rid="bibr54-15347354241252698" ref-type="bibr">54</xref>
	</sup> A
	moderate-intensity walking exercise program was reported to be a feasible and effective
	intervention method for managing fatigue,<sup><xref rid="bibr55-15347354241252698"
	ref-type="bibr">55</xref>,<xref rid="bibr56-15347354241252698" ref-type="bibr">56</xref></sup>
	anxiety, depression,<sup>
	<xref rid="bibr57-15347354241252698" ref-type="bibr">57</xref>
	</sup> and sleep
	in cancer survivors at different stages of cancer.<sup><xref
	rid="bibr58-15347354241252698" ref-type="bibr">58</xref>
	<xref
	rid="bibr59-15347354241252698" ref-type="bibr" />-<xref rid="bibr60-15347354241252698"
	ref-type="bibr">60</xref></sup> GQ exercise training also facilitates the inhaling of
	oxygen which is important for the homeostasis of oxygen-carbon dioxide in controlling
	cancer and ultimately survival, as supported by a 10-year longitudinal cohort study of 122
	lung and nasopharyngeal cancer patients which reported that improvements in End Tidal
	Breath Holding Time (ETBHT), alveolar O<sub>2</sub> (aO<sub>2</sub>) pressure, and
	alveolar CO<sub>2</sub> (aCO<sub>2</sub>) pressure capacity with GQ was associated with
	higher survival years, 5 years survival rate and survival probability.<sup>
	<xref rid="bibr61-15347354241252698" ref-type="bibr">61</xref>
	</sup> In the
	above-mentioned cohort study,<sup>
	<xref rid="bibr61-15347354241252698" ref-type="bibr">61</xref>
	</sup> GQ also
	demonstrated improvement in depression among cancer participants. Additionally, in breast
	cancer patients undergoing 5 to 6 weeks of radiotherapy, women with elevated
	depressive symptoms at the start of treatment showed significant enhancements in fatigue
	and QOL.<sup>
	<xref rid="bibr50-15347354241252698" ref-type="bibr">50</xref>
	</sup></p>
	<p>However, the impact of GQ on CRF, often associated with sleep and depression<sup><xref
	rid="bibr3-15347354241252698" ref-type="bibr">3</xref>,<xref
	rid="bibr26-15347354241252698" ref-type="bibr">26</xref>
	<xref
	rid="bibr27-15347354241252698" ref-type="bibr" />-<xref rid="bibr28-15347354241252698"
	ref-type="bibr">28</xref></sup> and its correlation with cortisol levels has not been
	explored.</p>
	<p>In addition to that, a qualitative study to evaluate the perception and acceptance of GQ
	is needed to explore the feasibility, adherence, and experience related to this complex
	intervention. It aims to understand the more subjective domains and identify potential
	factors for improving healthcare<sup>
	<xref rid="bibr62-15347354241252698" ref-type="bibr">62</xref>
	</sup> to
	address the multi-faceted needs of this population. Such research, however, has not been
	conducted yet.</p>
	<p>Therefore, the purpose of this paper is to describe the protocol of a mixed-method study
	comprising,</p>
	<list list-type="order" id="list1-15347354241252698">
	<list-item>
	<p>A randomized-controlled trial to evaluate the feasibility of GQ training and its
	effect on CRF, sleep, depression, and cortisol levels in breast, lung and colon cancer
	survivors and,</p>
	</list-item>
	<list-item>
	<p>Semi-structured interview with study participants from the randomized- controlled
	trial to understand their perceptions and experiences of GQ to identify: <list
	list-type="simple" id="list2-15347354241252698">
	<list-item>
	<p>(a) other physiological and psychological benefits gained from the GQ
	intervention,</p>
	</list-item>
	<list-item>
	<p>(b) the barriers to GQ participation, adherence, and recommendations for
	improvement.</p>
	</list-item>
	</list></p>
	</list-item>
	</list>
	<p>We hypothesized that</p>
	<list list-type="order" id="list3-15347354241252698">
	<list-item>
	<p>It is feasible for cancer survivor participants to engage in the GQ training and
	those who participated in the GQ training will experience positive impacts on CRF,
	sleep, depression, and cortisol level. Feasibility of this study is established at
	about 80% to 85% retention rate and 75% to 85% class attendance rate based on prior
	similar studies.<sup><xref rid="bibr63-15347354241252698" ref-type="bibr">63</xref>
	<xref
	rid="bibr64-15347354241252698" ref-type="bibr" />-<xref
	rid="bibr65-15347354241252698" ref-type="bibr">65</xref></sup></p>
	</list-item>
	<list-item>
	<p>The semi-structured interview will identify a broader spectrum of benefits and
	barriers to participation and adherence to GQ training to provide valuable insights
	for program enhancement.</p>
	</list-item>
	</list>
	</sec>
	<sec sec-type="methods" id="section6-15347354241252698">
	<title>Methods</title>
	<sec id="section7-15347354241252698">
	<title>Study Design</title>
	<sec id="section8-15347354241252698">
	<title>Intervention/clinical trial</title>
	<p>The primary objective of this study is to explore the feasibility of a GQ
	intervention in patients with various cancer types who experience CRF. This study
	includes the 3 most prevalent cancer types that is, breast, lung and colon cancers.
	This is a randomized-controlled trial that compares the GQ intervention group to a
	usual care waitlist control group receiving standard medical care allocated in a 1:1
	ratio to evaluate the feasibility and effects of a 12-week GQ intervention on 60
	eligible breast, lung, and colorectal cancer survivors’ fatigue, sleep quality,
	depression, and 24-hour urine cortisol change. Refer to <xref
	rid="fig1-15347354241252698" ref-type="fig">Figure 1</xref> for an overview of the
	study. This study protocol was developed based on the SPIRIT 2013 Statement (Standard
	Protocol Items: Recommendations for Interventional Trials) (<ext-link
	xlink:href="https://journals.sagepub.com/doi/suppl/10.1177/15347354241252698"
	ext-link-type="uri">Supplemental Material 1</ext-link>).<sup>
	<xref rid="bibr66-15347354241252698" ref-type="bibr">66</xref>
	</sup></p>
	<fig position="float" id="fig1-15347354241252698">
	<label>Figure 1.</label>
	<caption>
	<p>Participant flow diagram.</p>
	</caption>
	<graphic xlink:href="10.1177_15347354241252698-fig1" position="float" />
	</fig>
	</sec>
	<sec id="section9-15347354241252698">
	<title>Interview</title>
	<p>We will use a qualitative descriptive design, with a semi-structured interview to
	collect in-depth information to enhance our understanding of the perceptions and
	experiences of GQ participation of cancer survivors based on purposive sampling until
	data saturation is reached.</p>
	<p>The qualitative interview will be reported within the primary randomized feasibility
	trial according to the guidelines recommended in the CONSORT 2010 statement extension.<sup>
	<xref rid="bibr67-15347354241252698" ref-type="bibr">67</xref>
	</sup></p>
	</sec>
	</sec>
	<sec id="section10-15347354241252698">
	<title>Study Setting</title>
	<p>The trial is conducted at University Malaya Medical Centre (UMMC) in Kuala Lumpur,
	Malaysia. Participants are recruited by referrals from UMMC or online and print
	advertisements such as posting recruitment in UMMC, cancer support groups, GQ
	Association and GQ practice stations around Klang Valley, and social media platforms
	including X Corp (formerly known as Twitter) and Facebook.</p>
	</sec>
	<sec id="section11-15347354241252698">
	<title>Recruitment</title>
	<p>Recruitment started in October 2022. Upon first contact, the Researcher will screen
	potential breast, lung, or colon cancer survivors and provide information about the
	study to those who meet the eligibility criteria and indicate interest to participate.
