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Tai chi mind-body exercise in patients with COPD: study protocol for a randomized controlled trial
Trialsvolume 15, Article number: 337 (2014)
Chronic obstructive pulmonary disease (COPD) is a chronic, progressively debilitating condition that is prevalent in the US and worldwide. Patients suffer from progressive dyspnea and exercise intolerance. Physical exercise is beneficial, but conventional pulmonary rehabilitation programs are underutilized. There remains a need for novel interventions that improve symptoms, quality-of-life, and functional capacity. Tai chi is an increasingly popular mind-body exercise that includes physical exercise, breathing training, mindful awareness, and stress management--components that are essential to the self-management of COPD. There are, however, limited data on the effectiveness of tai chi as a therapeutic intervention in this population.
The Primary Aims are to evaluate the efficacy, safety, and feasibility of a 12-week tai chi program for patients with COPD. We utilize a randomized controlled trial design, with participants assigned in a 2:1 ratio to either a group tai chi program (N = 63) or a time/attention-matched education control (N = 31). Our primary outcomes are COPD-specific quality-of-life and exercise capacity. Secondary outcomes include dyspnea, mood, functional status, self-efficacy, and lung function. Cardiopulmonary exercise testing is done in a subset of patients (N = 50). To explore optimal training duration, a subgroup of patients in tai chi are randomly assigned to complete an additional 12 weeks training (total 24 weeks) (Exploratory Aim 1). To explore the impact of a simplified seated intervention including only a subset of tai chi’s training components, a third randomly assigned group (N = 31) receives a 12- week mind-body breathing program (N = 31) (Exploratory Aim 2).
Results of the BEAM study (Breathing, Education, Awareness, Movement) will provide preliminary evidence regarding the value of tai chi for improving quality of life and exercise capacity in patients with COPD, including information regarding optimal duration. They will also inform the feasibility and potential benefit of an alternative mind-body breathing intervention, and provide insight regarding how isolated mind-body exercise components contribute to the overall effects of tai chi. Should the results be positive, tai chi and related mind-body practices may offer a novel exercise option that is potentially accessible to a large proportion of patients with COPD.
This trial is registered in Clinical Trials.gov, ID number NCT01551953. Date of Registration March 1 2012.
Chronic obstructive pulmonary disease (COPD), a progressive syndrome of airflow limitation , is a major cause of morbidity and mortality. In the US, it is the third most common cause of death, and is the only major disease among the top ten that continues to increase in prevalence . In 2011, almost 13 million adults in the US were diagnosed with COPD, although close to 24 million have impaired lung function, indicating under-diagnosis [3, 4].
Despite advances in pharmacologic and surgical therapy, patients suffer from dyspnea and have substantial limitations in daily activities. Airflow limitation puts the respiratory muscles at a mechanical disadvantage, increasing the work of breathing and worsening exercise tolerance. COPD also has systemic consequences with increased oxidative stress and systemic inflammation, contributing to skeletal muscle dysfunction and atrophy. In addition, persons with COPD are significantly less active than healthy persons  even at the earliest stages of disease [5, 6]. In persons with COPD, decreased physical activity is associated with increased levels of systemic inflammation and increased risk of hospital admissions, acute exacerbations, and death, independent of lung function [7–10].
Moreover, anxiety and depression are prevalent among these patients , which can become additional barriers to participating in exercise and overall self--efficacy. Novel interventions that address complex, biopsychosocial issues of COPD and promote physical activity, could potentially improve symptoms, health-related quality-of-life (HRQL), functional capacity, and modify disease progression [2, 12].
Complementary and integrative forms of exercise, such as tai chi, have gained popularity in the general population to promote health. Tai chi (tai chi chuan or taijiquan), is a multicomponent gentle, mind-body exercise that has its roots in ancient Chinese martial arts. It employs regimens of flowing circular movements that integrate balance, flexibility, strength, and breath training, along with multiple cognitive tools (for example, focused internal awareness, positive imagery) [13, 14]. Tai chi’s role in conventional medical management of chronic disease is poorly understood.
Studies have investigated tai chi exercise for a variety of medical diseases including cardiovascular conditions (for example, coronary artery disease , heart failure [7, 16–18], hypertension [19, 20]), fall prevention and neuromuscular control [21–26], pain and rheumatological conditions [27–29], and cognitive function and psychological wellbeing [30, 31]. These studies support its potential health benefits and safety for chronic health conditions, and show promise as a novel, alternative, low-cost intervention for prevention and rehabilitation [32, 33].
