Article

Comparative Analysis of Functional Capacity Improvements Through 6MWD Testing Across Different Respiratory Conditions: Implications for Targeted Pulmonary Rehabilitation

Sneha Chacko1★, Gaurang Shah1★ Corresponding author

  1. 1Department of Pharmacology L. M. College of Pharmacy, Ahmedabad, Gujarat, INDIA, INDIA.

CORRESPONDENCE

Sneha Chacko

Assistant Professor, Department of Pharmacology L. M. College of Pharmacy Ahmedabad, Gujarat, INDIA.

saumyasneha@gmail.com

Received: 09-05-2025; Revised: 24-07-2025; Accepted: 12-09-2025.

Volume 16, Issue 1 · pp. 283–289 · PUBLISHED Jan-Mar 2026 · DOI: 10.5530/ijpi.20260451

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ABSTRACT

Background The 6-Min Walk Distance (6MWD) test is widely used to assess functional capacity in respiratory patients, but response patterns across different respiratory conditions remain poorly understood. Materials and Methods 115 patients (29 Asthma, 46 COPD, 40 ILD) underwent 6MWD testing before and after pulmonary rehabilitation. Changes in distance, heart rate, and oxygen saturation were analyzed across diagnostic groups. Results Mean 6MWD improved from 363.90 m to 375.26 m post-rehabilitation. Asthma patients showed the most significant improvement (30 m increase), followed by COPD (8 m increase), while ILD patients showed minimal change. Heart rate and SpO2 changes during testing showed no significant differences pre- and post-rehabilitation (p>0.05). Diagnostic category significantly influenced improvement patterns (p<0.05). Conclusion The effectiveness of pulmonary rehabilitation on functional capacity varies significantly across respiratory conditions, with asthma patients showing the most marked improvements. These findings suggest the need for condition-specific rehabilitation protocols and indicate that 6MWD improvements may not be a universally appropriate primary outcome measure across all respiratory conditions.

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INTRODUCTION

The 6-Min Walk Distance (6MWD) test is becoming a crucial assessment parameter when evaluating patients' functional ability with respiratory diseases (Holland et al., 2014a; Singh et al., 2014). Very much like habitual tasks 6MWD, a submaximal workout test, provides significant insights into patients’ practical restrictions and therapeutic effects (Dantes et al., 2019; Singh et al., 2014). Although pulmonary rehabilitation is widely implemented in several clinics, uncertainty persists regarding the influence of various respiratory impairments on test results, along with patterns of response (Candemir, 2018; Spruit et al., 2015).

The effectiveness of pulmonary rehabilitation in increasing exercise capacity, decreasing symptoms, and improving quality of life has been established in many pulmonary conditions (Mccarthy et al., 2015; Spruit et al., 2013). The degree of such changes and the underlying mechanisms, however, are likely to differ widely according to the primary pathophysiology involved in respiratory disease (McNamara et al., 2019). In contrast to the progressive airflow limitation in Chronic Obstructive Pulmonary Disease (COPD) or the restrictive ventilatory defects and gas exchange abnormalities in Interstitial Lung Disease (ILD), asthma represents a relatively unique pathophysiological state of reversible airflow limitation and airway hyperresponsiveness (Gloeckl et al., 2013; Raghu et al., 2015). These pathophysological differences have thrown into question the validity of standardized approaches to rehabilitation and the selection of outcome measures in different diagnostic groups (Dowman et al., 2014; Neder et al., 2019). While the 6MWD test has been established for multiple respiratory illnesses, it might reiterate diverse physiologic limitations and compensatory mechanisms among patients with ILD, COPD and asthma (Andrianopoulos et al., 2015; Bahmer et al., 2017).

Here, we aim to fill this knowledge gap by providing an evidence-based comparison of the functional capacity improvements to the 6MWD test across a heterogeneous cohort of asthmatic, COPD and ILD patients participating in a standardized pulmonary rehabilitation program. Through the analysis of variations in walking distance, changes in heart rate responses and changes in oxygen saturations through the course of exercise, we aim to identify physiological response patters specific to condition, which may inform a more tailored approach to rehabilitation. Understanding these differences might help develop more tailored rehabilitation approaches and matching outcomes based on diagnostic category (Holland et al., 2014b; Spruit et al., 2013).

