Skip to main content
Download PDF

Effectiveness of home-based pulmonary rehabilitation programs for patients with chronic obstructive pulmonary disease (COPD): systematic review

BMC Health Services Research volume 22, Article number: 557 (2022) Cite this article

Abstract

Background

Although pulmonary rehabilitation (PR) is considered a key component in managing chronic obstructive pulmonary disease (COPD) patients, uptake remains suboptimal. This systematic review aimed to determine the effectiveness of home-based PR (HBPR) programs for COPD patients.

Methods

A systematic review of scholarly literature published within the last 10 years from the conception of this project was conducted using internationally recognized guidelines. Search strategies were applied to electronic databases and clinical trial registries through March 2020 and updated in November 2021 to identify studies comparing HBPR with ‘usual care’ or outpatient pulmonary rehabilitation (OPR). To critically appraise randomized studies, the Cochrane Collaboration risk of bias tool (ROB) was used. The quality of non-randomized studies was evaluated using the ACROBAT-NRSI tool. The quality of evidence relating to key outcomes was assessed using Grading of Recommendations, Assessment, Development and Evaluations (GRADE) on health-related quality of life (HRQoL), exacerbation frequencies, COPD-related hospital admissions, and program adherence. Three independent reviewers assessed methodologic quality and reviewed the studies.

Results

Twelve randomized controlled trials (RCTs) and 2 comparative observational studies were included. While considerable evidence relating to the effectiveness of HBPR programs for COPD patients exist, overall quality is low. There were no differences between HBPR and OPR in terms of safety, HRQoL, functional exercise capacity and health care resource utilization. Compared to usual care, functional exercise capacity seemed to significantly improve after HBPR. While patient compliance with HBPR is good, two factors appeared to increase the ‘risk’ of non-compliance: expectations of patients to 1) complete daily diaries/activity logs and 2) engage in solely unsupervised exercise sessions.

Conclusion

The overall quality for most outcomes was low to very low; however, HBPR seems to offer comparable short-term benefits to OPR.

Peer Review reports

Background

Chronic Obstructive Pulmonary Disease (COPD) is a progressive lung disease and a leading cause of morbidity and mortality worldwide with substantial economic and social burdens on individuals and society [1,2,3]. While COPD outpatient pulmonary rehabilitation (OPR) programs are well established, uptake remains suboptimal, in part because of difficulties in access to patients who do not live near to OPR [3, 4]. Home-based pulmonary rehabilitation program (HBPR) may represent an important strategy to improve patient access to this vital program. The purpose of this systematic review was to determine the effectiveness of HBPR programs for COPD patients.

Methods

Search strategy

A comprehensive, structured search strategy was developed iteratively by an experienced medical information specialist in consultation with the research team. It was peer-reviewed by another senior information specialist for quality assurance using the Peer Review of Electronic Search Strategies (PRESS) checklist (online supplementary appendix 1). The initial searches were conducted from March 1st to March 13th, 2020 and updated in November 17th 2021. They were also supplemented by manual searches of reference lists from included studies.

Inclusion and exclusion criteria

Two reviewers independently screened the titles and abstracts of all citations. Full papers corresponding to potentially relevant citations were retrieved, divided among, and assessed by three reviewers for inclusion/exclusion according to criteria (Table 1). A pulmonary rehabilitation program was as defined by the American Thoracic Society and considered studies after 2009 in order to examine evidence reflecting current practice/guidelines [5]. Reviewers met to compare results and agree on the final set of studies to include. At both screening steps, consensus between reviewers was assessed using the Kappa statistics and found to be “substantial”.

Table 1 PICOS Elements of the effectiveness review
Full size table

Data extraction and synthesis

Extracted data were tabulated to identify trends or patterns across studies and facilitate qualitative and quantitative comparative analyses. Key characteristics of included studies, their quality, potential sources of bias, and findings were synthesized narratively. A narrative synthesis of effectiveness outcomes across the studies was undertaken. Where studies appeared similar enough in patient populations, designs, and outcomes, meta-analyses were performed. Forest plots were used to display individual and pooled results. Pooled risk ratios for categorical data and mean differences with 95% confidence intervals (CIs) for continuous outcomes were calculated. A p-value < 0.05 was considered statistically significant. For each pooled estimate, the I2 statistic was calculated to measure the amount of heterogeneity across combined studies. Where the value exceeded 50% (indicating substantial heterogeneity), the pooled estimate was not used in the interpretation of the results. Publication bias was evaluated using funnel plots, where sufficient data were available from the meta-analyses [6]. Multiple publications from the same study were linked together in the tables.