There have been few studies examining tai chi exercise specifically in patients with COPD. Recent meta-analyses suggest potential benefits for multiple outcomes including 6-minute walk distance, measures of dyspnea, spirometric indices, and quality of life. However, the evidence to date is preliminary and inconclusive due to small samples sizes and methodological flaws [34, 35]. Moreover, the majority of these studies have been conducted in Asia, and generalizability of these results to ethnically diverse Western populations is unclear.
This clinical investigation, the BEAM study (Breathing, Education, Awareness, Movement), expands current knowledge of the potential efficacy of tai chi as an intervention for improving quality of life and exercise capacity in patients with COPD. First, this study is a rigorous investigation in a Western population utilizing a novel intervention protocol. Second, it provides an important evaluation of dosage and optimal duration of tai chi. Third, the study preliminarily investigates an alternative, simplified mind-body breathing (MBB) intervention that isolates breathing and meditative subcomponents of the tai chi intervention. Results of this study will both provide information about the relevance of these components in an overall tai chi program and also evaluate MBB as an alternative meditative intervention. Collectively, the BEAM study addresses key gaps in current COPD care by evaluating a potentially safe, modality of physical activity that is enjoyable, easily accessible, may lead to longer-term adherence, and become readily incorporated into COPD self-management plans.
Tai chi components relevant to COPD
Tai chi is a multicomponent intervention that integrates a number of training elements that are relevant to the treatment of patients with COPD [33, 36]. Key elements included in our protocols include 1) physical exercise, 2) respiratory muscle training and breathing techniques, and 3) mindful awareness (Figure 1).
The importance of exercise in the management of patients with COPD has been well studied, although there is ongoing debate regarding the optimal types, intensity, and duration of exercise [37–44]. Conventional exercise programs, both high- and low-intensity (such as walking, cycle ergometer, strength training), have been shown to improve exercise endurance, shortness of breath, and quality of life, even in patients with severe disease and poor exercise tolerance . Most studies support that exercise leads to skeletal muscle adaptation, allowing more work to be performed.
Exercise may also desensitize patients to dyspnea. In addition, studies have suggested that unsupported upper extremity exercise (for example, against gravity) may offer additional benefits and effectively train patients in activities that mimic or are more similar to those required in daily living [39, 46, 47]. Although conventional pulmonary rehabilitation programs have been shown to be beneficial, only a small percentage of patients eligible for such programs actually participate and maintenance of physical activity is an ongoing challenge . Alternative exercise options that are easily implemented, and that promote long-term adherence and self-efficacy, are much needed.
Tai chi provides mild aerobic activity, core strength training, and lower extremity and unsupported upper extremity training. The physical activity of tai chi is estimated to be mild-moderate aerobic exercise, at 1.6 to 4.6 metabolic equivalents (METs) and 50 to 74% maximal heart rate, depending on the age of the individual and the intensity of practice [49, 50]. Previous literature suggests that it is safe in patients with chronic disease, including COPD, chronic heart failure, coronary artery disease (recovering from bypass surgery and myocardial infarction), as well as frailty, arthritis, and vestibular disease [51–53]. Studies also suggest that tai chi is accessible, enjoyable and has high rates of adherence; multiple comparative effectiveness studies have reported higher adherence to tai chi than the comparison group or exercise. Tai chi may provide a suitable range of exercise for those initiating physical activity or those transitioning to higher levels of activity, or as an adjunct to other forms of conventional activity.
Respiratory muscle training and breathing techniques
In COPD, respiratory muscle weakness and inefficiency contributes to breathlessness, and exercise impairment. Respiratory muscle training selectively works the inspiratory muscles to perform against loads, thereby increasing strength, endurance, and efficiency. Studies in patients with various respiratory disease, including COPD, have reported improvements in inspiratory muscle function (maximal inspiratory pressure), exercise performance (walk distance), and dyspnea related to daily activities [54–56].
Similarly, breathing retraining in COPD aims to teach patients to breathe more efficiently, replacing rapid shallow breathing patterns that may worsen gas exchange with slower breathing patterns that improve chest wall mechanics, allow more complete expiration, and decrease air trapping. Conventional breathing retraining, such as diaphragmatic and pursed-lip breathing, may improve symptoms, increase tidal volume and total ventilation, decrease respiratory rate, and improve gas exchange [57–59]. In addition, slow, deep breathing can also have beneficial effects on the autonomic nervous system which is increasingly recognized as highly relevant in COPD . Studies in COPD patients have suggested changes in sympathetic/parasympathetic balance in indices such as heart rate variability .