	Thereafter a Physician/Oncologist Screening Form, Participant Information Sheet, and 2
	copies of Participant Consent Form will be given, explained, and a separate date agreed
	for in-person enrollment.<sup>
	<xref rid="bibr67-15347354241252698" ref-type="bibr">67</xref>
	</sup></p>
	</sec>
	<sec id="section12-15347354241252698">
	<title>Inclusion Criteria</title>
	<list list-type="simple" id="list4-15347354241252698">
	<list-item>
	<p>(1) Age ≥ 18 years old;</p>
	</list-item>
	<list-item>
	<p>(2) *Cancer survivor diagnosed with breast, lung and colorectal cancer;</p>
	</list-item>
	<list-item>
	<p>(3) Able to read and answer questionnaires in English and/or Bahasa Malaysia
	language by oneself;</p>
	</list-item>
	<list-item>
	<p>(4) Suffering from moderate to severe fatigue as assessed by the simple
	fatigue scale; with severity score of 3 and above<sup>
	<xref rid="bibr68-15347354241252698" ref-type="bibr">68</xref>
	</sup>
	;</p>
	</list-item>
	<list-item>
	<p>(5) Able to use smart phones and the WeChat or WhatsApp application;</p>
	</list-item>
	<list-item>
	<p>(6) Life expectancy of more than 3 months;</p>
	</list-item>
	<list-item>
	<p>(7) Able to give informed consent;</p>
	</list-item>
	<list-item>
	<p>(8) Available and willing to comply with the study requirements.</p>
	</list-item>
	</list>
	<p>*A cancer survivor is defined as an individual diagnosed with cancer through the
	balance of life according to National Cancer Institute.<sup>
	<xref rid="bibr69-15347354241252698" ref-type="bibr">69</xref>
	</sup></p>
	<p>Including cancer survivors throughout the continuum of survivorship in our sample
	inclusion criteria allows us to capture a comprehensive spectrum of experiences. From
	those newly diagnosed to long-term survivors, each stage brings unique perspectives on
	GQ participation and its impact. This approach ensures a thorough exploration of how GQ
	intervention intersects with varying phases of the cancer journey, providing a rich
	understanding of the diverse narratives and challenges encountered across this
	continuum.</p>
	</sec>
	<sec id="section13-15347354241252698">
	<title>Exclusion Criteria</title>
	<list list-type="simple" id="list5-15347354241252698">
	<list-item>
	<p>(1) Cardiopulmonary disease, nerve, muscle, or joint disease, or other
	malignant tumors affecting movement;</p>
	</list-item>
	<list-item>
	<p>(2) Mental illness or serious cognitive impairment and defects in language
	that significantly impairs communication;</p>
	</list-item>
	<list-item>
	<p>(3) Post-operative heart, cerebral vessel, or other serious complications;</p>
	</list-item>
	<list-item>
	<p>(4) Neurological degenerative disease (e.g. dementia), reduced cognitive;
	capacity in any way that would affect ability to understand trial procedures and
	give informed consent;</p>
	</list-item>
	<list-item>
	<p>(5) Patients who are not able to walk;</p>
	</list-item>
	<list-item>
	<p>(6) Other medical conditions which would preclude study intervention or make
	study participation unsafe such as severe chronic heart failure.</p>
	</list-item>
	</list>
	</sec>
	<sec id="section14-15347354241252698">
	<title>Randomization and Blinding</title>
	<p>After informed consent, participants will be randomly assigned to either the GQ or
	usual care waitlist control group at a 1:1 ratio with the random sequence generated by
	an online computerized randomization system using minimization method<sup><xref
	rid="bibr70-15347354241252698" ref-type="bibr">70</xref>
	<xref
	rid="bibr71-15347354241252698" ref-type="bibr" />-<xref
	rid="bibr72-15347354241252698" ref-type="bibr">72</xref></sup> by an independent
	research assistant.</p>
	</sec>
	<sec id="section15-15347354241252698">
	<title>Intervention</title>
	<p>After being advised of group allocation, the study participant will be given a few days
	to decide on whether to proceed with enrollment. Incorporating a brief period for
	participants to reflect and opt-out after randomization supports ethical research
	practices, ensures ethical informed consent, reduces pressure, enhances retention, and
	respects participant autonomy in clinical trials or studies.</p>
	<sec id="section16-15347354241252698">
	<title>Guolin Qigong</title>
	<p>Participants in the intervention group will attend a 2-hour supervised face-to-face
	(F2F) GQ training class for 12 weeks with home-practice on non-class days.