Assessment of study quality

RCTs were appraised using the Cochrane Collaboration ROB tool [7]. The methodological quality of the non-RCT interventional and comparative observational studies were evaluated using the Cochrane Risk of Bias Assessment Tool for Non-Randomized Studies (ACROBAT-NRSI) [8]. The quality of evidence relating to key outcomes of interest were assessed using the Grading of Recommendations, Assessment, Development and Evaluations (GRADE) tool [9]. GRADE assessment was based on the following outcomes: health-related quality of life (HRQoL), frequency of exacerbations, and COPD-related hospital admissions.

Results

Search results

A total of 18,846 citations were identified and screened, 217 were retrieved for full consideration, and 14 studies included - 12 RCTs [10,11,12,13,14,15,16,17,18,19,20,21] and 2 comparative observational [22, 23] studies (from 18 papers). The PRISMA diagram for the review is shown in Fig. 1 (additional information in online supplementary appendix 2).

Fig. 1
figure 1

Preferred Reporting Items for Systematic Review and Meta-analysis (PRISMA) flow diagram for the systematic review and meta-analysis

Full size image

Characteristics of studies

Nine studies compared HBPR to ‘usual care’ [10, 11, 14,15,16,17,18, 20, 22], four to OPR [12, 13, 19, 21, 23], and one [19] compared HBPR to OPR or ‘usual care’. They were conducted between 2007 and 2017 in Australia (2 studies) [10, 12], Brazil (2) [16, 19], China (2) [14, 18], Iran (1) [15],Spain (2) [17, 22], the United States (1) [11], and the United Kingdom (4) [13, 20, 21, 23] (Table 2). Collectively, they included 2293 patients and all but four [10, 12, 13, 22] were conducted in single centers.

Table 2 Characteristics of included studies included in the systematic review
Full size table

HBPR program characteristics

All HBPR programs lasted at least 8 weeks. Except in three [11, 12, 18, 24,25,26,27] studies, programs began with one or more in-person training/education session(s) at an outpatient clinic or an initial in-home visit. The three [11, 12, 18, 24,25,26,27] exceptions delivered introductory sessions online or by video. Where described, sessions and in-home visits were conducted by nurses or physiotherapists. Additionally, all programs provided information booklets, manuals or workbooks and exercise prescription information, about which reported information varied. There were differences in specific components of and schedule for weekly in-home exercise, but most programs incorporated both strength and endurance training into activities to be performed unsupervised three times per week. However, four [12, 17, 22, 23] of the programs included supervised exercise. In the single [18] online HBPR, participation was monitored through the system itself, which collected log-on and log-off information. Patients logging on regularly were flagged and contacted by a nurse. Most programs asked patients to keep track of daily activities and symptoms in a diary or workbook. In one [15] case, patients used checklists. Programs employing special equipment or devices supplied them (hand and ankle weights [19], heart rate monitors [19], and pedometers [10, 12],). Weekly follow-up telephone calls by a nurse or physiotherapist to encourage or motivate patients and monitor progress were a part of almost all programs. Comparator interventions in studies were ‘usual care’ or OPR. ‘Usual care’, when described, varied significantly across studies, but typically comprised at least some form of in-person self-management/clinical needs assessment and advice on staying active and taking medications as prescribed, delivered through in-person education sessions and/or information booklets. OPR involved community-based supervised group sessions held two to three times weekly for seven to 12 weeks, and included exercise and education (online supplementary appendix 3, 4 and 5).

Risk of bias

Results of risk of bias assessment

The majority of RCTs provided a clear description of the objectives, interventions, outcomes and findings (online supplementary appendix 6). However, in two [15, 22] trials, ‘usual care’ was not defined. Four [10,11,12,13] of the RCTs had published or registered protocols pre-specifying outcomes, and in all five, such outcomes were the same as those reported in the trial results. In the remaining RCTs, it was not possible to determine if the results reflected all outcomes measured (Fig. 2).

Fig. 2
figure 2

Cochrane risk of bias summary for included RCTs. (1) random sequence generation (selection bias); (2) allocation concealment (selection bias); (3) blinding of participants and personnel (performance bias); (4) blinding of outcome assessment (detection bias) (patient reported outcomes); (5) blinding of outcome assessment (detection bias) (other outcomes); (6) incomplete outcome data (attrition bias); (7) selective reporting (reporting bias); (8) other bias

Full size image

All non-randomized studies [22, 23] provided a clear description of the objectives, interventions, differences in patient characteristics and potential confounding variables between the HBPR and comparator groups, outcomes and findings (online supplementary appendix 7) (Fig. 3).

Fig. 3
figure 3

ACROBAT-NRSI summary

Full size image

Of the 15 RCTs, eight [10,11,12,13, 17, 19,20,21] provided a clear description of the random sequence generation. In five [14,15,16,17, 19] RCTs, no details around allocation concealment were included. In the seven [10,11,12,13, 18, 20, 21] RCTs describing methods for ensuring blinding of patients and investigators, four [12, 18, 20, 21] used opaque sealed envelopes, two [11, 20] assigned the task to a researcher uninvolved in the trial, and two [10, 13] relied on web-based/online programs. In the two [10, 23] non-randomized studies, the risk of bias due to confounding was moderate, although known confounders were measured and controlled for through statistical analyses.