Efficient, intentional and mindful breathing is a key element of tai chi. The interventions employed in the BEAM study include elements of respiratory muscle and breathing retraining that similarly aim to increase muscle strength and endurance, decrease mechanical loads such as chest wall stiffness, and deepen and slow the respiratory rate, thereby increasing gas exchange efficiency. The MBB is taught and integrated within a broader context of relaxation, focused self-awareness, and imagery (see below), which may easily be adopted by patients and facilitate translation into usual breathing patterns during activities of daily life.
A fundamental component of tai chi is the deliberate attention to bodily sensation, movement, breath, and emotion, which fosters acute self-awareness, both physically and emotionally. Participants learn, for example, to discriminate areas with or without strain or tension, stronger or weaker regions, movements that feel graceful or fearful, or aspects of breathing that feel labored or unconstrained. This awareness may in turn complement other tai chi components that foster improved function (for example, improved posture, relaxation). Recent studies support that mindfulness training can impact interoceptive awareness of key COPD symptoms (such as dyspnea and cough) which may lead to better symptom management [62–64]. Inner awareness of moment-to-moment sensations also helps develop focused attention, providing a tool to manage distracting thoughts .
We hypothesize that increased awareness of postures and breathing, and the psychophysiology of when dyspnea starts, will allow participants to better anticipate and manage their symptoms, decreasing the risk of worsening dyspnea and precipitating further breathing difficulty and anxiety. This heightened mindfulness and self-awareness of breathing, body shape, and emotion may be important in facilitating change in pulmonary patients who have developed maladaptive physical and psychological patterns due to chronic dyspnea over time, and lead to better symptom management . In addition, it is increasingly recognized that patients with COPD are at high risk of developing symptoms of anxiety and depression . Anxiety over dyspnea-producing activities is common and may promote maladaptive sedentary lifestyles . Collectively, the mind-body approach of tai chi inherently addresses stress management which is an important component of COPD self-management.
The BEAM study is a pilot randomized controlled trial investigating tai chi exercise and MBB as an adjunct to standard care in patients with COPD. We will enroll a total of 125 participants, with participants randomized in a 2:1 ratio to either a 12-week tai chi program (n = 63) or a time- and attention-matched education control (n = 31).
The primary aims of this study are to evaluate the 1) efficacy and 2) safety and feasibility of a 12-week tai chi mind-body exercise for patients with COPD. To explore optimal training durations of tai chi, a subgroup of patients assigned to the tai chi program are randomly assigned to complete an additional 12 weeks of training (total 24 weeks) (Exploratory Aim 1). Additionally, to explore the impact of an alternative simplified seated intervention that includes a subset of tai chi training components, a third randomly assigned group (n = 31) receives a 12-week MBB program (n = 31) (Exploratory Aim 2) (Figure 2).
Our primary efficacy outcomes are COPD-specific quality-of-life (chronic respiratory questionnaire (CRQ)) and exercise capacity (6-minute-walk test). Secondary outcomes examining further psychosocial and physiological effects of tai chi include symptoms of dyspnea, fatigue, mood, functional status, strength and flexibility, self-efficacy, social support, and pulmonary function. Cardiopulmonary exercise testing is also done in a subset of patients (n = 50). Safety and feasibility will be assessed by successful recruitment and randomization, adherence to the protocol and attendance at classes (at least 70%), and demonstrated safety through systematic adverse events (AE) monitoring and reporting.
We hypothesize that there will be improved patient-centered outcomes (quality of life and exercise capacity) in the tai chi group as compared to education control and that the study will be feasible and safe in COPD. Those who receive continued tai chi in phase 2 will have increased 24-week adherence and improved outcomes. There may be similar benefit in the MBB group in symptoms of dyspnea and psychosocial measures, but the tai chi intervention will have trends towards more benefit on exercise capacity, cardiopulmonary function, strength, and flexibility.
Participants are being identified from the primary care and pulmonary clinics at two primary institutions: Beth Israel Deaconess Medical Center (BIDMC) and VA Boston Healthcare System. Additional recruitment sites include the pulmonary clinics at Brigham and Women’s Hospital and Boston Medical Center. Recruitment strategies include direct referral from physicians, and identification of eligible patients through hospital databases, and mailings. All recruitment and data collection procedures follow the Health Information Privacy and Accountability Act (HIPAA) guidelines to maintain patient confidentiality, and study procedures have been approved by each institution’s investigational review board. A list of the institutions and ethical boards providing approval is provided in Additional file 1.
Participants are eligible for the study if they: 1) have moderate-severe COPD as defined by global obstructive lung disease (GOLD) stage 2, 3, or 4, with symptoms of dyspnea (either forced expiratory volume in one second (FEV1) ≤80% and FEV1/forced vital capacity (FEV1/FVC) <0.70, or evidence of emphysema on computed tomography (CT); and 2) are aged ≥40 years.
