Open Access Highly Accessed Study protocol

The impact of physical activity on fatigue and quality of life in lung cancer patients: a randomised controlled trial protocol

Haryana M Dhillon14, Hidde P van der Ploeg23, Melanie L Bell4, Michael Boyer5, Stephen Clarke67 and Janette Vardy14568*

Author affiliations

1 Centre for Medical Psychology and Evidence-based Decision-making, University of Sydney, Sydney, Australia

2 Sydney School of Public Health, University of Sydney, Sydney, Australia

3 Department of Public and Occupational Health, VU University Medical Center Amsterdam, Amsterdam, The Netherlands

4 Psycho-Oncology Co-Operative Research Group (PoCoG), School of Psychology, Faculty of Science, University of Sydney, Sydney, Australia

5 Sydney Cancer Centre, Sydney, Australia

6 Sydney Medical School, University of Sydney, Sydney, Australia

7 Royal North Shore Hospital, St Leonards, Australia

8 Sydney Cancer Centre, Concord Repatriation General Hospital, Hospital Rd, Concord, NSW, 2137, Australia

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Citation and License

BMC Cancer 2012, 12:572  doi:10.1186/1471-2407-12-572


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2407/12/572


Received:4 July 2012
Accepted:26 November 2012
Published:5 December 2012

© 2012 Dhillon et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

People with lung cancer have substantial symptom burden and more unmet needs than the general cancer population. Physical activity (PA) has been shown to positively influence quality of life (QOL), fatigue and daily functioning in the curative treatment of people with breast and colorectal cancers and lung diseases, as well as in palliative settings. A randomised controlled trial (RCT) is needed to determine if lung cancer patients benefit from structured PA intervention. The

    P
hysical
    A
ctivity in
    L
ung Cancer (PAL) trial is designed to evaluate the impact of a 2-month PA intervention on fatigue and QOL in patients with non-resectable lung cancer. Biological mechanisms will also be studied.

Methods/design

A multi-centre RCT with patients randomised to usual care or a 2-month PA programme, involving supervised PA sessions including a behavioural change component and home-based PA. QOL questionnaires, disease and functional status and body composition will be assessed at baseline, 2, 4 and 6 months follow-up. The primary endpoint is comparative levels of fatigue between the 2 arms. Secondary endpoints include: QOL, functional abilities and physical function. Exploratory endpoints include: anxiety, depression, distress, dyspnoea, PA behaviour, fitness, hospitalisations, survival, cytokines and insulin-like growth factor levels.

Discussion

This study will provide high-level evidence of the effect of PA programmes on cancer-related fatigue and QOL in patients with advanced lung cancer. If positive, the study has the potential to change care for people with cancer using a simple, inexpensive intervention to improve their QOL and help them maintain independent function for as long as possible.

Trial registration

Australian New Zealand Clinical Trials Registry No. ACTRN12609000971235

Keywords:
Physical activity; Exercise; Fatigue; Quality of life; Lung cancer

Background

Lung cancer is the leading cause of cancer-related death worldwide. In the United States alone it was estimated there would be 226,160 new lung cancer cases and 160,340 lung cancer deaths in 2012 [1]. The majority (60%) of lung cancer patients present with advanced, incurable disease resulting in a median survival of only 9–12 months [2]. In this context, the aim of anti-cancer treatment is to improve or maintain quality of life (QOL) in addition to prolonging survival.

Fatigue is one of the most common and distressing patient-reported symptoms associated with cancer and its treatment [3-5]. People with lung cancer report a higher prevalence and longer duration of cancer-related fatigue, leading to more functional impairment when compared to other cancer patients [6]. There is growing evidence that physical activity can improve fatigue in people with cancer, [7-9] and in those with chronic obstructive pulmonary disease (COPD) [10]. However, no study has evaluated the benefits of a lifestyle physical activity programme for people with non-resectable lung cancer. This study will determine if physical activity improves fatigue, in people with non-resectable lung cancer.

