Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO ® clinical trial

Abstract

Background:

Exercise tolerance is an important endpoint in chronic obstructive pulmonary disease (COPD) clinical trials. Little is known about the comparative measurement properties of constant work rate cycle ergometry (CWRCE) and the endurance shuttle walking test (ESWT). The objective of this sub-analysis of the TORRACTO^® study was to directly compare the endurance measurement properties of CWRCE and ESWT in patients with COPD in a multicentre, multinational setting. We predicted that both tests would be similarly reliable, but that the ESWT would be more responsive to bronchodilation than CWRCE.

Methods:

This analysis included 151 patients who performed CWRCE and ESWT at baseline and week 6 after receiving once-daily placebo, tiotropium/olodaterol (T/O) 2.5/5 μg or T/O 5/5 μg. Reproducibility was assessed by comparing their respective performance at baseline and week 6 in the placebo group. Responsiveness to bronchodilation was assessed by comparing endurance time at week 6 with T/O with baseline values and placebo. The locus of symptom limitation and end-exercise Borg scales for breathing and leg discomfort for both tests were also analysed.

Results:

The intraclass correlation coefficients for CWRCE and ESWT were 0.56 [95% confidence interval (CI) 0.37–0.71] and 0.75 (95% CI 0.63–0.84). More patients were limited by breathing discomfort during the ESWT than during CWRCE, whereas more patients were limited by leg discomfort or breathing/leg discomfort during CWRCE than the ESWT (p <0.0001). Both tests were responsive to bronchodilator treatment: there was a 19% increase in endurance time from baseline at week 6 (p = 0.0006) assessed with CWRCE, and a 20% increase in endurance time assessed with ESWT (p = 0.0013).

Conclusions:

Both exercise tests performed well in a multicentre clinical trial. Although the locus of symptom limitation differed between the two tests, both were reliable and responsive to bronchodilation. For future clinical trials, the choice of test should depend on the study requirements.

ClinicalTrials.gov identifier:

NCT01525615.

The reviews of this paper are available via the supplemental material section.

Keywords

clinical trials COPD pharmacology exercise exercise testing physical activity

Introduction

Evaluating exercise tolerance is considered to be an essential component of disease assessment in chronic obstructive pulmonary disease (COPD).^1,2 Of the available exercise-testing protocols, constant work rate cycle ergometry (CWRCE) and the endurance shuttle walking test (ESWT) are gaining popularity, and are shown to be reliable and responsive to pharmacological and non-pharmacological intervention.^3–5

In a single-centre study, the ESWT was found to be more sensitive to bronchodilation than CWRCE in patients with COPD; differences in the occurrence of quadriceps muscle fatigue were offered by the authors as a potential explanation of the different responsiveness to change between cycling and walking.⁶ However, although several multicentre and multinational bronchodilator studies have been conducted using CWRCE,^7–15 there is currently only limited information for the ESWT in similar settings.^16–18 Furthermore, a direct comparison of ESWT and CWRCE in a multicentre setting is lacking. This knowledge could be important in the planning and design of future multicentre clinical trials assessing the impact of pharmacotherapy on exercise tolerance in COPD.

The TORRACTO^® study evaluated the effect of tiotropium/olodaterol (T/O) compared with placebo on endurance during CWRCE in patients with COPD after 12 weeks of treatment.¹⁹ Endurance during the ESWT was evaluated in a subset of patients.¹⁹ The objective of this analysis was to compare, for the first time, the measurement properties of CWRCE and ESWT in patients with COPD in a multicentre, multinational setting at baseline and after 6 weeks of treatment. Specifically, we compared the test–retest reproducibility and the responsiveness of CWRCE and the ESWT, testing the hypotheses that both tests would be similarly reliable, but that the ESWT would be more responsive to bronchodilation than CWRCE. We also compared the relative intensity of breathing discomfort and leg discomfort, as well as the locus of symptom limitation, during these two exercise testing modalities.

