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Journal of Education and Health Promotion logoLink to Journal of Education and Health Promotion
. 2024 Feb 7;13:31. doi: 10.4103/jehp.jehp_960_23

The evaluation of the effectiveness of a health promotion training on breast cancer survivors

Bahar Kefeli Çol 1,, Gülnihal Tufan 1, Dilek Kiliç 2
PMCID: PMC10967940  PMID: 38545312

Abstract

BACKGROUND:

Increased early diagnosis and improved treatment options have decreased the mortality rate of breast cancer and increased the survival rate. Healthy lifestyle behaviors are very important in breast cancer survivors as they reduce mortality and morbidity rates, cancer recurrence frequency, and side effects of treatment and improve health. This study was conducted to evaluate the effectiveness of a health promotion training intervention in breast cancer survival.

MATERIALS AND METHODS:

The study is a quasi-experimental, pre-test–post-test and single-group study. It was conducted with 43 women breast cancer survivors. The “Healthy Lifestyle Behaviors Scale II” was used to collect the data. Four sessions of training were given to the women once a week, and a 3-month post-training follow-up was performed. The t-test, Wilcoxon analysis, and Spearmen correlation analysis were used to evaluate the data.

RESULTS:

Pre-training and post-training scores in the sub-dimensions and total scores of the healthy lifestyle behavior scale showed that the training was highly effective. There was a significant increase in all sub-dimensions and total scale post-training scores (P < 0.05). In the correlation analysis, a negative correlation was found between age and physical activity, between elapsed time after diagnosis and nutrition, and between elapsed time after diagnosis and spiritual development (P < 0,05). However, there was a positive correlation between educational status and nutrition (P < 0.05).

CONCLUSIONS:

The results show that a health promotion training program covering physical activity/exercise, healthy nutrition, effective communication, coping with stress, and increasing health responsibility had positive effects on healthy lifestyle behaviors in this population, and age, educational status, and elapsed time after diagnosis influence healthy lifestyle behaviors in survival.

Keywords: Breast cancer, health promotion, survival, training

Background

Breast cancer is a global public health problem. The International Agency for Research on Cancer (IARC) estimates that there were more than 2.26 million new cases and approximately 685,000 deaths from breast cancer in 2020 worldwide.[1] World Health Organization (WHO) announced that 7.8 million women diagnosed with breast cancer in the last 5 years had survived by the end of 2020, making it the most common cancer in the world.[2] Currently, breast cancer mortality rates are decreasing, and survival rates are increasing thanks to early diagnosis and improved treatment options.[3,4] According to recent reports, breast cancer survival for at least 5 years after diagnosis is more than 90% in high-income countries.[2]

Recent literature reports that healthy lifestyle behaviors improve health and significantly reduce mortality and morbidity rates, cancer recurrence, and side effects of treatment during cancer survivorship.[5,6] The cancer survivor population needs information and counseling on diet, exercise, mental health, and so on. Therefore, it is a critical issue to focus on promoting healthy lifestyle behaviors in health services.[7,8]

Healthy lifestyle behaviors are defined as the individual’s taking control of behaviors that are effective in improving health and implementing them in daily life.[9] According to the health promotion model, physical activity, stress management, nutrition, health responsibility, inter-personal relationships, and spiritual development are among healthy lifestyle behaviors.[10] There is an increasing body of literature emphasizing the significance of healthy nutrition and physical activity to reduce the rate of recurrence and mortality and the side effects of cancer treatment and increase healthy survival.[11,12,13] However, studies also show that breast cancer survivors do not adhere to recommended dietary and physical activity guidelines.[14,15,16] In addition to daily stressors, breast cancer survivors often deal with the fear of recurrence or developing new cancer, which can lead to high levels of stress.[17,18] Coping with stress is effective in increasing the breast cancer survival rate.[17] A healthy lifestyle improves longer and healthier survival in breast cancer.[19,20] In breast cancer survival, women’s inter-personal relationships with their environment (spouse, family, friends, etc.) may have positive or negative effects, and supportive relationships may be effective in promoting healthy survival.[21,22]

Enhanced spiritual well-being is effective in providing a positive perspective in the face of traumatic and negative situations, reducing pain, and increasing life satisfaction and self-belief.[23,24] A study evaluating the role of spirituality highlighted that spirituality is the main coping mechanism used at all stages of the cancer journey.[25]

Unfortunately, the treatment of cancer patients often focuses only on the pharmacological problems of the disease. However, as mentioned above, a healthy lifestyle has positive effects on cancer and survival, and integrating healthy lifestyle behaviors into health services is essential for a holistic patient-centered approach.