	There will be 2 training classes per week for the first 2 weeks and once per
	week for the next 10 weeks.</p>
	<p>The GQ training involves a modified version of a Chinese medical qigong therapy often
	referred to as “walking qigong” developed by Guo Lin.<sup>
	<xref rid="bibr38-15347354241252698" ref-type="bibr">38</xref>
	</sup>
	GQ was developed specifically for cancer and consisted of several breathing and moving
	exercises. The GQ training in the current study includes the following 3 main
	exercises:</p>
	<list list-type="simple" id="list6-15347354241252698">
	<list-item>
	<p>1. Feng Hu Xi Zhi Ran Xing Gong (Natural Wind Breathing Walking)</p>
	</list-item>
	</list>
	<p>Participants walk in a circle, synchronizing their breathing, arm movements, and
	steps focusing on the movement of their body with the goal of calming one’s
	mind, relaxing various parts of the body and the mind, and revitalizing the
	“life-force,” that is, <italic toggle="yes">qi</italic>.</p>
	<list list-type="simple" id="list7-15347354241252698">
	<list-item>
	<p>2. Dian Bu Gong (Step Tap Method)</p>
	</list-item>
	</list>
	<p>A modified natural Wind Breathing Walking Exercise with additional step tap.</p>
	<list list-type="simple" id="list8-15347354241252698">
	<list-item>
	<p>3. Sheng Jiang Kai He Fa (Ascending, Descending, Opening, and Closing
	Method)</p>
	</list-item>
	</list>
	<p>A calming and relaxation method of synchronized arms and legs movements on the spot
	which can be practiced within limited space.</p>
	<p>Each main exercise has to be practiced separately as individual sets comprising 3
	parts:</p>
	<list list-type="simple" id="list9-15347354241252698">
	<list-item>
	<p>a. Preparatory relaxation exercise (gentle breathing and meditation;
	4 minutes):</p>
	</list-item>
	</list>
	<p>In relaxed standing posture, synchronize the breath with gentle arm movements in
	front of the abdomen (opening and closing of the Dantian). Dantian is a Chinese
	medicine concept that refers to the “elixir field” or “energy
	center.” It has different locations but often referred to the lower abdomen
	between the navel and pubic bone of the human body.<sup><xref
	rid="bibr73-15347354241252698" ref-type="bibr">73</xref>,<xref
	rid="bibr74-15347354241252698" ref-type="bibr">74</xref></sup></p>
	<list list-type="simple" id="list10-15347354241252698">
	<list-item>
	<p>b. Main exercise</p>
	</list-item>
	<list-item>
	<p>i. Feng Hu Xi Zhi Ran Xing Gong (Natural Wind Breathing Walking) or</p>
	</list-item>
	<list-item>
	<p>ii. Dian Bu Gong (Step Tap Method) or</p>
	</list-item>
	<list-item>
	<p>iii. Sheng Jiang Kai He Fa (Ascending, Descending, Opening, and Closing
	Method).</p>
	</list-item>
	<list-item>
	<p>c. Concluding exercise: breathing exercises, opening, and closing of the
	Dantian, and self-massage (3-6 minutes).<sup>
	<xref rid="bibr50-15347354241252698" ref-type="bibr">50</xref>
	</sup></p>
	</list-item>
	</list>
	<p>Please refer to <ext-link
	xlink:href="https://journals.sagepub.com/doi/suppl/10.1177/15347354241252698"
	ext-link-type="uri">Supplemental Material 2</ext-link> for detailed steps. All
	movements will include modifications to enhance safety. Participants will be advised
	to rest as and when necessary, according to their health status.</p>
	<p>The F2F GQ class will be taught by qualified GQ instructors who are both long-term
	cancer survivors with more than 20 years of GQ training experience to ensure
	the full potential of the GQ intervention. The Researcher, who is a registered Chinese
	Medicine practitioner in Malaysia and Australia with more than 20 years’
	experience in Qigong, will be in attendance during the F2F GQ class to ensure the safe
	and seamless facilitation of the training session.</p>
	<p>Home practice is recommended for non-class days according to individual health status
	and available time.<sup>
	<xref rid="bibr54-15347354241252698" ref-type="bibr">54</xref>
	</sup>
	Participants will be provided with class notes and video links (<ext-link
	xlink:href="https://journals.sagepub.com/doi/suppl/10.1177/15347354241252698"
	ext-link-type="uri">Supplemental Material 3</ext-link>) to promote and support home
	practice. Home practice after the intervention period is encouraged for incorporation
	into daily life to foster a healthy lifestyle.</p>
	</sec>
	</sec>
	<sec id="section17-15347354241252698">
	<title>Usual Care Waitlist Control</title>
	<p>Participants in the usual care waitlist control group will be advised to continue with
	their usual care routines and exercises and will be asked not to attend any other Qigong
	exercises. They will be offered to attend the same GQ training class after Week-16 of
	the GQ training of their cohort.</p>
	<p>However, to maintain integrity of the study, instructors will not be informed about the
	allocation of participants. Consequently, when instructors commence training of
	subsequent cohorts, they will be unaware of which participants belong to the
	intervention group (commencing from Week 1), and which are part of the control group
	(joining the GQ group in Week 1), given the GQ training will be offered continuously.
	This ensures the instructors are effectively blinded to the allocation to maintain
	impartiality in the delivery of the training and minimizes any potential biases that may
	arise from instructor knowledge of group allocation.</p>
	</sec>
	<sec id="section18-15347354241252698">
	<title>Study Assessments</title>
	<p>The variables under consideration will encompass basic demographic data, primary
	outcomes, and secondary outcomes. Basic characteristics will be collected at baseline
	(Week-1).</p>
	<p>Primary feasibility outcomes on adherence, attendance, and any adverse events will be
	recorded throughout the intervention period from Week-1 to Week-12 in the practice diary
	by the participants. Secondary patient-reported outcomes on fatigue, depression, and
	sleep will be measured at baseline (Week-1), mid-intervention (Week-6),
	post-intervention (Week-12), and 4 weeks after completion of intervention
	(Week-16). Urine samples (for urine cortisol test) to assess 24-hour urinary cortisol
	will be collected a day prior to enrollment date and post-intervention (Week-12).