Methods

Study design

TORRACTO^® (1237.15) [ClinicalTrials.gov identifier: NCT01525615] was a multicentre, multinational, randomised, double-blind, placebo-controlled, parallel-group trial to evaluate the effects of once-daily T/O (2.5/5 μg and 5/5 μg) compared with placebo on exercise tolerance after 12 weeks of treatment in patients with COPD (methods detailed in the work by Maltais et al.¹⁹). This secondary analysis of TORRACTO® involved patients in whom both the ESWT and the CWRCE tests were performed. In total, 25 centres participated in the ESWT sub-study (Supplemental Figure S1 and Table S1), and they received ethics approval for both the main study and the ESWT sub-study.

Table 1.

Baseline patient characteristics.

	Placebo (n = 47)	T/O (doses combined) (n = 104)
Male, n (%)	29 (61.7)	73 (70.2)
Mean (SD) age, years	61.1 (6.4)	64.9 (7.4)
Pre-bronchodilator
Mean (SD) FEV₁, l	1.471 (0.434)	1.351 (0.420)
Post-bronchodilator (albuterol)
Mean (SD) FEV₁, l	1.662 (0.419)	1.564 (0.440)
Mean (SD) predicted normal FEV₁, %	60.4 (11.6)	57.0 (13.4)
Mean (SD) FEV₁ change from pre-bronchodilator, l	0.191 (0.155)	0.213 (0.143)
Mean (SD) FEV₁/FVC, %	53.2 (9.8)	50.9 (10.8)
GOLD, n (%)
2	37 (78.7)	74 (71.2)
3	10 (21.3)	27 (26.0)
Mean (SD) body mass index, kg/m²	28.3 (5.2)	27.6 (5.0)
Current smoker, n (%)	22 (46.8)	36 (34.6)
Ex-smoker, n (%)	25 (53.2)	68 (65.4)
Mean (SD) smoking history, pack-years	45.8 (23.4)	50.9 (28.3)

FEV₁, forced expiratory volume in 1 s; FVC, forced vital capacity; GOLD, Global Initiative for Chronic Obstructive Lung Disease; SD, standard deviation; T/O, tiotropium/olodaterol.

Patients

Detailed description of the study population is reported elsewhere.¹⁹ Patients aged 40–75 years with a clinical diagnosis of COPD, a post-bronchodilator forced expiratory volume in 1 s (FEV₁) between ⩾30% and <80% predicted normal and a post-bronchodilator FEV₁/forced vital capacity (FVC) <70% were recruited. Key exclusion criteria were significant disease other than COPD, a history of asthma, myocardial infarction in the previous year, unstable or life-threatening cardiac arrhythmia, or hospitalisation for heart failure within the previous year.

The study was conducted in accordance with the Declaration of Helsinki and the International Conference on Harmonisation Tripartite Guideline for Good Clinical Practice. Before the study started, the protocol was reviewed and approved by the institutional review boards, and all patients were required to provide written informed consent.

Exercise testing

The specific details about exercise testing procedures have been previously reported¹⁹ and are included in the online supplement. Exercise tests were performed at screening and baseline, and 2 h after dosing at weeks 6 and 12. The CWRCE was always performed first, and the ESWT 2–4 days later, because the CWRCE was the study primary endpoint.

During both exercise testing procedures, patients rated the intensity of breathing discomfort and leg discomfort using the modified Borg scale at rest, at 2-min intervals during exercise and at the end of exercise. Immediately after completing exercise, subjects were asked to identify the primary reason for stopping exercise using a standardised questionnaire.²⁰

CWRCE

Patients performed incremental cycle ergometry to symptom limitation to determine peak work rate (Wpeak) at an initial screening visit. During the run-in period, two CWRCE tests to symptom limitation at 75% Wpeak were conducted: the first test was used to familiarise the patient with the exercise protocol, whereas the second test, conducted at least 4 days later, was a priori defined as the pre-treatment baseline. To avoid unduly long exercise tests that could lead to non-physiological exercise limitation (e.g. discomfort or tiredness), patients who cycled for >25 min at either of the two run-in CWRCE tests were not eligible for randomisation.