Six [10,11,12,13, 18, 21] RCTs reported that outcome assessors were blinded to the type of intervention. No information was provided in all but one [19] of the remaining trials. One [20] RCT explicitly stated that assessors were not blinded, rendering it at high risk for observer bias. None of the [10, 23] non-randomized studies mentioned blinding of assessors.

In five [10, 11, 13, 14, 19] RCTs, the risk of attrition bias was high but was low in six [12, 15,16,17,18, 21] RCTs, where missing data and reasons for withdrawals were similar between groups.

Results from GRADE assessment

GRADE assessment was conducted on selected outcomes (Tables 3 and 4). The GRADE level was ‘very low’ or ‘low’ for all outcomes in HBPR vs. ‘usual care’ studies and 2 of 3 outcomes in HBPR vs OPR studies (Tables 3 and 4).

Table 3 Studies comparing HBPR to ‘usual care’
Full size table
Table 4 Studies comparing HBPR to OPR
Full size table

Summary results of effectiveness

Safety

Three [11, 12, 21] studies reported adverse event rates, but none specified the type of adverse event. One [11] study comparing HBPR to usual care, and two [12, 21] studies comparing HBPR to OPR showed no statistically significant differences between groups (online supplementary appendix 8).

Health care resource utilization (hospital admissions, ER visits, and physician visits)

HBPR compared to ‘usual care’

In one of two [11, 22, 24, 25] studies comparing the percentage of patients with one or more COPD-related hospital admissions over a 12 to 18 month period, there were no statistically significant differences between groups. In the second [11, 24, 25] study, the percentage of patients with admission in the HBPR group was almost half that of the ‘usual care’ group (19% versus 30%; statistical significance of the difference not reported).

HBPR compared to OPR

One [12] study concluded that the impact of HBPR and OPR on health services utilization was similar.

Health-related quality of life (HRQoL)

Different disease-specific instruments were used, including the COPD assessment test (CAT), chronic respiratory disease questionnaire (CRQ), and the St. George’s respiratory questionnaire (SGRQ). Measurements were also at different points in time as the duration of rehabilitation programs varied among studies (online supplementary appendix 9, 10 and 11).

HBPR compared to usual care

In the study [14] using the CAT, short-term improvements in scores were statistically significantly greater in the HBPR group, but both groups experienced clinically meaningful improvements (a change in scores of at least 2 points [28]). However, 6 months after completion of HBPR, improvements from baseline were similar between groups. Two studies [10, 11, 24, 25] using CRQ found no statistically significant differences in changes between treatment groups on any of the 4 CRQ domains from baseline to several months after HBPR or ‘usual care’. However, in one [10], both groups reported clinically meaningful improvements in the dyspnea, fatigue and mastery domains at 2 and 6 months of follow-up (a change in score of at least 0.5 points). In the other [11, 24, 25], neither group experienced clinically meaningful improvements in the dyspnea domains. In contrast, the single study [20] that measured HRQoL directly following completion of HBPR reported statistically significant improvements in dyspnea, emotional function and fatigue among patients who had HBPR, but not among those who received ‘usual care’. In two [16, 17] of the three [16,17,18] studies using the SGRQ there were statistically significantly greater improvements in total scores (from baseline to end of treatment) with HBPR. However, for individual domains, scores varied between studies; in one study, changes in all domain scores were similar between groups and in the other, those for the ‘activity’ and ‘impact’ domains were greater among HBPR patients. The third [18] study assessed HRQoL 10 months post HBPR or ‘usual care’. There were no statistically significant differences between groups, except for social functioning and psychological disturbances resulting from COPD (i.e., ‘impact’ domain), which improved with HBPR and worsened with ‘usual care’.

HBPR compared to OPR

In one [13] study using CAT before and after completion of the programs, actual scores were not presented, but the reported p-value was not statistically significant (Fig. 4). Three [12, 21, 23] studies used CRQ and measured HRQoL at program completion, and meta-analyses were possible in 4 domains of the instrument: dyspnea, emotional, fatigue and mastery. Two [15, 26] found no statistically significant differences between groups in these domains after 2 months of pulmonary rehabilitation. By contrast, in the third [21] study, scores were statistically significantly lower in the emotional, fatigue and mastery domains among HBPR patients. However, 4 months after the end of the program, no statistically significant differences were reported.

Fig. 4
figure 4

Mean differences in health-related quality of life after completion of 2-month active pulmonary rehabilitation phase in studies comparing HBPR with OPR

Full size image

Adherence to/compliance with treatment

HBPR compared to usual care

With one exception [17], at least 79% of patients completed HBPR [10, 11, 15, 16, 18,19,20, 22, 24, 25] Of the three [17, 19, 20] studies reporting lower rates of adherence with HBPR, ‘usual care’ did not include an exercise component or diary for patients to log symptoms and/or activities on a daily basis.

