Abstract
Objectives:
To assess the feasibility, acceptability, and preliminary effectiveness of implementing a home-based aerobic and resistance exercise for patients with breast cancer receiving endocrine treatment in Indonesia.
Methods:
This is a mixed methods study with concurrent design consisting of quantitative single-arm pre-post intervention and qualitative study. We recruited patients with breast cancer (N = 36) receiving endocrine treatment and assigned 12 weeks of home-based pedometer-driven walking and resistance exercises using therapeutic bands. Descriptive statistics were used to assess the feasibility (recruitment, retention, and adherence) and safety. The modified Bruce treadmill test was used to measure predicted aerobic capacity (V̇O2 peak). Quality of life and fatigue were assessed using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire and fatigue severity scale. Measurements were performed at baseline and post-intervention and analyzed with the paired t-test or Wilcoxon test. Semi-structured interviews and thematic analysis were conducted post-intervention to explore patients’ acceptability.
Results:
The results showed a recruitment rate of 75%, retention rate of 89%, and adherence rates were 53% for aerobic and 78% for resistance exercise. No severe adverse events were reported. Post-intervention interviews identified positive attitudes toward the intervention, with low burden and high perceived benefit. Exercise duration and predicted V̇O2 peak increased significantly (+1.1 min, p = 0.001 and +2.3 ml/kg/min, p = 0.043), but no significant change was detected for Quality of Life (p > 0.050) or fatigue severity (p = 0.299).
Conclusions:
A home-based aerobic and resistance exercise was feasible when implemented in the context of routine care in our study population, improving predicted aerobic capacity. Further research is required to understand limited changes to Quality of Life and fatigue and adaptations to support implementation in additional sites in Indonesia.
Keywords: Exercise, breast neoplasms, physical fitness, walking, resistance exercise
Introduction
Female breast cancer (BC) is the most commonly diagnosed malignancy worldwide with 2.3 million new cases or 11.7% of all newly diagnosed cancers in 2020. In Indonesia, BC has the highest incidence (65.858 new cases, 16.6%) of all cancer types and is the second leading cause of cancer death (9.6%). 1 Specifically, in the region of Yogyakarta, a province in Java that has the highest cancer prevalence in the country, BC is dominated by late presentation of patients with advanced disease (59.4%).2,3 Similar to most countries, the highest prevalence of BC (86%) in Yogyakarta is hormone receptor-positive BC.4,5 This patient population generally receives endocrine treatment for a minimum duration of 5 years, which can result in a multitude of adverse health effects (e.g., pain, arthralgia, reduced muscle mass, and strength) up to 14 years after diagnosis. 6 Finding solutions to help patients to self-manage health problems associated with the disease and its treatment is imperative.
Physical activity can reduce many of the adverse effects resulting from treatment for BC and is a cost-effective, empowering approach that can support self-management.7,8 There is strong evidence that combined moderate-intensity aerobic and resistance exercise performed 2–3 times per week for at least 12 weeks can improve physical function and quality of life (QoL), prevent reoccurrence, prolong survival, and reduce fatigue both during and after BC treatment.7,9,10 Cancer patients are advised to perform 150 min of moderate intensity, or 75 min of vigorous physical activity weekly, as recommended by the American College of Sports Medicine (ACSM). 9 It also recommends performing muscle-strengthening exercises at least twice a week. However, many BC patients become physically inactive after breast surgery due to limited function and mobility of the upper extremity, 11 alongside increases in sedentary behavior mainly due to fatigue. 12 In many low- and middle-income countries (LMICs), increased levels of physical inactivity are exacerbated by a lack of access to high-quality facilities for rural residents, program availability, and lack of information and tailored advice. 13 Supporting patients to be active at the recommended level during and after treatment is therefore important for improving their overall health and well-being. However, there is limited research as to how to support patients in LMICs. Home-based programs may be an effective way to do this.
Exercise prescribed to patients with BC in the home environment has been found to result in significant improvements in aerobic capacity and QoL.11,14,15 Home-based programs are acceptable, convenient, and safe and can be delivered to patients using minimal resources.13,16 However, the bulk of the evidence in this area is heavily skewed toward patients who live in high-income countries (HICs)10,16 with limited research conducted in LMICs. Research findings from HICs may not be transferable to LMICs due to differences in demographic characteristics, health system capacity, sociocultural factors, and resource availability. 17 Furthermore, the word “exercise” and other related terms are not shown in the bibliometric network visualization indicating an under-explored research topic in Indonesia. 18 Home-based exercise programs in LMICs may be important for promoting physical activity in this population as lack of funding, paucity of trained rehabilitation specialists, and lack of a tailored physical activity plan often hinder supervised hospital-based program delivery. 19
Exercise interventions considering sociocultural factors are more effective in influencing health outcomes. It is important to evaluate participants’ acceptance of exercise intervention to assist with their needs and challenges to adhere to exercise intervention. 13 More knowledge about how our patients with BC accept and experience the quantitative change after completing home-based exercise intervention can enrich the findings from the quantitative measurements. This knowledge can provide a holistic picture of implementing a home-based exercise program for patients with BC in Indonesia and develop tailored interventions based on our patients’ experience and acceptance.
The purpose of this mixed methods study was the quantitative assessment of feasibility and preliminary effectiveness of a 12-week home-based exercise program, with qualitative description of how our patients with BC experience and accept the program implementation. We hypothesize that home-based aerobic and resistance exercise is feasible, acceptable, and effective for Indonesia BC patients.
Methods
Study participants and design
A mixed methods study using concurrent design was conducted from January to July 2022 in patients with BC receiving endocrine treatment. This study consisted of a single-arm pre-post intervention study used to evaluate the quantitative feasibility and preliminary effectiveness of participating in a home-based exercise program and a qualitative measure using a semi-structured interview to describe the intervention’s acceptability. Participants were recruited between 3 January and 8 April 2022. Data were collected using a range of device-based (i.e., pedometer, treadmill test) and subjective (i.e., questionnaires, recall interviews, self-reported diaries) measures.
This study enrolled BC patients aged 18–70 years, who had completed primary treatment and received endocrine treatment. Patients with stage I–III BC with Eastern Cooperative Oncology Group score ⩽1 were recruited using a consecutive sampling approach. They were included if they: (a) had completed primary treatment (e.g., surgery, chemotherapy, and radiotherapy); (b) were within 5 years of diagnosis; (c) received ongoing endocrine treatment; (d) were able to perform moderate-intensity physical activity as determined by their oncologist and care team; (e) were able to read and write in Bahasa, Indonesia; and (f) were willing to provide written informed consent. Patients were excluded from the study if they had an ejection fraction of <50%, evidence of cardiac disease, severe musculoskeletal problems, or other contraindications for exercise.
A previous study by Rogers et al. 20 reported a V̇O2 peak increase of 2.6 ml/kg/min after a 12-week physical activity intervention. Sample size calculation using power analysis based on that data, type-I error of 0.05, and type-II error of 0.80, estimated that 29 subjects were needed. We sought to enroll up to 36 patients, which also aligned with recommendations for a sample of 30 participants as a minimum sample size for designing pilot studies, assuming a 20% dropout rate. 21 For the qualitative interview, the sample size was determined based on the achievement of data saturation. Consecutive sampling was done after a 12-week intervention, and no participant refused to be interviewed. Since no new information was arising in the last participant’s interview, our sample consisting of 25 patients was deemed sufficient. 22 Participants were recruited from Dr Sardjito General Hospital, a tertiary referral hospital in Yogyakarta, Indonesia. Ethical approval was obtained from the Medical and Health Research Ethics Committee, Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia (reference number KE/FK/0184/EC/2021).
Study procedures
Potential participants meeting all eligibility criteria were approached by their oncologists (SHH, MSH) during a hospital appointment in the cancer clinic, and the study objectives were explained. All recruited participants signed a written informed consent form before participation. The intervention consisted of a 12-week, home-based, personalized moderate-intensity aerobic and resistance exercise program. All participants received a face-to-face 30-min instructional session with the clinical study coordinator (YKA) under cardiac prevention and rehabilitation consultant supervision (ABH), before they started the intervention. They were provided with a pre-packaged kit, which included a detailed written manual of the intervention, a pedometer (Yamax Digiwalker SW-200, Tokyo, Japan), a set of resistance bands (Happy Fit®, Jakarta, Indonesia), and a self-report diary.