For CWRCE, subjects performed 1 min of unloaded pedalling before the work rate was immediately increased to 75% Wpeak; subjects were encouraged to cycle to the point of symptom limitation. For all exercise tests, patients were instructed to self-select a comfortable pedalling rate from 50 to 90 revolutions per minute, and then to maintain that self-selected pedalling rate throughout exercise. Exercise endurance time (EET) was recorded as the time from the increase in work rate to the point of symptom limitation.

ESWT

An incremental shuttle walking test (ISWT)²¹ was conducted 2–4 days after the initial screening visit to estimate volume of oxygen (VO₂) peak.

Training and baseline ESWTs were performed at a walking speed corresponding to 85% of estimated VO₂ peak from ISWT.²² Patients with an EET ⩾15 min in the training or baseline ESWT were excluded from further participation in this sub-study. This 15-min limit was set to allow some space for improvement given that the recorded audio signal for the walking pace of the ESWT has a maximum duration of 20 min.

The ESWT was performed in an enclosed corridor on a flat 10 m course. After a 90 s warm-up at a slow pace, walking speed was set at the pace corresponding to 85% of estimated VO₂ peak (see online supplement for more detail). Subjects were instructed to walk for as long as possible at the speed dictated by the auditory signal. The EET, as well as the distance covered in that time, were recorded. The warm-up period was excluded from this analysis.

Statistical analysis

Although the comparison of tests was a secondary objective of the trial, the analyses presented herein are post hoc. Owing to the skewness of baseline endurance time during CWRCE and ESWT,^4,19,23 we transformed the endurance time in seconds to the logarithm to base 10 scale and also present results in the original units (EET in seconds). The reproducibility of the CWRCE and ESWT endurance times was evaluated by comparing values obtained at baseline and week 6 in the placebo group. The presence of a systematic bias and the agreement between the baseline and week 6 exercise tests were assessed using Bland–Altman plots,²⁴ whereas the linear correlation between exercise time during both CWRCEs and ESWTs was evaluated by the Pearson product-moment correlation. The CWRCE and ESWT performance reproducibility was also assessed with determination of the intraclass correlation coefficient (ICC).²⁵ The ability of the two exercise modalities to detect changes (responsiveness) with both doses of T/O versus baseline and placebo at week 6 was examined. Week 6 data are used in this analysis rather than week 12 data to enhance the chances that patients in the placebo group would have relatively stable measurements for the reproducibility analysis.

We compared the locus of symptom limitation between the two tests using a Bhapkar’s test for marginal homogeneity.

As per study design, patients involved in TORRACTO® could have a CWRCE EET up to 25 min and an ESWT EET up to 15 min at baseline. To take this difference in test duration into account, we excluded from the present analysis the small number of patients with a CWRCE EET at baseline between 15 and 25 min (n = 14). At week 6, the duration of the ESWT was limited at 20 min, and there was no limit on CWRCE.

For these analyses, we pooled the two T/O arms (2.5/5 µg and 5/5 µg). This was done to optimise the statistical power of this analysis, and is justified, considering that both doses of T/O improve CWRCE and ESWT EETs to a similar extent.^19,23

Results

Patient disposition and baseline characteristics

From the 165 patients who performed both CWRCE and ESWT in the TORRACTO^® study, 14 were excluded because their CWRCE EET at baseline was ⩾15 min, leaving 151 patients for this analysis (Supplemental Figure S1). Of these, 47 were treated with placebo and 104 with T/O (pooled 2.5/5 µg and 5/5 µg arms). Baseline characteristics were generally balanced across treatment groups (Table 1).

