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Qualitative research on the Belgian Cancer Rehabilitation Evaluation System (CARES): An evaluation of the content validity and feasibility

机译:比利时癌症康复评估系统的定性研究(关心):对内容有效性和可行性的评估

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Abstract Rationale, aims, and objectives The systematic assessment of cancer patients well‐being and care needs is internationally recommended to optimize comprehensive cancer care. The Cancer Rehabilitation Evaluation System (CARES) is a psychometrically robust quality of life and needs assessment tool of US origin, developed in the early 1990s. This article describes Belgian patients' view on the content validity and feasibility of the CARES for use in current cancer care. Methods Participants were cancer patients recruited through media. Data were gathered in 4 focus groups (n?=?26). The focus group discussions were facilitated with key questions. A moderator and an observer conducted and followed up the discussion. The audio file was transcribed verbatim and afterwards analyzed thematically. Results Participants experience concerns and needs in a wide range of life domains such as physical, emotional, cognitive, social, relational, sexual, financial, and work‐related and in the interaction with care professionals. According to participants, the items of the CARES are all relevant to capture the possible life disruption that cancer patients and survivors experience. One important theme is missing in the CARES, namely, the well‐being of loved ones. The completion time of the CARES was judged to be feasible, and according to participants, only a few items need a reformulation. Conclusions In general, the results of this study support the content validity and feasibility of the CARES. However, little adjustments in formulation and a few extra items are needed. The instrument can be used to obtain a comprehensive assessment of a cancer patients' overall well‐being and care needs to take dedicated action in care.
机译:摘要摘要理由,目标和目标系统评估癌症患者福祉和护理需求的系统评估是在国际上进行综合癌症护理的。癌症康复评估系统(关心)是在20世纪90年代初开发的美国来源的精神度稳健的生活质量和需求评估工具。本文介绍了比利时患者对当前癌症护理的关注内容有效性和可行性的看法。方法参与者是通过媒体招募的癌症患者。数据收集在4个焦点组中(n?=?26)。焦点小组讨论有助于关键问题。主持人和观察者进行并跟进讨论。音频文件是逐字转录的,然后在主题上进行分析。结果参与者在广泛的生命领域中经历担忧和需求,例如身体,情感,认知,社会,关系,性,财务和工作相关和与护理专业人士的互动。根据参与者的说法,关心的物品都是相关的,以捕捉癌症患者和幸存者经历的可能救生中断。关心中缺少一个重要的主题,即亲人的福祉。判断关心的完工时间是可行的,并且根据参与者,只有少数物品需要重新制作。结论一般来说,这项研究的结果支持关心的内容有效性和可行性。但是,需要对配方和一些额外的物品进行很少的调整。该仪器可用于获得对癌症患者的整体福祉和护理需要采取专门行动的综合评估。

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