Taking Charge: A Proposed Psychological Intervention to Improve Pulmonary Rehabilitation Outcomes for People with COPD
Received 22 June 2020
Accepted for publication 20 August 2020
Published 11 September 2020 Volume 2020:15 Pages 2127—2133
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Richard Russell
Amanda McNaughton,1,2 William Levack,3 Harry McNaughton2
1Department of Respiratory Medicine, Nottingham University Hospitals NHS Trust, Nottingham, UK; 2Medical Research Institute of New Zealand, Wellington, New Zealand; 3Department of Medicine, University of Otago, Wellington, New Zealand
Correspondence: Amanda McNaughton Email [email protected]
Abstract: Pulmonary rehabilitation (PR) is an important, evidence-based treatment that improves outcomes for people with COPD. Individualized exercise programmes aim to improve exercise capacity; self-management education and psychological support are also provided. Translating increased exercise capacity into sustained behavioural change of increased physical activity is difficult. Other unresolved problems with PR programmes include improving uptake, completion, response and sustaining long-term benefit. We offer a different perspective drawn from clinical experience of PR, quantitative and qualitative studies of singing groups for people with COPD, and stroke rehabilitation research that gives psychological factors a more central role in determining outcomes after PR. We discuss Take Charge; a simple but effective psychological intervention promoting self-management––that could be used as part of a PR programme or in situations where PR was declined or unavailable. This may be particularly relevant now when traditional face-to-face group programmes have been disrupted by COVID-19 precautions.
Keywords: pulmonary rehabilitation, self-management, self-efficacy, psychological
People living with chronic obstructive pulmonary disease (COPD) commonly carry substantial psychological morbidity along with their chest disease.1,2 Furthermore, psychological factors can influence uptake and outcomes of the most effective therapy available for people with COPD – pulmonary rehabilitation (PR).3,4 PR service providers aim to be “patient-centred” in their approach5,6 and "empower patients"7 with both personalized exercise prescription, self-management education and psychological supports. PR audit reports also recommend services be responsive to people from ethnic minorities.8 These goals are challenging, especially as face-to-face PR services are likely to remain significantly disrupted in a COVID-19 world. Interventions that help people with COPD self-manage their condition without face-to-face input would be a real advantage.
“Take Charge” is a psychological intervention that potentially meets all these criteria. It is low-cost, requires minimal training and is effective as an adjunct to community rehabilitation for people after acute stroke9– another group with significant psychological comorbidities that affect outcomes. It is also fully person-centred and of proven effectiveness in ethnic minority groups.10 With minor modifications from the version used in the stroke trials, Take Charge was used in a feasibility study for people with COPD following acute exacerbations requiring hospitalization.11 The stroke study booklet and training manual are available, free to use (www.mrinz.ac.nz/programmes/stroke).
In this article, we briefly describe the Take Charge intervention and evidence for benefit for people with stroke. We will draw parallels between the evidence concerning stroke rehabilitation and pulmonary rehabilitation, dominated in stroke by physical therapy approaches, and by exercise training in PR and suggest an alternative perspective based on hope, purpose and motivation. Finally, we will propose options for using Take Charge for people with COPD as part of pulmonary rehabilitation.
Learning from the Stroke Rehabilitation Literature
Although the abrupt onset of stroke requires a different model of rehabilitation from that of pulmonary rehabilitation (PR), PR and stroke rehabilitation (SR) share similarities. Both are supported by overwhelming evidence of effectiveness.12,13 Nearly 30 randomized controlled trials (RCTs) confirm a significant reduction in mortality of patients managed in inpatient stroke and stroke rehabilitation units compared to management in general medical wards.13 Both PR and SR are “black box” interventions – a complex mixture of components with considerable uncertainty as to which parts are critical to successful outcomes.14 Finally, both PR and SR aim for behaviour change on the part of participants which is likely influenced by the nature and strength of the relationship between participants and health professionals; an unequivocally “psychological” variable.
Following on from the SR trials, coordinated, therapist-led interventions are the recommended approach to stroke rehabilitation.15,16 However, large randomized controlled trials aimed at optimizing the timing, dose and specific type of therapy-led intervention (compared to “usual care”) have failed to show any additional benefit for patients at the level of independence or quality of life.17 This has led some to question the idea that the improved outcomes in the SR trials were solely the result of coordinated therapy.17 One alternative hypothesis is that SR has an important psychological component helping to increase motivation in the person with stroke. Most of the SR RCTs were conducted at a time when patients with stroke were managed on general medical wards, with no specific treatments apart from nursing care, and a significant expectation from health professionals, families and patients that this was a life-ending or life-changing event. A key component of stroke rehabilitation units was a shared enthusiasm for managing stroke, mobilizing patients and working with an expectation that there was “life after stroke”.18 It is possible that patients (and their families) with this hope of a positive future, simply did not die as frequently as those without it. Having hope could substantially affect engagement in physical therapy both in the hospital and at home, enhancing physical recovery. So enhancing personal motivation, in addition to a therapy-led rehabilitation approach, may improve outcomes, where a purely therapy-led approach does not.