In the primary health care system, public\community health nurses play a critical role in health protection and promotion.[26] In the holistic approach, nurses focus on assisting individuals, families, and communities to make health-related decisions or supporting their participation in health promotion activities.[27,28] In health promotion activities, nurses aim to change individuals’ behaviors and use health training, the most common health promotion intervention, to change health behaviors.[28,29]

Public health nurses need to include healthy lifestyle behaviors (physical activity, nutrition, health responsibility, and inter-personal relationships), which are effective in promoting the health of survivors of breast cancer, one of the critical population groups, in educational interventions. This study was conducted to evaluate the effectiveness of a health promotion training intervention in breast cancer survival.

Materials and Methods

Study design and setting

The study was conducted between 2014 and 2015 in a single group using pre-test–post-test and quasi-experimental methods.

Study participants and sampling

Forty-three volunteer women who completed chemotherapy and/or radiotherapy treatments in the oncology outpatient clinic of a training and research hospital were included in the sample.

The exclusion criteria include to have metastasized, inability to communicate verbally, an age under 18, and a history of psychiatric illness.

Data collection tool and technique

The data were collected using the Demographic Information Form and the Healthy Lifestyle Behavior Scale II with 52 items.

The research data were collected by the researcher through home visits and face-to-face interview technique. During the data collection in the pre-test phase, Demographic Information Form and the Healthy Lifestyle Behavior Scale II of women were used. Upon completion of the training program, the Healthy Lifestyle Behavior Scale II was administered to the women in order to gather post-test data.

The healthy lifestyle behavior scale II

Developed by Walker et al.[10] (1987) and revised in 1996 (Walker and Hill-Polerecky,[30] 1996), the scale measures health-promoting behaviors related to an individual’s healthy lifestyle. It has 52 items and 6 sub-factors. The sub-factors are spiritual development, health responsibility, physical activity, nutrition, inter-personal relationships, and stress management. The overall score of the scale gives the healthy lifestyle behaviors score. All items of the scale are positive and have a 4-point Likert scale: never (1), sometimes (2), often (3), and regularly (4). The minimum and maximum scores on the scale are 52 and 208. The validity and reliability study for the adaptation of the scale into Turkish was conducted by Bahar et al. in 2008.[31] In this study, the Cronbach’s alpha coefficient of the scale was found to be 0.92. The Cronbach’s alpha coefficient of the sub-scales varied between 0.68 and 0.82.

Research plan

The Healthy Lifestyle Behaviors Scale II was administered to the participants as a pre-test to assess their healthy lifestyle behaviors before the training program. Then, a training intervention lasting 50–60 minutes, one session per week for 4 weeks, was implemented during a home visit on the following healthy lifestyle behaviors. Post-test data were collected after the training.

The training topics were the importance of healthy lifestyle behaviors in survival, physical activity/exercise, coping with stress, nutrition, health responsibility, inter-personal relationships, and effective communication.

Statistical method

The Statistical Package for the Social Sciences SPSS (V22.0) package program was used for the statistical analysis of the data. Descriptive data were expressed as percentage, mean, and standard deviation. In the statistical analysis of quantitative data, t-tests and Wilcoxon analysis were performed. Spearman correlation analysis was used to evaluate the relationship between variables.

Ethical consideration

Ethical approval for this study was obtained from the Ethics Council of the University (Decision no: 2014\129). Informed consent was obtained from all the participants.

Results

According to the results, 39.5% of the women were in the 50–59 age group, 55.8% had primary education, and the elapsed time after diagnosis was 0–4 years for 65.1% [Table 1]. The mean score of the healthy lifestyle scale was 140.28 ± 19.5 before the training and 166.84 ± 15.25 after the training [Table 2].

Table 1.