Exclusion criteria are: 1) respiratory failure or GOLD stage 4 and inability to safely perform a 6-minute walk test or otherwise exercise safely as deemed by a physician; 2) COPD exacerbation requiring steroids, antibiotics, an emergency room (ER) visit or hospitalization within the past 2 weeks unless the physician deems the subject to be at clinical baseline; 3) planned thoracic surgery within the next 3 months; 4) hypoxemia on the walk test or cardiopulmonary exercise test (oxygen saturation <88% on supplemental oxygen); 5) inability to ambulate due to vascular or other neuromuscular conditions that would preclude a walk test; 6) clinical signs of unstable cardiovascular disease (that is, chest pain on the walk test or electrocardiogram changes on the cardiopulmonary exercise test); 7) severe cognitive dysfunction (mini-mental status exam score ≤24); 8) non-English speaking; 9) current active participation in a pulmonary rehabilitation program or current regular practice of tai chi; and 10) physician diagnosis of unstable/untreated clinical depression.
Written informed consent is obtained by the research assistant at the initial visit. Patients are asked to participate in a study examining three types of intervention involving exercise and/or education. In order to assess credibility of the three groups and clinical equipoise from the patient’s perspective, we employ an expectancy and treatment credibility assessment from Borkovec and Nau. This instrument provides a measure of how credible patients perceive a treatment to be, and has been used in prior trials to assess blinding .
Randomization and allocation concealment
Randomization occurs after baseline testing. Participants are randomized to one of three group classes: tai chi, MBB, or education, in a 2:1:1 ratio. Group assignments are generated by a permuted blocks method with randomly varying block size, and sealed in numbered, opaque envelopes. Intervention classes begin within 3 weeks of baseline testing. At the end of phase 1, participants in the tai chi group undergo a second randomization to either continue tai chi class once weekly, or to resume usual care. Participants are informed at baseline of the two randomization processes and that the intervention may be either 3 or 6 months long.
Tai chi, MBB, and education classes are conducted twice weekly for one hour each for the first 12 weeks. In the second 12 weeks of the study, participants in the tai chi class may be assigned to continue tai chi classes once weekly for an additional 12 weeks. Instructors who administer the tai chi and MBB interventions are senior tai chi students and certified graduates of a 2.5-year instructor training program that includes training in meditative breathing. The average training experience of the four study instructors is 19 years.
Importantly, the tai chi instructors also administer the education class to minimize the variability with respect to instructor type, personality, and training. Chairs are provided for seated warm-up, breathing exercises and resting, as well as for stability as needed when performing standing tai chi exercises. Subjects in tai chi and MBB groups receive a 45-minute video as well as a separate audio file of the exercises taught in class, and are given detailed instruction about specific exercises, and encouraged to practice outside of class three times a week (for at least 30 minutes).
Tai chi intervention
The 12-week tai chi intervention has been specifically designed for an older, physically limited population with COPD. In brief, this protocol was modified from a similar intervention that was developed in prior studies investigating tai chi for chronic heart failure [7, 68] and in a pilot study of COPD patients .
We convened an expert panel with representation from pulmonary medicine, exercise physiology, mind-body medicine, tai chi, and clinical trial methodology. We refined the intervention protocol using an iterative modified Delphi process (details to be reported elsewhere). In comparison to our intervention for persons with heart failure, the current tai chi protocol further emphasized the integration of multiple mindful breathing techniques as well as the addition of two warm-up exercises to improve awareness and flexibility of the spine, rib cage and upper torso.
The intervention emphasizes essential tai chi movements that are both easily comprehensible and can be done repetitively in a flowing manner. The five tai chi movements - ‘raising the power’ , ‘withdraw and push’ , ‘grasp the sparrow’s tail’ , ‘brush knee twist step’ , and ‘cloud hands’ - are based on the traditional Cheng Man-Ch’ing’s Yang-style short form . In addition to these five core movements, the intervention includes a complementary set of traditional tai chi warm-up exercises, including specific MBB techniques. These warm-ups focus on loosening the physical body, providing moderate aerobic activity, incorporating mindfulness and imagery into movement, promoting overall relaxation of body and mind, and generating awareness and efficiency of breathing.
The MBB techniques included within the tai chi protocol are described below. All components of the MBB intervention are included in the tai chi intervention. Within the tai chi protocol, breathing components are taught both in a seated position as in the MBB class, but also integrated into moving tai chi and warm-up exercises. We conclude each session with a brief cool-down exercise of seated self-massage of the face, abdomen, flanks, and mid-back.