MATERIALS AND METHODS

Study Design and Participants

This was a prospective cross-sectional study from June 2022 to June 2024 done at Sparsh Chest Disease Centre. Patients were recruited based on inclusion and exclusion criteria. All participants were enrolled in a standardised pulmonary rehabilitation program. The study protocol was approved by the institutional ethics committee (GCSMC/EC/Research project/APPROVE/2022 /352) and all participants provided written informed consent prior to enrolment.

6 Min Walk Distance Test Protocol

The 6MWD Test was carried out in compliance with guidelines laid down by the American Thoracic Society (ATS). Tests were conducted on a flat and straight 30 m walking course in an enclosed hallway. Participants were given standardized instructions urging them to walk as far as possible during this 6 min interval, while they could build in rest periods if needed. Consistent verbal encouragement was given at intervals standardized to the advice of the ATS in order not to influence test performance by investigator attitude. Each participant conducted the 6MWD Test twice. Once before the start of respiratory rehabilitation (pre-rehabilitation) and once after completing it (post-rehabilitation).

Pulmonary Rehabilitation Program

Each participant went through an eight-week standard pulmonary rehabilitation program It consisted of supervised exercise twice a week Each session ran for 1 hr and included:

Aerobic conditioning:, 30 min on the treadmill at levels of intensity tailored to each person so they correspond 60-80% heart rate control for that individual's heart rate intensity.

Resistance training:, Using arms and legs strengthening exercises such as free weights and resistance bands.

Flexibility exercises:, 10 min of stretching major muscle groups.

Educational components:, Weekly sessions addressing disease management, breathing techniques, and energy conservation strategies.

Throughout the program, exercise intensity was progressively increased depending on each person's tolerance to it. All sessions were run by experienced physiotherapists with qualifications in pulmonary rehabilitation.

Statistical analysis

Statistical analyses were conducted using version 25.0 of IBM SPSS software (Armonk, N.Y., USA: IBM Corp.). The Shapiro-Wilk test was used to determine whether the data distribution was normal. For every variable, descriptive statistics were calculated; continuous data were shown as means and standard deviations, while categorical data were shown as frequencies and percentages.

RESULTS

Demographic characteristics of participants of the study (n=115) by diagnostic group are shown in Table 1. There were 29 patients with asthma, 46 with COPD, and 40 with ILD. The majority of participants were female in all of the diagnostic categories, with females accounting for 75.9% (n=22) asthma patients, 82.6% (n=38) of COPD patients, and 72.5% (n=29) of ILD patients. In the analysis of the age distribution of study participants, the bulk of the recruited population in the asthma, COPD and ILD cohorts were in the 51-60 years age bracket (34.5%, 50.0% and 47.5% respectively). None of the individuals diagnosed in any category were under the age of 30 years. Distribution of BMI by classification was variable between groups. In asthmatics, the same proportions were identified as having healthy weight (18.5-24.9 kg/m²) or pre-obesity (25-29 kg/m²). Within the group with COPD, 34.8% (n=16) were classified as normal weight and 30.4% (n=14) as overweight. The largest portion of ILD patients were pre-obese (42.5%, n=17), followed by healthy weight (32.5%, n=13). Severe obesity (BMI ≥40 kg/m²) was uncommon among all groups (n=1 in ILD group).

Table 1: Demographic Details.
ParametersASTHMA (n=29)COPD (n=46)ILD (n=40)
Gender,
Male7811
Female223829
Age (Years),
Below 30000
31-40536
41-50869
51-60102319
61-705145
Above 71101
BMI (kg/m2),
Underweight (<18.5)001
Healthy (18.5-24.9)101613
Overweight (greater than or equal to 25)285
Pre-obese (25-29)101417
Obese class 1 (30-34)372
Obese class 2 (35-39)411
Obese class 3 (greater than or equal to 40)001

Table 2 shows the 6MWD parameter changes after pulmonary rehabilitation among asthma patients (n=29). The distribution of heart rates at baseline showed a significant shift post-rehabilitation (p100 bpm), 19 being in the normal heart range (60-100 bpm) at baseline compared to 2 and 27 respectively after rehabilitation. Baseline SpO2 was unchanged, all patients remained normal (88-92%) pre- and post-rehabilitation (p=1.0).