Determinant factors

Group (n=43)
S %
Age
  40-49 years 16 37.2
  50-59 years 17 39.5
  60-69 years 10 23.3
Education status
  Literate 11 25.6
  Primary education 24 55.8
  High school degree and ↑ 8 18.6
Number of children
  1 2 4.7
  2 17 39.5
  3 13 30.2
  4≤ 11 25.6
The stage at the time of diagnosis
  Stage I 9 20.9
  Stage II 25 58.2
  Stage III 9 20.9
Elapsed time since diagnosis
  0-4 years 28 65.1
  5+ years 15 34.9

Table 2.

Comparison of the pre-test–post-test average scores of the sub-dimensions of the SYBD scale

Participants (n=43) Pre-training Post-training P
Health Responsibility
  A.M±SD 26,26±5,62 29,88±3,71 Z=-5,318
  Median (min-max) 28 (12-34) 31 (19-34) 0,0001*
Physical Activity
  A.O±SD 10,21±4,41 18,51±3,28 Z=-5,657
  Med (min-max.) 8 (8-26) 19 (12-26) 0,0001*
Nutrition
  A.O±SD 22,16±5,21 28,4±3,52 t=-11,552
  Med (min-max.) 22 (11-34) 29 (20-35) 0,0001*
Spiritual Development
  A.O±SD 30,86±3,56 32,7±2,74 Z=-4,893
  Med (min-max) 32 (21-36) 33 (24-36) 0,0001*
Interpersonal relationships
  A.O±SD 29,88±4,74 31,51±3,94 Z=-4,498
  Med (min-max) 31 (17-36) 32 (20-36) 0,0001*
Stress Management
  A.O±SD 20,91±4,72 25,84±3,21 Z=-5,725
  Med (min-max) 21 (11-30) 27 (20-32) 0,0001*
Total
  A.O±SD 140,28±19,5 166,84±15,25 t=-16,070
  Med (min-max) 139 (91-177) 169 (123-194) 0,0001*

*P<0.05 statistically significant difference; t: Significance Test for the Difference Between Two Pairs; Z: Wilcoxon Paired Two Sample Test

In the Spearman correlation analysis performed after the training, there was a statistically negative and moderately significant relationship between age and physical activity scores, a positive and moderately significant relationship between educational status and nutrition, a negative and moderately significant relationship between elapsed time after diagnosis and nutrition, and a negative and weak significant relationship between elapsed time after diagnosis and spiritual development [Table 3].

Table 3.

Correlation coefficients between post-training demographic factors and HLBD scale sub-dimensions (Spearman)

Post-training r (P) Health Responsibility Physical Activity Nutrition Spiritual Development Interpersonal Relationships Stress Management Total
Age -0.179 (P=0.25) -0.312* (P=0.042) -0.121 (P=0.439) -0.056 (P=0.719) 0.219 (P=0.158) 0.116 (P=0.46) -0.039 (P=0.802)
Education status 0.183 (P=0.24) 0.181 (P=0.246) 0.309* (P=0.043) 0.177 (P=0.256) -0.198 (P=0.202) 0.073 (P=0.644) 0.139 (P=0.375)
Number of children -0.193 (P=0.215) -0.191 (P=0.221) -0.086 (P=0.584) -0.042 (P=0.787) 0.042 (P=0.788) 0.014 (P=0.929) -0.058 (P=0.712)
The stage at the time of diagnosis 0.044 (P=0.78) 0.143 (P=0.36) 0.116 (P=0.457) 0.042 (P=0.787) 0.022 (P=0.889) 0.108 (P=0.491) 0.112 (P=0.476)
Elapsed time since diagnosis 0.008 (P=0.958) -0.076 (P=0.63) -0.313* (P=0.041) -0.296* (P=0.05) -0.116 (P=0.458) -0.07 (P=0.654) -0.169 (P=0.278)

*P<0,05 statistically significant correlation (Spearman Correlation Analysis)

Discussion

In this study, the mean score for a health-promoting lifestyle was found to be moderate, similar to an earlier study, and the highest and lowest mean scores were obtained from spiritual development and physical activity, respectively.[32] Age, educational status, and elapsed time since diagnosis were found to be factors affecting healthy lifestyle behaviors.

