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首页> 外文期刊>Health expectations: an international journal of public participation in health care and health policy >Evaluation of a project to engage patients in the development of a patient‐reported measure for HIV care (the I‐Score Study)
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Evaluation of a project to engage patients in the development of a patient‐reported measure for HIV care (the I‐Score Study)

机译:评估使患者参与制定患者报告的 HIV 护理措施的项目的评估(I-Score研究)

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摘要

Background Patient engagement ( PE ), patients’ meaningful involvement in research through partnerships and sensitivity to their expertise, is receiving attention. However, PE initiatives are poorly reported and little is known about patients’ perspective on PE . Objective To document and evaluate the first phase (22?months) of a PE Project for the I‐Score Study which is developing a patient‐reported measure of HIV treatment adherence barriers, we describe the nature of PE conducted, determine the level of PE achieved and present its impacts from the engaged patients’ perspective. Setting and participants A Montreal‐based committee of ten people with HIV was recruited from community and clinical settings and participated in: I‐Score study decision making, knowledge dissemination, research on the experience of people with HIV and the PE project's evaluation. Methods The evaluation followed a convergent parallel mixed‐methods design. Data collection included participant observation, a satisfaction survey and meeting minutes/transcriptions. Analysis entailed reporting PE activities, generating descriptive statistics and thematically analysing qualitative material. Results PE consisted of twelve meetings, including two focus groups (needs assessment), in addition to four knowledge dissemination activities. PE levels showed an increase: the first four regular meetings entailed information/consultation, while subsequent meetings reached implication/collaboration. Regarding impacts, patients indicated high and stable satisfaction rates (M? =? 4.4/5; SD ?=?0.76). Furthermore, thematic analysis identified “positive interactions,” “co‐learning,” “self‐determination,” and “the collective management of confidentiality” as important PE impacts for engaged patients. Conclusion This PE Project evaluation highlighted growing engagement levels, high satisfaction rates and the importance of a patient‐centric approach to PE .
机译:背景技术患者参与度(PE),患者通过伙伴关系有意义地参与研究以及对其专业知识的敏感性正在受到关注。但是,关于体育活动的报道很少,而且对患者对体育的看法知之甚少。目的为了记录和评估I-Score研究的PE项目的第一阶段(22个月),该项目正在开发患者报告的HIV治疗依从性障碍测量方法,我们描述了PE的性质,确定PE的水平从参与患者的角度实现并展示了其影响。机构和参与者从社区和临床机构招募了一个由蒙特利尔的10名艾滋病毒感染者委员会组成的委员会,该委员会参加了以下活动:I-Score研究决策,知识传播,艾滋病毒感染者经验研究以及PE项目评估。方法评估遵循收敛的并行混合方法设计。数据收集包括参与者观察,满意度调查和会议记录/笔录。分析包括报告体育活动,生成描述性统计数据和对定性材料进行专题分析。结果PE除了四次知识传播活动外,还包括十二个会议,包括两个焦点小组(需求评估)。 PE水平有所提高:前四次例会需要信息/咨询,而随后的会议则涉及/合作。关于影响,患者显示出高而稳定的满意率(M i = 4.4 / 5; SD = 0.76)。此外,主题分析将“积极互动”,“共同学习”,“自决”和“机密性的集体管理”确定为参与患者的重要体育锻炼。结论本项PE项目评估突出了参与水平的提高,较高的满意度和以患者为中心的体育方法的重要性。

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