The aerobic exercise consisted of a walking program based on the number of steps per day, which was recorded using a pedometer. The pedometer elicited acceptable inter-unit reliability (p < 0.05) and excellent intra-trial reliability (interclass correlation ⩾ 0.75). 23 Patients were asked to wear the pedometer daily, except when they were sleeping, and were instructed to record their number of steps per day during the 12-week intervention. Patients’ average number of steps per day in the first week served as a baseline value. 24 The target of the aerobic exercise was individually tailored by adding 3000 accumulated steps above their baseline value on 5 days of the week. This value was based on the assumption that moderate brisk walking produces 100 steps a minute. Therefore, 3000 steps would equate to approximately 30 min of moderate-intensity aerobic activity, in line with ACSM recommendations. 24
The resistance exercise program consisted of two sets of biceps curl, triceps extension, chest press, shoulder flexion, shoulder press, lateral extension, seated row, and upright row, with 8–10 repetitions. 25 Patients were instructed to perform each exercise with an average total duration of 10 min on 2 days a week, based on current recommendations 7 at home. The exercises were individually tailored based on participants’ strength and range of movement using a set of three color-coded bands representing low, moderate, and high levels of resistance. The resistance program was focused on targeting the upper body, as the aerobic program focused on the lower body through walking. The participants recorded their resistance exercise frequency, duration, and intensity in a self-reported diary.
The study coordinator (YKA) explained and demonstrated the proper use of the resistance bands and how to safely perform the exercises during the initial 30-min instructional session. A video and written manual was developed and given to patients as guidance. It consisted of step-by-step instructions on how to complete the exercises, exercise frequency, repetition, and intensity (2–4 rating of perceived exertion on a 1–10 Borg scale).
The study coordinator monitored participation through weekly phone communication, recording any side effect occurrence and providing patients with a target for the following week. During participants’ visits to the hospital for their monthly check-ups, they were asked to perform each exercise so the study coordinator could assess their technique and adjust the level of intensity if required.
Measures
Demographic and clinical characteristics
Demographic data collected included age, educational background, employment, and marital status. Clinical data was also collected including body mass index, hypertension comorbidity, cancer stage, primary treatment received (e.g., surgery, chemotherapy, and radiation therapy), and details about the type of endocrine treatment (selective estrogen receptor modulators (SERMs), such as tamoxifen, and aromatase inhibitors (AIs), such as letrozole, anastrozole, and exemestane). Demographic and clinical data were extracted from the participant’s medical records at baseline.
Intervention feasibility
Intervention feasibility was determined by (a) recruitment (ratio of the number of participants recruited to the number of eligible participants approached), (b) retention (ratio of the number of participants who completed the 12-week program to the total number of participants enrolled in the study), (c) adherence (the ratio of the number of participants meeting at least 70% of prescribed activities calculated using steps per day, resistance exercise frequency, duration, and intensity to the total number of participants completing the 12-week program) defined as feasible if those rates were above 75% 26 , and (d) adverse events (e.g., dyspnea, tachycardia, nausea, pain, and myalgia) reported by participants. Adherence data was extracted from participant’s self-reported diary. Baseline demographic, clinical, and treatment factors were compared between adherent and non-adherent participants.
Intervention acceptability
Intervention acceptability was explored using semi-structured interviews with participants (N = 25) post-intervention to: (a) explore their experiences of participating in the intervention and; (b) understand the most prominent aspects of intervention acceptability. The first and last authors (YKA, an MD and graduate student in Master of Medical Science program, and SB, a PhD well-versed in qualitative research) developed the interview guide based on the main areas outlined in the theoretical framework of acceptability. 27 The interview guide was pilot-tested on the first four participants (16%), and minor revisions were made before implementing the final version. Before each interview, informed consent was obtained. Interviews were conducted by two members (AS, FB) of the Center of Health Behavior and Promotion, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada trained in qualitative interview techniques. All interviews were individual and face-to-face, took place in a private room in the cancer clinic, lasting approximately 25–40 min, and audiotaped. No non-participants were present during the interview.
Intervention effectiveness: Aerobic capacity
Participants’ aerobic capacity was assessed at baseline and after participation in the 12-week intervention. Aerobic capacity was determined with the modified Bruce treadmill test, which is a predictive submaximal exercise test deemed appropriate and safe for subjects with a low or unknown functional capacity. 28 A cardiac prevention and rehabilitation consultant (ABH) monitored and supervised all procedures. The treadmill test (Cardiac ScienceTM TM55, Hannover, Germany) was conducted at the Cardiac Rehabilitation Unit, Dr Sardjito General Hospital. Cardiac rehabilitation nurses (EW, DP) measured a participant’s blood pressure at rest, during the test stage, and recovery phase while their heart rate was automatically recorded using a treadmill test monitor. Treadmill speed and inclination were automatically increased every 3 min (test stage). The test was terminated when participants reached volitional fatigue. Exercise duration was recorded in minutes, and aerobic capacity was calculated as V̇O2 peak using the following equation: The predicted V̇O2 peak was used to determine participants’ physical fitness, which is classified as low, fair, average, and good based on the normative values for women from the ACSM. 28
Intervention effectiveness: QoL and fatigue
Quality of life and fatigue were assessed at baseline and after participation in the 12-week intervention using translated and validated Indonesian versions of the EORTC Quality of Life Questionnaire (QLQ-C30) 29 and Fatigue Severity Scale (FSS). 30 A member of the research team (NDS) administered the questionnaires in a private room at the hospital. The EORTC QLQ-C30 consists of global health status, functional scales, and symptom scales. A higher score indicates better health for global health status and functional scales but represents a higher level of burden for symptom scales. 31 The FSS is a nine-item questionnaire to assess the severity of fatigue symptoms and its impact on an individual’s daily functioning. A higher score of the FSS represented a more severe fatigue level and also was classified as no-to-mild fatigue (FSS < 4.0) and severe fatigue (FSS ⩾ 4.0). 32
Data analysis
Participants’ characteristics were calculated using means and standard deviation for numerical data and were described with frequencies and percentages for categorical data. Descriptive statistics were used to calculate the feasibility outcomes including recruitment, retention, adherence rate, and intervention safety. Baseline characteristics were compared between adherent and non-adherent participants using Chi-Square test.
Quantitative analysis
To analyze the effects of the 12-week home-based intervention on health outcomes, we used a paired t-test for treadmill test parameters, except for the physical fitness that was analyzed with the McNemar test as the data was non-parametric. As QoL and fatigue scores were not normally distributed, we used the Wilcoxon signed rank test for the analysis. Participants with complete evaluation data were further classified into two groups (with and without improvement) based on their aerobic capacity change after the 12-week intervention. Participants’ baseline characteristics were analyzed between groups using logistic regression. Participants with incomplete data were not included in the analysis. The p-value under 0.05 was considered statistically significant while p-value under 0.10 was considered a trend that may have clinical significance. Data were analyzed using STATA software, version 17 (Stata Corp., College Station, TX, USA).
Qualitative analysis
Interviews were audiotaped and transcribed verbatim. The analysis followed a deductive thematic approach 33 guided by the theoretical framework of acceptability. 27 The first author (YKA) reviewed all transcripts line by line to become familiar with the data and created descriptive codes. Text passages that had been coded multiple times were put together and designated as a potential sub-theme. These initial sub-themes were then grouped into the themes described in the theoretical framework of acceptability. The transcripts were then reread to make sure no information was left out. The last author was interested in this topic due to prior experience in physical activity research and assumed that this intervention was acceptable for study participants. However, alternative interpretations for the data that were generated were proposed and discussed with the research team using a collaborative procedure. 34 The analysis was conducted manually. Specific quotations were selected to illustrate each of the sub-themes. To ensure confidentiality, each participant was given an arbitrary number as their identifier in the transcripts.
Results
Patient characteristics
The mean age of participants (N = 36) was 52 ± 6.98 years old. All participants had mastectomy and chemotherapy, in which 89%–92% of patients also received radiation therapy. Endocrine therapy regimen used was tamoxifen (SERMs) in 48%–53% and AIs in 52%–55% of participants. The average endocrine therapy duration was 26.9–28.5 months at baseline. There was no baseline characteristics difference between recruited and interviewed participants (Table 1).
Table 1.