Physical activity is a significant modifiable lifestyle behavior influencing the health outcomes of cancer survivors.[33] However, a recent study shows that the physical activity level of women is low. Consistent with our study, it is reported that breast cancer survivors reduced their physical activities, mostly with a further decline in activity over 10 years or more.[15] Cancer survivors engage in less physical activity than others.[34] As noted in previous studies, low physical activity among breast cancer survivors may be due to the insecurity and uncertainty about how to perform certain exercises, fear of injury due to general health problems, physical limitations (e.g., lymphedema, fatigue, obesity, lack of time, weight gain after chemotherapy), and low confidence and understanding of the benefits of exercise.[34,35,36] DeNysschen et al.[16] (2015) showed that physical activity levels were low in breast cancer survivors, but most women were interested in increasing their activity levels. These findings suggest the need for educational interventions to increase physical activity in breast cancer survivors. Our study shows that health promotion training given to breast cancer survivors is effective in increasing physical activity levels.

The literature is consistent with this present study and shows that the level of physical activity after breast cancer decreases with increasing age.[37,38] Age is a determining factor in physical activity in cancer survivors. Therefore, public health nurses need to prepare interventions to promote physical activity in this population based on age.

Women experience stress/post-traumatic stress in breast cancer survival.[39,40] These data reveal that women need stress management programs. In our study, the stress management level of post-survival women was moderate and increased after the training provided. A stress management program is an effective strategy to help women exposed to stress.[41] Therefore, it is recommended that public health nurses include stress management in health promotion training programs for breast cancer survivorship.

Healthy eating is one of the most reported health-related lifestyle changes after a cancer diagnosis,[42] yet most survivors do not comply with healthy eating guidelines.[43] Breast cancer survivors do not follow dietary recommendations and have low fruit and vegetable intake and high dietary fat intake.[14,16] Unlike the literature, in the current study, the nutritional level was found to be moderate, which may be explained by the difficulty of maintaining healthy lifestyle behaviors like low diet quality in long-term cancer survivors compared to recently diagnosed patients.[43,44] The findings suggest that women survivors need training on topics like choosing and organizing their meals to increase the level of healthy eating.

Cancer survivors believe that nutrition is important, but health care teams often do not address nutrition issues, and healthy eating should be a core part of the cancer care process.[45,46] Breast cancer survivors were highly concerned about weight gain and needed individualized guidance.[47] In our study, health promotion training provided to breast cancer survivors is effective in healthy eating.

Low education level is a risk factor for breast cancer.[48] Research shows that individuals with low levels of education generally have a low tendency to eat healthily.[49,50] Similar to previous studies, in this study, as the education level of breast cancer survivors increased, their healthy eating habits also increased. A recent study supported the findings of the current study and showed that women’s healthy eating habits decreased as the time since diagnosis increased.[51] Public health nurses should prepare the content of the training program by considering the level of education of women and the elapsed time since diagnosis while providing nutrition education to surviving women.

In parallel to the impact of individual lifestyle choices on health, the role of personal responsibility is inevitably gaining importance.[52] Health responsibility is an effective factor for individuals to develop a healthy lifestyle such as healthy eating and adequate physical activity.[19] In the current study, women’s health responsibility was at a moderate level and health training was found to be effective in increasing women’s health responsibility. Positive inter-personal relationships with women’s environment (spouse, family, friends, etc.) are effective in healthy survival in breast cancer survival.[21,22] Women had moderate inter-personal relationships, and the health promotion training increased their inter-personal relationships in our study. Therefore, public health nurses should educate women about the importance of taking responsibility for their health, establishing healthy inter-personal relationships during their survival, and participating in supportive social, friend, and family relationships.

Spiritual development makes cancer diagnosis meaningful;[53] improves the psychological, spiritual, and general well-being of patients; reduces depression;[54] and boosts the enjoyment of life and peace of mind.[55] In the present study, women’s spiritual development was at a moderate level and increased after education, and spiritual development decreased with time after diagnosis. The present data show that women need spiritual development in the early survival period.

After these considerations on the positive effects of healthy lifestyle behaviors on breast cancer survival and the current results, it is concluded that this population needs interventions for health-promoting lifestyle behaviors. The health promotion training provided by public health nurses to this population is effective in increasing healthy lifestyle behaviors.

Limitation and recommendation

The limitation of this study was the selection of participants from one hospital. Other studies are recommended by selecting a sample group from more than one hospital.