Five patients (all in the T/O groups) reached test termination criteria on the ESWT at week 6 (i.e. EET = 20 min); their EET was thus recorded as 20 min. For comparison, two patients had an EET during CWRCE of ⩾20 min at week 6; for these individuals, the actual EET was used for analysis.

Distribution and comparison of exercise duration for CWRCE and ESWT at baseline and week 6

The distributions of the CWRCE and ESWT endurance times at baseline are presented in Figure 1(a,b). In both cases, the distribution of exercise duration showed a rightward skew toward long exercise duration. A scatter plot of exercise duration during cycling and walking at baseline and at week 6 is provided in Figure 1(c,d). The majority of patients exhibited a longer EET during cycling compared with walking.

Figure 1.

Distribution of CWRCE and ESWT endurance times at baseline, as well as exercise duration of cycling and walking at baseline and at 6 weeks.

Mean endurance time at baseline was 435 s during the CWRCE and 355 s during the ESWT.

Test–retest reproducibility of the CWRCE and ESWT

Mean values for the CWRCE and ESWT times obtained at baseline and week 6 in the placebo group are reported in Table 2. Scatter plots showing baseline and week 6 endurance time values for CWRCE and the ESWT in the placebo group are shown in Figure 2. Strong linear relationships were found for endurance times obtained at baseline and week 6 for both exercise modalities. Pearson correlation coefficients were 0.77 (p <0.0001) and 0.58 (p <0.0001) for walking and cycling, respectively [Figure 2(a,b)]. The reproducibility of ESWT and CWRCE performance was also confirmed with Bland–Altman plots [Figure 2(c,d)]. The variability of endurance time seems to increase over time during both ESWT and CWRCE; mean (SE) endurance time in the T/O arms was 471.49 (28.74) s on day 46 and 472.73 (30.50) s on day 88 during ESWT, and 561.50 (31.16) s on day 43 and 576.69 (36.28) s on day 85 for CWRCE.

Table 2.

Reproducibility: endurance time measured during CWRCE and ESWT at baseline and week 6 in the placebo group.

	Mean (SE) endurance time, s			Pearson correlation coefficient (p value)	Intraclass correlation coefficient (95% CI)
	Baseline	Week 6	Change from baseline	Pearson correlation coefficient (p value)	Intraclass correlation coefficient (95% CI)
CWRCE (n = 46)	468.9 (28.5)	425.2 (25.3)	−43.7 (24.8)	0.58 (<0.0001)	0.56 (0.37–0.71)
ESWT (n = 47)	352.6 (27.7)	375.6 (34.0)	23.0 (21.8)	0.77 (<0.0001)	0.75 (0.63–0.84)

CI, confidence interval; CWRCE, constant work rate cycle ergometry; ESWT, endurance shuttle walking test; s, seconds; SE, standard error of the mean.

Figure 2.

Baseline and week 6 endurance time values in the placebo group for ESWT and CWRCE, as well as Bland–Altman plots showing reproducibility of the ESWT and CWRCE.

The reproducibility of both exercise modalities assessed using ICC was 0.75 for the ESWT and 0.56 for CWRCE (Table 2). Although the ICC for CWRCE was numerically smaller, the difference did not reach statistical significance (there was an overlap in ICC 95% CIs between the tests).

Responsiveness of CWRCE and the ESWT to bronchodilation

The responsiveness of both exercise tests was addressed by pooling the data of the two T/O treatment groups. The arithmetic and geometric mean values for the endurance time at baseline and at week 6 for the two exercise modalities are presented in Table 3. Both tests were responsive to bronchodilator treatment; the improvement from baseline in exercise duration with T/O was similar for the two exercise testing modalities at week 6 (19% for cycling and 20% for walking, based on the geometric mean). There were also improvements with T/O compared with placebo at week 6 (22% for cycling and 17% for walking, based on the geometric means; Table 3).

Table 3.