HBPR compared to OPR

The percentage of patients completing HBPR was higher in three studies [12, 19, 21] but lower in two [13, 23], but the statistical significance was not reported. In one study [13], with lower adherence to HBPR, patients withdrew because it was too time-consuming or preferred a classroom setting or had computer problems affecting access (online supplementary appendix 12).

Frequency of exacerbations

HBPR compared ‘usual care’

Two studies [14, 22] showed no statistically significant differences in exacerbation rates during the rehabilitation phase between groups (online supplementary appendix 13).

Functional exercise capacity and activity levels

Different assessment tools were used to measure functional exercise capacity; the most commonly applied measure, the six-minute walk test. Others were the incremental shuttle walk test (ISWT) and the endurance shuttle walk test (ESWT).

HBPR compared to usual care

Across studies [11, 14, 18, 19, 22, 24, 25], the distance walked in 6 min statistically significantly increased among patients who received HBPR, indicating an improvement in exercise capacity. In some studies, it also increased among patients who received ‘usual care’, but the amount of increase was statistically significantly less than that reported for HBPR.

Five [10, 11, 14, 17, 19, 24, 25] out of six studies demonstrated that patients receiving HBPR had clinically meaningful improvements by the end of follow-up (change in distance of at least 30 m). However, one study [11, 24, 25] reported that at 18 months, only patients with serious COPD showed meaningful improvements in this test.

HBPR compared to OPR

In all four studies [13, 19, 21, 23], the distance walked in 6 min statistically significantly increased after HBPR and OPR, and the gains were similar between programs. However, one study [21] that measured ISWT reported no clinically meaningful improvements (change in distance of at least 48 m [29]) after HBPR or OPR.

Mental health

Studies used the Beck depression inventory, and the Hospital Anxiety and Depression scale (HADS) to assess changes in depression and anxiety (online supplementary appendix 14).

HBPR compared to ‘usual care’

In one [14] study, statistically significant improvements in scores on the Beck Depression Inventory were observed in both groups, but no statistical estimates of between-group measures were provided.

HBPR compared to OPR

Two [13, 21] of the five studies used the HADS. Within groups, post-program scores were similar to baseline, indicating that neither form of pulmonary rehabilitation reduced anxiety and depression among patients.

Self-efficacy

HBPR compared to ‘usual care’

One [15] study assessed self-efficacy changes between baseline and 2 months (the length of the active rehabilitation). HBPR patients had statistically significantly greater confidence in their ability to manage or avoid dyspnea during events across all five domains of the questionnaire compared to ‘usual care’.

HBPR compared to OPR

Three [12, 13, 21] studies used the PRAISE (Pulmonary Rehabilitation Adapted Index of Self-efficacy) tool [30]. However, only two [13, 21] reported statistical estimates of data variability between groups when administered to patients before and after the active rehabilitation phase (3 months in one study and 2 months in the other). Within and between groups, pre and post-treatment scores were similar, indicating that the confidence level among patients to self-manage their disease did not increase with HBPR or OPR (online supplementary appendix 15).

Discussion

This review examined the effectiveness of HBPR compared to usual care or OPR for safety, patient compliance, HRQoL, exercise capacity, self-efficacy, mental health, and health care resource utilization. Overall, HBPR appears to be comparable to standard OPR in terms of safety, HRQoL and exercise capacity. While there is considerable evidence supporting the effectiveness HBPR for COPD patients, study quality is low, and therefore findings should be interpreted with caution.

Although there have been previous reviews of HBPR published [31, 32], the current review included a larger number of primary studies and outcome measures. Only two common outcome measures were reported in all 3 of these reviews – HRQoL and exercise capacity, based on the CRQ and 6 min walk test, respectively. With respect to these two outcomes, Chen et al. also found that improvements after HBPR were similar to OPR [32]. By contrast, the earlier Liu et al. study reported improved HRQoL and functional capacity in the HBPR groups. However, it included patients in the control groups undergoing various types of interventions (including patients who did not have any form of exercise) [31]. In the present review, additional system outcomes, including measures of mental health and health resource utilization, have been included for the first time.

As HBPR takes place in the home with limited supervision, there could be a concern for patient safety. However, in the limited number of studies that reported on safety, importantly, there were no significant differences in reported adverse events between HBPR and OPR. This is consistent with a recent Cochrane review that did not identify any safety issues with telerehabilitation in patients with chronic respiratory diseases [33]. Combined, these results suggest that HBPR is safe and poses no greater risk than standard OPR.