Conclusion

Our study demonstrated that health promotion training given to women survivors of breast cancer is effective in increasing physical activity, healthy nutrition, developing positive inter-personal relationships, taking responsibility for their health, using effective stress coping methods, and spiritual development. Age influences physical activity, education level influences nutrition, and elapsed time since diagnosis influences nutrition and spiritual development. These results will guide the educational interventions that public health nurses will prepare to provide healthy lifestyle behaviors to survivors of breast cancer.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

Acknowledgment

The authors would like to thank all volunteering women who participated in the study for their valuable cooperation.

References

  • 1.The International Agency for Research on Cancer (IARC) Breast Cancer Awareness Month 2021. 2021 Available from: https://www.iarc.who.int/featured-news/breast-cancer-awareness-month-2021/#:~:text=IARC%20estimates%20that%20there%20were, cause%20of%20cancer%20death%20overall. [Last accessed on 2022 Aug 06] [Google Scholar]
  • 2.World Health Orgaization (WHO) Breast cancer. 2021 Available from: https://www.who.int/news-room/fact-sheets/detail/breast-cancer. [Last accessed on 2022 Aug 06] [Google Scholar]
  • 3.Narod SA, Iqbal J, Miller AB. Why have breast cancer mortality rates declined? J Cancer Policy. 2015;5:8–17. [Google Scholar]
  • 4.National Academies of Sciences, Engineering, and Medicine, Health and Medicine Division, Committee on a National Strategy for Cancer Control in the United States . Guiding Cancer Control: A Path to Transformation. In: Nass SJ, Amankwah FK, Madhavan G, Johns MME, editors. Washington (DC): National Academies Press (US); 2019. [PubMed] [Google Scholar]
  • 5.Jia T, Liu Y, Fan Y, Wang L, Jiang E. Association of healthy diet and physical activity with breast cancer: Lifestyle ınterventions and oncology education. Front Public Health. 2022;10:797794. doi: 10.3389/fpubh.2022.797794. doi: 10.3389/fpubh.2022.797794. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Hamer J, Warner E. Lifestyle modifications for patients with breast cancer to improve prognosis and optimize overall health. CMAJ. 2017;189:E268–74. doi: 10.1503/cmaj.160464. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.American Cancer Society Breast Cancer Facts and Figures 2019-2020. Available from: https://www.cancer.org/content/dam/cancer-org/research/cancer-facts-and-statistics/breast-cancer-facts-and-figures/breast-cancer-facts-and-figures-2019-2020.pdf. [Last accessed on 2022 Aug 06] [Google Scholar]
  • 8.Zebrack B. Information and service needs for young adult cancer survivors. Support Care Cancer. 2009;17:349–57. doi: 10.1007/s00520-008-0469-2. [DOI] [PubMed] [Google Scholar]
  • 9.Zeng W, Shang S, Fang Q, He S, Li J, Yao Y. Health promoting lifestyle behaviors and associated predictors among clinical nurses in China: A cross-sectional study. BMC Nursing. 2021;20:230. doi: 10.1186/s12912-021-00752-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Walker SN, Sechrist KR, Pender NJ. The health promoting lifestyle profile: Development and psychometric characteristics. Nurs Res. 1987;36:76–81. [PubMed] [Google Scholar]
  • 11.Zagalaz-Anula N, Mora-Rubio MJ, Obrero-Gaitán E, Del-Pino-Casado R. Recreational physical activity reduces breast cancer recurrence in female survivors of breast cancer: A meta-analysis. Eur J Oncol Nurs. 2022;59:102162. doi: 10.1016/j.ejon.2022.102162. doi: 10.1016/j.ejon. 2022.102162. [DOI] [PubMed] [Google Scholar]
  • 12.Spei ME, Samoli E, Bravi F, La Vecchia C, Bamia C, Benetou V. Physical activity in breast cancer survivors: A systematic review and meta-analysis on overall and breast cancer survival. Breast. 2019;44:144–52. doi: 10.1016/j.breast.2019.02.001. [DOI] [PubMed] [Google Scholar]