Demographics and clinical baseline characteristics.
| Variable | Recruited participants (N = 36), Mean ± SD or n (%) | Interviewed participants (N = 25), Mean ± SD or n (%) |
|---|---|---|
| Age (years) | 52 ± 6.98 | 52 ± 7.05 |
| Employment | ||
| Employed or self-employed | 18 (50.0) | 11 (44.0) |
| Housewife | 18 (50.0) | 14 (56.0) |
| Education | ||
| Less than high school | 11 (30.6) | 7 (28.0) |
| High school | 18 (50.0) | 14 (56.0) |
| College | 7 (19.4) | 4 (16.0) |
| Marital status | ||
| Married | 31 (86.1) | 22 (88.0) |
| Widowed | 3 (8.3) | 3 (12.0) |
| Single | 2 (5.6) | 0 (0) |
| BMI (kg/m2) | 24.68 ± 4.38 | 24.74 ± 4.26 |
| <23 kg/m2 | 14 (38.9) | 7 (28.0) |
| ⩾23 kg/m2 | 22 (61.1) | 18 (72.0) |
| Hypertension comorbidity | ||
| No | 27 (75.0) | 19 (76.0) |
| Yes | 9 (25.0) | 6 (24.0) |
| Stage | ||
| Stage I–II | 22 (61.1) | 16 (64.0) |
| Stage III | 14 (38.9) | 9 (36.0) |
| Primary treatment | ||
| Surgery | ||
| Lumpectomy and mastectomy | 18 (50.0) | 10 (40.0) |
| Mastectomy | 18 (50.0) | 15 (60.0) |
| Chemotherapy | 36 (100.0) | 25 (100.0) |
| Radiation therapy | 32 (88.9) | 23 (92.0) |
| Endocrine treatment | ||
| SERMs | 19 (52.8) | 12 (48.0) |
| Ais | 20 (55.5) | 13 (52.0) |
| Endocrine treatment duration (months) | 28.47 ± 14.62 | 26.89 ± 14.41 |
| ⩽24 months | 22 (61.1) | 16 (64.0) |
| >24 months | 14 (38.9) | 9 (36.0) |
SD: standard deviation; BMI: body mass index; SERMs: selective estrogen receptor modulators; AIs: aromatase inhibitors.
Intervention feasibility
Recruitment
During the recruitment period between 3 January and 8 April 2022, 48 eligible patients were approached and 36 patients agreed to participate in the study. Six patients declined due to being too busy to participate, two because they were not sure if they would be able to adhere to the intervention and four were reluctant to engage in the study, resulting in a 75% recruitment rate.
Retention and adherence
A total of four participants dropped out from the study due to schedule conflict (n = 1), sickness (n = 1), and did not attend post-intervention data collection (n = 2), resulting in a retention rate of 89% (Figure 1). However, one additional participant who completed the 12-week intervention has partial data, as they had to be excluded from the post-intervention treadmill test and aerobic capacity analysis due to newly acquired musculoskeletal problems. They were able to complete the questionnaires that were included in the analysis.
Figure 1.
Flow diagram of participants’ recruitment. From 48 approached eligible patients, 36 patients agreed to participate in the study. Four participants dropped out and one additional participant was excluded from the post-intervention treadmill test analysis. A total of 25 participants underwent semi-structured interview at the end of the study.
Fifty-three percent of participants adhered to the aerobic program, achieving at least 70% of the step/day target. The average number of steps per day significantly increased from baseline to week 12 (5694 ± 2820.98 vs 7728 ± 2509.34; p < 0.001) (Figure 2). Seventy-eight percent of participants adhered to at least 70% of the prescribed resistance exercise sessions. Participants reported an average of 10.3 ± 5.40 min duration and 2.2 ± 1.21 days a week resistance exercise frequency, with a rating of perceived exertion of 3 out of 10, indicating moderate intensity. Participants’ adherence was measured based on self-reported diary and weekly phone monitoring by the research team. There was no significant difference in baseline characteristics including demographic, clinical, and treatment factors, between adherent and non-adherent groups (Table 2).
Figure 2.

Participants’ steps per day during the 12-week physical activity intervention. Box plots demonstrated the participants’ steps per day during the 12-week study intervention. Horizontal line is the participants’ median target by adding 3000 steps/day (median 8800 steps/day).
Table 2.
Baseline characteristics influencing participants’ adherence.
| Variables | Aerobic exercise | p-Value | Resistance exercise | p-Value | ||
|---|---|---|---|---|---|---|
| Adherent | Non-adherent | Adherent | Non-adherent | |||
| Age | ||||||
| ⩽52 years | 10 (55.6) | 8 (44.4) | 0.755 | 12 (66.7) | 6 (33.3) | 0.075 |
| >52 years | 7 (50.0) | 7 (50.0) | 13 (92.9) | 1 (7.1) | ||
| Employment | ||||||
| Employed/self-employed | 8 (53.3) | 7 (46.7) | 0.982 | 10 (66.7) | 5 (33.3) | 0.141 |
| Housewife | 9 (52.9) | 8 (47.1) | 15 (88.2) | 2 (11.8) | ||
| Education | ||||||
| ⩾High school | 11 (47.8) | 12 (52.2) | 0.287 | 16 (69.6) | 7 (30.4) | 0.073 |
| <High school | 6 (66.7) | 3 (33.3) | 9 (100.0) | 0 (0.0) | ||
| Marital status | ||||||
| Married | 14 (51.8) | 13 (48.2) | 0.563 | 22 (81.5) | 5 (18.5) | 0.296 |
| Widowed, single | 3 (60.0) | 2 (40.0) | 3 (60.0) | 2 (40.0) | ||
| BMI (kg/m2) | ||||||
| <23 kg/m2 | 8 (61.5) | 5 (38.5) | 0.430 | 10 (76.9) | 3 (23.1) | 0.892 |
| ⩾23 kg/m2 | 9 (47.4) | 10 (52.6) | 15 (78.9) | 4 (21.1) | ||
| Stage | ||||||
| Stage I–II | 10 (50.0) | 10 (50.0) | 0.647 | 16 (80.0) | 4 (20.0) | 0.740 |
| Stage III | 7 (58.3) | 5 (41.7) | 9 (75.0) | 3 (25.0) | ||
| Endocrine treatment duration | ||||||
| ⩽24 months | 10 (47.6) | 11 (52.4) | 0.388 | 17 (80.9) | 4 (19.1) | 0.593 |
| >24 months | 7 (63.6) | 4 (36.4) | 8 (72.7) | 3 (27.3) | ||
BMI: body mass index.
Safety
No severe adverse events were reported. However, five patients (13.9%) reported myalgia after completing the resistance exercises. One participant reported pain, swelling, and discharge around post-mastectomy wounds after completing the 12-week intervention. All symptoms were relieved after a week of oral antibiotics treatment and twice-a-week wound debridement. Due to the absence of laboratory investigation, infection etiology could not be excluded and this case might not be related to study intervention.
Intervention acceptability
Findings on acceptability of the intervention are presented under three separate but interconnected themes including affective attitude, burden, and perceived effectiveness. Exemplary quotes are presented in Table 3 to represent participants’ affective and cognitive responses associated with participating in the home-based program.
Table 3.
Relevant quotations of acceptability themes from BC patients’ participation in home-based exercise intervention (N = 25).
