Randomized pilot test of a lifestyle physical activity intervention for breast cancer survivors

Randomized pilot test of a lifestyle physical activity intervention for breast cancer survivors

Patient Education and Counseling 64 (2006) 225–234 www.elsevier.com/locate/pateducou Randomized pilot test of a lifestyle physical activity intervent...

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Patient Education and Counseling 64 (2006) 225–234 www.elsevier.com/locate/pateducou

Randomized pilot test of a lifestyle physical activity intervention for breast cancer survivors Karen Basen-Engquist a,*, Cindy L. Carmack Taylor a, Carol Rosenblum a, Murray A. Smith a, Eileen H. Shinn a, Anthony Greisinger b, Xylina Gregg c, Pamela Massey a, Vicente Valero a, Edgardo Rivera a a

The University of Texas M.D. Anderson Cancer Center, USA b Kelsey Research Foundation, USA c Kelsey-Seybold Clinic, USA

Received 25 June 2005; received in revised form 10 February 2006; accepted 13 February 2006

Abstract Objective: This paper will report the results of a pilot test of a 6-month, 21-session intervention to increase breast cancer survivors’ physical activity by teaching them to incorporate short periods of moderate activity into their daily routines (lifestyle intervention). The effect of the intervention on physical performance, quality of life, and physical activity are reported. Methods: Sixty breast cancer survivors were randomized to either a lifestyle intervention or a standard care control group. Physical performance, quality of life (Medical outcomes study short form-36 [SF-36]), and physical activity (7-day recall and motivation readiness), were assessed at baseline and 6 months. Results: The lifestyle group had significantly better performance in the 6-min walk task than the controls ( p = 0.005) at 6 months. The intervention had positive effects on the bodily pain ( p = 0.020) and general health ( p = 0.006) subscales from the SF-36. The lifestyle group had a greater motivational readiness for physical activity at 6-month than standard care, but no significant differences were seen between the two in terms of number of minutes of moderate or more intense physical activity or number of days on which they did 30 min of moderate or more intense activity. Conclusions: Despite the small sample size, the lifestyle intervention showed promise for improving physical functioning and quality of life and increasing physical activity, and should be tested in a larger randomized trial. Practice Implications: If the lifestyle approach is shown to be effective in a larger trial, it represents a highly feasible intervention that it can be delivered to cancer survivors by health care institutions or community organizations without dedicated exercise facilities and equipment. # 2006 Elsevier Ireland Ltd. All rights reserved. Keywords: Breast cancer; Physical activity; Adherence; Cancer survivors; Quality of life; Physical functioning

1. Introduction Exercise improves breast cancer survivors’ physical and psychological functioning [1-4]; it may reduce the risk of cancer recurrence [5], second primary cancers and other chronic diseases [6-8], as well as prolong survival [5]. * Corresponding author at: Department of Behavioral Science, The University of Texas M.D. Anderson Cancer Center, P.O. Box 301439-Unit 1330, Houston, TX 77230-1439, USA. Tel.: +1 713 745 3123. E-mail address: [email protected] (K. Basen-Engquist).

Research with cancer survivors has demonstrated that exercise increases muscle strength [9] and cardiovascular fitness [10,11], improves physical functioning [11,12], helps to control body weight [11], decrease body fat [13,14], and lower blood pressure [15]. Exercise may also alleviate symptoms that interfere with the daily life of cancer patients and survivors, such as fatigue [9,10,16-19], nausea [18], and sleep disturbance [12]. Associations between exercise and emotional well-being have been documented in observational research [20,21] and quasi-experimental [18,22] and randomized studies [10,12,15,16] involving cancer patients

0738-3991/$ – see front matter # 2006 Elsevier Ireland Ltd. All rights reserved. doi:10.1016/j.pec.2006.02.006

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and survivors, although most trials have not controlled for the possible emotional benefits of factors other than exercise, such as attention from the intervention staff. There is emerging evidence that exercise and physical activity are beneficial for cancer survivors; the evidence is particularly compelling for breast cancer survivors [23]. Currently published clinical trials of exercise in cancer survivors have primarily prescribed uniform, structured, and often gym-based exercise programs that meet these requirements. Structured exercise interventions generally require participants to come to a center to exercise at a specified duration and frequency (e.g., 30 min four times per week). However, research in the general population indicates that structured exercise programs pose significant barriers to long-term adherence. If these barriers, which include a lack of access to facilities and equipment, lack of knowledge about appropriate exercise, and insufficient time for a regular schedule of exercise [24], interfere with adherence in healthy populations, they may be even more significant for cancer survivors or others with serious or chronic health problems. It is possible that different approaches will be needed to enhance wide scale adoption of physical activity in a cross-section of cancer survivors. The logical next step in developing physical activity interventions for cancer survivors, therefore, is to study methods to increase adherence to a physically active lifestyle by variably motivated, sedentary cancer survivors who may not have access to a gym, exercise equipment, or highly trained exercise professionals, and to test whether such interventions improve quality of life and physical functioning in cancer survivors. According to behavioral theory and empirical research concerning the adoption and maintenance of increased physical activity by healthy populations, interventions are more effective when they aim to teach cognitive and behavioral skills, provide social support, and increase selfefficacy [25–32]. It is likely that the same holds true for cancer survivors, although interventions for this population may require some modifications in message and methods. Theorybased research on variables affecting cancer survivors’ adoption and maintenance of physical activity is limited. Courneya and colleagues have conducted most of this research using the theory of planned behavior [33] to study cancer survivors’ adherence to physical activity. Briefly, this theory states that behavior is a function of the intention to perform a behavior and the person’s perceived behavioral control over the behavior (a construct similar to self-efficacy). Intention is formed by the attitudes held toward the behavior, the subjective norm (perception of how others want the person to act), and perceived behavioral control. Studies of several cancer survivor samples demonstrate that models of exercise behavior for cancer survivors differ somewhat from those of healthy individuals [34], particularly with regard to the beliefs about outcomes that are hypothesized to create attitudes [35,36], forming the basis for behavioral intent. Overall, the studies demonstrate significant variability in the degree to

