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BMJ 2007;334:517 (10 March), doi:10.1136/bmj.39094.648553.AE (published 16 February 2007)
Nanette Mutrie, professor of exercise and sport psychology1, Anna M Campbell, research fellow1, Fiona Whyte, Macmillan cancer lecturer2, Alex McConnachie, senior analyst3, Carol Emslie, research scientist4, Laura Lee, research assistant1, Nora Kearney, professor of cancer care5, Andrew Walker, health economist3, Diana Ritchie, consultant oncologist6
1 Department of Sport, Culture and the Arts, Strathclyde University, Glasgow G13 1PP, 2 Nursing and Midwifery School, University of Glasgow, Glasgow G12 8LW, 3 Robertson Centre for Biostatistics, University of Glasgow G12 8QQ, 4 MRC Social and Public Health Sciences Unit, Glasgow G12 8RZ, 5 Cancer Care Research Centre, Department of Nursing and Midwifery, University of Stirling, Stirling FK9 4LA, 6 Beatson Oncology Centre, Glasgow G11 6NT
Correspondence to: N Mutrie nanette.mutrie{at}strath.ac.uk
Design Pragmatic randomised controlled prospective open trial.
Setting Three National Health Service oncology clinics in Scotland and community exercise facilities.
Participants 203 women entered the study; 177 completed the six month follow-up.
Interventions Supervised 12 week group exercise programme in addition to usual care, compared with usual care.
Main outcome measures Functional assessment of cancer therapy (FACT) questionnaire, Beck depression inventory, positive and negative affect scale, body mass index, seven day recall of physical activity, 12 minute walk test, and assessment of shoulder mobility.
Results Mixed effects models with adjustment for baseline values, study site, treatment at baseline, and age gave intervention effect estimates (intervention minus control) at 12 weeks of 129 (95% confidence interval 83 to 176) for metres walked in 12 minutes, 182 (75 to 289) for minutes of moderate intensity activity reported in a week, 2.6 (1.6 to 3.7) for shoulder mobility, 2.5 (1.0 to 3.9) for breast cancer specific subscale of quality of life, and 4.0 (1.8 to 6.3) for positive mood. No significant effect was seen for general quality of life (FACT-G), which was the primary outcome. At the six month follow-up, most of these effects were maintained and an intervention effect for breast cancer specific quality of life emerged. No adverse effects were noted.
Conclusion Supervised group exercise provided functional and psychological benefit after a 12 week intervention and six months later. Clinicians should encourage activity for their patients. Policy makers should consider the inclusion of exercise opportunities in cancer rehabilitation services.
Trial registration Current controlled trials ISRCTN12587864 [controlled-trials.com] .
Physical activity levels reduce significantly for many women after a diagnosis of breast cancer and remain low after treatment is completed.56 A prospective observational study in survivors of breast cancer has indicated a 50% risk reduction in mortality among women who are regularly active compared with those who remained inactive post-diagnosis.7 A recent systematic review of the effects of exercise on breast cancer patients and survivors concluded that exercise is an effective intervention to improve quality of life, cardiorespiratory fitness, physical functioning, and fatigue.8 However, a more recent Cochrane review, which examined exercise interventions exclusively during treatment for breast cancer, found improvements in physical fitness and activities of daily life but no significant improvements in quality of life or fatigue.9 Little of the existing evidence comes from the UK or a National Health Service (NHS) setting.
We aimed to determine if participating in a supervised group exercise programme for women during treatment for early stage breast cancer had functional and psychological benefits. We tested the hypotheses that 12 weeks of supervised group exercise, as an adjunct to usual care, would improve quality of life for women during treatment for early stage breast cancer and that benefits would be maintained for six months after the intervention.
Protocol, assignment, and masking
This study was a two group (intervention and control) by three time points (baseline, 12 weeks, and six month follow-up) randomised controlled trial. After obtaining written informed consent and baseline measures, we randomly allocated women into one of two groups. The randomisation was stratified by hospital and treatment at baseline (chemotherapy, radiotherapy, or combination) and used randomised permuted blocks of length four and six (that is, for sequences of four or six women in each hospital-treatment combination, exactly half were allocated to each group). Randomisation was done by telephone to an interactive voice response system. We entered and managed all data in an anonymised format; we held data on patient contacts and other administrative data in a separate database. The study was a pragmatic, randomised, prospective, open trial. In exercise studies, blinding the participants to allocation is not possible. We took steps to blind the evaluation of outcomes by having questionnaire responses in sealed envelopes and ensuring that outcome measures were taken by researchers who were not involved in exercise classes. We sent a letter to general practitioners informing them of their patients' participation in the study.