EET in the tiotropium/olodaterol pooled group at week 6 versus baseline and in the tiotropium/olodaterol pooled group versus placebo group at week 6.

T/O at week 6 versus baseline
	Arithmetic mean					Geometric mean
	EET, s (SE)		Change from baseline			EET, s (SE)		Ratio of EET at week 6 versus baseline
	Baseline	Week 6	Mean	95% CI	p value	Baseline	Week 6	Mean	95% CI	p value
CWRCE (n = 103)	418.6 (18.8)	507.0 (27.0)	88.4	44.0–132.8	0.0001	372.0 (19.0)	441.7 (23.2)	1.187	1.078–1.308	0.0006
ESWT (n = 103)	358.6 (20.2)	457.2 (30.3)	98.6	48.7–148.6	0.0002	305.9 (17.3)	368.3 (24.1)	1.204	1.077–1.346	0.0013
T/O versus placebo at week 6
	Arithmetic mean					Geometric mean
	EET, s (SE)		Change from placebo			EET, s (SE)		Ratio of EET with T/O at week 6 versus placebo
	Placebo	T/O	Mean	95% CI	p value	Placebo	T/O	Mean	95% CI	p value
CWRCE	425.2 (25.3)	507.0 (27.0)	118.3	45.9–190.8	0.0015	390.3 (24.9)	441.7 (23.2)	1.223	1.054–1.420	0.0083
ESWT	375.6 (34.0)	457.2 (30.3)	76.3	−2.8–155.4	0.0585	316.0 (27.4)	368.3 (24.1)	1.165	0.979–1.387	0.0856

CI, confidence interval; CWRCE, constant work rate cycle ergometry; EET, exercise endurance time; ESWT, endurance shuttle walk test; s, seconds; SE, standard error of the mean; T/O, tiotropium/olodaterol.

Locus of symptom limitation

Figure 3 shows the locus of symptom limitation at baseline for all treated patients, that is, whether it was leg discomfort or breathing discomfort, or both, that caused a patient to stop cycling/walking. This differed between the two tests (Bhapkar’s test for marginal homogeneity p <0.0001); a higher proportion of patients were limited by breathing discomfort during the ESWT (57%) than during CWRCE (39%). Moreover, a higher proportion of patients during the CWRCE than during the ESWT were limited by either leg or leg and breathing discomfort.

Figure 3.

Locus of symptom limitation.

Furthermore, the mean (SD) Borg scale for leg discomfort at the end of exercise at baseline was numerically greater with CWRCE [6.54 (2.97)] than with the ESWT [5.23 (3.31)], whereas the Borg scale for breathing discomfort was similar after both tests [6.59 (2.54) for CWRCE; 6.52 (2.56) for the ESWT].

In an analysis of whether there was a difference in response to bronchodilators by the locus of symptom limitation at baseline, the greatest improvement from baseline with T/O in the ESWT was in patients with breathing discomfort at baseline, and there was no significant difference in patients with leg discomfort (Table 4). The same was true in the CWRCE: the greatest improvement from baseline with T/O occurred in patients who were limited by breathing discomfort at baseline, although CWRCE EET also improved significantly with T/O in patients limited by leg fatigue (Table 5).

Table 4.

Improvement in ESWT EET with T/O by baseline locus of symptom limitation.

	Arithmetic mean					Geometric mean
	EET, s (SE)		Change from baseline			EET, s (SE)		Ratio of EET at week 6 versus baseline
	Baseline	Week 6	Mean	95% CI	p value	Baseline	Week 6	Mean	95% CI	p value
Leg discomfort (n = 21)	409.0 (48.2)	394.1 (56.2)	−15.0	−83.7 to 53.8	0.6551	351.9 (44.7)	326.2 (44.4)	0.927	0.762–1.128	0.4300
Breathing discomfort (n = 60)	363.1 (28.0)	526.7 (44.0)	163.6	85.9–241.3	<0.0001	303.0 (24.3)	420.4 (38.0)	1.387	1.178–1.634	0.0002
Leg/breathing discomfort (n = 22)	298.2 (29.2)	328.0 (40.3)	29.8	−17.5 to 77.1	0.2048	274.7 (23.7)	288.0 (31.7)	1.048	0.894–1.229	0.5425

CI, confidence interval; EET, exercise endurance time; ESWT, endurance shuttle walking test; SE, standard error of the mean; T/O, tiotropium/olodaterol.