	Primary feasibility outcomes and secondary patient-reported outcomes will be assessed by
	an independent research assistant to minimize bias. A summary of the planned data
	collection is shown in <xref rid="fig2-15347354241252698" ref-type="fig">Figure 2</xref>
	.</p>
	<fig position="float" id="fig2-15347354241252698">
	<label>Figure 2.</label>
	<caption>
	<p>Schedule of enrollment, intervention and data collection</p>
	<p>Abbreviations: BFI, Brief Fatigue Inventory, CES-D, Centre for Epidemiologic
	Studies Depression; PSQI, Pittsburgh Sleep Quality Index.</p>
	</caption>
	<graphic xlink:href="10.1177_15347354241252698-fig2" position="float" />
	</fig>
	<sec id="section19-15347354241252698">
	<title>Basic demographic data</title>
	<p>Participants’ basic characteristics (sex, marital status, age) and cancer
	history will be collected using a self-designed questionnaire.</p>
	</sec>
	<sec id="section20-15347354241252698">
	<title>Feasibility outcomes</title>
	<p>Feasibility will be assessed based on recruitment rate, retention rate, class
	attendance, home practice adherence, the nature and extent of missing data, and
	safety. Safety will be monitored and assessed based on total number of Adverse Event
	and the presence of any Serious Adverse Event.<sup>
	<xref rid="bibr75-15347354241252698" ref-type="bibr">75</xref>
	</sup></p>
	</sec>
	<sec id="section21-15347354241252698">
	<title>Patient-reported outcomes and cortisol biomarker</title>
	<list list-type="simple" id="list11-15347354241252698">
	<list-item>
	<p>i. Patient-reported outcomes</p>
	</list-item>
	</list>
	<p>Participants will complete several patient-reported outcome measures to evaluate
	fatigue—Brief Fatigue Inventory (BFI),<sup>
	<xref rid="bibr68-15347354241252698" ref-type="bibr">68</xref>
	</sup>
	sleep quality—Pittsburgh Sleep Quality Index (PSQI)<sup>
	<xref rid="bibr76-15347354241252698" ref-type="bibr">76</xref>
	</sup>
	and depression—Centre for Epidemiologic Studies Depression (CES-D)<sup><xref
	rid="bibr77-15347354241252698" ref-type="bibr">77</xref>,<xref
	rid="bibr78-15347354241252698" ref-type="bibr">78</xref></sup> at Week-1, Week-6,
	Week-12, and Week-16.</p>
	<list list-type="simple" id="list12-15347354241252698">
	<list-item>
	<p>a. Fatigue—The Brief Fatigue Inventory (BFI)</p>
	</list-item>
	</list>
	<p>The BFI was developed for the rapid assessment of fatigue severity in cancer patients
	for use in both clinical screening and clinical trials. It is easy to administer, and
	patients can complete them easily as it has only 9 items with simple wordings that are
	easy to understand and translate.<sup>
	<xref rid="bibr68-15347354241252698" ref-type="bibr">68</xref>
	</sup>
	Items 1 to 3 rate participants’ worst, usual, and current fatigue during the
	past 24 hours using a visual analog scale (VAS) ranging from 0 (no fatigue) to
	10 (very severely fatigued). A composite fatigue severity score was obtained by
	averaging the 3 severity scores. The remaining 6 items rate the level at which
	patients` fatigue interferes with certain functions such as daily activity, work,
	walking ability, normal work, relations with others, and enjoyment in life. Each item
	is rated on a scale of 0 (does not interfere) to 10 (completely interferes). A
	composite fatigue interference score will be obtained by averaging the scores of the 6
	interference items. Severity scores of 1 to 3 suggest mild fatigue, 4 to 6 moderate,
	and 7 to 10 represent severe fatigue. The internal consistency Cronbach’s
	α at .96 supports the reliability of BFI which is correlated with measures of
	performance status (patients who are more ill reported higher levels of fatigue).<sup>
	<xref rid="bibr68-15347354241252698" ref-type="bibr">68</xref>
	</sup></p>
	<list list-type="simple" id="list13-15347354241252698">
	<list-item>
	<p>b. Sleep—Pittsburgh Sleep Quality Index (PSQI)</p>
	</list-item>
	</list>
	<p>The PSQI, proposed by Buysse et al<sup>
	<xref rid="bibr76-15347354241252698" ref-type="bibr">76</xref>
	</sup>
	in 1989, is currently the most commonly used scale for assessing sleep quality. The
	PSQI is a 19-item scale measuring 7 aspects of the sleep quality and disturbances,
	that is, subjective sleep quality, sleep latency, duration, efficiency, disturbances,
	use of sleep medication, and daytime sleep dysfunction, each weighted equally on a 0
	to 3 scale. The total score ranges between 0 and 21, with increasing scores indicating
	worse sleep quality.<sup>
	<xref rid="bibr76-15347354241252698" ref-type="bibr">76</xref>
	</sup>
	It has a sensitivity of 89.6% and a specificity of 86.5% to detect insomnia cases and
	is a useful first-line, easy-to-handle, and time-efficient questionnaire to evaluate
	sleep quality.<sup>
	<xref rid="bibr79-15347354241252698" ref-type="bibr">79</xref>
	</sup>
	The PSQI was reported to be a stable measure of sleep quality with high test-retest
	reliability and construct validity.<sup><xref rid="bibr79-15347354241252698"
	ref-type="bibr">79</xref>,<xref rid="bibr80-15347354241252698" ref-type="bibr">80</xref></sup></p>
	<list list-type="simple" id="list14-15347354241252698">
	<list-item>
	<p>c. Depression—Centre for Epidemiologic Studies Depression (CES-D)</p>
	</list-item>
	</list>
	<p>The CES-D is a short self-reported 20-item scale<sup>
	<xref rid="bibr81-15347354241252698" ref-type="bibr">81</xref>
	</sup>
	to be administered to measure depression symptoms at baseline, mid-intervention,
	post-intervention, and follow-up. The CES-D shows very high internal consistency and
	adequate test-retest repeatability.<sup>
	<xref rid="bibr81-15347354241252698" ref-type="bibr">81</xref>
	</sup>
	The score is the sum of all items, and the maximum score is 60.
	Scores ≥ 16 on the CES-D is considered as having
	“depressed symptoms.” The cut off score of 12 has been validated with
	DSM-III criteria for clinical depression.<sup><xref rid="bibr81-15347354241252698"
	ref-type="bibr">81</xref>,<xref rid="bibr82-15347354241252698" ref-type="bibr">82</xref></sup></p>
	<list list-type="simple" id="list15-15347354241252698">
	<list-item>
	<p>ii. Cortisol biomarker: 24-hour urine cortisol</p>
	</list-item>
	</list>
	<p>Urine sample will be collected at baseline (Week-1) and post-intervention (Week- 12).<sup>
	<xref rid="bibr83-15347354241252698" ref-type="bibr">83</xref>
	</sup>
	Participants are briefed on the urine collection procedure during assessment and
	advised to obtain the 2.5 L urine collection container from any nearby BP
	Laboratories before baseline (Week-1) and post-intervention (Week-12). We use 24-hour
	urinary cortisol as a non-invasive, integrated measure of cortisol stress hormone
	activity that could be collected in participants’ home environments.
