农村社区肿瘤项目对远程医疗癌症支持小组的看法。

IF 1.4 4区 医学 Q3 EDUCATION, SCIENTIFIC DISCIPLINES Journal of Cancer Education Pub Date : 2024-08-01 Epub Date: 2024-03-28 DOI:10.1007/s13187-024-02428-7
Bree E Holtz, Katharine M Mitchell, Deborah Strand, Kelly Hirko
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引用次数: 0

摘要

癌症同伴互助小组对于提高生活质量和延长癌症生存期至关重要。本研究以健康信念模型(HBM)和计划行为理论(TPB)为指导框架,考察了农村肿瘤项目中接受癌症治疗的个人对基于远程医疗的癌症互助小组的看法。我们向 34 名积极参加虚拟癌症支持小组的幸存者或正在接受癌症治疗的个人发放了在线调查问卷,回复率达到 79.4%(27 人参与)。调查融合了定量和定性方法,评估了人口统计学特征、远程医疗的总体满意度、对基于远程医疗的同伴支持的满意度以及感知到的社会支持。定量数据采用描述性统计进行分析,而定性回答则通过模板分析进行研究,重点关注 HBM 和 TPB 构建。参与者对远程保健普遍表示满意,并表示愿意再次使用远程保健服务。参与者认为远程保健方法易于使用,而且可以更广泛地接触癌症支持小组。远程保健的障碍包括缺乏人际联系、互联网接入和技术困难。研究结果强调了农村肿瘤环境中对基于远程医疗的癌症支持小组的细微看法。尽管认识到远程医疗的局限性,但参与者对其在促进获得支持方面的作用表示赞赏。研究结果为优化数字健康干预措施提供了宝贵的见解,强调需要采取一种平衡的方法,同时考虑远程医疗在癌症治疗中的潜力和挑战。这项研究为优化数字健康干预措施和确保为农村地区的癌症患者提供便捷、有效的支持提供了重要指导。
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Perceptions of Telehealth-Based Cancer Support Groups at a Rural Community Oncology Program.

Cancer peer support groups are crucial in improving quality of life outcomes and extending cancer survival. Using the Health Belief Model (HBM) and Theory of Planned Behavior (TPB) as guiding frameworks, this study examined perceptions of telehealth-based cancer support groups among individuals treated for cancer at a rural oncology program. We distributed online surveys to 34 survivors or individuals undergoing cancer treatment who actively participated in virtual cancer support groups, achieving a 79.4% response rate (27 participants). The survey, blending quantitative and qualitative methodologies, assessed demographic characteristics, overall telehealth satisfaction, satisfaction with telehealth-based peer support, and perceived social support. Quantitative data were analyzed using descriptive statistics, while qualitative responses were examined through template analysis, focusing on the HBM and TPB constructs. Participants expressed general satisfaction with telehealth and indicated a willingness to use telehealth services again. Participants cited ease of use and broader access to cancer support groups with telehealth approaches. Barriers to telehealth included the lack of interpersonal connection, internet access, and technical difficulties. The findings underscore the nuanced perceptions of telehealth-based cancer support groups in a rural oncology setting. Despite acknowledging telehealth's limitations, participants appreciated its role in facilitating access to support. The findings provide valuable insights for optimizing digital health interventions, emphasizing the need for a balanced approach that considers both the potential and the challenges of telehealth in cancer care. This study offers critical guidance in optimizing digital health interventions and ensuring accessible, effective support for cancer patients in rural areas.

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来源期刊
Journal of Cancer Education
Journal of Cancer Education 医学-医学:信息
CiteScore
3.40
自引率
6.20%
发文量
122
审稿时长
4-8 weeks
期刊介绍: The Journal of Cancer Education, the official journal of the American Association for Cancer Education (AACE) and the European Association for Cancer Education (EACE), is an international, quarterly journal dedicated to the publication of original contributions dealing with the varied aspects of cancer education for physicians, dentists, nurses, students, social workers and other allied health professionals, patients, the general public, and anyone interested in effective education about cancer related issues. Articles featured include reports of original results of educational research, as well as discussions of current problems and techniques in cancer education. Manuscripts are welcome on such subjects as educational methods, instruments, and program evaluation. Suitable topics include teaching of basic science aspects of cancer; the assessment of attitudes toward cancer patient management; the teaching of diagnostic skills relevant to cancer; the evaluation of undergraduate, postgraduate, or continuing education programs; and articles about all aspects of cancer education from prevention to palliative care. We encourage contributions to a special column called Reflections; these articles should relate to the human aspects of dealing with cancer, cancer patients, and their families and finding meaning and support in these efforts. Letters to the Editor (600 words or less) dealing with published articles or matters of current interest are also invited. Also featured are commentary; book and media reviews; and announcements of educational programs, fellowships, and grants. Articles should be limited to no more than ten double-spaced typed pages, and there should be no more than three tables or figures and 25 references. We also encourage brief reports of five typewritten pages or less, with no more than one figure or table and 15 references.
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