Table 2: Effects of Pulmonary Rehabilitation on 6MWD Parameters in Asthma Patients (n=29).
6 Min Walk Test Recording of Asthma Patients (n=29)
ParametersPrePostp value
BaselineHR GroupBradycardia (Below 60)004.556067412e-9
Normal Range (60-100)1927
Tachycardia (Above 100)102
SPO2 GroupNormal* (88-92)29291
Hypoxic (88-85)00
Severly Hypoxic (less than 85)00
End of testHR GroupBradycardia (Below 60)020.2712958233
Normal Range (60-100)45
Tachycardia (Above 100)2522
SPO2 GroupNormal* (88-92)24290.053
Hypoxic (88-85)20
Severly Hypoxic (less than 85)30
Serial 6MWDDistance Group<40022180.1258119093
Normal711
Lowest Saturation GroupNormal* (88-92)21270.000001160491812
Hypoxic (88-85)21
Severly Hypoxic (less than 85)61

At the end of 6MWD, no statistically significant changes in heart rate distribution were noted post rehabilitation (p=0.271). There was a small increase in number of patients with bradycardia (0 to 2) and normal heart rate (from 4 to 5) with corresponding decrease in number of patients with tachycardia (from 25 to 22). Notably, end-test SpO2 was improved with borderline significance (p=0.053) with every patient achieving normal levels at end-test following rehabilitation compared to pre-rehabilitation when 2 and 3 patients had hypoxia (85-88%) and severe hypoxia (<85%) during exercise, respectively.

Almost walking distance showed a non-significant trend toward improvement (p=0.126), with the number of patients reaching normal distance (≥400m) increased from 7 to 11. The lowest saturation measurements showed the greatest improvement with a highly significant decrease in oxygen desaturation events (p<0.000002). After rehabilitation, 27 patients (51%) had normal saturation during the test compared to only 21 patients before rehabilitation, and severe hypoxia was observed in only 1 patient as opposed to 6 patients before rehabilitation.

Table 3 gives the analysis of the 6MWD parameters before and after pulmonary rehabilitation in COLD patients (n=46) all baseline measurement showed that SpO2 distribution after rehabilitation (p=1.0 for both parameters) still had no significant change without any different heart rates. By contrast our patients at their worst could still maintain normal oxygen saturation each time before and after rehabilitation. As the analysis shows, from 35 patients experienced tachycardia to 40 patients and one patient developed bradycardia post-rehabilitation; this was not apparent before rehabilitation. Even more impressively, end-test SpO2 showed significant improvement (p=0.004). All 46 patients maintained normal oxygen saturation post-rehabilitation compared to pre-rehabilitation, when 4 patients experienced hypoxia and 2 patients experienced severe hypoxia. Walking distance analysis demonstrated a significant improvement following rehabilitation (p=0.013). The number of patients able to make good distance (≥400m) doubled from 8-16. The most striking change, however, was in lowest saturation measurements during the test. Oxygen desaturation underwent a highly significant reduction (p<0.001). Post-rehabilitation, 38 patients kept normal saturation throughout the test compared with just 18 pre-rehabilitation.

Table 3: Pre and Post Pulmonary Rehabilitation 6MWD Outcomes in COPD Patients (n=46).
6 Min Walk Test Recording OF Copd Patients (n=46)
ParametersPREPOSTp value
BaselineHR GroupBradycardia (Below 60)001
Normal Range (60-100)3333
Tachycardia (Above 100)1313
SPO2 GroupNormal* (88-92)46461
Hypoxic (88-85)00
Severly Hypoxic (less than 85)00
End of testHR GroupBradycardia (Below 60)010.01212482834
Normal Range (60-100)115
Tachycardia (Above 100)3540
SPO2 GroupNormal* (88-92)40460.004
Hypoxic (88-85)40
Severly Hypoxic (less than 85)20
Serial 6MWDDistance Group<40038300.01326565341
Normal816
Lowest Saturation GroupNormal* (88-92)18380
Hypoxic (88-85)126
Severly Hypoxic (less than 85)162