Evidence to support this hypothesis comes from two large RCTs involving 572 participants after stroke, testing a psychological intervention aimed at increasing personal motivation.9,10 The Take Charge intervention was tested in the early community phase of stroke rehabilitation, 2–16 weeks after acute stroke, in addition to usual community stroke rehabilitation. One of these studies was with participants from ethnic minority populations.10 This very brief intervention (one or two 60 minute sessions in the person’s home) uses simple images and prompts, to help the person look beyond their medical condition – in this case, stroke - and transform from a “stroke person” into “the real ‘me’ who happens to have had a stroke” (see Figure 1).9 Twelve months after stroke, people exposed to the Take Charge intervention in the Taking Charge after Stroke (TaCAS) trial9 were performing significantly more advanced activities of daily living, were less likely to be dependent on another person for help, and reported better quality of life. These are the first trials of a specific stroke rehabilitation intervention that have shown a sustained benefit at the level of independence or quality of life.17
Figure 1 Taking Charge: aiming for transformation from a patient defined by their medical condition to the person they really are, who happens to have a medical condition.
“Taking Charge” embraces four fundamental components: a sense of autonomy, a sense of purpose, a sense of competence or mastery and connectedness with others. These components have been extensively studied in the fields of education and psychology as part of Self-Determination Theory.20 A facilitator, trained to be completely non-directive, guides the person through the Taking Charge booklet. The first three pages concentrate on sense of purpose, personal identity and hopes for the future, modified as necessary for the specific medical condition of interest (see Figure 2). Further pages consider the issues of importance for the person (eg physical activity, mood, finances, supports, information, disease prevention) with a structure that allows them to break down their hopes for the future into “do-able” steps and identify their key support person/people. All ideas come from the person or their family, and the facilitator is trained not to provide ‘helpful suggestions’ ie this is all about the unique individual and is therefore fully person-centred.
Figure 2 The first page of the Take Charge booklet from a feasibility study for people with exacerbations of COPD requiring hospitalization11 showing the translation from the “Taking Charge” concept in Figure 1 to a specific medical condition, in this case, COPD. The words “matua”, “whaea”, “koro”, and “kuia” are in the Māori language, with English equivalents of parent, mother, male and female elders/grandparents.
PR is also a complex intervention. Exercise-training is a core component of PR programmes; guidelines indicate minimum levels of both dose and frequency, tailored to the individual, aiming to increase exercise capacity.21,22 There is growing evidence of both the importance of increased physical activity as part of the efficacy of PR, and the substantial independent contribution this makes to health and survival.23–25 Translating a personalized exercise programme into the sustained behavioural change of increased physical activity remains a significant challenge for PR. This will be potentially more difficult in COVID-19 pandemic environments.26 Other problems with PR include gross under-utilization of PR (low rates of PR referral, uptake and completion) and considerable heterogeneity in patient responses to PR, as measured by exercise capacity, breathlessness scores, and health-related quality of life.27,28 Universal barriers to attendance include: travel and transport, depression, comorbidities, reduced perceived benefit, and socio-economic deprivation; others are patient or place-specific, eg ethnicity.29,30 There is evidence that adaptive coping strategies to ill-health affect response to PR.31 But although anxiety (36%) and depression (40%) are common in patients with COPD, there is no evidence that these conditions impact on rates of completion or response to PR.1,2,32
So how can we facilitate behaviour change to increase physical activity? Various groups have studied the use of counselling, coaching and goal setting after PR, generally showing small improvements in physical activity.34,35 The barriers and enablers to increasing physical activity for people living with COPD are complex and varied, including physical, environmental and psychosocial factors.