The content of this class is based on information from the American Thoracic Society, American College Chest Physicians, and the Global Obstructive Lung Disease Patient Guide[69–74]. Educational modules include: anatomy of the lungs, COPD, managing COPD symptoms, smoking cessation, diagnostic tests, understanding COPD meds, managing acute exacerbations, managing stress, exercise, nutrition, sleep, mental health, oxygen therapy, surgical options, pulmonary rehabilitation, and advance care planning. Time is spent with both didactic as well as informal group discussion moderated by the instructor. The instructors have explicit instructions to moderate discussions and not make any recommendations regarding an individual’s treatment.
The MBB intervention is comprised of the breathing techniques of the tai chi exercise program; however, all techniques are performed in a seated position. This intervention removes some elements of physical activity (no aerobic activity, no lower extremity strengthening and stretching, less core strengthening), while retaining breathing and mindful awareness.
The overall goals of the breathing intervention are to increase the efficiency of gas exchange, enhance awareness/mindfulness of the mechanics of breathing, and promote relaxation of both physical body and mind. Four traditional inter-related techniques are taught; detailed descriptions of these can be found in traditional and modern tai chi and qigong publications [75–78]. 1) renewing the body with breath is a simple relaxation technique that employs the breath and imagery as a focusing tool to release physical and emotional tensions; 2) mindful breathing cultivates inner awareness of the breath as air and its consequent internal pneumatic and hydraulic pressures travel from the nostrils to the lower abdomen, and back out; 3) ocean breathing emphasizes diaphragmatic breathing and expansion and contraction of the lower abdomen; and 4) balloon breathing emphasizes effortless inhalations and a prolonged exhalation cycle relative to inhalation.
Each of the techniques was chosen to emphasize different aspects of MBB relevant to COPD rehabilitation. The expectation is that over time these methods will become integrated into usual breathing patterns during daily activities. Subjects in class are explicitly taught to incorporate the techniques into simple activities of daily living (for example, while reading or talking on the phone). The protocol also begins with the same series of seated warm-up exercises that are employed in the tai chi intervention that particularly target awareness and flexibility of the upper torso and rib cage. Subjects who complete all study requirements have the option of joining a class of their choice (one of the two groups to which they were not randomized). These subjects do not undergo additional testing but are monitored for AEs.
All research staff performing outcome testing are blinded to participants’ intervention allocations. Table 1 details the schedule of evaluations.
Six-minute walk test
This is a standardized assessment that measures the maximum distance walked in 6 minutes . Subjects are read standardized, scripted instructions and informed when there are 3 minutes and 1 minute before the end of the test. Subjects are allowed to stop as often as they need and to use supplemental oxygen if usually prescribed for activity. The 6-minute walk test has been shown to be an independent correlate of COPD prognosis and survival [80, 81].
Disease-specific HRQL measure
The main HRQL measure is the disease-specific chronic respiratory disease questionnaire (CRQ). This validated instrument is one of the most commonly employed health status measures for COPD. It consists of 20 items covering four domains - dyspnea, fatigue, emotional function and mastery. Items are scaled on a 7-point modified Likert scale, with higher scores indicating better HRQL . We use the self-administered, standardized version. Our main outcome is a total CRQ score calculated by the sum of individual responses divided by the number answered (mean response).
Cardiopulmonary exercise test
In a random subset (n = 50 total), participants perform a symptom-limited exercise test using a bicycle ramp protocol to determine peak oxygen uptake (VO2) and exercise endurance. Testing is done on an electronically calibrated upright bicycle, with expired gas analysis under continuous electrocardiographic monitoring. Breathlessness and leg fatigue are measured using the Borg scale of 1 to 10 during the test. Breath-by-breath respiratory gas analysis is performed using a SensorMedics (Yorba Linda, CA, USA) metabolic cart. Peak values are averaged from the final 20 seconds of the test. Peak VO2 has been shown to correlate with cardiac output and skeletal muscle blood flow and predict mortality in COPD .
Strength and flexibility
The chair stand test assesses lower body strength and endurance. Subjects are instructed to rise to a full standing position and then return to a seated position with arms folded across their bodies as many times as possible within 30 seconds. This validated test has been used in numerous populations with age and gender specific normative data available . The chair sit and reach assesses lower body flexibility, primarily the hamstring, and is a modification of the original sit and reach, developed for use in older or deconditioned populations to decrease risk of injury in those with back pain or limited range of motion .