which attitude, subjective norm, or self-efficacy predict the intention to exercise. Research on the theory of planned behavior enhances our understanding of some of the factors associated with the adoption of physical activity and helps identify appropriate intervention messages for particular populations. However, it does not specify methods for changing behavior or behavioral correlates [37]. Therefore we looked to intervention approaches that have been used with healthy but sedentary populations to identify an intervention approach that would be more likely to be adopted by cancer survivors outside the setting of a clinical trial. Recognition of barriers to long-term participation in structured exercise programs, in concert with the demonstrated health benefits of even short bouts of moderate activity [38], led to development of the lifestyle approach to increasing physical activity. Participants in this type of intervention learn cognitive and behavioral skills and ways to incorporate moderate physical activity into their daily routine by: (a) accumulating short bouts of moderate to vigorous activity throughout the day; (b) integrating activity into daily routines, like performing household or occupational work at moderate intensity, walking briskly for brief periods, climbing stairs; (c) performing activities they choose, as opposed to prescribed exercise [39]. These interventions have effectively increased physical activity and decreased cardiovascular risk factors in healthy populations [26,27,28], obese women [40,41], and overweight men and women [42]. However, this approach has rarely been tested to determine whether it produces improvements in quality of life, nor has it been tested in cancer survivor populations. Therefore, we aimed to test the effect of a lifestyle physical activity intervention on quality of life and physical functioning of breast cancer survivors. Interventions using the lifestyle approach to increasing physical activity, if effective with cancer survivors, could be highly disseminable because they do not require a highly trained personnel or specialized facilities to implement. We conducted with randomized pilot test in order to determine if a large scale randomized controlled trial of a lifestyle physical activity intervention was warranted. We hypothesized that breast cancer survivors assigned to the lifestyle physical activity intervention would show greater improvements in physical performance and quality of life than survivors assigned to a standard care control group. Secondarily, we hypothesized that the lifestyle group would show greater increases in physical activity and more favorable improvements in body composition than the control group.

2. Methods 2.1. Design and sample Participants were randomized to either the 6-month lifestyle physical activity program (Active for Life After Cancer) or to a standard care condition. They completed

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baseline and 6-month assessments of physical performance, quality of life, and physical activity. Women were eligible for the study if they were within 7 years of a breast cancer diagnosis, no longer receiving treatment for breast cancer (except hormone therapy), and not engaging in focused moderate physical activity for 30 min or more a day most days of the week. Participants received clearance from their physicians to ensure that they had no medical conditions contraindicating moderately intensive exercise. The protocol was approved by the M.D. Anderson Cancer Center Institutional Review Board, and participants provided informed consent before completing assessments. Participants were recruited from February to August 2003 from the M.D. Anderson Cancer Center Breast Center, Kelsey-Seybold Clinic (a large, multispeciality clinic), the Houston chapter of the Sisters’ Network (a support and advocacy group for African-American breast cancer survivors), and The Rose, a community agency sponsoring support groups for breast cancer survivors. Study recruitment included mailing letters of invitation to M.D. Anderson patients who had been identified by a previous crosssectional survey, to support group members from Sisters’ Network and The Rose, and breast cancer survivors who were patients at Kelsey Seybold Clinic. In addition, we advertised the study through M.D. Anderson publications. 2.2. Procedures Assessment and intervention for the study were conducted from April 2003 to April 2004. 2.2.1. Randomization After baseline assessment, participants were assigned to study arms using a form of adaptive randomization called minimization, which is similar to stratification in that participants’ characteristics are used to assign them to the treatment conditions [43]. In minimization, before a participant is assigned to a treatment group, the numbers of participants in each treatment group with similar covariate characteristics are totaled. Totals are based on the marginal sums of the covariates, so that each covariate is considered separately. The treatment assignment for a participant is then determined according to which treatment group would provide the best overall balance with respect to those covariates. Covariates used in the randomization of participants to our study conditions were baseline physical functioning and vitality (from the self-report Medical outcomes study short form-36 [SF-36] questionnaire), motivational readiness for physical activity, body mass index (BMI), disease stage at diagnosis, time since diagnosis, age, race, and whether the participant had received chemotherapy. 2.2.2. Intervention The lifestyle physical activity intervention was originally developed for healthy individuals in Project Active at the