	Participants are instructed to collect all urine for 24 hours from 8:00am a day
	prior to baseline (Week-1) and post-intervention (Week-12) to 8:00am the next mornings
	and to send the urine sample collected to the nearest BP Laboratories the next morning
	itself. If the 2.5L collection container is completely full, subjects are advised to
	use a clean mineral water bottle to collect any specimen in excess of the 2.5 L
	collection. If subjects are unable to collect all urine for any reason, their samples
	will be deemed inadequate and no urinary cortisol data will be recorded for these
	subjects.</p>
	<p>The 24-hour urine cortisol test provides a more accurate estimate of overall cortisol
	secretion<sup>
	<xref rid="bibr84-15347354241252698" ref-type="bibr">84</xref>
	</sup>
	to assess urinary-free cortisol (UFC) over a 24-hour period and provides an index of
	(unbound serum cortisol) the total amount of cortisol released by the adrenals. The
	24-hour collection time reflects the amount of cortisol that is released over a
	complete circadian cycle, which is a physiologically meaningful unit of time. An
	integrated mean of cortisol levels over a 24-hour period is thought to provide a
	moderately stable measure of adrenocortical output.<sup>
	<xref rid="bibr85-15347354241252698" ref-type="bibr">85</xref>
	</sup>
	Urinary cortisol output will be analyzed by chemiluminescent microparticle immunoassay
	(CMIA) at BP Laboratories, headquartered in Shah Alam, Selangor Darul Ehsan, Malaysia.</p>
	</sec>
	<sec id="section22-15347354241252698">
	<title>Qualitative interview</title>
	<p>Semi-structured interviews will be conducted to inform interpretation of quantitative
	results and participants’ acceptance, experience, and subjective perception of
	the study as well as to find out areas for further improvement<sup>
	<xref rid="bibr86-15347354241252698" ref-type="bibr">86</xref>
	</sup>
	after Week-16.</p>
	<p>A prepared interview guide (<ext-link
	xlink:href="https://journals.sagepub.com/doi/suppl/10.1177/15347354241252698"
	ext-link-type="uri">Supplemental Material 4</ext-link>) is designed to delve into
	participants’ experiences and will be used in the interview to cover 3 primary
	themes: the experiences of practicing GQ, changes in the physical and emotional state,
	and suitability of GQ for cancer survivors. Examples of questions to be asked are
	“How do you feel about the 12 weeks of Guolin Qigong study?,”
	“Have you had other benefits from this Guolin Qigong study?,” and
	“Would you recommend Guolin Qigong to other cancer survivors? Why? Why
	not?.”</p>
	<p>Each interview will take approximately 45 minutes and will be audio-recorded
	and transcribed verbatim by the Researcher.</p>
	</sec>
	</sec>
	</sec>
	<sec id="section23-15347354241252698">
	<title>Protocol Amendments</title>
	<p>The Researcher is responsible for submitting materials to the human ethics committee.</p>
	<sec id="section24-15347354241252698">
	<title>Trial Monitoring</title>
	<p>The Researcher will report progress of the trial to the panel of supervisors on a
	quarterly basis. Annual reports will be submitted to the human ethics committee to
	monitor the trial progress and outcomes. Participants in the GQ group will be advised to
	record any perceived adverse events in the practice diary and this will be recorded in
	participants’ Adverse Event Form by the Researcher. The severity, expectedness
	and causal relationship with GQ intervention will be assessed for every adverse event
	according to guidelines for safety reporting.<sup><xref rid="bibr75-15347354241252698"
	ref-type="bibr">75</xref>,<xref rid="bibr87-15347354241252698" ref-type="bibr">87</xref></sup></p>
	<p>The schedule of the enrollment, intervention, and data collection is shown in <xref
	rid="fig2-15347354241252698" ref-type="fig">Figure 2</xref>.</p>
	</sec>
	<sec id="section25-15347354241252698">
	<title>Sample Size</title>
	<p>Using a small effect size (0.2)<sup>
	<xref rid="bibr65-15347354241252698" ref-type="bibr">65</xref>
	</sup>
	rather than a medium effect size (0.5)<sup>
	<xref rid="bibr64-15347354241252698" ref-type="bibr">64</xref>
	</sup> to
	achieve a more conservative estimation, the sample size is 25 cases in each group with
	90% power and two-sided 5% significance trial design.<sup>
	<xref rid="bibr88-15347354241252698" ref-type="bibr">88</xref>
	</sup>
	Allowing for a drop-out of about 20% based on previous studies,<sup><xref
	rid="bibr89-15347354241252698" ref-type="bibr">89</xref>
	<xref
	rid="bibr90-15347354241252698" ref-type="bibr" /><xref
	rid="bibr91-15347354241252698" ref-type="bibr" />-<xref
	rid="bibr92-15347354241252698" ref-type="bibr">92</xref></sup> a total sample of 60
	(30 in each group) would be required.</p>
	</sec>
	<sec id="section26-15347354241252698">
	<title>Data Collection</title>
	<p>De-identified information will be collected and managed by assigning an identification
	code to each participant. Demographic information, medical history, any occurrence of
	adverse events, practice adherence and intervention outcomes during the study will be
	collected and recorded on paper or electronic file.</p>
	<p>Demographic information and medical history will first be collected by the Researcher.
	De-identified Practice Diary, Brief Fatigue Index, Pittsburgh Sleep Quality Index, and
	Centre for Epidemiologic Studies Depression will be collected at Week-1, Week-6,
	Week-12, and Week-16, while the 24-hour urine cortisol results will be collected by the
	research assistant at Week-1 and Week-12. Interviews will be conducted by the Researcher
	after Week-16, audio-recorded, de-identified, and transcribed verbatim.</p>
	<p>During the study, all data will be recorded in participant source document files in
	paper format (sociodemographic data, feasibility and clinical data), administered by
	independent research assistants and will be transferred to an electronic format for
	storage and analysis. The 2 independent research assistants will verify and check the
	data collected by each other. After all data are confirmed and checked the research
	assistants will extract the data into an Excel sheet for analysis.</p>
	<p>After participants have been randomized, dropout and premature termination or
	withdrawal from the 2 groups at any point will be recorded along with relevant reasons.