Table 4, it presents the changes of the 6MWD parameter after pulmonary rehabilitation in ILD patients (n=40). Heart rate distributions in baseline showed an almost non-significant increase from those patients tending toward supraventricular tachycardia (p=0.053). Baseline SpO2 was consistent before and after intervention, and it remained that the entire group of subjects had 88-92% per cent saturation. (p=1.0) There were no significant changes in end-test heart rate distribution after rehabilitation (p=0.573), with all 3 groups that existed before intervention being maintained simultaneously afterwards. On the other hand, end-test SpO2 showed a significant inferior change over time (p=0.010). After rehabilitation, fewer patients had normal saturation (18 versus 27 pre-rehabilitation) and more experienced hypoxia (7 versus 2) or even severe hypoxia (15 versus 11). Two. There was no statistically significant change in walking distance after rehabilitation (p=0.740). Only a marginal increase was seen from before to after the intervention with respect percentage of people who achieved a normal distance at baseline from 13 to 14. In spite of the overall distance walked remaining largely unchanged, however, lowest saturation measurements during the test did show a statistically significant shift in distribution (p=0.016). Post-rehabilitation, more people had severe hypoxia during test (27 versus 22 pre-rehabilitation), fewer moderate hypoxias (5 versus 11). The number of people who kept normal saturation throughout test also increased slightly from 7 to 8.

Table 4: Analysis of 6MWD Parameters Pre and Post Pulmonary Rehabilitation in ILD Patients (n=40).
6 Min Walk Test Recording of Ild Patients (n=40)
ParametersPrePostp value
BaselineHR GroupBradycardia (Below 60)000.05280751142
Normal Range (60-100)3024
Tachycardia (Above 100)1016
SPO2 GroupNormal* (88-92)40401
Hypoxic (88-85)00
Severly Hypoxic (less than 85)00
End of testHR GroupBradycardia (Below 60)110.5728434234
Normal Range (60-100)64
Tachycardia (Above 100)3335
SPO2 GroupNormal* (88-92)27180.01036782914
Hypoxic (88-85)27
Severly Hypoxic (less than 85)1115
Serial 6MWDDistance Group<40027260.7402692788
Normal1314
Lowest Saturation GroupNormal* (88-92)780.01615601322
Hypoxic (88-85)115
Severly Hypoxic (less than 85)2227

DISCUSSION

The results of this study demonstrate the heterogeneous nature of improvements in functional exercise capacity following pulmonary rehabilitation in people with various respiratory diseases. Asthmatics had the highest 6MWD mean improvement of 30 m and patients with COPD had more modest improvement (8 m), and ILD patients exhibited little change in walking distance. At the same time, these differential responses speak to the importance of the underlying pathophysiological interpretation towards both the understanding of our data as well as the development of intervention protocols.

Improved responsiveness in asthma patients fits with prior studies noting that exercise limitations may be more fully reversible in this population than with other chronic lung diseases (Carson et al., 2013; Tan et al., 2017). The traditional pathophysiology of asthma (with characteristics of reversible airflow obstruction and airway hyperresponsiveness) could allow for greater improvements in exercise capacity with interventions aimed at both the elements affecting respiratory mechanics and systemic deconditioning (Cordova-Rivera et al., 2018; Trevor et al., 2015). Moreover, asthma patients in our cohort were younger than the COPD or ILD patients, which might have also contributed to the greater physiological reserves they possessed.

In light of this, the modest gains achieved in COPD patients (of 8 m) were below the widely accepted Minimal Clinically Important Difference (MCID) threshold of the 6MWD of 25-30 m in COPD populations (Spruit et al., 2015). However, in our study, we discovered considerable advances in mean exercise oxygen saturation patterns in this group and a significant transition from moderate to severe hypoxia during testing for patients that transitioned from hypoxia to normal (Polkey et al., 2013; Singh et al., 2014). Increasing aerobic capacity with no greater mobility increase implies that during exercise, pulmonary rehabilitation has most likely improved ventilation-perfusion matching and oxygen utilization in diagnosed COPD patients (Gloeckl et al., 2013; Neder et al., 2019).

The minimal improvement in 6MWD noted in patients with ILD should be interpreted with caution. ILD is defined as a heterogeneous group of disorders characterized by lung parenchymal inflammation and fibrosis, leading to restrictive ventilatory defects and severe gas exchange abnormalities. However, the ILD patients reported a greater degree of oxygen desaturation following rehabilitation (Dantes et al., 2019; Raghu et al., 2015). Such paradoxical responses are indicative of the complex pathophysiology of exercise limitation in ILD, and highlight the fact that "one size" pulmonary rehabilitation may not be appropriate for this patient group (Dowman et al., 2014; Vainshelboim, 2016).