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Cooper Institute [26,27], modified for use with prostate cancer patients [44], and further modified for use with breast cancer survivors for this pilot test. Participants in the lifestyle program attended 90-min group meetings each week for 16 weeks, and every other week for 8 weeks (21 sessions total). Behavior change methods were based on the transtheoretical model [45–49], which emphasizes that individuals adopt behavior change in stages (precontemplation, contemplation, preparation, adoption, and maintenance) and that different types of intervention methods are effective at different stages. Participants were taught to assess their motivational readiness for physical activity, which they did every 4–5 weeks, and they received booklets about increasing physical activity matched to their stage of readiness. The intervention sessions emphasized information and skills such as benefits of physical activity, making small changes, overcoming barriers, goal-setting, rewarding yourself, and self-monitoring. Several methods of selfmonitoring were used, including recording minutes of activity and recording steps using a pedometer. Information and skills were sequenced so that cognitive methods (e.g., recognizing benefits of physical activity) were presented in the earlier sessions, and behavioral methods (e.g., monitoring steps, rewarding yourself) were presented in later sessions. Group sizes ranged from 7 to 15 participants. Group meetings were held at a local church or at the KelseySeybold clinic. The first 50 min of each session were spent teaching cognitive behavioral skills related to exercise and providing brief opportunities (2–10 min) to practice moderately intensive activity such as walking. After a 10min break, the group reconvened for a presentation or guided discussion on a breast cancer-related topic; written informational materials relevant to the topic of discussion were provided. The written materials dealt with topics relevant to breast cancer survivorship but did not address physical activity. During the 6-month intervention period the standard care participants received two mailings of the same written material, but did not meet as a group. 2.3. Measures Baseline and 6-month assessments included self-report questionnaires concerning quality of life and motivational readiness, five physical performance tests, a 7-day physical activity recall interview, and lymphedema assessment. Staff conducting the assessments were blind to the participants’ study condition. 2.3.1. Physical performance Physical performance tests developed by Simmonds [50] were conducted at baseline and 6 months. Participants completed a 6-min endurance walk test (walking as far as comfortably possible in 6 min); a 50-foot walk test (walking 50 feet as fast as comfortably possible); a timed sit-to-stand test (standing and sitting twice as fast as comfortable — after

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a few minutes’ rest, the test is repeated and the average score recorded); a timed reach-up test (standing and reaching up with both hands as far as possible and returning hands to side — three repetitions are done at the maximum distance reached and the time recorded); and a forward-reach test (with heels on the floor, reaching forward as far as possible — distance is recorded at the farthest point before the participant loses her balance). 2.3.2. Quality of life (QOL) Participants completed the SF-36 [51,52], a 36-item selfreport measure of health-related quality of life based on eight health concepts: physical function, social function, pain, mental health, energy and fatigue, general health perceptions, role limitations caused by physical problems, and role limitations caused by emotional problems [53]. Internal consistency reliability for the eight scales is high, ranging from 0.78 to 0.93. 2.3.3. Physical activity The 7-day physical activity recall questionnaire (7DPARQ) is an interviewer-administered measure assessing physical activity during the past week. Information on the amount of time spent sleeping, and in moderate, hard, and very hard activities is gathered in the interview. The 7DPARQ has established validity and reliability [54,55]. As another measure of physical activity, motivational readiness was measured by defining moderate lifestyle physical activity of 30 min a day or more on most days of the week, and asking the participant to respond if she was active according to that definition. She could respond (1) yes, for more than 6 months (maintenance stage); (2) yes, for less than 6 months (adoption stage); (3) no, but I intend to in the next 30 days (preparation stage); (4) no, but I intend to in the next 6 months (contemplation stage); or (5) no, and I do not intend to in the next 6 months (precontemplation). A similar question was used by Marcus et al. [46] to assess motivational readiness for exercise. 2.3.4. Body composition and lymphedema Body mass index (BMI) was calculated from height and weight measurements. Height, weight, and hip and waist circumference were measured without shoes, with the participant wearing a light gown. Hip and waist circumference were measured as the participant stood with feet together, hands at sides, and abdomen relaxed. Waist circumference was measured at the narrowest part of the torso, at the end of a normal expiration, without compressing the skin. Hip circumference was measured similarly at the point of greatest extension of the buttocks. Lymphedema was assessed by a physical therapist who measured arm girth circumferentially at predetermined bilateral points. Jobst measuring tapes were used to take circumferential measurements every inch and a half, starting at the elbow and moving toward the shoulder and toward the wrist.

2.3.5. Patient satisfaction A brief questionnaire measuring patient satisfaction was administered to participants in the lifestyle program during the last session of the program. This questionnaire was based on one used in our previous trial of the Active for Life program in prostate cancer patients [56]. 2.4. Analysis Between-group differences in physical performance, quality of life, physical activity, and body composition were tested in a 2 (study condition) by 2 (cohort) analysis of variance; the analysis controlled for baseline values of the outcomes tested, age, time since diagnosis, BMI, education, baseline motivational readiness, baseline self-reported physical functioning, and whether the participant had received chemotherapy. All participants who were randomized were included in the analysis, regardless of their attendance at the intervention sessions. Data for participants who did not complete the 6-month assessment were imputed based on regression models predicting outcomes in the remaining sample, using covariates and design variables.