	Participants can choose to withdraw and will not be affected at any time while declining
	to participate or withdrawing from the trial. In some cases, participants will
	discontinue the intervention, such as illness, progression of their disease, or
	inability to engage despite adjustment of the program. Participants who withdraw from
	the intervention during the trial will not be replaced.</p>
	<p>Interviews will be conducted after Week-16 in person or online via Zoom by the
	Researcher at an appointed time. Interview sessions will be audio recorded and
	transcribed verbatim using NVivo or the recording feature available in Zoom, ensuring
	accurate documentation, and stored in electronic files for analysis.</p>
	</sec>
	<sec id="section27-15347354241252698">
	<title>Data Management</title>
	<p>De-identified electronic data will be stored on a password-protected computer. Files
	will be accessible for review only to the research team. Specific requests will be
	needed from the supervisory panel for any access by any other person. All completed
	forms and study information will be de-identified and stored in a locked filing cabinet
	together with consent forms at UMMC.</p>
	<p>The information collected will be securely locked and only accessible to the research
	personnel. The data will be de-identified for analysis and once date is coded, all
	identifiable information will be destroyed. All data collected in the study will be
	destroyed 7 years after publication.</p>
	</sec>
	</sec>
	<sec id="section28-15347354241252698">
	<title>Data Analysis</title>
	<sec id="section29-15347354241252698">
	<title>Quantitative Data</title>
	<p>Data analysis will be conducted by an independent statistician. Data analysis will be
	by intention to treat using last observation carried forward (LOCF).<sup>
	<xref rid="bibr93-15347354241252698" ref-type="bibr">93</xref>
	</sup> The
	normality of the study data will be checked by examining the mean, median, skewness, and
	kurtosis including graphical representation of the box plot, normal Q-Q Plot or
	histogram. Continuous data will be summarized using descriptive statistics including the
	number of observations used in the calculation (<italic toggle="yes">n</italic>), mean,
	standard deviation (SD), minimum, median and maximum. Categorical data will be
	summarized as counts and percentages of each category. Between group comparison will be
	conducted using the t test, chi-square test, or Fisher exact test, as
	appropriate. We will report the results for two-sided 5% tests for the primary trial
	outcome. We will use generalized linear mixed model (GLMM). The outcomes of the model
	will be BFI, PSQI, CES-D scores, and 24-hour urine cortisol test results. Models will
	include the treatment group as a fixed effect, with time as a random effect to account
	for the repeated measurements. Analyses will be conducted to identify the baseline
	characteristics of the participants who may benefit most from the intervention. Model
	assumptions will be checked and appropriate adjustments to the analysis will be made
	where necessary. STATA<sup>®</sup> software version 17.1 (2021; Stata Corporation,
	College Station, TX, USA) will be used for all analyses. Cohen’s D will be
	calculated as the absolute differences between the mean change in the variable divided
	by pooled variance of the change.</p>
	</sec>
	<sec id="section30-15347354241252698">
	<title>Qualitative Data</title>
	<p>The researcher will conduct an interview consisting of 6 pre-determined open-ended
	questions (Refer <ext-link
	xlink:href="https://journals.sagepub.com/doi/suppl/10.1177/15347354241252698"
	ext-link-type="uri">Supplemental Material 4</ext-link>) that were identified from
	literature review and based on research questions outlined in the study. Probing
	questions will only be asked where clarification or expansion of expressed ideas is
	required. Interviews will be conducted until data saturation is reached. Interview
	transcripts will be analyzed using the inductive qualitative content analysis approach
	to provide a comprehensive descriptive summary of the interviewee’s experience
	and perception of GQ in everyday terms.<sup>
	<xref rid="bibr94-15347354241252698" ref-type="bibr">94</xref>
	</sup> All
	audio recordings of the interview will be transcribed verbatim with NVivo or Zoom.
	First, to obtain an overall impression, the transcribed materials will be read several
	times thoroughly. Then, sentences or phrases will be condensed and divided into
	ideas/meaning units. The ideas/meaning units are further condensed, abstracted, and
	conceived into the categories. All categories will be put together and compared, based
	on differences and similarities and group together to create themes. This iterative
	approach to analysis will be conducted until no new ideas/codes emerge and saturation is
	achieved. A second reviewer will review each phase of the process. A summary of each
	theme and supporting quotes from participants will be generated and shared with the
	study team to review independently. Data analysis will be repeated in this manner until
	a final consensus is reached on final themes to ensure validity.<sup><xref
	rid="bibr95-15347354241252698" ref-type="bibr">95</xref>,<xref
	rid="bibr96-15347354241252698" ref-type="bibr">96</xref></sup> The Consolidated
	Criteria for Reporting Qualitative Research (COREQ)<sup>
	<xref rid="bibr62-15347354241252698" ref-type="bibr">62</xref>
	</sup> will
	be used for reporting the findings.</p>
	</sec>
	<sec id="section31-15347354241252698">
	<title>Trial Registration and Ethical Issues</title>
	<p>This study has been registered with ANZCTR (ACTRN12622000688785p), was approved by
	Medical Research Ethic Committee of University Malaya Medical Centre (MREC ID NO:
	2022323-11092) and recognized by Western Sydney University Human Research Ethics
	Committee (RH15124).</p>
	</sec>
	<sec id="section32-15347354241252698">
	<title>Dissemination</title>
	<p>The results of this study will be reported in a PhD thesis by the first author and
	submitted for publication following the rules of CONSORT in a peer-reviewed journal or
	presentation using de-identified or non-identifiable information. Sensitive information
	including participants’ details will not be disclosed and will be treated
	strictly under the privacy and confidentiality act of Malaysia and Australia.</p>
	</sec>
	</sec>
	<sec sec-type="discussion" id="section33-15347354241252698">
	<title>Discussion</title>
	<p>CRF is endemic in cancer survivors with disabling effects on quality of life,
	co-morbidities, independent living, and work productivity. It includes physiological
	changes associated with cancer diagnosis and treatment such as cortisol dysregulation,
	sleep disorders, depression, and functional disability, which further contribute to the
	burden of CRF. Despite the high incidence of CRF and its symptom clusters involving sleep
	quality and depression, there is no effective pharmacological intervention to prevent or
	alleviate these symptoms,<sup>
