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临床试验/NCT07575581
NCT07575581已完成不适用

From Translation to Validation: Psychometric Evaluation of the EVARUCI Scale in Turkish Intensive Care Units

Istanbul University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年10月1日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
1

研究概览

简要总结

International guidelines recommend the use of Pressure Injury risk assessment tools. According to these guidelines, a systematic approach to assessing risk for PI development is essential. Although several tools have been developed, no single clinical pathway is considered superior. Instead, a comprehensive evaluation of risk factors, combined with visual skin assessment, is recommended. The aim of this study was to evaluate the applicability of the EVARUCI Scale in a Turkish intensive care unit setting by performing cross-cultural adaptation and linguistic validation, and to examine its validity and reliability through psychometric testing.

详细描述

A scoping review examining pressure injury risk assessment tools in critically ill patients across eight databases reported that the Risk Assessment Scale for Pressure Ulcers in Intensive Care demonstrated superior performance indicators, while the CALCULATE scale was highlighted as a recent, appropriate, simple, and user-friendly instrument, although both still require further refinement. In a study by Guerrero-Toapanta et al., EVARUCI was found to be a suitable tool for assessing PI risk in ICU patients, with the optimal assessment time identified as 48 hours after admission. The aim of this study was to evaluate the applicability of the EVARUCI Scale in a Turkish intensive care unit setting by performing cross-cultural adaptation and linguistic validation, and to examine its validity and reliability through psychometric testing.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who are 18 years or older
  • without a pressure injury at the time of ICU admission
  • expected to stay in the ICU for at least 72 hours who consent to participate in the study (or whose family members consent) included in the study.

排除标准

  • Patients or their family members who did not consent to participate
  • Patients who transferred to another hospital during their ICU stay, excluded from the study.

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nurten Ozen

Associate Professor

Istanbul University

研究点 (1)

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