3. Results 3.1. Recruitment The combined recruitment efforts (M.D. Anderson, Kelsey-Seybold, support groups, and advertising) yielded 364 breast cancer survivors to be contacted for telephone screening. Fig. 1 provides the information on the outcomes of the screening process. Participants were recruited and randomized in two cohorts; when approximately 45 interested and eligible women were identified, they were contacted to schedule baseline assessments and then allocated to study condition. In total, 74 women completed baseline assessments; 14 were excluded after baseline (13 were too active to benefit from participation in the study, and one would be out of the country for most of the next 6 months). The remaining 60 survivors were allocated to the study conditions — 35 to the lifestyle program and 25 to standard care. More women were assigned to the lifestyle program to ensure that we would have an adequate number of women (at least seven) in each intervention group, and also to maximize the amount of process data we would obtain about the conduct of the lifestyle physical activity intervention. In the lifestyle program condition, retention at 6 months was 80%; four participants withdrew before the intervention began (primarily because of schedule conflicts with meeting times), and three more withdrew during the intervention. Retention in standard care was 92% at 6 months; one participant withdrew immediately after randomization because she had wanted to be in the lifestyle program, and another participant died before the 6-month assessment.

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Fig. 1. Patient recruitment, screening, allocation to study condition, and retention by study condition.

3.2. Characteristics of sample Baseline clinical, demographic, and outcome variables for the two study conditions are provided in Table 1. The sample was diverse with regard to ethnicity and disease stage. The participants in the two conditions did not differ significantly on any of the variables measured at baseline. 3.3. Process data Of the 35 women who were randomized to the Lifestyle program, four dropped out before starting the program and

an additional three participants dropped out during the intervention; these three participants attended 2, 4, and 5 sessions each. Among those who started the intervention, the mean number of sessions attended was 14.6 out of 21 (standard deviation = 5.1), with a range of 2–21 sessions. At the end of the lifestyle program, participants completed a program evaluation. Results indicated they were satisfied with the program format; ratings (from 1 to 5) indicated the content was more than expected (mean = 4.6) and the number of sessions and session length were considered ‘‘just right’’ (means = 3.3 and 3.0, respectively). Ratings were positive with regards to feelings towards group members

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Table 1 Demographic, medical, and baseline assessments by group Lifestyle Standard pa intervention N (%) care N (%)

Table 2 Differences in performance tests between lifestyle intervention and standard care participants at 6 months Performance test

Group

Adjusted meana

Standard error

F

p

Six-min walk

Lifestyle Standard care

1643 ft. 1546 ft.

20.7 25.5

8.5

0.005

Fifty-foot walk

Lifestyle Standard care

9.0 s 9.0 s

0.1 0.2

0.01

0.924

Forward-reach

Lifestyle Standard care

31.9 cm 31.9 cm

0.9 0.8

0

0.996

Sit-to-stand test

Lifestyle Standard care

3.1 s 3.3 s

0.1 0.1

0.6

0.427

Timed reach-up

Lifestyle Standard care

4.5 4.7

0.1 0.2

1.1

0.294

Demographic and medical variables Disease stage DCIS Stage I Stage II Stage III Stage IV Missing

0.61 9 9 7 8 1 1

(27) (27) (21) (24) (3)

4 8 8 3 1 1

(17) (33) (33) (13) (4)

Type of Surgery Breast-conserving Mastectomy BCT, then mastectomy

13 (37) 17 (49) 5 (14)

11 (44) 7 (28) 7 (28)

Adjuvant Treatment None Radiation Chemotherapy Radiation + chemotherapy

3 8 8 16

(9) (23) (23) (46)

4 5 5 11

(16) (20) (20) (44)

Race/ethnicity African-American American Indian Asian Latina White

11 1 2 1 57

(31) (3) (6) (3) (20)

8 1 0 2 14

(32) (4) (0) (8) (56)

Education High school diploma 2 (6) Technical/vocational program 0 (0) Some college/2 year degree 14 (41) Four-year degree 9 (27) Masters degree 7 (21) Doctoral degree 2 (6)

3 1 6 4 8 3

(12) (4) (24) (16) (32) (12)

Time from diagnosis (months) Age BMI

0.21

0.85

0.69

Mean (S.D.)

Mean (S.D.) 37.1 (14.1) 54.4 (11.7) 30.0 (5.8)

Adjusted for baseline value, age, education, time since diagnosis, received chemotherapy, body mass index (BMI), baseline physical functioning, and baseline stage of change.

were no other significant differences between the two groups in the physical performance tests at the 6-month assessment. 3.5. Quality of life

0.38

39.2 (16.7) 55.7 (11.1) 28.8 (5.3)

a

0.61 0.66 0.39

The lifestyle program group reported better quality of life in several areas at the 6-month assessment (Table 3). Lifestyle participants had significantly higher scores (indicating better QOL) on scales measuring general health ( p = 0.006) and bodily pain ( p = 0.020). Differences in role

Table 3 Differences in quality of life (QOL) between lifestyle intervention and standard care participants at 6 months QOL dimension

Group

Adjusted meana

Standard error

F

p

Physical functioning

Lifestyle Standard care

82.5 77.4

2.4 2.4

2.8

0.101

Mental health

Lifestyle Standard care

78.2 77.2

2.0 2.5

0.1

0.750

Vitality

Lifestyle Standard care

60.9 58.1

2.2 2.8

0.6

0.449

Role limitationsphysical

Lifestyle Standard care

86.1 73.0

4.2 5.1

3.8

0.056

Bodily pain

Lifestyle Standard care

79.7 72.1

2.0 2.4

5.8

0.020

General health

Lifestyle Standard care

77.4 67.1

2.2 2.8

8.4

0.006

Social functioning

Lifestyle Standard Care

84.6 84.9

3.2 4.0

0

0.963

Role limitationsemotional

Lifestyle Standard care

81.2 79.4

5.1 6.2

1.5

0.228

a

p-Value for significance of baseline differences between groups, as tested using x2 (categorical data) or t-test (continuous data).