| Themes and subthemes | Illustrative quotes/Key quotations |
|---|---|
| Affective attitude | |
| Enjoying intervention activities | “Yes, I enjoyed it [the exercise program] and was happy to do it. I even felt guilty when I could not do the program.” (P18) |
| “It [the exercise program] is fun! The exercise was a challenge for me but I was happy to do it.” (P23) | |
| Goal-setting as motivation and challenge to overcome | “The weekly targets pushed me to do more exercise. My exercise target was increased every week. I often wondered whether I could reach the target or not and it turned out, that I could.” (P19) |
| Sense of reassurance from regular contact with the research team | “I was happy that someone paid attention and routinely reminded me to do the exercises. When I had a question about how to do an exercise, I could ask her [the researcher] so I didn’t get lost at home.” (P09) |
| Convenient instrument | “Every day we used a pedometer and only took it off when going to the bathroom or sleeping. I didn’t mind it [wearing the pedometer].” (P24) |
| Disadvantages of aerobic exercise (walking) | “I didn’t like walking, even before participating in this program. My foot hurt when I walked too far or too long. Actually, I realized the importance of walking as an aerobic exercise. However, I still couldn’t perform adequate walking.” (P25) |
| Disadvantages of resistance exercise | “After using the resistance band, it hurt here (pointing at her arm). So, I decided to stop doing the exercise.” (P13) |
| Burden | |
| Straightforward and effortless | “It [exercise program] was simple and easy especially after you have practiced the exercises a couple of times.” (P01) |
| “Walking is easy. As for resistance exercise, I had to memorize the movements.” (P12) | |
| Flexibility | “There was no obligation to do it [exercise] in the morning. Sometimes I did it in the afternoon, sometimes before I went to bed. When I wanted to exercise, I just used the resistance band. So, I didn’t feel burdened, no. . .” (P01) |
| Adapting to a novel exercise program | “At first, I felt stressed. But after I went through it [the exercises] and learned the technique, I was able to relax and keep my mind calm, no problem.” (P21) |
| Feeling burdened targets | “Whenever the doctor reminded me about this program, my mind became troubled. I felt like I had to chase targets, targets, and targets.” (P13) |
| Perceived effectiveness | |
| Improved fitness and stamina | “Most importantly, my fitness has improved. Now I don’t easily pant while walking.” (P08) |
| Reduced fatigue | “Before this [program], I felt my body was fatigued and tired easily. After participating in this program, I am not as easily tired.” (P10) |
| Developing a new habit | “My [past] experience was that I usually didn’t do exercise. Since I was given this program, I made time for exercise.” (P09) |
| Improved arm strength and range of movement | “After surgery, my arm movement was very limited. Now, I can move my arm more freely.” (P12) |
| “Resistance exercise helped me improve my arm’s range of movement. I can lift my arm and bring my arm behind my back. Before [participating in the program], I couldn’t move my arm behind my back and buttoning up my shirt was difficult. Now, I can do it comfortably.” (P20) | |
| “I can lift my arm! Before, I got tired only from combing my hair.” (P08) | |
| Improved physical symptoms | “Pain around my post-surgery area is reduced.” (P22) |
| “I feel my appetite is increasing.” (P14) | |
| “Tingling in my hands are reduced so I can work more comfortably with longer duration.” (P11) | |
| Improved psychological well-being | “Before I was more concerned about my disease, whether I can be cured or not. But now, I feel happier.” (P20) |
| Increased physical self-efficacy | “I gained more confidence since practicing the resistance exercise. Even though I can’t do it 100%, I am confident because I know I can do it.” (P07) |
Affective attitude
Most participants reported enjoying participation in the program, with some describing that goal-setting (i.e., target step counts) served as a motivation and challenge that encouraged them to do more. Furthermore, regular contact with the research team provided many participants with a sense of reassurance that they were completing the exercises correctly. However, one participant recounted experiencing discomfort while walking (e.g., knee and foot pain), which had a negative impact on her ability to complete the walking sets.
Burden
The combined aerobic and resistance program was, for the most part, described as straightforward to complete and was not considered to be burdensome. Walking was typically perceived as simple and easy to do, while resistance exercise required participants to concentrate on proper technique. Participants spoke about the benefit and ease of being able to complete the exercises in the home setting, providing them with flexibility in when and where to do the exercises. However, for most participants, there was an initial period at the start of the program that was perceived as stressful. This was due to having to learn new exercises alongside becoming familiar and comfortable with apparatuses such as resistance bands and belt-worn pedometers. In contrast with the vast majority of participants who believed goal-setting was a motivation for them, one participant reported feeling burdened by the need to achieve a weekly exercise target.
Perceived effectiveness
Most of the participants reported feeling that their fitness and stamina improved, and also felt less tired (fatigue), following participation in the program. For some, participating in this program was novel since they did not regularly exercise or participated in no exercise at all. Participants reported positive physical changes including improved range of movement and upper body strength, reduced post-surgical pain, and symptom improvements including increased appetite and reduced tingling in their arm. Psychological improvements were also noted by some participants, such as increased physical self-efficacy and overall well-being.
Intervention effectiveness
Aerobic capacity
At baseline, we found 18 participants (58.1%) had low fitness, 9 (29%) fair fitness, 3 (9.7%) average fitness, and only one participant (3.2%) had good physical fitness, based on the normative values from ACSM. 26 After the 12-week home-based intervention, the number of participants with low and fair physical fitness was reduced (54.8% and 19.4%), while the number of participants with average and good physical fitness was increased (16.1% and 9.7%) (Figure 3). Additionally, the 12-week home-based aerobic and resistance exercise intervention significantly increased test duration and aerobic capacity in predicted V̇O2 peak (+1.1 min, p = 0.001 and +2.3 ml/kg/min, p = 0.043, respectively) (Table 4).
Figure 3.

Participants’ physical fitness before and after the 12-week physical activity intervention. A Sankey diagram described participants’ physical fitness before and after the 12-week study intervention. Physical fitness was classified as low, fair, average, and good fitness based on aerobic capacity and age. Line thickness indicates participants’ proportion.
Table 4.
Modified Bruce treadmill test results before and after intervention (N = 31).
| Parameters | Before intervention (mean ± SD) | After intervention (mean ± SD) | p-Value |
|---|---|---|---|
| Test duration (min) | 9.89 ± 2.38 | 10.99 ± 2.24 | 0.001 |
| Aerobic capacity | |||
| V̇O2 peak (ml/kg/min) | 21.24 ± 6.83 | 23.54 ± 6.55 | 0.043 |
| Rest HR (bpm) | 93.84 ± 14.65 | 91.52 ± 15.14 | 0.372 |
| Rest SBP (mmHg) | 119.68 ± 13.54 | 119.68 ± 12.51 | 0.942 |
| Rest DBP (mmHg) | 72.90 ± 5.88 | 74.19 ± 6.20 | 0.285 |
| Peak HR (bpm) | 149.23 ± 19.84 | 148.00 ± 18.25 | 0.702 |
| Peak SBP (mmHg) | 162.58 ± 20.16 | 159.35 ± 23.65 | 0.108 |
| Peak DBP (mmHg) | 75.80 ± 6.72 | 76.13 ± 7.61 | 0.781 |
SD: standard deviation; V̇O2peak: peak oxygen uptake; HR: heart rate; bpm: beat per minutes; SBP: systolic blood pressure; DBP: diastolic blood pressure.
Twelve participants (38.7%) demonstrated improvement in aerobic capacity after a 12-week intervention, while the rest (n = 19; 61.3%) remained the same or declined. From logistic regression, we found that hypertension comorbidity and low physical fitness at the baseline were significantly associated with aerobic capacity improvement (p = 0.031 and 0.033) (Table 5). Adherence rates to the intervention were not significantly associated with aerobic capacity improvement (p = 0.246 and 0.798).
Table 5.
Participants’ baseline characteristics influencing aerobic capacity improvement (N = 31).
| Factors | With improvement n (%) | Without improvement n (%) | OR | p-Value | 95% CI |
|---|---|---|---|---|---|
| N | 12 | 19 | |||
| Age | |||||
| ⩽52 years | 5 (41.7) | 13 (68.4) | Ref | ||
| >52 years | 7 (58.3) | 6 (31.6) | 0.33 | 0.147 | 0.07– 1.48 |
| BMI | |||||
| <23 kg/m2 | 4 (33.3) | 8 (42.1) | Ref | ||
| ⩾23 kg/m2 | 8 (66.7) | 11 (57.9) | 0.69 | 0.626 | 0.15–3.10 |
| Hypertension comorbidity | |||||
| No | 7 (58.3) | 18 (94.7) | Ref | ||
| Yes | 5 (41.7) | 1 (5.3) | 0.08 | 0.031 | 0.01–0.79 |
| Stage | |||||
| Stage I–II | 6 (50.0) | 13 (68.4) | Ref | ||
| Stage III | 6 (50.0) | 6 (31.6) | 0.46 | 0.309 | 0.10–2.04 |
| Endocrine treatment duration | |||||
| ⩽24 months | 9 (75.0) | 11 (57.9) | Ref | ||
| >24 months | 3 (25.0) | 8 (42.1) | 2.18 | 0.337 | 0.44–10.73 |
| Physical fitness | |||||
| Low | 10 (83.3) | 8 (42.1) | Ref | ||
| Fair, average, good | 2 (16.7) | 11 (57.9) | 0.14 | 0.033 | 0.02–0.85 |
| Aerobic exercise adherence | |||||
| Adherent | 5 (41.7) | 12 (63.2) | Ref | ||
| Non-adherent | 7 (58.3) | 7 (36.8) | 0.42 | 0.246 | 0.09–1.83 |
| Resistance exercise adherence | |||||
| Adherent | 9 (75.0) | 15 (78.9) | Ref | ||
| Non-adherent | 3 (25.0) | 4 (21.1) | 0.80 | 0.798 | 0.14–4.42 |
OR: odds ratio; CI: confidence interval; BMI: body mass index.