Adherence to PR is key to achieve improvements in health outcomes and to facilitate behaviour change. HBPR has the advantage over traditional in-person PR in that barriers such as daily commute and weather should not affect adherence. Home-based programs could also be provided to rural and remote areas without space and workforce resources for a OPR. Further, the COVID-19 pandemic has forced heath systems to introduce home-based programs, including pulmonary rehabilitation programs. As a result, it has become evident that there might be additional groups of COPD patients who might benefit from HBPR. However, the risk of non-compliance to HBPR in the studies reviewed was associated with two PR program factors: 1) if there are expectations of patients to complete daily diaries/activity logs, or 2) if the program engaged in solely unsupervised exercise sessions. Requiring patients to fill out daily logs could become burdensome and represent an additional barrier to participation. Technological advances, e.g., remote-wireless activity monitors, may reduce this challenge in the future. Supervision/feedback during the exercise sessions would provide social interaction and positive reinforcement opportunities, which are key mechanisms for enhancing self-efficacy [34]. Self-efficacy has been shown to predict attendance at PR [35] and long-term adherence to exercise programs [36]. Further, supervision would increase the likelihood that the patient is following all components of their exercise program (e.g. target exercise intensity), which would maximize benefits from PR and the likelihood that patients would perceive such benefits. Patients have reported that expectations of benefits are critical for their engagement in PR and exercise programs [37,38,39,40].

The inclusion of an individualized exercise plan appeared to facilitate greater improvements in exercise capacity with HBPR. An individualized exercise plan would require a thorough patient assessment, including evaluation of exercise capacity, at the start of rehab, as well as an exercise program be developed based on fundamental exercise principles. These are entirely consistent with recently published quality indicators for PR [41]. Similar to the supervision component discussed previously, an individualized exercise plan will facilitate an exercise program with the appropriate aerobic stimulus/training load. Aerobic training load has been shown to be an important determinant in improvement in exercise tolerance with PR [42]. Combined, these findings support the need for individualized exercise programs in order to maximize health outcomes in patients participating in HBPR.

This review demonstrates that neither HBPR nor OPR appear to reduce health care resource utilization. Across the studies comparing HBPR to ‘usual care,’ the findings varied, but there were no statistically significant differences between groups, except in terms of the 6 min walk test. The one study that assessed the statistical significance of differences in hospital admissions suggests that the impact of HBPR and OPR on health services utilization was similar.

Limitations

This systematic review has several limitations. First, there is the possible risk of bias due to missing information in the included studies. Furthermore, included studies provided limited descriptions of the study randomization process, and the studies varied in components of the interventions. Second, the study was restricted to English language studies, which might have led to the exclusion of possibly relevant studies. The review was also limited to work published in 2009 or later, and therefore some papers published before that time [43] were excluded. Also, it was not possible to perform a meta-analysis on most outcomes due to a high level of heterogeneity and limited data.

Conclusion

In conclusion, HBPR is an alternative approach which appears as safe as OPR, and HBPR outcomes were similar to standard pulmonary rehabilitation programs. Although there is a considerable amount of evidence relating to these programs’ effectiveness for COPD patients, its quality is low and should be interpreted with caution.

Availability of data and materials

All data relevant to the study are included in the article or uploaded as supplementary information.

References

  1. Sullivan S, Ramsey S, Lee T. The economic burden of COPD. Chronic Obstr Pulm Dis. 2000;117(2):5s–9s. https://doi.org/10.1002/9780470755976.ch64.

    Article  CAS  Google Scholar 

  2. Iheanacho I, Zhang S, King D, Rizzo M, Ismaila AS. Economic burden of chronic obstructive pulmonary disease (COPD): a systematic literature review. Int J COPD. 2020;15:439–60. https://doi.org/10.2147/COPD.S234942.

    Article  Google Scholar 

  3. Global Initiative For Chronic Obstructive Lung Disease. Global strategy for the diagnosis, managment, and prevention of chronic obstructive pulmonary disease (2019 Report); 2019.

    Google Scholar 

  4. Bolton CE, Waters CS, Peirce S, Elwyn G. Insufficient evidence of benefit: a systematic review of home telemonitoring for COPD. J Eval Clin Pract. 2011;17(6):1216–22. https://doi.org/10.1111/j.1365-2753.2010.01536.x.

    Article  PubMed  Google Scholar 

  5. Spruit MA, Singh SJ, Garvey C, et al. An official American thoracic society/European respiratory society statement: key concepts and advances in pulmonary rehabilitation. Am J Respir Crit Care Med. 2013;188(8). https://doi.org/10.1164/rccm.201309-1634ST.

  6. Banks GC, Kepes S, Banks KP. Publication Bias: the antagonist of Meta-analytic reviews and effective policymaking. Educ Eval Policy Anal. 2012;34(3):259–77. https://doi.org/10.3102/0162373712446144.