The University of California, San Diego (UCSD) shortness of breath questionnaire is a 24-item self-administered instrument that assesses the degree to which patients feel short of breath while performing 21 different activities of daily living. Respondents rate symptoms on a 6-point scale from not at all to maximally or unable to do because of breathlessness . The Modified Medical Research Council (MMRC) dyspnea scale is a 4-point scale assessing dyspnea severity, with a score of 4 indicating that the patient is too breathless to leave the house or becomes breathless when dressing or undressing. This scale predicts the likelihood of survival among patients with COPD and correlates well with other scales and health status scores . This scale is one of the four components of the body mass: airflow obstruction: dyspnea: exercise capacity (BODE) index, a validated multidimensional grading system for COPD that has been shown to be a better predictor of mortality than FEV1 alone .
The COPD self-efficacy scale (CSES) was developed to identify situations during which patients with COPD lack confidence in their ability to manage or to avoid breathing difficulties. The situations include times of negative affect (when I feel down or depressed), intense emotions, physical exertion, at-risk behaviors (when I overeat), or adverse weather/environmental conditions. Patients rate the level of confidence they feel, ranging from not confident at all to very confident, in managing or avoiding breathing difficulties during 24 different situations. The CSES has high internal consistency (r = 0.95) and test-retest reliability (r = 0.77) .
The Center of Epidemiology Studies-depression scale (CES-D) is a general measure of psychological impairment, primarily depressive symptoms, that has been used extensively in epidemiology studies . It is a validated instrument consisting of 20 items, including feelings of depression, worthlessness, loneliness, energy level and fear. Participants are asked to report how often they experienced the symptom during the past week using a 4-point ordinal scale (rarely or none of the time; some or little of the time (1 to 2 days); occasionally or moderate amount of the time (3 to 4 days); most or all of the time (5 to 7 days). A score <15 indicates no depression. The CES-D has high internal consistency (r = 0.90) and a test-retest reliability of 0.51 [91, 92].
Physical function and fatigue
We use the PROMIS Physical Function-Short Form 10a questionnaire to track patients’ physical functioning, and the PROMIS Fatigue Short Form 7a to track patients’ fatigue. The Patient-Reported Outcome Measurement Information System (PROMIS®) instruments funded by the National Institutes of Health are based on modern measurement theory and include the application of mixed methods approaches for instrument development. Both forms are short validated instrument with seven to ten items, each with five response options on an ordinal scale (not at all, a little bit, somewhat, quite a bit, very much) [93, 94].
Perceived stress and social support
The perceived stress scale is a measure of the degree to which situations in one's life are appraised as stressful. We will use the 10-item version of this instrument which we have used in our prior tai chi trials and which has been shown to have good reliability and validity . The multidimensional scale of perceived social support is a validated instrument that will be used to assess the degree of perceived social support provided in each group. It consists of 12 items covering subscale areas of family, friends, and significant others .
Pulmonary function tests
Spirometry and lung volume measurements will be performed using rolling-seal volume displacement spirometers (Collins CPL Raptor, Louisville, CO, USA), following American Thoracic Society standards for quality and reproducibility . Lung volumes are performed via plethysmography. Lung volumes, such as total lung capacity (TLC) and functional residual capacity, add information about hyperinflation from COPD that may negatively affect respiratory muscle function. The inspiratory-to-total lung capacity ratio (IC/TLC) may be a particularly useful index of resting airflow limitation and lung hyperinflation that correlates with exercise capacity .
Other data collection
To track participants’ level of physical activity outside of exercise classes, we use the Community Health Activities Model Program for Seniors (CHAMPS) physical activity questionnaire for older adults . CHAMPS is a 41-item validated instrument in the elderly, which covers physical activity from several domains, including leisure, household, and occupational. Weekly frequency and total time spent allows estimation of caloric expenditure. In addition, we use the Moy physical activity checklist specifically to measure activity in patients with COPD . A higher number of daily checklist activities performed is associated with better indices of COPD health, including higher FEV1 and lower BODE index.
We also perform semi-structured qualitative exit interviews with participants in all groups to further explore areas not captured in our standardized quantitative instruments. Questions probe participants’ experiences with the program overall; changes in physical, mental, or social function specific to the intervention; changes in illness perception; experiences with practicing the intervention; and expectations and beliefs about mind-body therapies. These open-ended questions may yield additional insights into understanding the mechanism of a mind-body exercise program. Each interview session is audio recorded, then transcribed verbatim.