Quality of life and fatigue
The mean of each QoL domain and FSS at baseline and post-intervention was presented in Table 6. There were no significant changes in all QoL domains before and after the 12-week intervention (p > 0.050). However, most domains in the functional scale were slightly higher in post-intervention evaluation, and appetite loss was trending toward improvement (p = 0.083). The exercise intervention appeared to decrease fatigue severity although statistical significance was not reached (p = 0.299).
Table 6.
Quality of life and fatigue before and after intervention (N = 32).
| Domain | Before intervention | After intervention | p-Value |
|---|---|---|---|
| EORTC QLQ C-30 (mean ± SD) | |||
| Global health status/QoL | 82.16 ± 15.67 | 82.03 ± 15.85 | 0.741 |
| Functional scales | |||
| Physical | 61.25 ± 6.44 | 62.29 ± 8.05 | 0.246 |
| Role | 61.46 ± 13.01 | 63.54 ± 7.84 | 0.669 |
| Emotional | 53.39 ± 17.05 | 55.21 ± 19.37 | 0.202 |
| Cognitive | 54.69 ± 17.06 | 55.73 ± 16.18 | 0.574 |
| Social | 66.67 ± 0.00 | 65.63 ± 5.89 | 0.317 |
| Symptom scales | |||
| Fatigue | 11.46 ± 14.79 | 13.54 ± 21.81 | 0.456 |
| Nausea and vomiting | 1.01 ± 4.04 | 1.56 ± 4.93 | 0.563 |
| Pain | 4.69 ± 11.39 | 5.73 ± 13.12 | 0.686 |
| Dyspnea | 0.00 ± 0.00 | 2.08 ± 8.19 | 0.157 |
| Insomnia | 8.33 ± 20.74 | 11.46 ± 20.05 | 0.220 |
| Appetite loss | 5.21 ± 19.14 | 0.00 ± 0.00 | 0.083 |
| Constipation | 3.12 ± 9.87 | 4.17 ± 11.20 | 0.654 |
| Diarrhea | 1.04 ± 5.89 | 0.00 ± 0.00 | 0.317 |
| Financial difficulties | 6.25 ± 17.84 | 5.21 ± 14.93 | 0.438 |
| Fatigue severity scale (FSS) | |||
| Fatigue severity (mean ± SD) | 3.56 ± 1.79 | 3.31 ± 1.72 | 0.299 |
| Fatigue severity category (n (%)) | |||
| No-mild fatigue (FSS < 4) | 16 (50.0) | 17 (53.1) | 0.739 |
| Severe fatigue (FSS ⩾ 4) | 16 (50.0) | 15 (46.9) | |
SD: standard deviation; EORTC QLQ-C30: European organization for research and treatment of cancer quality of life core questionnaire; QoL: quality of life; FSS: fatigue severity scale.
Discussion
This study reports on the feasibility, acceptability, and preliminary effectiveness of a home-based exercise program delivered during endocrine treatment for patients with BC. This is the first study to implement a combined aerobic and resistance exercise intervention in BC care in Indonesia. It is also one of few studies that have used a personalized exercise program in a home setting in an LMIC. In addition, few studies in LMICs have used a predictive submaximal exercise test to assess changes in physical fitness. Our study demonstrated that participation in a 12-week home-based exercise was feasible and acceptable. Moreover, preliminary findings point toward significant increases in predicted V̇O2 peak and exercise duration suggesting that the program may be beneficial for patients receiving endocrine treatment in Indonesia.
Despite a considerable amount of research investigating the impact of exercise on outcomes for patients with BC, studies that focus on home-based interventions that can be embedded in a real-world setting are scarce. 35 In Indonesia, evidence-based interventions that are affordable, accessible, low burden for healthcare professionals and can be delivered as an integrated pathway are needed to improve outcomes for patients with BC. Most countries in low resources settings struggle to deliver exercise interventions due to a lack of resources, space, equipment, and trained professionals. 36 Our study is one of the first studies to identify and analyze indicators addressing the possibility of delivering home-based exercise (e.g., feasibility and acceptability) in the context of cancer care in Indonesia.
The recruitment and retention rates (75% and 89%) in our study are consistent with rates observed in studies conducted in high-income country settings (ranging from 76.5% to 97%).11,15,37 Adherence to resistance exercise in this study (78%) was considered high, supported by a previous review suggesting 71%–88% as high adherence levels for home-based aerobic and resistance intervention in HICs. 16 However, adherence to the aerobic program (53%) was lower than other walking-based interventions,38,39 but followed similar trends as found by Pinto et al., 40 where walking was highest in the first 4 weeks of the intervention and then declined until week 12 due to the increased exercise targets and a reduction in its novelty over time. Previous studies found that education level, BMI, history of multimodal treatment, and physical fatigue were predictors of adherence rate41,42 even though our analyses revealed no association between participants’ characteristics and adherence rate. However, Witlox et al. 41 supported that possible predictors of adherence were not identical across the study population. Our study, as reported elsewhere in the literature, highlights the acceptability of home-based exercise programs during the treatment for BC.43,44 Participants reported that exercises were easy and enjoyable. Overall, the absence of serious adverse events in the present study indicates that home-based aerobic and resistance exercise have an acceptable safety profile. Whilst five patients (13.9%) reported myalgia after participating in resistance exercise, its reported prevalence in this study aligns with similar studies (13.3% and 16.1%).20,45 While myalgia can be caused by caused by unaccustomed exercise 46 and is a common side effect of endocrine treatment. 47 Future research should investigate pain exacerbation with exercise in patients receiving endocrine treatment who have not previously performed resistance exercise.
Our study expands on previous research by exploring the feasibility and acceptability of a home-based exercise program in the context of an LMIC setting and provides new insight into women’s cognitive and emotional responses to an intervention delivered by healthcare professionals in Indonesia. In this study, we found that home-based aerobic and resistance exercise is acceptable, with perceived benefits (including improved physical fitness, arm strength and movement, and psychological well-being), goal-setting, and reassurance feeling as the major enabling factors. On the contrary, we found pain experienced during and after exercising as a barrier that led to low intervention adherence. The inclusion of participant interviews provides insights into the mechanisms that may be underpinning the emotional experience of engaging with exercise, and participants’ perceptions of the burden and effectiveness associated with the intervention. Strategies to mitigate barriers (e.g., offering individualized types of therapeutic exercises) and maintain or enhance participation in exercise are needed in future work to improve adherence and increase intervention uptake.48,49
The home-based aerobic and resistance exercise was beneficial, demonstrating a remarkable increase in the predicted V̇O2 peak and treadmill test duration, in line with previous studies in HICs.11,15,26,39,45 An increase of 3.5 ml/kg/min V̇O2 peak, representing aerobic capacity improvement, is associated with reduced mortality in patients with BC. 12 Patients with BC and moderate aerobic capacity demonstrated a 33% lower risk of mortality. 50 In addition, a meta-analysis reported that participation in a home-based exercise intervention results in QoL improvement and is an efficacious option for those with limited access to exercise facilities. 51 However, this study failed to show a significant QoL improvement, probably due to a high QoL level at the baseline. We identified differing levels of improvement regarding aerobic capacity. In this study, participants who did not experience an improvement in aerobic capacity, sometimes referred to as “non-responders,” had better physical fitness compared to the responders who mostly (83.3%) had low physical fitness. These last two findings may indicate little opportunities to improve or a ceiling effect. We could not further analyze this ceiling effect in the absence of a control group. In addition, considering that this study used a home-based intervention, the overall exercise dose was relatively low. However, based on our aerobic capacity finding, the low-dose exercise still had significant benefits, particularly among responders, even though the magnitude was lower compared to moderate-to-high dose programs usually delivered in a supervised setting. 52 Studies with control groups are needed, as well as exploring tailoring of intervention dose in response to participant baseline physical fitness level.