    Article  Google Scholar 

  7. Sterne JAC, Savović J, Page MJ, et al. RoB 2: a revised tool for assessing risk of bias in randomised trials. BMJ. 2019;366:1–8. https://doi.org/10.1136/bmj.l4898.

    Article  Google Scholar 

  8. Sterne JAC, Higgins JPT RB on B of the DG for A-N, Sterne J, Higgins J, Reeves B, on behalf of the development group for ACROBAT-NRSI. A Cochrane Risk Of Bias Assessment Tool: for Non-Randomized Studies of Interventions (ACROBAT-NRSI). Version 100. 2014;(September):Version 1.0.0.

  9. Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009;6(7). https://doi.org/10.1371/journal.pmed.1000097.

  10. Lahham A, McDonald CF, Moore R, et al. The impact of home-based pulmonary rehabilitation on people with mild chronic obstructive pulmonary disease: a randomised controlled trial. Clin Respir J. 2020;14(4):335–44. https://doi.org/10.1111/crj.13138.

    Article  PubMed  Google Scholar 

  11. Coultas DB, Jackson BE, Russo R, et al. Home-based physical activity coaching, physical activity, and health care utilization in chronic obstructive pulmonary disease chronic obstructive pulmonary disease self-management activation research trial secondary outcomes. Ann Am Thorac Soc. 2018;15(4):470–8. https://doi.org/10.1513/AnnalsATS.201704-308OC.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Holland AE, Mahal A, Hill CJ, et al. Home-based rehabilitation for COPD using minimal resources: a randomised, controlled equivalence trial. Thorax. 2017;72(1):57–65. https://doi.org/10.1136/thoraxjnl-2016-208514.

    Article  PubMed  Google Scholar 

  13. Chaplin E, Hewitt S, Apps L, et al. Interactive web-based pulmonary rehabilitation programme: a randomised controlled feasibility trial. BMJ Open. 2017;7(3):1–10. https://doi.org/10.1136/bmjopen-2016-013682.

    Article  Google Scholar 

  14. Li Y, Feng J, Li Y, Jia W, Qian H. A new pulmonary rehabilitation maintenance strategy through home-visiting and phone contact in COPD. Patient Prefer Adherence. 2018;12:97–104. https://doi.org/10.2147/PPA.S150679.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Khoshkesht S, Zakerimoghadam M, Ghiyasvandian S, Kazemnejad A, Hashemian M. The effect of comorbidity severity on pulmonary rehabilitation outcomes in chronic obstructive pulmonary disease patients. J Pak Med Assoc. 2015;65(10):1041–6. https://doi.org/10.1177/1479972318809472.

    Article  PubMed  Google Scholar 

  16. Pradella CO, Belmonte GM, Maia MN, et al. Home-based pulmonary rehabilitation for subjects with COPD: a randomized study. Respir Care. 2015;60(4):526–32. https://doi.org/10.4187/respcare.02994.

    Article  PubMed  Google Scholar 

  17. De Sousa Pinto JM, Martín-Nogueras AM, Calvo-Arenillas JI, Ramos-González J. Clinical benefits of home-based pulmonary rehabilitation in patients with chronic obstructive pulmonary disease. J Cardiopulm Rehabil Prev. 2014;34(5):355–9. https://doi.org/10.1097/HCR.0000000000000061.

    Article  PubMed  Google Scholar 

  18. Liu F, Cai H, Tang Q, et al. Effects of an animated diagram and video-based online breathing program for dyspnea in patients with stable COPD. Patient Prefer Adherence. 2013;7:905–13. https://doi.org/10.2147/PPA.S43305.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Mendes De Oliveira JC, Studart Leitão Filho FS, Malosa Sampaio LM, et al. Outpatient vs. home-based pulmonary rehabilitation in COPD: a randomized controlled trial. Multidiscip Respir Med. 2010;5(6):401–8. https://doi.org/10.1186/2049-6958-5-6-401.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Moore J, Fiddler H, Seymour J, et al. Effect of a home exercise video programme in patients with chronic obstructive pulmonary disease. J Rehabil Med. 2009;41(3):195–200. https://doi.org/10.2340/16501977-0308.

    Article  PubMed  Google Scholar 

  21. Horton EJ, Mitchell KE, Johnson-Warrington V, et al. Comparison of a structured home-based rehabilitation programme with conventional supervised pulmonary rehabilitation: a randomised non-inferiority trial. Thorax. 2018;73(1):29–36. https://doi.org/10.1136/thoraxjnl-2016-208506.

    Article  PubMed  Google Scholar 

  22. Lalmolda C, Coll-Fernández R, Martínez N, et al. Effect of a rehabilitation-based chronic disease management program targeting severe COPD exacerbations on readmission patterns. Int J COPD. 2017;12:2531–8. https://doi.org/10.2147/COPD.S138451.