(mean = 3.9, with five indicating ‘‘as close as I feel towards my family’’). Ratings also indicated high levels of comfort in talking openly in the group (mean = 4.1) and an increased in willingness to discuss breast cancer with others (mean = 4.3). Participants reported they would definitely recommend the program to other breast cancer survivors (mean = 5.0). They also reported the program increased their activity (mean = 4.6) and their physical (mean = 4.4) and emotional (4.0) well-being. 3.4. Physical performance At the follow-up assessment, the lifestyle group performed significantly better than standard care in the 6 minutes walk test ( p = 0.005), walking 97 feet farther in 6 minutes than standard care participants (Table 2). There

a

Adjusted for baseline value, age, education, time since diagnosis, received chemotherapy, body mass index (BMI), baseline physical functioning, and baseline stage of change.

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limitations due to physical problems and physical functioning ( p = 0.056 and 0.101, respectively) showed a trend toward significant differences. No significant differences between conditions were seen in scores of mental health, vitality, social functioning, and role limitations as a result of emotional problems.

the number of increases: right arm, Mann–Whitney U = 222.5, p = 0.124 (two-tailed); left arm, Mann–Whitney U = 252.5, p = 0.411 (two-tailed).

3.6. Physical activity

4.1. Discussion

At the 6-month assessment the lifestyle participants reported greater motivational readiness for physical activity than did standard care participants (Table 4; p = 0.024). The average stage of motivational readiness at baseline for participants in both study conditions was between preparation and action; at the 6-month assessment the lifestyle intervention participants’ stage of readiness was between action and maintenance, while that of the standard care participants did not change. There were no significant differences between the study conditions in the number of minutes spent in moderate or more intense physical activity and the number of days on which they did 30 min of such activity.

The randomized pilot study demonstrated that the lifestyle physical activity intervention produced improvements in some performance measures of physical functioning and physical aspects of quality of life, above and beyond those of a standard care comparison group. The lifestyle intervention condition participants also reported greater motivational readiness for physical activity than the standard care group; however, the reports of activity in the past 7 days do not reflect these differences. We assessed the effect of the lifestyle intervention on participants’ physical performance of tasks reflecting several dimensions of physical functioning. The intervention group performed better than the control condition on the 6-minute walk, indicating improvements in endurance. Tasks that were more reflective of strength (50-foot walk, sit-to-stand test), flexibility (repeated reach-up), and balance (forward-reach) showed no statistically significant changes. This was not surprising, given that the main emphasis of the lifestyle intervention was to increase walking activities. Participants were taught multiple ways to incorporate activity in their daily life, but most involved walking or other cardiovascular activity. As one way of monitoring activity, participants received pedometers and recorded their number of steps; other options for monitoring activity were provided, but most participants chose to use the pedometer. Flexibility and resistance exercises were taught, but the amount of time spent on them was brief. Most exercise interventions programs for cancer patients and survivors have emphasized cardiovascular activity [10–11,17,57,58], either walking or using a cycle ergometer, and the fitness outcomes have been related to cardiovascular fitness. A notable exception is a study by Segal et al. [9] of a strengthtraining intervention for androgen-ablated prostate cancer patients, which successfully increased participants’ strength and decreased their fatigue. With regard to quality of life improvements, only dimensions related to physical well-being were affected by the intervention (physical functioning, role limitations due to physical problems, and bodily pain), in contrast to other studies of exercise intervention in which improvements in emotional well-being were found as well [10,12,16,22]. However, the evidence of improved emotional well-being by exercise intervention is not consistent for cancer patients and survivors. One of the larger randomized trials [11] found that exercise had no effect on emotional well-being, and many of the studies found effects on some emotion/mood-related variables but not

3.7. Body composition and lymphedema There were no significant differences between the two study conditions at the 6-month assessment in BMI, hip circumference, or waist circumference. However, there was a significant intervention condition x cohort interaction in BMI ( p = 0.048); in cohort 1 the BMI was lower in the lifestyle intervention than standard care, while in cohort 2 they were nearly identical. To assess whether the intervention increased the risk of lymphedema, the number of increases in arm circumference greater than 2 cm was calculated for each participant. The study conditions demonstrated no significant differences in

Table 4 Differences in physical activity between lifestyle intervention and standard care participants at 6 months Physical Activity Variable

Group

Stage of changeb

Lifestyle Standard care

Minutes of moderate or more intense activity

Lifestyle Standard care

Days with 30 min of moderate and more intense activity

Lifestyle Standard care

a

Adjusted Meana 1.8 2.4 428 404 4.0 cm 4.2 cm

Standard Error 0.2 0.2 43 53 0.3 0.4

F

p

5.4

0.024

0.1

0.733

0.1

0.761

Adjusted for baseline value, age, education, time since diagnosis, received chemotherapy, body mass index (BMI), baseline physical functioning, and baseline stage of change. b 1: Maintenance, 2: action, 3: preparation, 4: contemplation, and 5: precontemplation.