In the past five years several large observational studies have reported that physical activity reduces the risk of cancer recurrence, death from cancer, and death from all causes for breast and colon cancer patients [11-16]. These studies have shown consistently that more than 9 metabolic equivalent task (MET) hours/week of physical activity (e.g. walking at a moderate pace for 2.5 hours/week) is associated with improved health outcomes. This is similar to the health guidelines of 150 minutes of moderate intensity physical activity per week or 60 minutes of vigorous physical activity per week [17].

A burgeoning literature has examined the effects of physical activity on supportive care outcomes in people with cancer including physical fitness, physical function, fatigue and QOL [8,18-21]. Observed benefits of physical activity include improved cardiovascular and pulmonary function, musculoskeletal strength, maintenance of mobility and independence, and improved psychological well-being and QOL [9,22,23]. Systematic reviews and meta-analyses have concluded that physical activity interventions during and after cancer therapies often result in meaningful and reliable improvements in several supportive care outcomes [8,9,19,20,22-25]. These benefits include observed changes in physiologic measures, objective performance indicators, self-reported functioning and symptoms, psychological well-being and overall QOL. However, these studies did not include people with advanced lung cancer.

A large body of evidence documents the benefits of physical activity as a component of pulmonary and cardiac rehabilitation in similar clinical populations, which demonstrate improved QOL, functional status, and symptom control including dyspnoea in patients with COPD. A Cochrane review of 31 randomised controlled trials in chronic obstructive pulmonary disease patients found those receiving pulmonary rehabilitation had statistically and clinically significant improvements in QOL, including dyspnoea, fatigue and patient control over disease [10].

Despite the benefits of physical activity, only 20-32% of all cancer survivors report meeting physical activity guidelines [18,26-28]. A recent study in lung cancer survivors found that 73% did not meet the United States physical activity guidelines, and 51% did not participate in any moderate or vigorous physical activity at all [29]. Lung cancer survivors who met the physical activity guidelines reported significantly better QOL across multiple domains compared to those who did not meet the guidelines [30]. This suggests that there are considerable opportunities for improving the physical activity behaviour of lung cancer patients and possibly improving their QOL.

Most physical activity studies have been performed in cancer populations with potentially curative disease, particularly breast and colorectal cancer survivors. By comparison, people with advanced incurable lung cancer are older (median age of 70 years) and more likely to have co-morbidities such as chronic obstructive pulmonary disease and cardiovascular disease. However, physical activity has been found to be beneficial in older cancer patients, [3] and in a palliative population [21]. Cardiopulmonary exercise testing in people with advanced cancer, including lung cancer, has been shown to be safe and feasible, which suggests that most people would be able to follow a programme emphasising moderate intensity physical activity [31].

The biological mechanisms by which physical activity may modify cancer risk or disease progression, or improve symptom control, include changes in insulin-like growth factor (IGF) levels, immune regulation, sex and metabolic hormone levels, prostaglandin ratio and obesity [16,32-35]. More specific to lung cancer, physical activity improves pulmonary function and perfusion, [36] and it is hypothesised that physical activity may up-regulate antioxidants and free scavengers to help counteract the effects of cigarette smoke [37]. Physical activity may also decrease the risk of pneumonia and venothrombotic events, thereby improving overall survival and QOL in patients with non-resectable lung cancer.

Our aim is to evaluate a physical activity programme in people with non-resectable lung cancer to determine if it improves fatigue and quality of life. Our hypotheses are that people who undergo the physical activity intervention compared to those who do not, will: 1) report less fatigue; 2) have better health-related quality of life; 3) have improved overall survival; and, 4) have less decline in their level of physical function over time.

Methods/design

This multi-site, randomised controlled trial is being led by the Survivorship Research Group (SuRG) at the University of Sydney, Australia. Funding was obtained from a Young Investigator Award from the Lance Armstrong Foundation. The study was prospectively registered with the Australian New Zealand Clinical Trials Registry, registration number ACTRN12609000971235. Ethics approval has been obtained from Concord Repatriation General Hospital Human Research Ethics Committee for each participating institution under the New South Wales Health multi-site ethics approval scheme (HREC reference number: 08/CRGH/242).

