Accessibility, Availability, and Potential Benefits of Psycho-Oncology Services: The Perspective of Community-Based Physicians Providing Cancer Survivorship Care
Open accessAbstract
Background: As persons of trust, community-based physicians providing survivorship care (e.g., general practitioners [GPs]) often serve as the primary contacts for cancer survivors disclosing distress. From the perspective of physicians providing survivorship care for cancer patients, this study explores (a) the accessibility, availability, and potential benefits of psycho-oncology services; (b) whether physicians themselves provide psychosocial support; and (c) predictors for impeded referrals of survivors to services. Methods: In a cross-sectional survey, all GPs and community-based specialists in a defined region were interviewed. In addition to descriptive analyses, categorical data were investigated by applying chi-square tests. Predictors for impeded referrals were explored through logistic regression. Results: Of 683 responding physicians, the vast majority stated that survivors benefit from psycho-oncology services (96.8%), but the physicians also articulated that insufficient coverage of psycho-oncology services (90.9%) was often accompanied by impeded referrals (77.7%). A substantial proportion (14.9%) of physicians did not offer any psychosocial support. The odds of physicians in rural areas reporting impeded referrals were 1.91 times greater than the odds of physicians in large urban areas making a similar report (95% confidence interval [1.07, 3.40]). Conclusion: Most community-based physicians providing survivorship care regard psycho-oncology services as highly beneficial. However, a large number of physicians report tremendous difficulty referring patients. Focusing on those physicians not providing any psychosocial support, health policy approaches should specifically (a) raise awareness of the role of physicians as persons of trust for survivors, (b) highlight the effectiveness of psycho-oncology services, and (c) encourage a proactive attitude toward the assessment of unmet needs and the initiation of comprehensive care.
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Access to in-person supportive care is often limited by clinician shortages, financial constraints, and time available to attend therapy sessions.
“Access to in-person supportive care is often limited by clinician shortages, financial constraints, and time available to attend therapy sessions [9-13].”
From Co-Designing the MOSAIC mHealth App With Breast Cancer Survivors: User-Centered Design Approach (2024) · cites this paper as [11]
The Availability and Accessibility section reports insufficient local psycho-oncology coverage and difficult access to psychotherapists, supporting the clinician-shortage portion of the claim. The Discussion mentions long wait lists, but does not identify financial constraints or patients’ time to attend therapy sessions as barriers; it describes the German care setting as providing free healthcare. (LLM, conf=0.88)
Experimental — accuracy not yet measuredBreast cancer survivors in this study recognized the current limitations of in-person psychosocial support, particularly a shortage of mental health clinicians trained to meet the unique needs of cancer survivors.
“Breast cancer survivors in this study recognized the current limitations of in-person psychosocial support [9,71], particularly a shortage of mental health clinicians trained to meet the unique needs of cancer survivors [11,72,73].”
From Co-Designing the MOSAIC mHealth App With Breast Cancer Survivors: User-Centered Design Approach (2024) · cites this paper as [11]
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“…(Haun et al., 2018), e.g. by lack of transportation, living in a rural area, suffering from physical disabilities, or information deficits, which prevent cancer patients from taking advantage of face-to-face support (Zimmermann-Schlegel et al., 2017; Sakellariou et al., 2019; Neumann et al., 2010).”
BackgroundCo-Designing the MOSAIC mHealth App With Breast Cancer Survivors: User-Centered Design Approach
Nuseibeh, B. Z., Johns, S. A., Shih, P. C., Lewis, G. F., Gowan, T. M., & Jordan, E. J. (2024) · JMIR Formative Research · doi:10.2196/59426 · Cited by 5 · see citing works
- Authors
- Zimmermann-Schlegel, V., Hartmann, M., Sklenarova, H., Herzog, W., & Haun, M. W.
- Affiliations
- Department of General Internal Medicine and Psychosomatics Heidelberg University Hospital, Germany
- University Hospital Heidelberg (DE)
- University of Regensburg (DE)
- Corresponding author
- Haun, Markus W.
- Venue
- The Oncologist
- Publisher
- Oxford University Press (OUP)
- Published
- 2017-04-24
- Volume
- 22
- Issue
- 6
- Pages
- 719-727
- ISSN
- 1083-7159 (ISSN-L)
- 1549-490X
- PMC
- PMC5469591
- OpenAlex
- W2609367840
- Cited by
- 35
- References
- 51
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 1 · 2023: 6 · 2022: 8 · 2021: 6 · 2020: 3 · 2019: 2 · 2018: 2 · 2017: 1
- FWCI
- 0.96
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- The Oncologist (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- University of Regensburg Publication Server (University of Regensburg) (submittedVersion)
- Funders
- Bundesministerium für Gesundheit
- Topics
- Health Sciences › Medicine › Oncology › Cancer survivorship and care
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative and Oncologic Care
- Health Sciences › Health Professions › General Health Professions › Health Policy Implementation Science
- Keywords
- survivorship care, community-based physicians, general practitioners, referral barriers, psychosocial support, access to services, urban-rural differences, physician attitudes, health policy
- MeSH terms
- Psycho-Oncology, Survivorship, Female, Humans, Male, Neoplasms, Practice Patterns, Physicians', Physicians, Surveys and Questionnaires, Survivors
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