  • 13.Lahart IM, Metsios GS, Nevill AM, Carmichael AR. Physical activity, risk of death and recurrence in breast cancer survivors: A systematic review and meta-analysis of epidemiological studies. Acta Oncol. 2015;54:635–54. doi: 10.3109/0284186X.2014.998275. [DOI] [PubMed] [Google Scholar]
  • 14.Shi Z, Rundle A, Genkinger JM, Cheung YK, Ergas IJ, Roh JM, et al. Distinct trajectories of fruits and vegetables, dietary fat, and alcohol intake following a breast cancer diagnosis: The pathways study. Breast Cancer Res Treat. 2020;179:229–40. doi: 10.1007/s10549-019-05457-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.McTiernan A. Weight, physical activity and breast cancer survival. Proc Nutr Soc. 2018;77:403–11. doi: 10.1017/S0029665118000010. [DOI] [PubMed] [Google Scholar]
  • 16.DeNysschen C, Brown JK, Baker M, Wilding G, Tetewsky S, Cho MH, et al. Healthy lifestyle behaviors of breast cancer survivors. Clin Nurs Res. 2015;24:504–25. doi: 10.1177/1054773814553298. [DOI] [PubMed] [Google Scholar]
  • 17.Mutwiri MN, Muraya MM, Gitonga LK. Modelling the effects of mindfulness based stress on breast cancer survival rate among women in Meru and Nyeri Counties, Kenya, using cox proportional hazard model. Asian J Probab Stat. 2022;16:1–8. doi: 10.9734/AJPAS/2022/v16i130390. [Google Scholar]
  • 18.Dinkel A, Herschbach P. Fear of progression in cancer patients and survivors. Recent Results Cancer Res. 2018;210:13–33. doi: 10.1007/978-3-319-64310-6_2. [DOI] [PubMed] [Google Scholar]
  • 19.Karavasiloglou N, Pestoni G, Wanner M, Faeh D, Rohrmann S. Healthy lifestyle is inversely associated with mortality in cancer survivors: Results from the third national health and nutrition examination survey (NHANES III) PLoS One. 2019;14:e0218048. doi: 10.1371/journal.pone.0218048. doi: 10.1371/journal.pone.0218048. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Li Q, Lesseur C, Neugut AI, Santella RM, Parada H, Jr, Teitelbaum S, et al. The associations of healthy lifestyle index with breast cancer incidence and mortality in a population-based study. Breast Cancer. 2022;29:957–66. doi: 10.1007/s12282-022-01374-w. [DOI] [PubMed] [Google Scholar]
  • 21.Cohee AA, Krueger EF, Vachon EA, Cottingham AH, Stutz PV, Alwine JS, et al. Breast cancer survivors’ perceptions of their partners’ interest in cancer-focused psychosocial interventions. J Psychosoc Oncol Res Pract. 2021;3:e042. [Google Scholar]
  • 22.Valente M, Chirico I, Ottoboni G, Chattat R. Relationship dynamics among couples dealing with breast cancer: A systematic review. Int J Environ Res Public Health. 2021;18:7288. doi: 10.3390/ijerph18147288. doi: 10.3390/ijerph18147288. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Mathad MD, Rajesh SK, Pradhan B. Spiritual well-being and its relationship with mindfulness, self-compassion and satisfaction with life in baccalaureate nursing students: A correlation study. J Religion Health. 2019;58:554–65. doi: 10.1007/s10943-017-0532-8. [DOI] [PubMed] [Google Scholar]
  • 24.Maazallahi M, Ghonchepour A, Sohrabi M, Golestani Z, Parandeh Afshar P, Malakoutikhah A, et al. Spiritual well-being among medical and nonmedical science students. Scientifica (Cairo) 2021;2021:6614961. doi: 10.1155/2021/6614961. doi: 10.1155/2021/6614961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Tate JD. The role of spirituality in the breast cancer experiences of African American women. J Holist Nurs. 2011;29:249–55. doi: 10.1177/0898010111398655. [DOI] [PubMed] [Google Scholar]
  • 26.World Health Organization Enhancing the Role of Community Health Nursing for Universal Health Coverage. World Health Organization; 2017 Available from: https://apps.who.int/iris/handle/10665/255047. [Last accessed on 2022 Aug 28]. License: CC BY-NC-SA 3.0 IGO. [Google Scholar]
  • 27.Hassmiller SB. Leveraging public health nursing to build a culture of health. Am J Prev Med. 2014;47(5 Suppl 3):S391–2. doi: 10.1016/j.amepre.2014.07.027. doi: 10.1016/j.amepre.2014.07.027. [DOI] [PubMed] [Google Scholar]