Participants are recruited from lung cancer clinics at 4 Sydney hospitals, commencing May 2009 until achievement of planned sample size.

Consenting, medically fit people with non-resectable lung cancer, including non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) are randomised to usual care or a 2-month physical activity intervention (Figure 1). People with Stage III NSCLC or locally advanced SCLC being treated with curative intent must have completed combination chemo-radiotherapy a minimum of 4 weeks prior to randomisation, and have an incomplete response on staging CT scans. People with metastatic disease being treated palliatively may be receiving chemotherapy, radiotherapy and/or biological agents. All subjects must be medically fit to participate in a physical activity program, as assessed by the Physical Activity Readiness Questionnaire (PAR-Q) [38] and their treating physician. Major exclusion criteria are: Eastern Co-operative Oncology Group (ECOG) performance status ≥3, life expectancy < 6 months or insufficient English fluency to complete the questionnaires. Complete inclusion and exclusion criteria are outlined in Table 1. Randomisation is stratified for disease stage (locally advanced: NSCLC Stage III/ limited SCLC without a complete response to treatment versus metastatic disease: NSCLC Stage IV and extensive SCLC), ECOG performance status (0–1 versus 2), and cancer centre. It is performed by an external academic organisation using an interactive voice response system.

thumbnailFigure 1. Study flowchart. PRO = patient reported outcomes.

Table 1. Study inclusion and exclusion criteria

Control – standard of care

All participants will have routine follow-up as per local cancer centre practice and receive cancer-specific education materials regarding nutrition (Eat For Health) and exercise (Move Your Body) published by Cancer Council Australia (http://www.cancer.org.au/home.htm webcite) to encourage adoption of a healthy lifestyle.

Intervention

Theoretical framework

The physical activity programme is based on the Theory of Planned Behaviour, [39] and modelled after the successful behaviour change programme developed by the Diabetes Prevention Programme [40].

Participants randomised to the physical activity intervention arm will participate in a 2-month individualised physical activity and behavioural support programme with a Physical Activity Consultant (PAC).

The goal of the intervention will be to increase the participant’s physical activity over the 2-month intervention by a minimum of 3 MET hours per week compared to baseline. While this may be less than the recommended physical activity guidelines for some participants, those capable of increasing their MET hours further will be encouraged to do so.

The physical activity program will consist of supervised physical activity (30 to 45 minutes duration) and behaviour support sessions (15 to 30 minutes) once a week for 8 weeks, as well as unsupervised home physical activity sessions. The physical activity program (including supervised and unsupervised sessions) will be tailored to the participant’s baseline fitness, performance status and physical activity preferences, and take account of personal facilitators and barriers to physical activity. The study emphasises aerobic physical activity. Consequently it is expected that most participants will engage in walking as their preferred form of physical activity; however, other forms of aerobic activity such as swimming, cycling or running are acceptable. The program also incorporates advice about resistance exercises to encourage participants to maintain muscle function and strength.

The weekly structured sessions include physical activity as well as behaviour support sessions that use behaviour lifestyle change principles. It is the behaviour support sessions that will be the primary focus of the program promoting unsupervised physical activity. A full list of behaviour change session titles and their learning goals is outlined in Table 2. Participants will be supplied with a physical activity and behaviour change guidebook titled “Exercising with Lung Cancer”, a pedometer and physical activity diary for use throughout the intervention.