Adherence is defined as greater or equal to 70% of intervention classes attended. During phase 1 in the first 12 weeks, compliance with home practice in the tai chi and MBB arms is tracked through home practice logs that are completed at each class. During phase 2 in the second 12 weeks, those not randomized to continued classes are queried about home practice once a month by phone.
Safety and adverse event monitoring
Interview data are used to document patients’ use of health care during the study period. Medical record review is conducted for details of hospitalizations for AE reporting. At each testing visit at baseline, 12 and 24 weeks, we ask specifically about medical symptoms in the past 12 weeks such as muscle strain, fainting/loss of consciousness, dizziness, worsening shortness of breath or COPD exacerbation, worsening fatigue, falls, palpitations, psychological stress, or other AEs. For any symptom ascertained, we further document the patient’s perception of relatedness to the intervention or testing, severity, any required change in medications, and any further medical care, hospitalization or ER visit. For hospitalizations and ER visits, we further ascertain discharge diagnosis and results of major cardiopulmonary tests or procedures performed. During the intervention, occurrences of adverse events are also queried by instructors and captured in the attendance log, which subjects complete during each class. If a potential AE is reported, study staff contact the participant for further details to determine if a reportable AE has occurred and if so, document the type, whether expected or not, relatedness to the study, and severity. Serious AEs are defined according to our institutional review board’s policy to be an event that is life-threatening, requires hospitalization, results in persistent or significant disability/incapacity or death. Incidents are reported to the IRB, our sponsor, and our Data Safety and Monitoring Board (DSMB) as appropriate.
Sample size and power
This study is powered on our pre-specified primary outcomes of overall CRQ (chronic respiratory questionnaire) score and 6-minute walk-test distance. Our effect estimates and standard deviations are based on pilot data of 12-weeks of tai chi versus usual care in patients with COPD . Enrollment of 125 participants will provide approximately 93% power to detect differences between groups of approximately 50 meters change in the 6-minute walk test and 0.9 point change in total CRQ score (mean response value). Our primary comparison will be between the tai chi and education groups, from baseline to 12 weeks in phase 1. It is widely accepted that a change in the 6-minute walk test of 54 meters is clinically significant [81, 101–104]. For the CRQ, Redelmeir et al. reported that a 0.5 point change is clinically meaningful . Our study has over 96% power to detect a difference of 54 meters and 99% power to detect a difference of 68 meters (the difference observed in our pilot). These calculations allow for a 5% loss of statistical efficiency of the nonparametric test compared to a t-test (for the 6-minute walk), 10% dropout rate, and a conservative Bonferroni correction for multiple outcomes.
For our exploratory dosage aim, we expect to have about 82% power to detect differences between groups of a 50-meter change in 6-minute walk and 0.9 point change in total CRQ. This sample size of 21 per group (12 weeks versus 24 weeks of tai chi) accounts for a 5% loss of statistical efficiency. We expect to have limited power for our second exploratory aim comparing tai chi to the MBB group.
Prior to analyzing the outcomes, we will examine baseline demographic, functional, and clinical variables as well as known prognostic factors (such as baseline GOLD stage and baseline peak VO2) by randomized group. Our primary analyses will examine changes between baseline and 12 weeks.
Changes in total scores on the CRQ will be analyzed using analysis of covariance (ANCOVA), comparing the change from baseline to 12 weeks among the two treatment groups tai chi versus education, adjusted for the baseline value of the outcome (and, if necessary, baseline characteristics found poorly balanced between groups). For the 6-minute walk, the change from baseline to 12 weeks is known to be skewed, so we will use a nonparametric approach and use a Wilcoxon rank sum test to compare the two treatment groups at α = 0.05 (without the Bonferroni correction, given the pilot feasibility nature of the study). As complements to these main approaches, we may use bootstrap analysis to evaluate confidence intervals and the cumulative distribution function with evaluation of the area under the curve for each study arm to show the distribution of patients who improve.
Study feasibility will be established if we can report that a reasonable proportion of eligible patients are willing to participate (>10%), that we can recruit participants at a reasonable rate (approximately 5 patients per month), and that patients once enrolled will adhere to our study protocol (with at least 70% attendance). Safety will be evaluated through descriptive statistics of AEs and frequencies will be reported per type according to grade and severity per arm. The intervention will be considered safe if there are no serious AEs related to the intervention.
The basic analytic approach for secondary efficacy measures will be parallel to the approach for the primary measures, comparing change in outcome from baseline to 12 weeks among the two treatment groups. However, for these secondary measures, we do not anticipate using an adjustment for multiple outcomes. As secondary analyses, we also plan to analyze the change in each of the four CRQ subdomains (dyspnea, fatigue, emotion, mastery) using the same methods.