The UK Medical Research Council intervention development framework consists of four phases to increase the uptake of successfully tested interventions, 53 namely intervention development, feasibility, evaluation, and implementation order. Our study assessed intervention feasibility and acceptability at the patient level and suggested that different outcomes are probably associated with the participant’s physical fitness level at baseline and total exercise dose. Intervention refinement after confirming the dose-response interaction, acceptability from the provider level, and cost considerations are essential before testing the intervention in the evaluation phase. Continuous evaluation before incorporating an intervention into routine care is needed since other BC populations in different hospitals or regions may have different acceptability rates, barriers, or enabling factors. Effective implementation also requires rehabilitation professionals training, public awareness education, and collaboration with other institutions or hospital to facilitate knowledge and resource transfer. 36
This is the first study that evaluates the feasibility and acceptability using theoretical framework analysis on home-based exercise intervention in LMICs. Previous studies in India 54 and Indonesia 55 did not report feasibility data. Measuring and reporting the implementation outcomes are important to maximize the use and impact of an intervention study in real-world setting.35,53 This study has already used mixed methods study to measure feasibility, acceptability, and preliminary effectiveness that reflect intervention appropriateness. 35 Additionally, a predictive submaximal treadmill test was used to assess aerobic capacity, which was perceived to be safer compared to field-based tests and timed up-and-go test 56 and more convenient compared to a cycle ergometer. 57 The modified Bruce treadmill test that we used has proven valid. 58 Furthermore, our study combined aerobic and resistance exercise in a home-based setting and demonstrated a positive effect on the aerobic capacity outcome. Most previous studies have adopted a single training modality, mainly aerobic exercise.55,59,60
Our study has limitations. First, even though implementing home-based exercise intervention was novel for Indonesian BC patients, as well as other LMICs, this kind of study was already conducted mainly in HICs.11,15,26,39,45 In addition, other studies incorporated other aspects alongside exercise intervention, such as nutritional and psychological education, 61 or assessed different outcomes, for example, lymphedema. 62 Second, a self-reported diary was used to capture patients’ adherence that may have introduced recall bias with consequential over- or under-reporting. 58 Weekly phone calls to monitor and document self-reported data from the prior week were conducted to minimize this bias. This study lacked a resistance test despite the use of a combined aerobic and resistance exercise intervention. Handgrip strength, one-repetition maximum, and multiple repetition test are commonly used evaluation methods in resistance exercise 25 , but appropriate equipment and gym facilities were not available to implement these measures. Lastly, even though we already incorporated some implementation outcomes, we have not analyzed the intervention acceptability beyond the patient level, the degree of intervention adoption, and cost-effectiveness. 35 Future studies need to address these concerns to promote home-based aerobic and resistance exercise implementation into cancer routine care in Indonesia.
Conclusion
This first study to implement a home-based combined aerobic and resistance exercise intervention in BC care in Indonesia demonstrates its feasibility, acceptability, safety, and preliminary effectiveness. Our work has begun to identify mechanisms that may be influencing the positive outcomes experienced by participants, but further intervention mapping and testing are required to support its development and understand its delivery and performance when tested in additional sites. Future research is required to determine appropriate approaches to tailoring the content of aerobic and resistance exercise programs in response to baseline levels of physical fitness to avoid ceiling effects.
Supplemental Material
Supplemental material, sj-docx-1-smo-10.1177_20503121241272706 for Feasibility, acceptability, and preliminary effectiveness of implementing a 12-week home-based aerobic and resistance exercise program for breast cancer patients receiving endocrine treatment in Indonesia: A mixed methods study by Yufi Kartika Astari, Susanna Hilda Hutajulu, Yayi Suryo Prabandari, Bagas Suryo Bintoro, Rakhmat Ari Wibowo, Mardiah Suci Hardianti, Anggoro Budi Hartopo, Katie M Di Sebastiano, Matthew John Allsop and Shaunna Burke in SAGE Open Medicine
Supplemental material, sj-docx-2-smo-10.1177_20503121241272706 for Feasibility, acceptability, and preliminary effectiveness of implementing a 12-week home-based aerobic and resistance exercise program for breast cancer patients receiving endocrine treatment in Indonesia: A mixed methods study by Yufi Kartika Astari, Susanna Hilda Hutajulu, Yayi Suryo Prabandari, Bagas Suryo Bintoro, Rakhmat Ari Wibowo, Mardiah Suci Hardianti, Anggoro Budi Hartopo, Katie M Di Sebastiano, Matthew John Allsop and Shaunna Burke in SAGE Open Medicine
Supplemental material, sj-docx-3-smo-10.1177_20503121241272706 for Feasibility, acceptability, and preliminary effectiveness of implementing a 12-week home-based aerobic and resistance exercise program for breast cancer patients receiving endocrine treatment in Indonesia: A mixed methods study by Yufi Kartika Astari, Susanna Hilda Hutajulu, Yayi Suryo Prabandari, Bagas Suryo Bintoro, Rakhmat Ari Wibowo, Mardiah Suci Hardianti, Anggoro Budi Hartopo, Katie M Di Sebastiano, Matthew John Allsop and Shaunna Burke in SAGE Open Medicine
Supplemental material, sj-docx-4-smo-10.1177_20503121241272706 for Feasibility, acceptability, and preliminary effectiveness of implementing a 12-week home-based aerobic and resistance exercise program for breast cancer patients receiving endocrine treatment in Indonesia: A mixed methods study by Yufi Kartika Astari, Susanna Hilda Hutajulu, Yayi Suryo Prabandari, Bagas Suryo Bintoro, Rakhmat Ari Wibowo, Mardiah Suci Hardianti, Anggoro Budi Hartopo, Katie M Di Sebastiano, Matthew John Allsop and Shaunna Burke in SAGE Open Medicine
Supplemental material, sj-docx-5-smo-10.1177_20503121241272706 for Feasibility, acceptability, and preliminary effectiveness of implementing a 12-week home-based aerobic and resistance exercise program for breast cancer patients receiving endocrine treatment in Indonesia: A mixed methods study by Yufi Kartika Astari, Susanna Hilda Hutajulu, Yayi Suryo Prabandari, Bagas Suryo Bintoro, Rakhmat Ari Wibowo, Mardiah Suci Hardianti, Anggoro Budi Hartopo, Katie M Di Sebastiano, Matthew John Allsop and Shaunna Burke in SAGE Open Medicine
Acknowledgments
We are grateful to Norma Dewi Suryani, Refdiana Dewi, Riani Witaningrum, Anton Sudiyanto, Fahmi Baiquni, and Juan Adrian Wiranata for technical assistance. We also gratefully thanked our cardiac rehabilitation nurses, Endang Warijanti and Diah Perwitasari.
Footnotes
Availability of data and materials: The data sets analyzed in the current study are accessible from the corresponding author on fair request.
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding: The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by University of Leeds (2021); The Indonesian Ministry of Research, Technology and Higher Education (grant number 1951/UN1/DITLIT/Dit-Lit/PT.01.03.2022, 2022); and Universitas Gadjah Mada (grant numbers 348/UN1/FKKMK/PPKE/PT/2022 and 3550/UN1.P.III/Dit-Lit/PT.01.05/2022, 2022). All funders did not play any role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Ethics approval: Ethical approval for this study was obtained from the Medical and Health Research Ethics Committee, Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia (reference number KE/FK/0184/EC/2021).
Informed consent: Written informed consent was obtained from all subjects before the study.
Trial registration: Not applicable.
ORCID iDs: Yufi Kartika Astari
https://orcid.org/0000-0003-0999-8826
Susanna Hilda Hutajulu
https://orcid.org/0000-0001-9236-9435
Matthew John Allsop
https://orcid.org/0000-0002-7399-0194
Supplemental material: Supplemental material for this article is available online.
References
- 1. Sung H, Ferlay J, Siegel RL, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2021; 71: 209–249. [DOI] [PubMed] [Google Scholar]
- 2. Sinaga ES, Ahmad RA, Hutajulu SH. Ketahanan hidup 5 tahun pada pasien kanker payudara. Berita Kedokteran Masyarakat 2017; 33: 67–72. [Google Scholar]
- 3. Registry JC. Laporan data registrasi kanker berbasis rumah sakit periode maret 2022. (Report of hospital-based cancer registry in March 2022), https://canreg.fk.ugm.ac.id/laporan-data/registrasi-kanker-berbasis-rumah-sakit-dr-sardjito-fkkmk-ugm/rkbr-maret-2022/ (2022, accessed 22 July 2022).