It is important to mention that there were no significant differences in heart rate parameters in any of the diagnostic groups. Improvements in exercise capacity following pulmonary rehabilitation may have a cardiovascular component, with reports of increases in stroke volume and cardiac output. Physiological adaptations were previously attributed to improved walking distance in several trials, but our results show these changes, especially in asthma patients, can be explained by improved ventilatory efficiency, reduced dynamic hyperinflation and/or peripheral muscle function rather than cardiovascular adaptations as previously suggested (Langer et al., 2014; Spruit et al., 2015).

The meaningful effect of diagnostic category on improvement patterns (p<0.05) reinforces the necessity for condition-specific approaches to rehabilitation design and outcomes. We believe our data better describes the role of the 6MWD test and reveal that its clinical applicability in COPD is not necessarily shared with other respiratory disorders (Dowman et al., 2014; Holland et al., 2014a). This is of clinical and research significance as introduced a potential break in the one size fits all approach commonly observed in pulmonary rehabilitation settings.

Some limitations need to be recognized. One limitation of the study is that the ILD cohort consists of multiple specific ILD conditions with differing prognoses and responses to treatment, which are heterogeneous within each diagnostic category and may have biased the results (Raghu et al., 2015). Furthermore, there may not have been an ideal standardized rehabilitation protocol designed for each diagnostic category that was applied in this study. The subsequent studies should aim to develop condition-specific rehabilitation protocols tailored to the specific pathophysiological limitations of each respiratory condition (Dowman et al., 2014; Spruit et al., 2013).

This last point is particularly critical if clinical services are to maximize the potential response of patients with different diagnoses to pulmonary rehabilitation as characterized by an improvement in the clinical outcome. Overall, the promising improvements seen in patients with asthma demonstrate that exercise-based interventions may be particularly beneficial in this cohort, whereas the diminished response in patients with ILD suggests that different and/or tailored approaches may be more appropriate for this group. These findings add to the increasing amount of evidence for next steps into tailored pulmonary rehabilitation strategies based on underlying pathophysiology rather than one-size-fits-all protocols across all chronic respiratory conditions (McNamara et al., 2019; Spruit et al., 2015).

CONCLUSION

According to the new study, there are different patterns of improvement in functional capacity by respiratory disease after pulmonary rehabilitation. Patients with asthma showed the greatest gains in 6MWD (an average of 30 m more), while those of COPD had modest increases for walking distance (8 m up), and ILD patients hardly changed. This verifies the view that pulmonary rehabilitation was effective for improving functional capacity of different underlying respiratory diseases was markedly different in these groups of patients.

Despite this fact, significant changes in oxygen saturation parameters materialized across the different diagnostic groups-however the patterns were quite distinct. Asthma and COPD patients both produced noticeable increases (p<0.000002) in minimum saturation readings during testing, but those with ILD showed signs that end-test SpO2 fell extremely off (p<0.010). Whether in these two different oxygenation parameters-from heart rates to SpO2 and saturation-we find that when looking at responses people still reflect the physiology specific to their disease in each very case.

In the meantime, responses of heart rate showed less consistent patterns by group a point which might suggest that improvements in walking distance are hardly to do with the central cardio-vascular system itself and rely more on peripheral muscle function than efficient ventilation. In particular, it is worth noticing that the changes in oxygen saturation patterns of 6MWD as an outcome parameter whose acceptance needs to be reconsidered for all respiratory conditions.

These findings underscore the need for pulmonary rehabilitation programs to have specific goals tailored to the different conditions of patients and suggest that 6MWD improvements may not be a universally appropriate primary outcome measure across all respiratory disease. The profound differences in response patterns between patients with asthma, COPD, and ILD highlight the need for rehabilitation efforts tailored to the specific pathophysiological peculiarities of each illness. For future research, the focus should be placed firmly on developing and validating condition-specific rehabilitation protocols in order to optimize functional outcomes for patients with different respiratory problems.

REFERENCES

As published

Showing references and in-text citations exactly as published.