In addition, we will use linear regression models using primary study outcomes (change in 6-minute walk and CRQ score) as dependent variables and scores on psychosocial assessments and functional tests as potential mediators to examine whether clinical outcome is associated with these psychosocial or physiological parameters. Separate exploratory models will be developed for each primary outcome, providing insight into potential mechanisms of effect.
Qualitative exit interviews will be professionally transcribed from audio recordings and coded using an inductive approach informed by grounded theory methods. We will identify passages in the transcripts that represent common themes or content categories relating to positive, negative, and neutral aspects of patients’ experiences with tai chi, MBB, and education control. Data will be analyzed and presented descriptively according to content categories (as above) [105–108]. We will also examine a per-protocol analysis of our primary outcomes for aim 1, where non-adherers will be excluded (secondary analysis). Non-adherence will be defined as attendance at less than 70% of classes.
Exploratory aim 1 (dosage)
With respect to examining dosage of tai chi, we will compare the change in all outcomes between the two tai chi groups (12-week versus extended 24-week intervention) using ANCOVA and the Wilcoxon rank sum test as appropriate, similar to our primary aims. We will further assess adherence to the continued classes from 12 to 24 weeks. We will also analyze home practice hours (in both groups), and total practice hours (class plus home practice in the 24-week class group) and compare groups using the Wilcoxon rank sum test. Clinical data obtained through patient interview will be analyzed using descriptive statistics.
Particularly in the intervention groups, we will describe patient attendance at classes and compliance with home practice, and examine whether compliance or dosage is associated with clinical outcome.
Exploratory aim 2 (MBB)
We will obtain the point estimates for the change in outcomes, that is, mean change in CRQ and median change in the 6-minute walk between baseline and 12 weeks in the MBB group. We expect these means/medians to be intermediate between changes in the tai chi group and changes in the education group. Even though we are not powered to detect differences between groups, we will conduct exploratory analyses to gather preliminary estimates of effect. We will use ANCOVA and Wilcoxon rank sum tests, similar to the first aim, to compare change in the CRQ and the 6-minute walk, between the MBB group and education, and between the MBB group and tai chi. We will establish overall feasibility and adherence of the MBB group by assessing willingness to participate and attendance at classes.
Results of this innovative study will establish feasibility and provide preliminary evidence on the efficacy of tai chi exercise to improve quality of life and exercise capacity in patients with COPD. In addition, we will capture information on potential physiological and psychosocial mechanistic pathways. The development and exploration of a seated intervention that emphasizes meditative breathing provides further insight into mechanisms of tai chi by isolating relevant elements of the larger, multicomponent intervention. Finally, the extension of intervention duration from 12 to 24 weeks will help to inform issues of optimal dosage for this population.
This study is currently ongoing with active recruitment.
analysis of covariance
breathing: education: awareness: movement
Beth Israel Deaconess Medical Center
body mass: airflow obstruction: dyspnea: exercise capacity
Center of Epidemiology Studies-depression scale
Community Health Activities Model Program for Seniors physical activity questionnaire for older adults
chronic obstructive pulmonary disease
chronic respiratory disease questionnaire
chronic obstructive pulmonary disease self-efficacy scale
Data Safety and Monitoring Board
forced expiratory volume in one second/forced vital capacity
global Obstructive Lung Disease
Health Information Privacy and Accountability Act
inspiratory-to-total lung capacity ratio
Institutional Review Board
Modified Medical Research Council
Patient-Reported Outcome Measurement Information System
total lung capacity
peak oxygen uptake.
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We would like to thank Amy Brown, Elizabeth Kacel, Caroline Chan, Cecilia Griggs, Danielle Berkowitz, Morgann Young, Danielle Mullin, Diana Homsy, Ana Kantorowski, and Merilee Teylan for their assistance in implementing this study. This study was supported by an award from the National Center for Complementary and Alternative Medicine (NCCAM) at the National Institutes of Health (NIH) (R01AT005436). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NCCAM or the NIH.
Peter Wayne is the founder and sole owner of the Tree of Life Tai Chi Center. Peter Wayne’s interests were reviewed and are managed by the Brigham and Women’s Hospital and Partners HealthCare in accordance with their conflict of interest policy.
GY conceived of the study, led in its design and coordination and drafted the manuscript. PW participated in study design and coordination and assisted in drafting the manuscript. DL participated in study coordination and assisted in editing the manuscript. DR participated in the design of the study and assisted in coordination. RD participated in design of the study and development of the statistical analysis plan. MM participated in design and coordination of the study and assisted in drafting the manuscript. All authors read and approved the final manuscript.