- 4. Hennigs A, Riedel F, Gondos A, et al. Prognosis of breast cancer molecular subtypes in routine clinical care: a large prospective cohort study. BMC Cancer 2016; 16: 1–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Anwar SL, Tampubolon G, Van Hemelrijck M, et al. Determinants of cancer screening awareness and participation among Indonesian women. BMC Cancer 2018; 18: 1–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Heins MJ, de Ligt KM, Verloop J, et al. Adverse health effects after breast cancer up to 14 years after diagnosis. Breast 2022; 61: 22–28. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Campbell KL, Winters-Stone K, Wiskemann J, et al. Exercise guidelines for cancer survivors: Consensus statement from international multidisciplinary roundtable. Med Sci Sports Exerc 2019; 51: 2375. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. Gordon LG, Eakin EG, Spence RR, et al. Cost-effectiveness analysis from a randomized controlled trial of tailored exercise prescription for women with breast cancer with 8-year follow-up. Int J Environ Res Public Health 2020; 17: 8608. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. McNeely M, Campbell K, Rowe B, et al. Effects of exercise on breast cancer patients and survivors: a systematic review and meta-analysis. CMAJ 2006; 175: 35–41. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Lahart IM, Metsios GS, Nevill AM, et al. Physical activity for women with breast cancer after adjuvant therapy. Cochrane Database Syst Rev 2018; 1: Cd011292. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11. Spector D, Deal AM, Amos KD, et al. A pilot study of a home-based motivational exercise program for African American breast cancer survivors: clinical and quality-of-life outcomes. Integr Cancer Ther 2014; 13: 121–132. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. de Jesus Leite MAF, Puga GM, Arantes FJ, et al. Effects of combined and resistance training on the inflammatory profile in breast cancer survivors: a systematic review. Complement Ther Med 2018; 36: 73–81. [DOI] [PubMed] [Google Scholar]
- 13. Burse NR, Bhuiyan N, Mama SK, et al. Physical activity barriers and resources among black women with a history of breast and endometrial cancer: a systematic review. J Cancer Surv 2020; 14: 556–577. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Do J, Cho Y, Jeon J. Effects of a 4-week multimodal rehabilitation program on quality of life, cardiopulmonary function, and fatigue in breast cancer patients. J Breast Cancer 2015; 18: 87–96. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Ligibel JA, Partridge A, Giobbie-Hurder A, et al. Physical and psychological outcomes among women in a telephone-based exercise intervention during adjuvant therapy for early stage breast cancer. J Womens Health (Larchmt) 2010; 19: 1553–1559. [DOI] [PubMed] [Google Scholar]
- 16. Batalik L, Winnige P, Dosbaba F, et al. Home-based aerobic and resistance exercise interventions in cancer patients and survivors: a systematic review. Cancers 2021; 13: 1915. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17. Pramesh C, Badwe RA, Bhoo-Pathy N, et al. Priorities for cancer research in low-and middle-income countries: a global perspective. Nat Med 2022; 28: 649–657. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Puspitaningtyas H, Espressivo A, Hutajulu SH, et al. Mapping and visualization of cancer research in Indonesia: a scientometric analysis. Cancer Control 2021; 28: 10732748211053464. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Leite VF, Cecatto RB, Battistella LR, et al. Establishing a cancer rehabilitation service in a middle-income country: an experience from Brazil. Curr Phys Med Rehab Rep 2022; 10(4): 339–344. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Rogers LQ, Courneya KS, Anton PM, et al. Effects of the BEAT cancer physical activity behavior change intervention on physical activity, aerobic fitness, and quality of life in breast cancer survivors: a multicenter randomized controlled trial. Breast Cancer Res Treat 2015; 149: 109–119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21. Lancaster GA, Dodd S, Williamson PR. Design and analysis of pilot studies: recommendations for good practice. J Eval Clin Pract 2004; 10: 307–312. [DOI] [PubMed] [Google Scholar]
- 22. Fusch PI, Ness LR. Are we there yet? Data saturation in qualitative research. Qual Rep 2015; 20(9): 1408–1416. [Google Scholar]
- 23. Corry K, Mummery W, Behan R, et al. Pedometer reliability, validity and feasibility report, 2010. CQ University, https://hdl.handle.net/10018/9197412010 (2010). [Google Scholar]
- 24. Baker G, Gray S, Wright A, et al. The effect of a pedometer-based community walking intervention “Walking for Wellbeing in the West” on physical activity levels and health outcomes: a 12-week randomized controlled trial. Int J Behav Nutr Phys Act 2008; 5: 44. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25. Montaño-Rojas LS, Romero-Pérez EM, Medina-Pérez C, et al. Resistance training in breast cancer survivors: a systematic review of exercise programs. Int J Environ Res Public Health 2020; 17: 20200907. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26. De Jesus S, Fitzgeorge L, Unsworth K, et al. Feasibility of an exercise intervention for fatigued breast cancer patients at a community-based cardiac rehabilitation program. Cancer Manag Res 2017; 9: 29–39. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27. Sekhon M, Cartwright M, Francis JJ. Acceptability of healthcare interventions: an overview of reviews and development of a theoretical framework. BMC Health Serv Res 2017; 17: 1–13. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. Pedoman Uji Latih jantung: Prosedur dan Interpretasi . Jakarta: PERKI, 2016. [Google Scholar]
- 29. Perwitasari DA, Atthobari J, Dwiprahasto I, et al. Translation and validation of EORTC QLQ-C30 into Indonesian version for cancer patients in Indonesia. Japan J Clin Oncol 2011; 41: 519–529. [DOI] [PubMed] [Google Scholar]
- 30. Rifaâ A, Kalim H, Handono K, et al. Validity and reliability fatigue severity scale in patients with systemic lupus erythematosus (SLE) in Indonesia. Indones J Rheumatol 2016; 8:231067. [Google Scholar]
- 31. Fayers P, Aaronson NK, Bjordal K, et al. The EORTC QLQ-C30 scoring manual (3rd edition). Brussels: European Organization for Research and Treatment of Cancer, 2001. [Google Scholar]
- 32. Krupp LB, Coyle PK, Doscher C, et al. Fatigue therapy in multiple sclerosis: results of a double-blind, randomized, parallel trial of amantadine, pemoline, and placebo. Neurology 1995; 45: 1956–1961. [DOI] [PubMed] [Google Scholar]
- 33. Braun V, Clarke V. Using thematic analysis in psychology. Qualit Res Psychol 2006; 3: 77–101. [Google Scholar]
- 34. Smith B, McGannon KR. Developing rigor in qualitative research: problems and opportunities within sport and exercise psychology. Int Rev Sport Exerc Psychol 2018; 11: 101–121. [Google Scholar]
- 35. Czosnek L, Richards J, Zopf E, et al. Exercise interventions for people diagnosed with cancer: a systematic review of implementation outcomes. BMC Cancer 2021; 21: 1–25. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Anwar SL, Adistyawan G, Wulaningsih W, et al. Rehabilitation for cancer survivors: how we can reduce the healthcare service inequality in low-and middle-income countries. Am J Phys Med Rehab 2018; 97: 764–771. [DOI] [PubMed] [Google Scholar]
- 37. Uhm KE, Yoo JS, Chung SH, et al. Effects of exercise intervention in breast cancer patients: is mobile health (mHealth) with pedometer more effective than conventional program using brochure? Breast Cancer Res Treat 2017; 161: 443–452. [DOI] [PubMed] [Google Scholar]
- 38. Sturgeon KM, Smith AM, Federici EH, et al. Feasibility of a tailored home-based exercise intervention during neoadjuvant chemotherapy in breast cancer patients. BMC Sports Sci Med Rehabil 2022; 14: 31. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39. Cornette T, Vincent F, Mandigout S, et al. Effects of home-based exercise training on VO2 in breast cancer patients under adjuvant or neoadjuvant chemotherapy (SAPA): a randomized controlled trial. Eur J Phys Rehabil Med 2016; 52: 223–232. [PubMed] [Google Scholar]