	<xref rid="bibr68-15347354241252698" ref-type="bibr">68</xref>
	</sup>
	highlighting the need to study CRF and its related symptom clusters to understand the
	common biological mechanisms to improve quality of life of cancer survivors. Numerous
	studies have reported certain psychological and physiological benefits of Qigong for
	cancer survivors, promising potential in the realm of cancer medicine. While its
	definitive impact requires further extensive research, some studies suggest benefits such
	as enhanced physical functioning, stress reduction, improved mental health, immune
	enhancement, and improved quality of life, and that it may complement conventional
	medicine as adjunct therapy by providing a holistic approach to cancer care.<sup><xref
	rid="bibr29-15347354241252698" ref-type="bibr">29</xref>,<xref
	rid="bibr33-15347354241252698" ref-type="bibr">33</xref>
	<xref
	rid="bibr34-15347354241252698" ref-type="bibr" /><xref rid="bibr35-15347354241252698"
	ref-type="bibr" /><xref rid="bibr36-15347354241252698" ref-type="bibr" /><xref
	rid="bibr37-15347354241252698" ref-type="bibr" /><xref rid="bibr38-15347354241252698"
	ref-type="bibr" /><xref rid="bibr39-15347354241252698" ref-type="bibr" /><xref
	rid="bibr40-15347354241252698" ref-type="bibr" /><xref rid="bibr41-15347354241252698"
	ref-type="bibr" /><xref rid="bibr42-15347354241252698" ref-type="bibr" /><xref
	rid="bibr43-15347354241252698" ref-type="bibr" />-<xref rid="bibr44-15347354241252698"
	ref-type="bibr">44</xref></sup> As research progresses, understanding its potential
	role in cancer medicine could open doors to more comprehensive and patient-centric
	approaches to healthcare. In this regard, GQ emerges as a unique mind-body exercise that
	combines moderate and adaptive walking exercise with a pronounced focus on a specialized
	breathing technique.<sup>
	<xref rid="bibr97-15347354241252698" ref-type="bibr">97</xref>
	</sup> While
	walking has been reported to improve cancer-related symptoms,<sup><xref
	rid="bibr57-15347354241252698" ref-type="bibr">57</xref>
	<xref
	rid="bibr58-15347354241252698" ref-type="bibr" /><xref rid="bibr59-15347354241252698"
	ref-type="bibr" />-<xref rid="bibr60-15347354241252698" ref-type="bibr">60</xref></sup>
	the incorporation of breathing technique of GQ serves to foster oxygen-carbon dioxide
	homeostasis—an essential factor in cancer control and ultimately survival.<sup><xref
	rid="bibr60-15347354241252698" ref-type="bibr">60</xref>,<xref
	rid="bibr61-15347354241252698" ref-type="bibr">61</xref></sup> As such GQ stands as a
	promising avenue for addressing the cluster of symptoms associated with CRF, encompassing
	sleep disorder, depression, and alterations in cortisol. However, despite this promising
	potential, the comprehensive exploration of GQ’s benefits remains a yet untapped
	opportunity.</p>
	<p>Therefore, our hypothesis posits that the current study of GQ is a feasible intervention
	that holds potential to ameliorate CRF, enhance sleep quality, alleviate depression, and
	regulate cortisol levels among breast, lung, and colon cancer survivors, while
	concurrently unveiling a comprehensive spectrum of benefits and barriers related to
	participation and adherence to GQ training, offering invaluable insights for optimizing
	and enriching the program.</p>
	<p>This is the first mixed-method study comprising a randomized-controlled trial and semi
	structured interview to evaluate the feasibility and benefits of GQ on CRF symptom cluster
	among cancer survivors. The quantitative data from the randomized-controlled trial
	complements the qualitative insights to be obtained through interviews, allowing for a
	comprehensive exploration of the subjective domains of feasibility, adherence, barriers
	and participants’ perceptions, experiences of GQ to help improve healthcare and
	identify factors for enhancing GQ intervention effectiveness.</p>
	<p>Moreover, the composition of this multidisciplinary study team comprising experts from
	Western Medicine and Chinese Medicine integrating their expertise from different
	perspectives will lead to robust study design, enhanced participant care, rigorous data
	analysis and comprehensive interpretation of results.</p>
	</sec>
	<sec id="section34-15347354241252698">
	<title>Limitations</title>
	<p>The nature of the intervention precludes blinding of both participants and researcher.
	While the researcher remains unblinded as this trial is open-label, the instructors will
	not be aware of intervention allocation to minimize bias. Although including cancer
	survivors across all stages enables a diverse assessment of feasibility, it potentially
	limits the generalizability of the results though sub-group analysis will be conducted.
	Furthermore, the reliance on self-reported data for secondary outcomes emphasizes the
	necessity for incorporating objective measures like actigraphy, polysomnography, and
	established scales such as the Hamilton Depression Rating Scale to ensure a comprehensive
	evaluation of GQ’s impact on CRF, sleep quality, and depression. Additionally, the
	predominant participation of Asian Chinese individuals highlights the need for expanded
	research to comprehend GQ’s feasibility and effects among cancer survivors from
	various ethnic and racial backgrounds. These limitations underscore the challenges
	inherent in the study’s design and demographics, emphasizing the importance of
	integrating objective measures and broadening participant diversity for more conclusive
	and inclusive findings.</p>
	<p>Despite the limitations, exploring GQ as a potential intervention to address existing
	gaps in effective treatment for CRF and its related symptom cluster of sleep quality and
	depression in cancer survivors demonstrates a forward-thinking approach in the field of
	oncology. It expands on the knowledge base and promotes innovative thinking, fostering the
	development of novel interventions with potential contribution to the advancement of
	oncology care.</p>
	</sec>
	<sec sec-type="conclusions" id="section35-15347354241252698">
	<title>Conclusion</title>
	<p>The insights gained from this study may guide future design and implementation of
	evidence based mind-body interventions to improve cancer survivorship.</p>
	</sec>
	<sec sec-type="supplementary-material" id="section36-15347354241252698"
	specific-use="figshare">
	<title>Supplemental Material</title>
	<supplementary-material id="suppl1-15347354241252698" position="float"
	content-type="local-data">
	<caption>
	<title>sj-docx-2-ict-10.1177_15347354241252698 – Supplemental material for
	Exploring Guolin Qigong (Mind-Body Exercise) for Improving Cancer Related Fatigue in
	Cancer Survivors: A Mixed Method Randomized Controlled Trial Protocol</title>
	</caption>
	<media xlink:href="sj-docx-2-ict-10.1177_15347354241252698.docx" />
	<p>Supplemental material, sj-docx-2-ict-10.1177_15347354241252698 for Exploring Guolin
	Qigong (Mind-Body Exercise) for Improving Cancer Related Fatigue in Cancer Survivors: A