4. Discussion and conclusion

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others [10,16]. Furthermore, in a mediational analysis, Courneya et al. [10] found that the differences in self-esteem and happiness (the two emotional variables significantly influenced by their exercise intervention) were not mediated by changes in fitness, indicating that either other facets of exercise (e.g., distraction from negative mood) were responsible for the changes, or that certain aspects of the intervention (e.g., attention from intervention staff) affected emotional well-being. The diversity of exercise interventions for cancer patients and survivors may account for the lack of consistency in findings of emotional benefits. One unexpected finding was that the intervention was related to improvements in motivational readiness, but not physical activity as reported in the past 7 days. Both study conditions reported increases in physical activity on the 7day recall interviews. According to exploratory paired t-tests to test within-group differences, the lifestyle intervention group increased the number of days on which they did moderate or more intense activity (from 3 to 4, p = 0.016), but their increase in total minutes of activity, from 345 to 432, was not statistically significant ( p = 0.13). The standard care group increased number of days (from 3 to 4.3, p = 0.024) and total minutes of activity (from 248 to 430, p = 0.003). One explanation for this result may be that assessing physical performance and physical activity was as effective as a 6-month intervention in increasing physical activity. However, this seems unlikely given the difficulty most sedentary people experience in adopting and sustaining a physically active lifestyle. An alternative explanation is also possible. About 2 weeks before the 6-month assessment of our second cohort of participants, research results presented at the American Association of Cancer Research (AACR) meeting showing that breast cancer survivors who exercised were less likely to die of breast cancer [58] received widespread media attention. This information may have caused women in standard care to start exercising, whereas it would have had less effect on the women in the intervention group who had already increased their activity levels. Several findings support this explanation. First, the lifestyle group reported greater motivational readiness than the standard care group, indicating that the intervention participants had been active longer and more regularly than those in standard care. Second, standard care participants in the second cohort, whose behavior could have been affected by the news coverage of the 2004 AACR results, had a larger increase in activity (248 min) than standard care participants in the first cohort (62 min) whose assessments preceded the news coverage. Finally, the standard care participants showed no physical performance improvement, which indicated that although they may have increased activity, the change was not sustained long enough to produce changes in endurance. There is no indication that lifestyle physical activity poses a risk of increasing lymphedema or other adverse outcomes in breast cancer survivors. The intervention group did not show a significantly larger number of increases in arm circumfer-

ence (more than 2 cm) than the standard care condition. In this pilot trial, one participant died, and one experienced a recurrence of cancer; both were in standard care. These events could not be attributed to the lifestyle intervention. 4.2. Conclusion The lifestyle physical activity intervention showed promise in its ability to improve endurance and physical aspects of quality of life and to induce changes in physical activity. Although the pilot test involved a small sample and thus had limited power for detecting differences between groups, the results provided a preliminary indication that the lifestyle program may be efficacious and should be rigorously tested in a larger randomized controlled trial. Comparison of the lifestyle physical activity program to a structured approach also should be tested with the goal of examining quality of life outcomes and long-term physical activity adherence. 4.3. Practice implications The results of this study indicate further research of the lifestyle approach is warranted. If this approach to increasing physical activity is shown to be effective in a larger trial, it represents a highly feasible intervention that can be delivered to cancer survivors by health care institutions or community organizations without dedicated exercise facilities and equipment. While our study was limited to breast cancer survivors, lifestyle physical activity interventions may also be beneficial for survivors of other types of cancer, or for individuals with other chronic diseases and conditions who might benefit from a more physically active lifestyle.

Acknowledgement This research was supported by grant R21 CA89519 and R25 CA57730 from the National Cancer Institute.

References [1] Courneya KS. Exercise in cancer survivors: an overview of research. Med Sci Sports Exerc 2003;35:1846–52. [2] Courneya KS. Exercise interventions during cancer treatment: biopsychosocial outcomes. Exerc Sport Sci Rev 2001;29:60–4. [3] Courneya KS, Friedenreich CM. Physical exercise and quality of life following cancer diagnosis: a literature review. Ann Behav Med 1999; 21:171–9. [4] Courneya KS, Keats MR, Turner AR. Physical exercise and quality of life in cancer patients following high dose chemotherapy and autologous bone marrow transplantation. Psycho-Oncology 2000; 9:127–36. [5] Holmes MD, Chen WY, Feskanich D, Kroenkeand CH, Colditz GA. Physical activity and survival after breast cancer diagnosis. J Am Med Assoc 2005;293(20):2479–86.