- 40. Pinto BM, Rabin C, Dunsiger S. Home-based exercise among cancer survivors: adherence and its predictors. Psychooncology 2009; 18: 369–376. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41. Witlox L, Velthuis MJ, Boer JH, et al. Attendance and compliance with an exercise program during localized breast cancer treatment in a randomized controlled trial: the PACT study. PLoS One 2019; 14: e0215517. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42. Coletta AM, Marquez G, Thomas P, et al. Clinical factors associated with adherence to aerobic and resistance physical activity guidelines among cancer prevention patients and survivors. PLoS One 2019; 14: e0220814. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43. Ingram C, Wessel J, Courneya KS. Women’s perceptions of home-based exercise performed during adjuvant chemotherapy for breast cancer. Eur J Oncol Nurs 2010; 14: 238–243. [DOI] [PubMed] [Google Scholar]
- 44. Schneider C, Reimann S, Schmid J, et al. Qualitative analysis of facilitators and barriers to center- and home-based exercise training in breast cancer patients—a Swiss tertiary center experience. Swiss Med Wkly 2022; 152: w30155. [DOI] [PubMed] [Google Scholar]
- 45. Vincent F, Deluche E, Bonis J, et al. Home-based physical activity in patients with breast cancer: during and/or after chemotherapy? Impact on cardiorespiratory fitness. A 3-Arm Randomized Controlled Trial (APAC). Integr Cancer Ther 2020; 19: 1534735420969818. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46. Vasconcelos ES. Inflammatory response induced by resistance exercise. MOJ Immunol 2018; 6: 110–113. [Google Scholar]
- 47. Yamamoto Y, Iwase H. Safety profiles of aromatase inhibitors and selective estrogen-receptor modulators in the treatment of early breast cancer. Int J Clin Oncol 2008; 13: 384–394. [DOI] [PubMed] [Google Scholar]
- 48. Beckenstein H, Slim M, Kim H, et al. Acceptability of a structured diet and exercise weight loss intervention in breast cancer survivors living with an overweight condition or obesity: a qualitative analysis. Cancer Rep 2021; 4: e1337. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49. Bauer MS, Kirchner J. Implementation science: what is it and why should I care? Psychiatry Res 2020; 283: 112376. [DOI] [PubMed] [Google Scholar]
- 50. Peel JB, Sui X, Adams SA, et al. A prospective study of cardiorespiratory fitness and breast cancer mortality. Med Sci Sports Exerc 2009; 41: 742–748. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51. Bates-Fraser LC, Riley S, Stopforth C, et al. Home-based exercise improves quality of life in breast and prostate cancer survivors: a meta-analysis. PLoS One 2023; 18: e0284427. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52. van Waart H, Stuiver MM, van Harten WH, et al. Effect of low-intensity physical activity and moderate- to high-intensity physical exercise during adjuvant chemotherapy on physical fitness, fatigue, and chemotherapy completion rates: results of the PACES randomized clinical trial. J Clin Oncol 2015; 33: 1918–1927. [DOI] [PubMed] [Google Scholar]
- 53. Skivington K, Matthews L, Simpson SA, et al. A new framework for developing and evaluating complex interventions: update of medical research council guidance. BMJ 2021; 374: n2061. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54. Gandhi A, Samuel SR, Kumar KV, et al. Effect of a pedometer-based exercise program on cancer related fatigue and quality of life among patients with breast cancer receiving chemotherapy. Asian Pac J Cancer Prev 2020; 21: 1813–1818. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55. Dewi L, Sukartini T, Kurniawati N, et al. The effects of home-based exercise training on physical performance, fatigue and quality of life in breast cancer patient receiving chemotherapy: a pilot study. Int J Psychosoc Rehab 2020; 24: 9184–9191. [Google Scholar]
- 56. Roy B, Fountaine CJ, Liguori G, et al. ACSM’s guidelines for exercise testing and prescription. Philadelphia, PA: Lippincott Williams & Wilkins, 2013. [Google Scholar]
- 57. Arena R, Myers J, Williams MA, et al. Assessment of functional capacity in clinical and research settings: a scientific statement from the American Heart Association Committee on Exercise, Rehabilitation, and Prevention of the Council on Clinical Cardiology and the Council on Cardiovascular Nursing. Circulation 2007; 116: 329–343. [DOI] [PubMed] [Google Scholar]
- 58. Musanti R. A study of exercise modality and physical self-esteem in breast cancer survivors. Med Sci Sports Exerc 2012; 44: 352–361. [DOI] [PubMed] [Google Scholar]
- 59. Gokal K, Wallis D, Ahmed S, et al. Effects of a self-managed home-based walking intervention on psychosocial health outcomes for breast cancer patients receiving chemotherapy: a randomized controlled trial. Support Care Cancer 2016; 24: 1139–1166. [DOI] [PubMed] [Google Scholar]
- 60. VanderWalde NA, Martin MY, Kocak M, et al. Randomized phase II study of a home-based walking intervention for radiation-related fatigue among older patients with breast cancer. J Geriatr Oncol 2021; 12: 227–234. [DOI] [PubMed] [Google Scholar]
- 61. Wolff J, Wuelfing P, Koenig A, et al. App-based lifestyle coaching (PINK!) accompanying breast cancer patients and survivors to reduce psychological distress and fatigue and improve physical activity: a feasibility pilot study. Breast Care (Basel) 2023; 18: 354–365. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62. Baumann FT, Reike A, Hallek M, et al. Does exercise have a preventive effect on secondary lymphedema in breast cancer patients following local treatment? A systematic review. Breast Care (Basel) 2018; 13: 380–385. [DOI] [PMC free article] [PubMed] [Google Scholar]
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Supplementary Materials
Supplemental material, sj-docx-1-smo-10.1177_20503121241272706 for Feasibility, acceptability, and preliminary effectiveness of implementing a 12-week home-based aerobic and resistance exercise program for breast cancer patients receiving endocrine treatment in Indonesia: A mixed methods study by Yufi Kartika Astari, Susanna Hilda Hutajulu, Yayi Suryo Prabandari, Bagas Suryo Bintoro, Rakhmat Ari Wibowo, Mardiah Suci Hardianti, Anggoro Budi Hartopo, Katie M Di Sebastiano, Matthew John Allsop and Shaunna Burke in SAGE Open Medicine
Supplemental material, sj-docx-2-smo-10.1177_20503121241272706 for Feasibility, acceptability, and preliminary effectiveness of implementing a 12-week home-based aerobic and resistance exercise program for breast cancer patients receiving endocrine treatment in Indonesia: A mixed methods study by Yufi Kartika Astari, Susanna Hilda Hutajulu, Yayi Suryo Prabandari, Bagas Suryo Bintoro, Rakhmat Ari Wibowo, Mardiah Suci Hardianti, Anggoro Budi Hartopo, Katie M Di Sebastiano, Matthew John Allsop and Shaunna Burke in SAGE Open Medicine
Supplemental material, sj-docx-3-smo-10.1177_20503121241272706 for Feasibility, acceptability, and preliminary effectiveness of implementing a 12-week home-based aerobic and resistance exercise program for breast cancer patients receiving endocrine treatment in Indonesia: A mixed methods study by Yufi Kartika Astari, Susanna Hilda Hutajulu, Yayi Suryo Prabandari, Bagas Suryo Bintoro, Rakhmat Ari Wibowo, Mardiah Suci Hardianti, Anggoro Budi Hartopo, Katie M Di Sebastiano, Matthew John Allsop and Shaunna Burke in SAGE Open Medicine
Supplemental material, sj-docx-4-smo-10.1177_20503121241272706 for Feasibility, acceptability, and preliminary effectiveness of implementing a 12-week home-based aerobic and resistance exercise program for breast cancer patients receiving endocrine treatment in Indonesia: A mixed methods study by Yufi Kartika Astari, Susanna Hilda Hutajulu, Yayi Suryo Prabandari, Bagas Suryo Bintoro, Rakhmat Ari Wibowo, Mardiah Suci Hardianti, Anggoro Budi Hartopo, Katie M Di Sebastiano, Matthew John Allsop and Shaunna Burke in SAGE Open Medicine
Supplemental material, sj-docx-5-smo-10.1177_20503121241272706 for Feasibility, acceptability, and preliminary effectiveness of implementing a 12-week home-based aerobic and resistance exercise program for breast cancer patients receiving endocrine treatment in Indonesia: A mixed methods study by Yufi Kartika Astari, Susanna Hilda Hutajulu, Yayi Suryo Prabandari, Bagas Suryo Bintoro, Rakhmat Ari Wibowo, Mardiah Suci Hardianti, Anggoro Budi Hartopo, Katie M Di Sebastiano, Matthew John Allsop and Shaunna Burke in SAGE Open Medicine