    Article  CAS  Google Scholar 

  23. Nolan CM, Kaliaraju D, Jones SE, et al. Home versus outpatient pulmonary rehabilitation in COPD: A propensity-matched cohort study. Thorax. 2019:996–8. https://doi.org/10.1136/thoraxjnl-2018-212765.

  24. Coultas DB, Jackson BE, Russo R, et al. A lifestyle physical activity intervention for patients with chronic obstructive pulmonary disease a randomized controlled trial. Ann Am Thorac Soc. 2016;13(5):617–26. https://doi.org/10.1513/AnnalsATS.201508-508OC.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Ashmore J, Russo R, Peoples J, et al. Chronic obstructive pulmonary disease Self-management activation research trial (COPD-SMART): design and methods. Contemp Clin Trials. 2013;35(2):77–86. https://doi.org/10.1016/j.cct.2013.05.004.Chronic.

    Article  PubMed  PubMed Central  Google Scholar 

  26. NCT01423227. Benefits and costs of home-based pulmonary rehabilitation in Chronic Obstructive Pulmonary Disease. Clinicaltrials.gov.

  27. Holland AE, Mahal A, Hill CJ, et al. Benefits and costs of home-based pulmonary rehabilitation in chronic obstructive pulmonary disease - a multi-centre randomised controlled equivalence trial. BMC Pulm Med. 2013;13(1):1. https://doi.org/10.1186/1471-2466-13-57.

    Article  Google Scholar 

  28. Kon SSC, Canavan JL, Jones SE, et al. Minimum clinically important difference for the COPD assessment test: a prospective analysis. Lancet Respir Med. 2014;2(3):195–203. https://doi.org/10.1016/S2213-2600(14)70001-3.

    Article  PubMed  Google Scholar 

  29. Singh SJ, Jones PW, Evans R, Morgan MDL. Minimum clinically important improvement for the incremental shuttle walking test. Thorax. 2008;63(9):775 LP–777. https://doi.org/10.1136/thx.2007.081208.

    Article  Google Scholar 

  30. Vincent E, Sewell L, Wagg K, Deacon S, Williams J, Singh S. Measuring a change in self-efficacy following pulmonary rehabilitation: an evaluation of the PRAISE tool. Chest. 2011;140(6):1534–9. https://doi.org/10.1378/chest.10-2649.

    Article  PubMed  Google Scholar 

  31. Liu X-L, Tan J-Y, Wang T, et al. Effectiveness of home-based pulmonary rehabilitation for patients with chronic obstructive pulmonary disease: a meta-analysis of randomized controlled trials. Rehabil Nurs Off J Assoc Rehabil Nurses. 2014;39(1):36–59. https://doi.org/10.1002/rnj.112.

    Article  Google Scholar 

  32. Chen Y-Y, Yang X-X, Meng F-J. Home versus Centre-based pulmonary rehabilitation for patients with chronic obstructive pulmonary disease: a systematic review and meta-analysis. TMR Integr Med. 2020;4 https://www.tmrjournals.cn/public/articlePDF/20201205/7fe2774a7b137c5f73b49be31624ede2.pdf.

  33. Cox NS, Dal Corso S, Hansen H, et al. Telerehabilitation for chronic respiratory disease. Cochrane Database Syst Rev. 2021;2021(1). https://doi.org/10.1002/14651858.CD013040.pub2.

  34. Bandura A. Self-efficacy: the exercise of control. New York: W H Freeman/Times Books/ Henry Holt & Co; 1997.

  35. Selzler AM, Rodgers WM, Berry TR, Stickland MK. The importance of exercise self-efficacy for clinical outcomes in pulmonary rehabilitation. Rehabil Psychol. 2016;61(4):380–8. https://doi.org/10.1037/rep0000106.

    Article  PubMed  Google Scholar 

  36. Selzler A-M, Rodgers WM, Berry TR, McFadden K, Husband C, Hall C. Reciprocal relationships between self-efficacy, outcome satisfaction, and attendance at an exercise programme. Br J Health Psychol. 2019;24(1):123–40. https://doi.org/10.1111/bjhp.12343.

    Article  PubMed  Google Scholar 

  37. Taylor R, Dawson S, Roberts N, Sridhar M, Partridge MR. Why do patients decline to take part in a research project involving pulmonary rehabilitation? Respir Med. 2007;101(9):1942–6. https://doi.org/10.1016/j.rmed.2007.04.012.

    Article  PubMed  Google Scholar 

  38. Hayton C, Clark A, Olive S, et al. Barriers to pulmonary rehabilitation: characteristics that predict patient attendance and adherence. Respir Med. 2013;107(3):401–7. https://doi.org/10.1016/j.rmed.2012.11.016.

    Article  PubMed  Google Scholar 

  39. Keating A, Lee AL, Holland AE. Lack of perceived benefit and inadequate transport influence uptake and completion of pulmonary rehabilitation in people with Chronic Obstructive Pulmonary Disease: a qualitative study. 2011;57. https://doi.org/10.1016/S1836-9553(11)70040-6.