  • 28.Kemppainen V, Tossavainen K, Turunen H. Nurses’ roles in health promotion practice: An integrative review. Health Promot Int. 2013;28:490–501. doi: 10.1093/heapro/das034. [DOI] [PubMed] [Google Scholar]
  • 29.Iriarte-Roteta A, Lopez-Dicastillo O, Mujika A, Ruiz-Zaldibar C, Hernantes N, Bermejo-Martins E, et al. Nurses’ role in health promotion and prevention: A critical interpretive synthesis. J Clin Nurs. 2020;29:3937–49. doi: 10.1111/jocn.15441. [DOI] [PubMed] [Google Scholar]
  • 30.Walker SN, Hill-Polerecky DM. Psychometric Evaluation of the Health Promoting Lifestyle Profile II. Unpublished manuscript, University of Nebraska Medical Center; 1996 Available from: https://deepblue.lib.umich.edu/bitstream/handle/2027.42/85349/HPLP_II-Dimensions.pdf?sequen-ce=2. [Last accessed on 2022 Aug 06] [Google Scholar]
  • 31.Bahar Z, Beşer A, Gördes N, Ersin F, Kıssal A. Healthy life style behavior scale II: A reliability and validity study. [Sağlıklı yaşam biçimi davranışları ölçeği II’nin geçerlik ve güvenirlik çalışması] Cumhuriyet Üniversitesi Hemşirelik Yüksekokulu Dergisi. 2008;12:1. [Google Scholar]
  • 32.Hamed Bieyabanie M, Mirghafourvand M. Health Promoting lifestyle and its relationship with self-efficacy in Iranian mastectomized women. Asian Pac J Cancer Prev. 2020;21:1667–72. doi: 10.31557/APJCP.2020.21.6.1667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Kanera IM, Bolman CA, Mesters I, Willems RA, Beaulen AA, Lechner L. Prevalence and correlates of healthy lifestyle behaviors among early cancer survivors. BMC Cancer. 2016;16:1–18. doi: 10.1186/s12885-015-2019-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Cao C, Friedenreich CM, Yang L. Association of daily sitting time and leisure-time physical activity with survival among US cancer survivors. JAMA Oncol. 2022;8:395–403. doi: 10.1001/jamaoncol.2021.6590. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Pudkasam S, Polman R, Pitcher M, Fisher M, Chinlumprasert N, Stojanovska L, et al. Physical activity and breast cancer survivors: Importance of adherence, motivational interviewing and psychological health. Maturitas. 2018;116:66–72. doi: 10.1016/j.maturitas.2018.07.010. [DOI] [PubMed] [Google Scholar]
  • 36.Aycinena AC, Valdovinos C, Crew KD, Tsai WY, Mata JM, Sandoval R, et al. Barriers to recruitment and adherence in a randomized controlled diet and exercise weight loss ıntervention among minority breast cancer survivors. J Immigr Minor Health. 2017;19:120–9. doi: 10.1007/s10903-015-0310-1. [DOI] [PubMed] [Google Scholar]
  • 37.Forbes CC, Blanchard CM, Mummery WK, Courneya K. Prevalence and correlates of strength exercise among breast, prostate, and colorectal cancer survivors. Oncol Nurs Forum. 2015;42:118–27. doi: 10.1188/15.ONF.42-02AP. [DOI] [PubMed] [Google Scholar]
  • 38.Kim BH, Lee H. Prevalence and correlates of physical activity and sitting time in cancer survivors: 2009–2013 Korea national health and nutrition examination survey. Asian Pac J Cancer Prev. 2016;17:5295–302. doi: 10.22034/APJCP.2016.17.12.5295. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Swartzman S, Booth JN, Munro A, Sani F. Posttraumatic stress disorder after cancer diagnosis in adults: A meta-analysis. Depress Anxiety. 2017;34:327–39. doi: 10.1002/da.22542. [DOI] [PubMed] [Google Scholar]
  • 40.Carreira H, Williams R, Müller M, Harewood R, Stanway S, Bhaskaran K. Associations between breast cancer survivorship and adverse mental health outcomes: A systematic review. J Natl Cancer Inst. 2018;110:1311–27. doi: 10.1093/jnci/djy177. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Azriful, Mallapiang F, Nildawati, Alam S, Jusriani R, Muis M. Stress management for breast cancer survivor in South Sulawesi Province Indonesia. Gac Sanit. 2021;35:183–5. doi: 10.1016/j.gaceta.2021.07.011. [DOI] [PubMed] [Google Scholar]