	Mixed Method Randomized Controlled Trial Protocol by Sara L. K. Low, Gwo Fuang Ho,
	Bingkai Liu, Eng-Siew Koh, Yutong Fei, Chiah Shean Teo and Xiaoshu Zhu in Integrative
	Cancer Therapies</p>
	</supplementary-material>
	<supplementary-material id="suppl2-15347354241252698" position="float"
	content-type="local-data">
	<caption>
	<title>sj-docx-3-ict-10.1177_15347354241252698 – Supplemental material for
	Exploring Guolin Qigong (Mind-Body Exercise) for Improving Cancer Related Fatigue in
	Cancer Survivors: A Mixed Method Randomized Controlled Trial Protocol</title>
	</caption>
	<media xlink:href="sj-docx-3-ict-10.1177_15347354241252698.docx" />
	<p>Supplemental material, sj-docx-3-ict-10.1177_15347354241252698 for Exploring Guolin
	Qigong (Mind-Body Exercise) for Improving Cancer Related Fatigue in Cancer Survivors: A
	Mixed Method Randomized Controlled Trial Protocol by Sara L. K. Low, Gwo Fuang Ho,
	Bingkai Liu, Eng-Siew Koh, Yutong Fei, Chiah Shean Teo and Xiaoshu Zhu in Integrative
	Cancer Therapies</p>
	</supplementary-material>
	<supplementary-material id="suppl3-15347354241252698" position="float"
	content-type="local-data">
	<caption>
	<title>sj-docx-4-ict-10.1177_15347354241252698 – Supplemental material for
	Exploring Guolin Qigong (Mind-Body Exercise) for Improving Cancer Related Fatigue in
	Cancer Survivors: A Mixed Method Randomized Controlled Trial Protocol</title>
	</caption>
	<media xlink:href="sj-docx-4-ict-10.1177_15347354241252698.docx" />
	<p>Supplemental material, sj-docx-4-ict-10.1177_15347354241252698 for Exploring Guolin
	Qigong (Mind-Body Exercise) for Improving Cancer Related Fatigue in Cancer Survivors: A
	Mixed Method Randomized Controlled Trial Protocol by Sara L. K. Low, Gwo Fuang Ho,
	Bingkai Liu, Eng-Siew Koh, Yutong Fei, Chiah Shean Teo and Xiaoshu Zhu in Integrative
	Cancer Therapies</p>
	</supplementary-material>
	<supplementary-material id="suppl4-15347354241252698" position="float"
	content-type="local-data">
	<caption>
	<title>sj-pdf-1-ict-10.1177_15347354241252698 – Supplemental material for
	Exploring Guolin Qigong (Mind-Body Exercise) for Improving Cancer Related Fatigue in
	Cancer Survivors: A Mixed Method Randomized Controlled Trial Protocol</title>
	</caption>
	<media xlink:href="sj-pdf-1-ict-10.1177_15347354241252698.pdf" />
	<p>Supplemental material, sj-pdf-1-ict-10.1177_15347354241252698 for Exploring Guolin
	Qigong (Mind-Body Exercise) for Improving Cancer Related Fatigue in Cancer Survivors: A
	Mixed Method Randomized Controlled Trial Protocol by Sara L. K. Low, Gwo Fuang Ho,
	Bingkai Liu, Eng-Siew Koh, Yutong Fei, Chiah Shean Teo and Xiaoshu Zhu in Integrative
	Cancer Therapies</p>
	</supplementary-material>
	</sec>
	</body>
	<back>
	<ack>
	<p>We thank Cansurvive Centre Malaysia Berhad and Breast Cancer Women Association for their
	invaluable support in promoting the study through their membership base. We also wish to
	express our gratitude to the two Guolin Qigong instructors, Wong Wei Ming of Shah Alam
	Guolin Qigong Paradise, Selangor and Chan Lan Fong of Lake Garden Guolin Qigong, Kuala
	Lumpur for their unwavering passion and dedication in teaching participants throughout the
	duration of the program. Their commitment to the Guolin Qigong classes over most weekends
	exemplifies their exceptional dedication to the research study. We are also immensely
	thankful to the courageous and resilient cancer survivors who generously share their
	personal experiences of their journey to recovery, providing encouragement and hope to the
	study participants.</p>
	</ack>
	<fn-group>
	<fn fn-type="con">
	<p><bold>Author Contributions:</bold> Conceptualization and design: Sara LK Low, Xiaoshu
	Zhu, Gwo Fuang Ho, BingKai Liu, Eng-Siew Koh, and Yutong Fei. Recruitment: Sara LK Low,
	Gwo Fuang Ho, Chiah Shean Teo. Investigating : Sara LK Low. Project Administration: Sara
	LK Low. Supervision: Xiaoshu Zhu, Gwo Fuang Ho, BingKai Liu, Eng-Siew Koh, and Yutong
	Fei. Writing- original draft: Sara LK Low. Writing-review and editing: Sara LK Low, Gwo
	Fuang Ho, BingKai Liu, Eng-Siew Koh, Chiah Shean Teo, Yutong Fei, Xiaoshu Zhu. All
	authors read and approved the final manuscript.</p>
	</fn>
	<fn fn-type="other">
	<p><bold>Availability of Data and Materials:</bold> The datasets used and/or analyzed
	during the current study are available from the corresponding author on reasonable
	request.</p>
	</fn>
	<fn fn-type="other">
	<p><bold>Consent for Publication:</bold> Consent for publication is not required as there
	is no details on individuals reported within the manuscript.</p>
	</fn>
	<fn fn-type="COI-statement">
	<p>The author(s) declared no potential conflicts of interest with respect to the research,
	authorship, and/or publication of this article.</p>
	</fn>
	<fn fn-type="financial-disclosure">
	<p><bold>Funding:</bold> The author(s) disclosed receipt of the following financial
	support for the research, authorship, and/or publication of this article: This paper is
	part of a PhD study and it is supported by the School of Health Science, Western Sydney
	University and Chinese Medicine Centre (an international collaboration between Western
	Sydney University and Beijing University of Chinese Medicine). Professor Xiaoshu Zhu and
	Professor Yutong Fei who are the supervisors of the first author of this manuscript are
	employed as academic by these institutes respectively.</p>
	</fn>
	<fn fn-type="other">
	<p><bold>Trial Status:</bold> Recruitment of participants started on October 2022. The
	trial is currently underway and expected to be completed by end of 2025. The protocol is
	version no.3 dated 16 May 2022.</p>
	</fn>
	<fn fn-type="other">
	<p><bold>Ethics Approval and Consent to Participate:</bold> This study has been approved
	by Medical Research Ethic Committee of University Malaya Medical Centre (MREC ID NO:
	2022323-11092) and recognized by Western Sydney University Human Research Ethics
	Committee (RH15124). All methods will be conducted in accordance with the ethical
	standards of the declaration of Helsinki. Informed consent will be obtained from all
	subjects.</p>
	</fn>
	<fn fn-type="other">
	<p><bold>ORCID iDs:</bold> Sara L. K. Low <inline-graphic
	xlink:href="10.1177_15347354241252698-img1.jpg" />
	<ext-link
	xlink:href="https://orcid.org/0000-0001-6296-6052" ext-link-type="uri">
	https://orcid.org/0000-0001-6296-6052</ext-link></p>
	<p>Chiah Shean Teo <inline-graphic xlink:href="10.1177_15347354241252698-img1.jpg" />
	<ext-link
	xlink:href="https://orcid.org/0000-0003-1071-443X" ext-link-type="uri">
	https://orcid.org/0000-0003-1071-443X</ext-link></p>
	<p>Xiaoshu Zhu <inline-graphic xlink:href="10.1177_15347354241252698-img1.jpg" />
	<ext-link
	xlink:href="https://orcid.org/0000-0002-2909-5926" ext-link-type="uri">
	https://orcid.org/0000-0002-2909-5926</ext-link></p>
	</fn>
	<fn fn-type="supplementary-material">
	<p><bold>Supplemental Material:</bold> Supplemental material for this article is available
	online.</p>
	</fn>
	</fn-group>
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