  1. 1.Andrianopoulos, V.; Holland, A. E.; Singh, S. J.; Franssen, F. M. E.; Pennings, H.-J.; Michels, A. J. et al. 6 min walk distance in patients with chronic obstructive pulmonary disease: Which reference equations should we use?. Chronic Respiratory Disease. 2015;12(2):111–119. https://doi.org/10.1177/1479972315575201DOIGOOGLE SCHOLAR
  2. 2.Bahmer, T.; Waschki, B.; Schatz, F.; Herzmann, C.; Zabel, P.; Kirsten, A.-M. et al. Physical activity, airway resistance and small airway dysfunction in severe asthma. In The European Respiratory Journal. 2017;49(1):Article 1601827. https://doi.org/10.1183/13993003.01827-2016DOIGOOGLE SCHOLAR
  3. 3.Candemir, I.. Advances in pulmonary rehabilitation for chronic obstructive pulmonary disease and associated conditions. In COPD - An Update in Pathogenesis and Clinical Management. InTech. 2018. https://doi.org/10.5772/intechopen.70920DOIGOOGLE SCHOLAR
  4. 4.Carson, K. V.; Chandratilleke, M. G.; Picot, J.; Brinn, M. P.; Esterman, A. J.; Smith, B. J.. Physical training for asthma. In The Cochrane Database of Systematic Reviews. John Wiley & Sons Limited. 2013;2013(9):Article CD001116. https://doi.org/10.1002/14651858.CD001116.pub4DOIGOOGLE SCHOLAR
  5. 5.Cordova-Rivera, L.; Gibson, P. G.; Gardiner, P. A.; Powell, H.; McDonald, V. M.. Physical activity and exercise capacity in severe asthma: Key clinical associations. The Journal of Allergy and Clinical Immunology. in Practice. 2018;6(3):814–822. https://doi.org/10.1016/j.jaip.2017.09.022DOIGOOGLE SCHOLAR
  6. 6.Dantes, E.; Tudorache, E.; Adina Man, M.. The role of pulmonary rehabilitation in patients with idiopathic pulmonary fibrosis. In. Interstitial lung diseases. IntechOpen. 2019. https://doi.org/10.5772/intechopen.84283DOIGOOGLE SCHOLAR
  7. 7.Dowman, L.; Hill, C. J.; Holland, A. E.. Pulmonary rehabilitation for interstitial lung disease. In The Cochrane Database of Systematic Reviews. John Wiley & Sons Limited. 2014;2014(10):Article CD006322. https://doi.org/10.1002/14651858.CD006322.pub3DOIGOOGLE SCHOLAR
  8. 8.Gloeckl, R.; Marinov, B.; Pitta, F.. Practical recommendations for exercise training in patients with COPD. European Respiratory Review. 2013;22(128):178–186. https://doi.org/10.1183/09059180.00000513DOIGOOGLE SCHOLAR
  9. 9.Holland, A. E.; Spruit, M. A.; Troosters, T.; Puhan, M. A.; Pepin, V.; Saey, D. et al. An official European Respiratory Society/American Thoracic Society technical standard: Field walking tests in chronic respiratory disease. The European Respiratory Journal. 2014a;44(6):1428–1446. https://doi.org/10.1183/09031936.00150314DOIGOOGLE SCHOLAR
  10. 10.Langer, D.; Ciavaglia, C. E.; Neder, J. A.; Webb, K. A.; O’Donnell, D. E.. Lung hyperinflation in chronic obstructive pulmonary disease: Mechanisms, clinical implications and treatment. In Expert Review of Respiratory Medicine. Expert Reviews Ltd. 2014;8(6):731–749. https://doi.org/10.1586/17476348.2014.949676DOIGOOGLE SCHOLAR
  11. 11.Mccarthy, B.; Casey, D.; Devane, D.; Murphy, K.; Murphy, E.; Lacasse, Y.. Pulmonary rehabilitation for chronic obstructive pulmonary disease. In The Cochrane Database of Systematic Reviews. John Wiley & Sons Limited. 2015;2015(2):Article CD003793. https://doi.org/10.1002/14651858.CD003793.pub3DOIGOOGLE SCHOLAR
  12. 12.McNamara, R. J.; Dale, M.; McKeough, Z. J.. Innovative strategies to improve the reach and engagement in pulmonary rehabilitation. In Journal of Thoracic Disease. AME Publishing Company. 2019;11(Suppl. 17):S2192–S2199. https://doi.org/10.21037/jtd.2019.10.29DOIGOOGLE SCHOLAR