Table 5.

Improvement in CWRCE EET with T/O by baseline locus of symptom limitation.

	Arithmetic mean					Geometric mean
	EET, s (SE)		Change from baseline			EET, s (SE)		Ratio of EET at week 6 versus baseline
	Baseline	Week 6	Mean	95% CI	p value	Baseline	Week 6	Mean	95% CI	p value
Leg discomfort (n = 27)	432.7 (34.0)	492.6 (40.8)	59.9	0.7–119.0	0.0474	398.3 (32.6)	448.5 (39.5)	1.126	1.007–1.258	0.0376
Breathing discomfort (n = 40)	378.7 (30.4)	515.7 (53.8)	137.0	45.7–228.2	0.0043	324.1 (31.0)	425.4 (42.0)	1.313	1.074–1.604	0.0091
Leg/breathing discomfort (n = 36)	452.3 (32.6)	508.1 (39.5)	55.8	−10.8 to 122.4	0.0978	411.9 (30.7)	455.2 (36.7)	1.105	0.950–1.285	0.1876

CI, confidence interval; CWRCE, constant work rate cycle ergometry; EET, exercise endurance time; SE, standard error of the mean; T/O, tiotropium/olodaterol.

Discussion

The TORRACTO^® study provided an opportunity to directly compare the measurement properties of the ESWT and CWRCE in a multicentre trial. More patients stopped the ESWT due to breathing discomfort than those in CWRCE, although both tests were similarly responsive to bronchodilator treatment. Notably, there were large improvements in walking and cycling duration in individuals in whom breathing discomfort was the primary reason for exercise termination. Overall, both tests were reliable and responsive, and are suitable for use in a multicentre trial setting.

The reproducibility of the CWRCE was lower in our study (ICC = 0.56) compared with previous studies that considered shorter intervals in assessing the reproducibility (ICC = 0.84⁴ and ICC = 0.85²⁶). Reasons for this discrepancy between studies are unclear but a number of factors may have contributed. Implementing exercise testing procedures across several clinical research centres is challenging, and despite efforts to standardise procedures, it is conceivable that variation in EET reproducibility across studies may be related to technical issues associated with the measurements. In the present study, repeated tests were separated by a 6-week period, whereas previous studies looked at variability between two tests with a shorter interval (5 days⁴ and within 2 weeks²⁶). Differences in study population may also contribute to different reproducibility between studies. For example, in TORRACTO®, there was no requirement for resting hyperinflation to be present, whereas in a combined exercise data set of two large clinical trials,⁴ patients had resting hyperinflation. Pre-bronchodilator FEV₁ % predicted in the current study was 52% predicted, compared with 42% and 40% predicted in previous studies. Finally, the previous analysis had a larger sample size (n = 463)⁴ than in the present analysis.

Both CWRCE and the ESWT are constant work-rate tests and are therefore subject to a similar profile of physiological demands. The CWRCE is shown to be responsive and reproducible,^5,26 and has become a standard method for evaluating the efficacy of long-acting bronchodilators in patients with COPD. It allows the measurement of physiological variables using standard cardiopulmonary test equipment. However, CWRCE may not reflect typical daily activity of patients with COPD, so the ESWT^22,27 may have value in this regard. Ambulatory activities such as climbing stairs and walking are affected earlier in the disease progression in patients with COPD.^28,29

