Abstract
Purpose
Most breast cancer survivors have challenges with adopting healthy lifestyle behaviors. This may be due to contextual challenges that result from the complex nature of the evidence. To address this gap, we explored the experiences of breast cancer survivors of color and oncology healthcare providers.
Methods
Content analysis with inductive and deductive approaches was used for semi-structured interviews with 26 female breast cancer survivors and 10 oncology healthcare providers from Greater New Haven, Connecticut.
Results
Survivors identified substantial confusion on the evidence regarding lifestyle behaviors and breast cancer, stemming from inadequate healthcare provider counseling and an overreliance on informal sources of information. Providers identified lack of evidence-based knowledge as a barrier to counseling on these topics. There was a mixed perspective regarding the consistency of evidence, stemming from a combination of gaps in the available evidence and accessing evidence-based knowledge from a wide range of professional resources. Some providers perceived the guidelines as consistent; others felt guidelines were constantly changing, impacting how and on what they counseled. Therefore, many healthcare providers in oncology care relied on generic messaging on lifestyle behaviors after a cancer diagnosis.
Conclusions
Inconsistent information sources, the rapidly changing evidence, and gaps in the current evidence contribute to generic messaging about lifestyle behaviors and may inhibit a survivor’s ability to engage in behavior change. Consistent and uniform healthy lifestyle guidelines for cancer outcomes may address both provider and patient level barriers to knowledge.
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Acknowledgements
Many thanks to each participant that shared their time and story with our research team and made this research possible.
Funding
Margaret S. Pichardo was funded for this study by the National Institutes of Health—National Cancer Institute, Award (# R01CA207753), and the Yale Center for the Study of Race, Indigeneity and Transnational Migration (RITM) Research Award. Denise Esserman was partially funded by the Yale Clinical and Translational Science Award (UL1 TR001863).
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Contributions
Margaret S. Pichardo, Melinda L. Irwin, and Yamile Molina contributed to the study conception and design. Material preparation and data collection were performed by Margaret S. Pichardo. Data analysis was performed by Margaret S. Pichardo, Abigail Ginader, and Thai Hien Nguyen. The first draft of the manuscript was written by Margaret S. Pichardo, and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript. Funding support and resources acquisition for this study were provided by Melinda L. Irwin and Tara Sanft.
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The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Yale Human Investigation Committee (HIC # 2000025065).
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Verbal informed consent was obtained from all individual participants included in the study.
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The authors declare no competing interests.
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Appendix. Sample questions from semi-structure interview guide for survivors and healthcare providers
Appendix. Sample questions from semi-structure interview guide for survivors and healthcare providers
Survivors
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1.
What support with nutrition and exercise did you receive from your community? Friends? Family?
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2.
How could your community have supported you with nutrition and exercise?
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3.
Thinking back to when you were receiving cancer treatment, what has changed about your eating habits since you were diagnosed?
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a.
Specific foods? Drinking? Exercise? Smoking?
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b.
Why did you change your habits?
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c.
What changes were easy or difficult to implement?
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d.
What made them easy or difficult?
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e.
Did you feel supported to make these changes? By who?
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a.
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4.
Thinking back to when you were receiving cancer treatment, what information did you receive about nutrition and exercise during treatment?
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a.
What resources did you have to support you to eat healthier and exercise while you were receiving treatment?
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b.
How did your doctors support you to eat healthier and be active?
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a.
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5.
Thinking back to the time after you had completed your cancer treatment, did you receive a survivorship care plan after completing treatment?
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a.
What did you like or dislike about your care plan?
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b.
Did your care plan include counseling on nutrition and exercise?
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c.
What resources did you have to support you to eat healthier and exercise?
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d.
How did your doctors support you to eat healthier and be active?
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a.
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6.
Thinking about the present, how do you make decisions about what foods to eat and what to avoid?
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a.
What are things that you believe to cause cancer?
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b.
What are your beliefs regarding unhealthy foods and breast cancer?
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c.
What makes food healthy or unhealthy?
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a.
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7.
Thinking about the present, how do you make decisions about whether to engage in exercise or not?
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8.
How could your care team have supported you with nutrition and exercise after you completed your treatment?
Healthcare providers
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1.
What do you think is your role in providing lifestyle counseling to survivors?
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2.
Tell me about a time when you offered counseling on diet and exercise to a patient of color?
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a.
What difficulties, if any, did you experience?
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a.
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3.
In your daily work, what makes it difficult to counsel patients on lifestyle?
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a.
What resources are available to support your ability to counsel patients on lifestyle behaviors?
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b.
What would make it easier for you to regularly counsel patients on lifestyle?
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a.
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4.
How do you confirm that patients have received information about lifestyle behaviors?
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5.
What resources do you have to offer breast cancer survivors regarding lifestyle behaviors?
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6.
Where do you get information about the current evidence regarding diet/exercise and cancer?
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7.
What barriers do you think women of color face to adopt healthy lifestyles?
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Pichardo, M.S., Irwin, M.L., Sanft, T. et al. A qualitative study identifying challenges resulting from complex evidence on lifestyle factors and cancer: perspectives from Black and Latina cancer survivors and healthcare providers. Support Care Cancer 31, 111 (2023). https://doi.org/10.1007/s00520-022-07539-9
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DOI: https://doi.org/10.1007/s00520-022-07539-9