葡萄牙适应和验证患者报告的经验措施,为类风湿关节炎患者:一项协议研究。

Porto biomedical journal Pub Date : 2022-09-09 eCollection Date: 2022-07-01 DOI:10.1097/j.pbj.0000000000000192
Daniela Oliveira, Miguel Bernardes, Carlos Vaz, Lúcia Costa, João Almeida Fonseca, Cristina Jácome
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引用次数: 0

摘要

背景:在以患者为中心的护理模式中,在评估护理质量时,越来越多的人关注患者报告的经验措施。英国已经开发了一种针对类风湿关节炎(RA)患者的特定患者报告经验测量方法——类风湿关节炎患者报告经验测量质量委托。这种患者报告的经验措施在葡萄牙可能是可行的,但需要一个适应和验证过程。因此,本研究的目的将是翻译和跨文化改编葡萄牙语版本的《类风湿关节炎患者报告体验测量质量委托》,通过定性方法评估其内容和面部效度,并通过临床现场测试评估其心理测量特性。方法:采用定性与定量相结合的多方法研究方法。本研究将包括来自单一风湿病中心的RA患者。计划三个连续阶段:类风湿关节炎患者报告经验量表的质量翻译和文化适应的调试;类风湿关节炎患者报告经验量表的质量调试,通过至少10名患者的2个焦点小组评估内容和面部效度;类风湿关节炎患者报告经验量表的质量调试,通过50名患者的横断面研究进行现场测试。结论:通过让类风湿性关节炎患者参与类风湿关节炎患者报告经验测量质量的验证和实施,我们希望证明这种特定的患者报告经验测量对改善为类风湿性关节炎患者提供的医疗保健的有用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Portuguese adaptation and validation of a patient-reported experience measure for patients with rheumatoid arthritis: A protocol study.

Background: There is a growing attention to patient-reported experience measures in assessing the quality of care in patient-centered care models. A specific patient-reported experience measure for patients with rheumatoid arthritis (RA) has been developed in the United Kingdom-Commissioning for Quality in Rheumatoid Arthritis Patient-Reported Experience Measure. This patient-reported experience measure might be feasible to be used in Portugal, yet an adaptation and validation process is needed. Therefore, the aims of this study will be to translate and cross-culturally adapt the Portuguese version of the Commissioning for Quality in Rheumatoid Arthritis Patient-Reported Experience Measure, evaluate its content and face validity through a qualitative approach, and evaluate its psychometric properties through a clinical field testing.

Methods: This study is based on a multimethod approach combining qualitative and quantitative approaches. This study will include patients with RA from a single rheumatology center. Three sequential phases are planned: Commissioning for Quality in Rheumatoid Arthritis Patient-Reported Experience Measure translation and cultural adaptation, Commissioning for Quality in Rheumatoid Arthritis Patient-Reported Experience Measure content and face validity assessed through 2 focus groups with at least 10 patients, and the Commissioning for Quality in Rheumatoid Arthritis Patient-Reported Experience Measure field testing through a cross-sectional study with 50 patients.

Conclusions: By involving patients with RA in the validation and implementation of the Commissioning for Quality in Rheumatoid Arthritis Patient-Reported Experience Measure, we expect to demonstrate the usefulness of this specific patient-reported experience measure to improve health care provided to patients with RA.

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