K. Basen-Engquist et al. / Patient Education and Counseling 64 (2006) 225–234 [6] LaCroix AZ, Leveille SG, Hecht JA, Grothausand LC, Wagner EH. Does walking decrease the risk of cardiovascular disease hospitalizations and death in older adults? J Am Geriatr Soc 1996;44:113–20. [7] Helmrich SP, Ragland DR, Leungand RW, Paffenbarger RS. Physical activity and reduced occurrence of non-insulin-dependent diabetes mellitus. New Engl J Med 1991;325(3):147–52. [8] Devogelaer JP, de Deuxchaisnes CN. Therapy and the 1990s: osteoporosis. Brit J Rheumatol 1993;32:48–55. [9] Segal RJ, Reid RD, Courneya KS, Malone SC, Parliament MB, Scott CG, Venner PM, Quinney HA, Jones LW, Slovinec D’Angelo ME, Wells GA. Resistance exercise in men receiving androgen deprivation therapy for prostate cancer. J Clin Oncol 2003;21(9):1653–9. [10] Courneya KS, Mackey JR, Bell GJ, Jones LW, Field CJ, Fairey AS. Randomized controlled trial of exercise training in postmenopausal breast cancer survivors: Cardiopulmonary and quality of life outcomes. J Clin Oncol 2003;21(9):1660–8. [11] Segal R, Evans W, Johnson D, Smith J, Colletta S, Gayton J, Wells WSG, Reid R. Structured exercise improves physical functioning in women with stage I and II breast cancer: Results of a randomized controlled trial. J Clin Oncol 2001;19(3):657–65. [12] Mock V, Dow KH, Meares CJ, Grimm PM, Dienemann JA, HaisfieldWolfe ME, Quitasol W, Mitchell S, ChakravarthyA, Gage I. Effects of exercise on fatigue, physical functioning, and emotional distress during radiation therapy for breast cancer. Oncol Nurs Forum 1997;24(6):991–1000. [13] Winningham ML, MacVicar MG, Bondoc M, Anderson JL, Minton JP. Effect of aerobic exercise on body weight and composition in patients with breast cancer on adjuvant chemotherapy. Oncol Nurs Forum 1989;16(5):683–9. [14] Courneya KS, Friedenreich CM, Sela RA, Quinney HA, Rhodes RE, Handman M. The group psychotherapy and home-based physical exercise (Group-Hope) trial in cancer survivors: Physical fitness and quality of life outcomes. Psycho-Oncology 2003;12: 357–74. [15] Pinto BM, Clark MM, Maruyama NC, Feder SI. Psychological and fitness changes associated with exercise participation among women with breast cancer. Psycho-Oncology 2003;12:118–26. [16] Dimeo FC, Stieglitz R, Novelli-Fischer U, Fetscherand S, Keul J. Effects of physical activity on the fatigue and psychologic status of cancer patients during chemotherapy. Cancer 1999;85(10):2273–7. [17] Dimeo F, Fetscher S, Lange W, Mertelsmann R, Keul J. Effects of aerobic exercise on the physical performance and incidence of treatment-related complications after high-dose chemotherapy. Blood 1997;90(9):3390–4. [18] MacVicar MG, Winningham ML. Promoting the functional capacity of cancer patients. Cancer Bull 1986;38:235–9. [19] Mock V, Burke MB, Sheehan P, Creaton EM, Winningham ML, McKenney-Tedder S, Schwager LP, Liebman M. A nursing rehabilitation program for women with breast cancer receiving adjuvant chemotherapy. Oncol Nurs Forum 1994;21(5):899–908. [20] Young-McCaughan S, Sexton DL. A retrospective investigation of the relationship between aerobic exercise and quality of life in women with breast cancer. Oncol Nurs Forum 1991;18:751–7. [21] Courneya KS, Friedenreich CM. Relationship between exercise during treatment and current quality of life among survivors of breast cancer. J Psychosoc Oncol 1997;15:35–57. [22] Segar ML, Katch VL, Roth RS, Garcia AW, Portner TL, Glickman SG, Haslanger S, Wilkins EG. The effect of aerobic exercise on self-esteem and depressive and anxiety symptoms among breast cancer survivors. Oncol Nurs Forum 1998;25(1):107–13. [23] Galvao DA, Newton RU. Review of exercise intervention studies in cancer patients. J Clin Oncol 2005;23:899–909. [24] Sherwood NE, Jeffery RW. The behavioral determinants of exercise: implications for physical activity interventions. Ann Rev Nutr 2000;20:21–44. [25] Bandura A. Self-efficacy: the exercise of control New York, NY: W.H. Freeman and Company; 1997.