COPD and Pulmonary Rehabilitation: The Psychosocial Dimension
Living with COPD has social and psychological consequences besides physical constraints. Anxiety, depression, impaired ability to work, problems with sexual function and limitations in social activities impact on wellbeing. An individual’s symptoms of breathlessness, and level of disability are complex. The Breathe Oxford group argue that this is beyond the complicated pathophysiology, incorporating prior experiences and expectations as well as the personal perception of body signals.35 Most PR programmes include an educational component usually concentrating on self-management, including how to manage breathlessness, medication adherence, inhaler technique, action plans for exacerbations and nutrition, as well as promotion of mental health and facilitation of advanced care plans. Delivered as education, they are by definition health-professional-centred, and in terms of sustained behavioural change, their effectiveness is variable.36,37
Outside of PR, many non-pharmacological interventions have shown positive outcomes in terms of mood for people with COPD, including home-based cognitive behavioural therapy, mindfulness, motivational interviewing and singing.38–45
Two randomized controlled trials of singing group interventions in COPD report improvements in quality of life and reduction in anxiety, although not in lung function.41,42 In our singing group study, there was a significant reduction in the Hospital Anxiety and Depression Scale (HADS) anxiety score between baseline and one year, as well as a significant increase in 6MWT.43 One explanation for the improvement in 6MWT after singing group programmes is that participants are personally motivated – they attempt more themselves (autonomy), have realistic personal goals for improvement (competence/mastery), look forward to the activity and the future (purpose), and feel more socially connected – all components of Take Charge.9 In our qualitative study of a COPD singing group, it was clear that social connection in a safe place was a key priority for participants,44 confirmed in other studies of PR.32 The participants in these studies appreciated the camaraderie of the singing group, with the once-weekly sessions at a community venue being a crucial part of their social schedule. Many of the group overcame significant barriers – transport, weather, intermittent ill-health, exercise restriction – to attend at unexpectedly high rates (85%) over a full year.43 We think that the social connection component of the singing group, while at the same time doing something that is both challenging and enjoyable, was influential in maintaining the high attendance rate as well as the improved outcomes.
The Importance of Social Connection, Mood and Hope
The importance of social connection for health and wellbeing is well established. Social isolation, loneliness, and living alone are associated with a 26–32% increased likelihood of mortality in the general population,46 and there is no reason to think the COPD population is any different.1 Furthermore, in the general population, social isolation has a significant bidirectional relationship with depression and anxiety.47 It makes sense that the same should hold for people with COPD.
Just as people with stroke managed on dedicated stroke rehabilitation wards may be more likely to hope (and believe) in a “life after stroke”, we feel one of the key contributors to the consistent benefits of PR, cognitive behavioural therapy and community activities such as COPD singing groups, is that involvement provides a person with COPD the hope (and belief) in “life beyond COPD”. For people living with progressive dyspnoea and exercise limitation, often accompanied by social isolation, that hope may be the catalyst for engaging in physical and social activities that were previously thought “too hard”.48 Other evidence supports this view.49 Arnold and colleagues showed that improvements in quality of life scores after PR were associated with increases in measures of self-efficacy and suggested that “focussing more explicitly on the enhancement of perceptions of personal control in COPD patients may be an important aim of pulmonary rehabilitation”.50
A “Take Charge” Approach for People with COPD?
There is nothing stroke-specific about Take Charge and early qualitative work showed that patients with a range of medical conditions valued this idea.51 Morgan and others have called for a more “person-centred” approach to the person with COPD without being specific about how to go about this.5 Take Charge is such a person-centred intervention. A feasibility study using a modified Take Charge intervention for people with a recent exacerbation of COPD requiring hospitalization is complete, and results are awaited.11 In that study, there was no problem modifying Take Charge for people with COPD. Building on that work, Take Charge could be tested as an adjunct to standard PR programmes, or for people who decline PR, as a standalone intervention. Meantime, some services wanting to provide a validated tool for person-centred interaction, might choose to incorporate the Take Charge approach into existing PR programmes, at minimal cost. Service configurations have changed dramatically with the advent of COVID-19, both for people with stroke and COPD. Although Take Charge has, so far, only been tested face-to-face, it is possible to deliver the facilitator input by telephone, video link or online chat with the person interacting with a hard copy of the booklet. In a COVID-19 world of limited face-to-face interactions and restrictions on group activities, the built-in social interaction of a regular PR group or singing group will be diminished. There will be a greater onus on the individual with COPD to undertake some or all components of a PR programme on their own. An intervention like Take Charge that explicitly encourages self-management, along with identification of key supporters would be a significant advantage.
The psychological dimension of PR may be crucial to its effectiveness and enhancing that effect is worthy of further consideration by providers, audit authorities and researchers. A better understanding of this idea and trials of focussed psychosocial interventions may allow a broader range of effective interventions for people with COPD. Our view is we should help the person with COPD get as much out of their life as they want rather than settling for self-management of their condition alone– ie to become “a person who happens to have COPD” rather than remain a “COPD patient”. The Take Charge intervention is one option to help make this happen.
The authors report no conflicts of interest in this work.
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