Table 2. Behaviour support sessions

Assessments

Outcomes will be assessed at baseline (prior to randomisation), 2, 4 and 6 months (Figure 1). Baseline assessments involve a medical history and examination. At all assessments, disease and treatment status will be recorded and subjects will complete patient reported outcome (PRO) questionnaires, a standardised fitness test (6 Minute Walk Test, [41] Senior’s Fitness Test, [41] hand grip strength [42]), and donate blood for biomarker analysis. All subjects will wear an Actigraph GT1M accelerometer [43] (Actigraph LLC, Pensacola, FL, USA) on the right hip to objectively determine physical activity for 7 full days prior to each assessment. Survival status will be obtained from the medical records, with follow up until the time of the final analysis.

Primary and secondary endpoints

The primary endpoint will be the level of self-reported fatigue as assessed by the Functional Assessment of Cancer Therapy - fatigue (FACT-F) subscale [44,45]. The primary outcome will be a comparison of fatigue in the intervention and control arms at the conclusion of the intervention (i.e. at the 2-month assessment).

Secondary endpoints will include the following Patient Reported Outcomes:

• QOL (European Organisation for Research and Treatment of Cancer –Quality of life questionnaire – Core (EORTC-QLQ-C30) and Lung module (LC-13 subscale) [46],

• activities of daily living and instrumental activities of daily living[47].

• physical function (6 Minute Walk Test) [41].

Other exploratory endpoints relating to physical activity and fitness will include:

• anxiety and depression (General Health Questionnaire 12) [48];

• distress (Distress Thermometer) [49],

• perceived cognitive function (FACT-Cognition v3) [50],

• sleep quality (Pittsburgh Sleep Quality Index) [51],

• dyspnoea (University of California San Diego Shortness of Breath Questionnaire [52] and physical activity and sedentary behaviour (Actigraph GT1M accelerometer; Active Australia questionnaire [53], sedentary behaviour questionnaire [54]);

• physical activity attitudes (Social Cognitive Determinants of Exercise questionnaire) [30,55]

• physical fitness (6 Minute Walk Test, Seniors Fitness Test, [41] hand grip strength);

• pulmonary function (Forced Expiratory Volume in 1 second, Forced Vital Capacity);

• general health, functional and performance status (anthropmetric measurements, Colinet co-morbidity score [56], ECOG performance status, admissions to hospital/hospice and survival data); and

• mechanisms and prognostic biomarkers (Glasgow Prognostic Score [C-reactive protein, albumin], selected cytokine levels, insulin-like growth factors).

Table 3 gives an overview of all outcome assessments.

Table 3. Assessments

Statistical analysis

Sample size

A sample size of 72 evaluable participants (36/arm) provides 80% power (two-tailed α 0.05) to detect a difference of 6 points (FACT-F subscale range: 0–52) in the primary outcome measure of fatigue between the two treatment arms at 2 months and assuming a standard deviation of 9 [57]. This is a standardized effect size of 0.67, thus each of the secondary outcomes is also powered at this level. Due to the poor prognosis for this patient population we need to increase our enrolment by 30% to account for attrition. Therefore, in total we will aim to recruit ~102 patients.

Statistical analyses

We report only on analyses for the primary and three secondary outcomes: fatigue, quality of life, activities of daily living, and the six minute walk test. Because of the potential for informative dropout, rigorous methods which account for missing data will be employed. There are three type of missing data. Data are missing completely at random (MCAR) if missing values and observed value are not systematically different. Data are missing at random (MAR) if any systematic differences can be explained by observed outcome or covariate data. Data are missing not at random (MNAR) when systematic differences exist, even after adjusting for previously observed data. A MAR primary analysis followed by sensitivity analyses are recommended by experts in the field of missing data [58].

Thus, our main analyses will use linear mixed models for all outcomes, which are unbiased for data which are MCAR or MAR and are consistent with the intention-to-treat principle [58-60]. Mixed model account for covariance between repeated measures on patients and allow for: 1) comparing patterns of change over time by testing the intervention group by time interaction; and 2) estimating and testing differences between groups at time points of interest via linear contrasts. Unadjusted and adjusted main analyses will be carried out, with adjustment for baseline measures including sex, age, disease stage, and the baseline outcome.