233

[26] Dunn AL, Marcus BH, Kampert JB, Garcia ME, Kohland HW, Blair SN. Reduction in cardiovascular disease risk factors: 6-month results from Project Active. Prev Med 1997;26:1–9. [27] Dunn AL, Garcia ME, Marcus BH, Kampert JB, Kohl III HW, Blair SN. Six-month physical activity and fitness changes in Project Active, a randomized trial. Med Sci Sports Exerc 1998;30(7):1076–83. [28] Dunn AL, Marcus BH, Kampert JB, Garcia ME, Kohl III HW, Blair SN. Comparison of lifestyle and structured interventions to increase physical activity and cardiorespiratory fitness. J Am Med Assoc 1999; 281(4):327–34. [29] Rejeski WJ, Brawley LR, Ambrosius WT, Brubaker PH, Focht BC, Foy CG, Fox LD. Older adults with chronic disease: Benefits of groupmediated counseling in the promotion of physically active lifestyles. Health Psychol 2003;22(4):414–23. [30] McAuley E, Coumeya KS, Rudolph DL, Lox CL. Enhancing exercise adherence in middle-aged males and females. Prev Med 1994;23: 498–506. [31] Steptoe A, Rink E, Kerry S. Psychosocial predictors of changes in physical activity in overweight sedentary adults following counseling in primary care. Prev Med 2000;31:183–94. [32] Carlson J, Johnson J, Franklin B, VanderLaan R. Program participation, exercise adherence, cardiovascular outcomes, and program cost of traditional versus modified cardiac rehabilitation. Am J Cardiol 2000;86:17–23. [33] Ajzen I. The theory of planned behavior. Organizational behavior and human decision processes 1991;50:1–33. [34] Rhodes RE, Courneya KS. Investigating multiple components of attitude, subjective norm, and perceived control: an examination of the theory of planned behaviour in the exercise domain. Brit J Soc Psychol 2003;42:129–46. [35] Courneya KS, Friedenreich CM. Determinants of exercise during colorectal cancer treatment: an application of the theory of planned behavior. Oncol Nurs Forum 1997;24:1715–7. [36] Courneya KS, Friedenreich CM. Utility of the theory of planned behavior for understanding exercise during breast cancer treatment. Psycho-Oncology 1999;8:112–22. [37] Bartholomew LK, Parcel GS, Kok G, Gottlieb NH. Intervention Mapping: designing theory- and evidence-based health promotion .programs Mountain View, CA: Mayfield Publishing Company; 2001 [38] DeBusk RF, Stenestrand U, Sheehan M, Haskell WL. Training effects of long versus short bouts of exercise in healthy subjects. Am J Cardiol 1990;65:1010–3. [39] Dunn AL, Andersen RE, Jakicic JM. Lifestyle physical activity interventions: history, short- and long-term effects, and recommendations. Am J Prev Med 1998;15:398–412. [40] Andersen RE, Wadden TA, Bartlett SJ, Zemel B, Verde TJ, Franckowiak SC. Effects of lifestyle activity vs structured aerobic exercise in obese women. J Am Med Assoc 1999;281(4):335–40. [41] Dallow C, Anderson J. Using self-efficacy and a transtheoretical model to develop a physical activity intervention for obese women. Am J Health Promot 2003;17:373–81. [42] Andersen RE, Franckowiak SC, Bartlett SJ, Fontaine KR. Physiologic changes after diet combined with structured aerobic exercise or lifestyle activity. Metabolism 2002;51(12):1528–33. [43] Pocock SJ. Clinical trials: a practical approach New York, NY: John Wiley & Sons; 1993. [44] Carmack Taylor CL, Smith MA, de Moor C, Dunn AL, Pettaway C, Sellin R, Chamsangavej C, Hansen MC, Gritz ER. Quality of life intervention for prostate cancer patients: design and baseline characteristics of the Active for Life after cancer trial. Control Clin Trials 2004;25:265–85. [45] Marcus BH, Rossi JS, Selby VC, Niaura RS, Abrams DB. The stages and processes of exercise adoption and maintenance in a worksite sample. Health Psychol 1992;11(6):386–95. [46] Marcus BH, Selby VC, Niaura RS, Rossi JS. Self-efficacy and the stages of exercise behavior change. Res Quart Exerc Sport 1992;63(1): 60–6.

234

K. Basen-Engquist et al. / Patient Education and Counseling 64 (2006) 225–234

[47] Marcus BH, Banspach SW, Lefebvre RC, Rossi JS, Carleton RA, Abrams DB. Using the stages of change model to increase the adoption of physical activity among community participants. Am J Health Promot 1992;6:424–9. [48] Marcus BH, Owen N. Motivational readiness, self-efficacy and decision making for exercise. J Appl Soc Psychol 1992;22:3–16. [49] Pinto BM, Frierson GM, Rabin C, Trunzo JJ, Marcus BH. Home-based physical activity intervention for breast cancer patients. J Clin Oncol 2005;23(15):3577–87. [50] Simmonds MJ. Physical function in patients with cancer: psychometric characteristics and clinical usefulness of a physical performance test battery. J Pain Symptom Manage 2002;24: 404–14. [51] Ware JE, Kosinski M, Bayliss MS, McHomey CA, Rogers WH, Raczek A. Comparison of methods for the scoring and statistical analysis of SF-36 health profile and summary measures: Summary of results from the Medical Outcomes Study. Med Care 1995;33(4): AS264–79. [52] Ware Jr JE, Kosinski M, Keller SD. SF-36 physical and mental health summary scales: a user’s manual Boston, Massachusetts: The Health Institute, New England Medical Center; 1994.

[53] McHorney CA, Ware JE, Raczek AE. The MOS 36-item short-form health survey (SF-36). Part II. Psychometric and clinical tests of validity in measuring physical and mental health constructs. Med Care 1993;31:247–63. [54] Blair SN, Haskell WL, Ho P, Paffenbarger Jr RS, Vranizan KM, Farquhar JW, Wood PD. Assessment of habitual physical activity by seven-day recall in a community survey and controlled experiments. Am J Epidemiol 1985;122:794–804. [55] Sallis JF, Haskell WL, Wood PD, Fortman SP, Rogers T, Blair SN, Paffenberger Jr RS. Physical activity assessment methodology in the Five-City project. Am J Epidemiol 1985;121:91–106. [56] Carmack Taylor CL, Gritz ER, Basen-Engquist K. Active for life after cancer: a randomized trial examining a lifestyle physical activity program for prostate cancer patients. Psycho-oncology (in press). [57] Dimeo FC, Tilmann MH, Bertz H, Kanz L, Mertelsmann R, Keul J. Aerobic exercise in the rehabilitation of cancer patients after high dose chemotherapy and autologous peripheral stem cell transplantation. Cancer 1997;79(9):1717–22. [58] Holmes MD, Chen WY, Feskanich D, Colditz GA. Physical activity and survival after breast cancer diagnosis. Proceedings of the AACR. 2004. p. 45 (abstract number 1462).