The ESWT is increasingly used in COPD studies.^6,17 The ESWT has been shown to be a more sensitive test than CWRCE to assess bronchodilation in a single-centre study in patients with COPD.⁶ In this study, Pepin et al. showed that the ESWT was a sensitive test to detect changes in exercise tolerance after bronchodilation, whereas CWRCE time did not improve significantly after bronchodilation despite a significant increase in FEV₁.⁶ The occurrence and extent of quadriceps muscle fatigue was proposed as a potential explanation for the difference in sensitivity between the ESWT and CWRCE in detecting improvements following bronchodilator therapy, as it was more pronounced and frequent after cycling than after walking.^6,30 Similarly, we found that the greatest improvement from baseline with T/O occurred in patients who were limited by breathlessness with both exercise methodologies. This may have implications for the selection of participants in clinical trials evaluating the impact of bronchodilation on exercise duration. For example, selecting study participants who are primarily limited by dyspnoea would be an ideal experimental set-up to highlight the potential of bronchodilators to enhance exercise endurance.

Considering that the greatest improvement in exercise duration with T/O occurred in patients limited by dyspnoea, and that this symptom was also a more frequent locus of symptom limitation during the ESWT, one would expect this exercise modality to be more responsive than CWRCE but this was not the case in the present clinical trial. This is because, in contrast to what was seen during the ESWT, patients limited by leg fatigue also improved their cycling exercise duration with T/O. The reason for this disparity in exercise response to T/O in those limited by leg fatigue between the two exercise modalities is uncertain but it contributed to the overall similar responsiveness of the two exercise modalities in the present investigation.

A potential weakness of using this study to compare the two exercise tests is that different upper limits were used for the two different tests; we have accounted for this by excluding all patients with EET ⩾15 min at baseline. Unlike a previous comparison of walking and cycling exercise tests,⁶ cardiopulmonary monitoring data are not reported here because it was not done in the ESWTs. The European Respiratory Society recommends that the target duration for endurance time should be between 3 and 8 min; this was not true of the testing protocols used here, but this should be considered in the design of future trials.³¹

Another issue to consider is that there was no predetermined upper limit of exercise duration at week 6 with the CWRCE, but the ESWT was capped at 20 min. In theory, this could have influenced both the reproducibility and responsiveness data for the ESWT. For example, having participants in the placebo group reaching the maximum allowable limit of 20 min at week 6 would tend to decrease the difference between the baseline and week 6 ESWT duration, thus artificially improving the reproducibility data. Only one individual in the placebo group reached the ESWT exercise duration upper limit at week 6. Conversely, fixing an upper limit for the ESWT exercise duration could reduce the magnitude of responsiveness of the test following bronchodilator treatment. In the study, five patients allocated to T/O reached the 20 min ESWT maximum duration after 6 weeks of treatment, and the test was therefore terminated by the investigators. Had we allowed these individuals to continue the walking test, the magnitude of improvement in ESWT seen with T/O would have been larger. Our estimate of the responsiveness of the ESWT is thus conservative.

CWRCE and the ESWT both performed well in the context of a multicentre clinical trial. The locus of symptom limitation differed between the two tests; however, both tests were reliable and responsive to bronchodilation. For future trial design, the choice of test should depend upon the requirements of the study, including the need to collect physiological response data, which can be done more conveniently during stationary cycling.

Supplemental Material

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Supplemental material, Author_Response_1 for Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO® clinical trial by François Maltais, Denis E. O’Donnell, Alan Hamilton, Yihua Zhao and Richard Casaburi in Therapeutic Advances in Respiratory Disease

Supplemental Material

Reviewer_1_v.1 – Supplemental material for Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO® clinical trial

Supplemental material, Reviewer_1_v.1 for Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO® clinical trial by François Maltais, Denis E. O’Donnell, Alan Hamilton, Yihua Zhao and Richard Casaburi in Therapeutic Advances in Respiratory Disease

Supplemental Material

Reviewer_2_v.1 – Supplemental material for Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO® clinical trial

