首页> 美国卫生研究院文献>Health Expectations : An International Journal of Public Participation in Health Care and Health Policy >What is involvement in research and what does it achieve? Reflections on a pilot study of the personal costs of stroke
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What is involvement in research and what does it achieve? Reflections on a pilot study of the personal costs of stroke

机译:研究涉及什么以及它取得了什么成就?关于中风个人成本试点研究的思考

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摘要

>Background  Health researchers are encouraged to involve service users as partners in their research. There is a need to increase the evidence base of involvement, including an accumulation of empirical accounts of involvement practices, demonstrating how involvement influences research and refinement of the concept itself. >Aims  To report the development of a pilot study by academic researchers and stroke service users belonging to a user research group to investigate costs of stroke to individuals and families; to reflect on what this example of user involvement achieved and implications for what involvement means. >Methods  We conducted a 2‐year ethnographic study that included participant observation, formal and informal interviews with professionals and user group members and documentary analysis. Data were systematically recorded to permit description of processes and reflexive analysis. >Results and conclusions  We report on five stages of the research process from service user identification of a research question to interpretation of pilot study findings. Professional researchers led the research process and developed a novel method to involve stroke service users in the development of a questionnaire. Some academic colleagues questioned the value of the proposed investigation as it did not appear to conform to implicit criteria of quality research. We argue that the moral status that user involvement has acquired means that academics’ concerns about quality did not prevent the pilot study from being conducted. We suggest that much of what was undertaken might be considered standard good practice in developing new research studies but also identify additional benefits of user involvement. Implications for conceptual development and evaluation are discussed.
机译:>背景鼓励卫生研究人员让服务用户作为合作伙伴参与他们的研究。有必要增加参与的证据基础,包括对参与实践的经验说明的积累,以证明参与如何影响概念本身的研究和改进。 >目标:报告学术研究人员和隶属于用户研究小组的卒中服务用户进行的一项先导研究的进展情况,以调查卒中给个人和家庭带来的成本;反思这个用户参与示例所取得的成就以及对参与意义的暗示。 >方法我们进行了为期2年的人种志研究,其中包括参与者观察,与专业人员和用户组成员进行的正式和非正式访谈以及文献分析。系统地记录数据以允许描述过程和进行反思性分析。 >结果与结论我们报告了研究过程的五个阶段,从服务用户对研究问题的识别到对试验研究结果的解释。专业的研究人员领导了研究过程,并开发了一种新颖的方法,使中风服务用户参与调查表的编制。一些学术同事质疑提议的调查的价值,因为它似乎不符合质量研究的隐含标准。我们认为,用户参与所获得的道德地位意味着学者对质量的关注并没有阻止试点研究的进行。我们建议,在进行新的研究时,所做的许多事情可能被视为标准的良好做法,但同时也可以确定用户参与的其他好处。讨论了对概念发展和评估的含义。

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