Outcome measures
The primary outcome measure was quality of life, as measured by the functional assessment of cancer therapygeneral (FACT-G) questionnaire.11 This questionnaire comprises four core domains of quality of lifephysical (FACT-GP), functional (FACT-GF), social (FACT-GS), and emotional (FACT-GE)and is considered appropriate for use with cancer patients. Breast cancer, fatigue, and endocrine symptoms subscales have been developed and, when added to the FACT-G score, are described as FACT-B, FACT-F, and FACT-ES.1213 Secondary outcomes were the Beck depression inventory, the positive and negative affect scale, body mass index, seven day recall of physical activity (Scottish physical activity questionnaire), performance in a 12 minute walk test, and score on a shoulder mobility test.1415161718
Intervention
Women assigned to the intervention group received usual care from their healthcare team and, in addition, were invited to attend a supervised group exercise programme. The exercise programme ran for 12 weeks, and women were encouraged to attend two classes and do one additional exercise session at home each week. Fourteen exercise classes led by specifically trained exercise specialists took place in eight community exercise facilities that were all accessible by public transport. Classes were timetabled at various times in the day and evening. The exercise intervention was based on guidelines for prescription of exercise for cancer patients and survivors.19 The classes consisted of a warm-up of 5-10 minutes, 20 minutes of exercise (for example walking, cycling, low level aerobics, muscle strengthening exercises, or circuits of specifically tailored exercises), and a cool-down and relaxation period. The exercise class lasted 45 minutes in total. Women were monitored throughout the class to ensure that they were exercising at a moderate level (50-75% of age adjusted maximum heart rate). Each week, for six weeks, a specific theme was covered in group discussion after the exercise (for example, the health benefits of exercise, enhancing self efficacy, setting goals) and supported with specifically constructed materials. These themes were guided by a model of behaviour change and were designed to promote independent exercise after the intervention.20 We repeated the six week block on a rolling basis, allowing all participants to hear the same themes. At the end of the 12 week intervention, the women were helped to construct an individual exercise programme and invited to join a local general practice exercise referral scheme. Further details of the intervention and the expertise of the staff are available on our website (www.strath.ac.uk/sca/staff/mutrie_n.html).
Women assigned to the control group received usual care from the healthcare team and completed all outcome measures on the same time frame as the intervention group. After randomisation, this group received a two page leaflet entitled "Exercise after cancer diagnosis," which provided safe guidelines. After the six month follow-up, these women were helped to construct their own personalised exercise plan and invited to join a local general practice exercise referral scheme.
Statistical power and analysis
With 91 participants in each group, the study was designed to have 90% power at a 5% level of significance to detect an intervention effect of approximately 7.5 units on the change in FACT-G score after 12 weeks, assuming a standard deviation of this outcome of 15 units. We based this change on findings from our pilot study.21 The primary analysis, and the main analysis applied to each secondary outcome, was to test whether significant differences existed between the exercise group and control group in outcomes at the end of the 12 week intervention period and at six months post-intervention, adjusting for the stratification variables (study site and treatment at baseline), age, and baseline value of the outcome. We did the analysis on an intention to treat basis, in the sense that we took no account of adherence to the intervention. We used all available data.
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Intervention effect estimates for the six month follow-up data were 105 (60 to 151) for metres walked in 12 minutes, 2.5 (1.4 to 3.6) for shoulder mobility, 1.5 (0.1 to 2.9) for breast cancer specific subscale quality of life (when this subscale is added to the FACT-G a significant effect (4.9, 0.2 to 9.6) for FACT-B emerges), 1.4 (0.3 to 2.5) for the social domain (FACT-GS), and 3.9 (1.6 to 6.1) for positive mood. At the follow-up we also saw non-significant trends towards improvements on the primary outcome (FACT-G; +3.6 points, P=0.053), the functional domain of the FACT-G score (FACT-GF; +1.1 points, P=0.067), and depression (1.8 points, P=0.064) in favour of the intervention.
Figure 3
shows the use of health services in the study up to the six month post-intervention follow-up. Ten per cent of patients in the intervention group and 20% in the control group reported at least one night in hospital, and 72% and 84% reported at least one visit to their general practitioner. The intervention group reported fewer nights in hospital (Mann-Whitney test, P=0.044) and fewer visits to their general practitioner (P=0.011) than the control group.
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Strengths and weaknesses
This is the first full scale randomised controlled trial in the UK of a group based exercise programme for breast cancer patients during treatment and has the largest sample size of published exercise trials in breast cancer. The study had an appropriate range and number of participants and is unique in including a follow-up. The dropout rate from the trial was 14%, which is similar to other studies on exercise in cancer.23
One weakness is that we do not know which aspect of the group exercise experience provided most benefit. Our qualitative data suggest that the group itself was an important aspect and that exercise in standard settings did not provide the same benefits.24 However, studies that have used appropriate comparison groups to rule out a placebo effect suggest that these beneficial effects cannot be completely attributed to non-specific characteristics of the programme (such as increased attention from fitness instructors) or support received from fellow patients.2225 In addition, improvements in the 12 minute walk and shoulder mobility tests in favour of the intervention group are more directly attributable to the exercise than to the group effect.
Meaning
A diagnosis of cancer can signal a "teachable moment," and patients often show an enhanced motivation to change lifestyle behaviours.26 Women benefited from the provision of exercise classes, and these benefits may be caused by the exercise itself, by the group experience, or by a combination of both. Clinicians should encourage activity for patients with cancer, and policy makers should consider including opportunities for exercise in cancer rehabilitation services, similar to the exercise component in cardiac rehabilitation. Further research is needed on the effects of exercise on patients with and survivors of cancers other than breast cancer. In addition, home based programmes need to be evaluated, as many women could not attend exercise classes because of the distance they needed to travel; this would also allow a test of exercise alone without the group effect.
Conclusion
Supervised group exercise in addition to usual care for women receiving treatment for early stage breast cancer provided functional and psychological benefit at the end of a 12 week programme and at the six month follow-up.
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Funding: Cancer Research UK. The funders were independent from the conduct and outcomes of this study. CE is funded by the UK Medical Research Council.
Competing interests: None declared.
Ethical approval: West ethics committee of Greater Glasgow Health Board (LREC Ref:03/22(2)).
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