Supplemental material, Reviewer_2_v.1 for Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO® clinical trial by François Maltais, Denis E. O’Donnell, Alan Hamilton, Yihua Zhao and Richard Casaburi in Therapeutic Advances in Respiratory Disease

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Reviewer_2_v.2 – Supplemental material for Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO® clinical trial

Supplemental material, Reviewer_2_v.2 for Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO® clinical trial by François Maltais, Denis E. O’Donnell, Alan Hamilton, Yihua Zhao and Richard Casaburi in Therapeutic Advances in Respiratory Disease

Supplemental Material

Reviewer_3_v.1 – Supplemental material for Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO® clinical trial

Supplemental material, Reviewer_3_v.1 for Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO® clinical trial by François Maltais, Denis E. O’Donnell, Alan Hamilton, Yihua Zhao and Richard Casaburi in Therapeutic Advances in Respiratory Disease

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Supplemental material, Supplement for Comparative measurement properties of constant work rate cycling and the endurance shuttle walking test in COPD: the TORRACTO® clinical trial by François Maltais, Denis E. O’Donnell, Alan Hamilton, Yihua Zhao and Richard Casaburi in Therapeutic Advances in Respiratory Disease

Footnotes

Acknowledgements

The authors meet criteria for authorship as recommended by the International Committee of Medical Journal Editors. They take full responsibility for the scope, direction, content of and editorial decisions relating to the manuscript, were involved at all stages of development and have approved the submitted manuscript. The authors received no compensation related to the development of the manuscript.

Author contribution(s)

François Maltais: Conceptualization; Data curation; Formal analysis; Funding acquisition; Investigation; Methodology; Project administration; Resources; Software; Supervision; Validation; Visualization; Writing-original draft; Writing-review & editing.

Denis E. O’Donnell: Conceptualization; Data curation; Formal analysis; Funding acquisition; Investigation; Methodology; Project administration; Resources; Software; Supervision; Validation; Visualization; Writing-original draft; Writing-review & editing.

Alan Hamilton: Conceptualization; Data curation; Formal analysis; Funding acquisition; Investigation; Methodology; Project administration; Resources; Software; Supervision; Validation; Visualization; Writing-original draft; Writing-review & editing.

Yihua Zhao: Conceptualization; Data curation; Formal analysis; Funding acquisition; Investigation; Methodology; Project administration; Resources; Software; Supervision; Validation; Visualization; Writing-original draft; Writing-review & editing.

Richard Casaburi: Conceptualization; Data curation; Formal analysis; Funding acquisition; Investigation; Methodology; Project administration; Resources; Software; Supervision; Validation; Visualization; Writing-original draft; Writing-review & editing.

Conflict of interest statement

FM has received research grants for participating in multicentre trials for AstraZeneca, Boehringer Ingelheim, GSK, Sanofi, and Novartis, and has received unrestricted research grants and personal fees from Boehringer Ingelheim, Grifols, and Novartis. DEOD reports grants from AstraZeneca and grants from Boehringer Ingelheim during the conduct of the study; and personal fees from AstraZeneca, Boehringer Ingelheim and Novartis outside the submitted work. RC reports grants and personal fees from Boehringer Ingelheim Pharma, AstraZeneca Pharma, GlaxoSmithKline Pharma and Astellas, personal fees from Regeneron Pharma, Genentech Pharma, and Theravance, outside the submitted work. AH and YZ are employees of Boehringer Ingelheim.

Funding

The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: this work was supported by Boehringer Ingelheim Pharma GmbH & Co. KG. Medical writing assistance was provided by Rob Kite of Complete HealthVizion and Claire Scofield of MediTech Media, which was contracted and compensated by Boehringer Ingelheim Pharma GmbH & Co. KG.

ORCID iD

François Maltais

Supplemental material

The reviews of this paper are available via the supplemental material section.

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Supplementary Material

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