  • 42.Hawkins NA, Smith T, Zhao L, Rodriguez J, Berkowitz Z, Stein KD. Health-related behavior change after cancer: Results of the American cancer society’s studies of cancer survivors (SCS) J Cancer Surviv. 2010;4:20–32. doi: 10.1007/s11764-009-0104-3. [DOI] [PubMed] [Google Scholar]
  • 43.Gu Q, Dummer TBJ, Spinelli JJ, Murphy RA. Diet quality among cancer survivors and participants without cancer: A population-based, cross-sectional study in the atlantic partnership for tomorrow’s health project. Nutrients. 2019;11:3027. doi: 10.3390/nu11123027. doi: 10.3390/nu11123027. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Wang Z, McLoone P, Morrison DS. Diet, exercise, obesity, smoking and alcohol consumption in cancer survivors and the general population: A comparative study of 16 282 individuals. Br J Cancer. 2015;112:572–5. doi: 10.1038/bjc.2014.598. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Sullivan ES, Rice N, Kingston E, Kelly A, Reynolds JV, Feighan J, et al. A national survey of oncology survivors examining nutrition attitudes, problems and behaviours, and access to dietetic care throughout the cancer journey. Clin Nutr ESPEN. 2021;41:331–9. doi: 10.1016/j.clnesp.2020.10.023. [DOI] [PubMed] [Google Scholar]
  • 46.Keaver L. Irish cancer patients and survivors have a positive view of the role of nutritional care in cancer management from diagnosis through survivorship. Ir J Med Sci. 2021;190:1387–90. doi: 10.1007/s11845-020-02488-w. [DOI] [PubMed] [Google Scholar]
  • 47.O’Callaghan N, Douglas P, Keaver L. Nutrition practices among adult cancer survivors living on the Island of Ireland: A cross-sectional study. Nutrients. 2022;14:767. doi: 10.3390/nu14040767. doi: 10.3390/nu14040767. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Balekouzou A, Yin P, Afewerky HK, Bekolo C, Pamatika CM, Nambei SW, et al. Behavioral risk factors of breast cancer in Bangui of Central African Republic: A retrospective case-control study. PLoS One. 2017;12:e0171154. doi: 10.1371/journal.pone.0171154. doi: 10.1371/journal.pone.0171154. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Hiza HA, Casavale KO, Guenther PM, Davis CA. Diet quality of Americans differs by age, sex, race/ethnicity, income, and education level. J Acad Nutr Diet. 2013;113:297–306. doi: 10.1016/j.jand.2012.08.011. [DOI] [PubMed] [Google Scholar]
  • 50.Kane K, Ilic S, Paden H, Lustberg M, Grenade C, Bhatt A, et al. An Evaluation of factors predicting diet quality among cancer patients. Nutrients. 2018;10:1019. doi: 10.3390/nu10081019. doi: 10.3390/nu10081019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Lei YY, Ho SC, Cheng A, Kwok C, Cheung KL, He YQ, et al. Dietary changes in the first 3 years after breast cancer diagnosis: A prospective Chinese breast cancer cohort study. Cancer Manag Res. 2018;10:4073–84. doi: 10.2147/CMAR.S168562. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Brown RC. Moral responsibility for (un)healthy behaviour. J Med Ethics. 2013;39:695–8. doi: 10.1136/medethics-2012-100774. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Devi MK, Fong KCK. Spiritual experiences of women with breast cancer in Singapore: A qualitative study. Asia Pac J Oncol Nurs. 2019;6:145–50. doi: 10.4103/apjon.apjon_77_18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Bekelman DB, Dy SM, Becker DM, Wittstein IS, Hendricks DE, Yamashita TE, et al. Spiritual well-being and depression in patients with heart failure. J Gen Intern Med. 2007;22:470–7. doi: 10.1007/s11606-006-0044-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Salsman JM, Pustejovsky JE, Jim HS, Munoz AR, Merluzzi TV, George L, et al. A meta-analytic approach to examining the correlation between religion/spirituality and mental health in cancer. Cancer. 2015;121:3769–78. doi: 10.1002/cncr.29350. [DOI] [PMC free article] [PubMed] [Google Scholar]

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