患者和非正式护理人员参与研究框架(PAICPAIR)

Katrine Staats, E. Grov, B. Husebø, Oscar Tranvåg
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引用次数: 9

摘要

“用户参与”一词经常应用于研究中。然而,患者和非正式护理人员作为共同研究人员参与有关危及生命的疾病患者的研究的框架很少。博士项目“带着尊严死去——为患有不治之症的居家老年妇女提供维护尊严的护理”从研究过程的早期阶段就与患者和非正式护理人员进行了彻底的合作。提出了患者和非正式护理人员参与研究的框架(PAICPAIR)——通过促进患有不治之症、危及生命的疾病的弱势群体作为共同研究人员的积极参与,为民主、平等和研究质量创造更坚实的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Framework for Patient and Informal Caregiver Participation in Research (PAICPAIR)
The term user involvement is frequently applied in research. Frameworks for patient and informal caregiver participation as coresearchers in studies concerning patients with life-threatening illness are however sparse. The PhD project Dying With Dignity—Dignity-Preserving Care for Older Women Living at Home With Incurable Cancer has implemented a thorough cooperation with patients and informal caregivers from the early stages of the research process. A framework for Patient and Informal Caregiver Participation In Research (PAICPAIR) is suggested—creating a stronger foundation for democracy, equality, and research quality by also promoting active participation among vulnerable people experiencing incurable, life-threatening illness, as coresearchers.
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