  40. Mathar H, Fastholm P, Lange P, Larsen NS. Why do patients decline participation in offered pulmonary rehabilitation? A qualitative study. Clin Rehabil. 2017;31(12):1674–83. https://doi.org/10.1177/0269215517708821.

    Article  PubMed  Google Scholar 

  41. Dechman G, Cheung W, Ryerson CJ, et al. Quality indicators for pulmonary rehabilitation programs in Canada: a Canadian thoracic society expert working group report. Can J Respir Crit Care, Sleep Med. 2019;3(4):199–209. https://doi.org/10.1080/24745332.2019.1643610.

    Article  Google Scholar 

  42. Huynh VC, Fuhr DP, Byers BW, Selzler A-M, Moore LE, Stickland MK. Influence of disease severity and exercise limitation on exercise training intensity and load and health benefits from pulmonary rehabilitation in patients with COPD. J Cardiopulm Rehabil Prev. 2018;38(5):320–6. https://doi.org/10.1097/HCR.0000000000000321.

    Article  PubMed  Google Scholar 

  43. Maltais F, Bourbeau J, Shapiro S, et al. Effects of home-based pulmonary rehabilitation in patients with chronic obstructive pulmonary disease. Ann Intern Med. 2008;149(12):869. https://doi.org/10.7326/0003-4819-149-12-200812160-00006.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported by a financial contribution from the Government of Alberta. The views expressed herein do not necessarily represent the official policy of the Government of Alberta. The Health Technology & Policy Unit, School of Public Health, University of Alberta, receives a multiyear unrestricted grant from Alberta Health to conduct health evidence reviews to inform policy decisions in the province. We would also like to acknowledge Dr. Serena Humphries and Susan Cleary for their contributions to the early work on this project.

Funding

The study received a grant from the Government of Alberta (grant number 008560). The funders had no role in the design and conduction of this study.

Author information

Authors and Affiliations

  1. School of Public Health, Health Technology and Policy Unit, 3-021 Research Transition Facility, University of Alberta, Edmonton, Alberta, T6G 2V2, Canada

    Tania Stafinski, Fernanda Inagaki Nagase, Melita Avdagovska & Devidas Menon

  2. Alberta Health Services, Edmonton, Alberta, Canada

    Michael K. Stickland

  3. Division of Pulmonary Medicine, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, Alberta, Canada

    Michael K. Stickland

  4. G.F. MacDonald Centre for Lung Health, Covenant Health, Edmonton, Alberta, Canada

    Michael K. Stickland

Authors
  1. Tania Stafinski
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Fernanda Inagaki Nagase
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Melita Avdagovska
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Michael K. Stickland
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Devidas Menon
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

In terms of contributions, TS, FN and DM conceived the presented idea, initiated the project and were responsible for the design of the protocol. TS, FN and MA did the review, data extraction, synthesis of results and quality assessment of studies. TS, FN, MA, MS and DM contributed to the analysis of the results. All authors have read and approved the manuscript.

Corresponding author

Correspondence to Devidas Menon.

Ethics declarations

Ethics approval and consent to participate

The University of Alberta’s Research Ethics Office waived ethical approval.

Consent for publication

Not required.

Competing interests

All authors declare no conflicts of interest.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Supplementary Appendix 1.

Literature search results. Supplementary Appendix 2. Summary of included studies of home-based pulmonary rehabilitation. Supplementary Appendix 3. Characteristics of patient populations across included studies. Supplementary Appendix 4. Summary of HBPR comparator interventions in included studies. Supplementary Appendix 5. Home based pulmonary rehabilitation program components. Supplementary Appendix 6. Risk of bias in RCTs. Supplementary Appendix 7. Risk of bias in non-randomized studies. Supplementary Appendix 8. Adverse events and deaths during follow-up period. Supplementary Appendix 9. Health-related quality of life –CAT, AQ 20, or VSRQ. Supplementary Appendix 10. Health related quality of life - Chronic Respiratory Disease Questionnaire (CRQ). Supplementary Appendix 11. Health related quality of life – St George’s Respiratory Questionnaire. Supplementary Appendix 12. Patient adherence to/compliance with HBPR or comparator. Supplementary Appendix 13. Frequency of exacerbations, hospital admissions and ER visits. Supplementary Appendix 14. Mental health. Supplementary Appendix 15. Self-efficacy.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Stafinski, T., Nagase, F.I., Avdagovska, M. et al. Effectiveness of home-based pulmonary rehabilitation programs for patients with chronic obstructive pulmonary disease (COPD): systematic review. BMC Health Serv Res 22, 557 (2022). https://doi.org/10.1186/s12913-022-07779-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12913-022-07779-9

Keywords

BMC Health Services Research

ISSN: 1472-6963

Contact us