  13. 13.Neder, J. A.; Marillier, M.; Bernard, A.-C.; James, M. D.; Milne, K. M.; O’Donnell, D. E.. The integrative physiology of exercise training in patients with COPD. In COPD. Taylor & Francis Limited. 2019;16(2):182–195. https://doi.org/10.1080/15412555.2019.1606189DOIGOOGLE SCHOLAR
  14. 14.Polkey, M. I.; Spruit, M. A.; Edwards, L. D.; Watkins, M. L.; Pinto-Plata, V.; Vestbo, J. et al. 6-min-walk test in chronic obstructive pulmonary disease: Minimal clinically important difference for death or hospitalization. American Journal of Respiratory and Critical Care Medicine. 2013;187(4):382–386. https://doi.org/10.1164/rccm.201209-1596OCDOIGOOGLE SCHOLAR
  15. 15.Raghu, G.; Rochwerg, B.; Zhang, Y.; Garcia, C. A. C.; Azuma, A.; Behr, J. et al. An official ATS/ERS/JRS/ALAT clinical practice guideline: Treatment of idiopathic pulmonary fibrosis: An update of the 2011 clinical practice guideline. American Journal of Respiratory and Critical Care Medicine. 2015;192(2):e3–e19. https://doi.org/10.1164/rccm.201506-1063STDOIGOOGLE SCHOLAR
  16. 16.Singh, S. J.; Puhan, M. A.; Andrianopoulos, V.; Hernandes, N. A.; Mitchell, K. E.; Hill, C. J. et al. An official systematic review of the European Respiratory Society/American Thoracic Society: Measurement properties of field walking tests in chronic respiratory disease. In The European Respiratory Journal. 2014;44(6):1447–1478. https://doi.org/10.1183/09031936.00150414DOIGOOGLE SCHOLAR
  17. 17.Spruit, M. A.; Pitta, F.; McAuley, E.; ZuWallack, R. L.; Nici, L.. Pulmonary rehabilitation and physical activity in patients with chronic obstructive pulmonary disease. In American Journal of Respiratory and Critical Care Medicine. 2015;192(8):924–933. https://doi.org/10.1164/rccm.201505-0929CIDOIGOOGLE SCHOLAR
  18. 18.Spruit, M. A.; Singh, S. J.; Garvey, C.; ZuWallack, R.; Nici, L.; Rochester, C. et al. An official American Thoracic Society/European Respiratory Society statement: Key concepts and advances in pulmonary rehabilitation. American Journal of Respiratory and Critical Care Medicine. 2013;188(8):e13–e64. https://doi.org/10.1164/rccm.201309-1634STDOIGOOGLE SCHOLAR
  19. 19.Tan, J. H. Y.; Chew, W. M.; Lapperre, T. S.; Tan, G. L.; Loo, C. M.; Koh, M. S.. Role of bronchoprovocation tests in identifying exercise-induced bronchoconstriction in a non-athletic population: A pilot study. Journal of Thoracic Disease. 2017;9(3):537–542. https://doi.org/10.21037/jtd.2017.02.70DOIGOOGLE SCHOLAR
  20. 20.Trevor, J. L.; Bhatt, S. P.; Wells, J. M.; Kirkpatrick, D.; Schumann, C.; Hitchcock, J. et al. Benefits of completing pulmonary rehabilitation in patients with asthma. The Journal of Asthma. 2015;52(9):969–973. https://doi.org/10.3109/02770903.2015.1025410DOIGOOGLE SCHOLAR
  21. 21.Vainshelboim, B.. Exercise training in idiopathic pulmonary fibrosis: Is it of benefit?. In Breathe. European Respiratory Society. 2016;12(2):130–138. https://doi.org/10.1183/20734735.006916DOIGOOGLE SCHOLAR

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Chacko, S., & Shah, G. (2026). Comparative Analysis of Functional Capacity Improvements Through 6MWD Testing Across Different Respiratory Conditions: Implications for Targeted Pulmonary Rehabilitation. International Journal of Pharmaceutical Investigation, 16(1), 283–289. https://doi.org/10.5530/ijpi.20260451