Patterns of missing data will be assessed to consider potential missing data mechanisms and baseline characteristics of patients lost to follow-up at 2, 4 and 6 months will be compared to patients who completed follow-up to assess patterns of loss to follow-up. Sensitivity analyses will be carried out using multiple imputation, which will include auxiliary data such as ECOG performance status and baseline secondary outcomes such as physical activity measures.

Overall survival is an exploratory endpoint, because the study has limited power to evaluate this. Patients alive at final analysis or who have become lost to follow up will be censored at their last contact date. Overall survival will be described by the Kaplan-Meier method. A stratified log-rank test adjusting for the stratification factors of disease stage (locally advanced vs metastatic) and ECOG performance status (0+1 vs 2) at randomisation will be used to compare overall survival between the two arms.

Discussion

Advanced lung cancer is incurable, and is the leading cause of cancer deaths world-wide. The goal of treatment is to improve QOL, maintain physical function and prolong life. Treatments to date have focused on disease modifying anti-cancer therapies (e.g. chemotherapy or radiation). A focus on the person and their functional status reflects an innovative approach to therapy, maximising their ability to live with miminal effects of the disease for as long as possible.

A physically active lifestyle improves fatigue and QOL in other cancer populations, particularly in early stage disease, but this type of intervention has not been evaluated in advanced lung cancer, where people are generally older with a higher burden of co-morbid illnesses than other cancer groups. This intervention has the potential to change standard care with a simple, safe, relatively inexpensive treatment that could improve the QOL of people with lung cancer and help them to maintain independent function for as long as possible. This study will determine whether a physical activity programme reduces the number of days participants spend in hospital for symptom control and end of life care. It will obtain unique data about the impact of physical activity on cytokines and the insulin pathway and the influence of each of these biomarkers on prognosis. It will provide preliminary evidence on whether physical activity can impact on survival in people with lung cancer.

One of the greatest challenges to implementation of physical activity programmes has been availability of adequate support and resources to promote and maintain adherence with physical activity. If a randomised controlled trial demonstrated a significant benefit for people with lung cancer this would not only provide great impetus to patients to increase their physical activity and oncologists to promote it, but provide an evidence base to support a change in policy and practice to ensure patients engage with a physical activity consultant to design and follow-up a personalised physical activity programme. The intervention under study has been designed to ensure it can be offered in a hospital or community setting.

Conclusions

Physical activity has been associated with many health benefits. This study will provide high-level evidence of the effectiveness of physical activity programmes to improve cancer fatigue and QOL in a cancer population with substantial symptom burden and high unmet needs. It will determine the feasibility of delivering exercise programmes in an advanced lung cancer population, and be powered to evaluate whether physical activity improves fatigue and QOL in this patient population. In addition, it will obtain important data about the impact of physical activity on physical function, body composition, mood, perceived cognitive function, dyspnoea, cytokines and the insulin pathway, and their influence on prognosis. The study outcomes have the potential to change standard care, with a non-toxic and inexpensive treatment, which can improve quality of life of people with lung cancer and help them achieve the highest possible level of independent function for as long as possible [61].

Competing interests

None of the authors has a conflict of interest to declare.

Authors’ contributions

HD and JV devised the study concept and design. All authors contributed to the study protocol. M.Bell was responsible for overseeing the statistical section. HD, HvP, M.Bell and JV wrote the manuscript. All authors read and approved the final manuscript.

Acknowledgements

The study has received funding from the Lance Armstrong Foundation / National Lung Cancer Alliance Partnership.

A/Prof. Janette Vardy is funded by the Cancer Institute NSW and Dr Haryana Dhillon received funding from the Australasian Lung Trials Group and Psycho-Oncology Co-Operative Research Group (PoCoG). Dr Hidde van der Ploeg was supported by an Australian National Health and Medical Research Council programme grant (#301200).

An equipment grant was received from the Sydney Cancer Centre Foundation for purchase of gymnasium equipment for use by trial participants.

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