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临床试验/NCT05155150
NCT05155150招募中不适用

Improving Shared-Decision Making in the Intensive Care Unit Using Patient-reported Outcome Information

Radboud University Medical Center2 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2021年11月9日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
160
试验地点
2
主要终点
Patient reported experience measure (PREM)

研究概览

简要总结

The aim of this study is to evaluate the effect of incorporation of outcome information in the Intensive Care Unit (ICU) decision-making process on patient and family reported outcomes and experiences of patients, relatives and ICU clinicians in a randomized clinical trial design in the Jeroen Bosch Ziekenhuis and Radboudumc in the Netherlands.

详细描述

Background Due to advances in critical care medicine, more patients survive their critical illness. However, many Intensive Care Unit (ICU) survivors suffer from physical, cognitive and/or mental problems impacting patients' quality of life (QoL). Because of a lack of long-term outcome information, ICU physicians make decisions regarding ICU treatment based on their clinical experience and intuition. Moreover, patients and relatives are often not involved in the decision-making process.

To improve the ICU decision-making process and to make it more substantiated, the use of patient-reported outcome measures (PROMs) is of utmost importance. Therefore, the Radboudumc, in collaboration with six regional hospitals, including Jeroen Bosch Ziekenhuis (JBZ), set up a large-scale prospective cohort study, MONITOR-IC (www.monitor-ic.nl), to study long-term outcomes of ICU survivors', their QoL and their needs.

This research sets out to evaluate the effect of incorporation of outcome information in the ICU decision-making process on patient and family reported outcomes and experiences of patients, relatives and ICU clinicians in a randomized clinical trial design in the Jeroen Bosch Ziekenhuis and Radboudumc in the Netherlands.

Methods A prediction model for long-term QoL was previously developed using physiological, pathological, drug and treatment data from patients' electronic health record combined with PROMs from one centre of the MONITOR-IC. It was externally validated with the data of six other centres and an E-health tool was developed, incorporating this prediction model. For this research, the E-health tool will be incorporated in family meetings.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients admitted to the ICU for 12 hours or more
  • •Patients (or their legal representative) provide written informed consent

排除标准

  • •Patients admitted to the ICU due to a COVID-19 infection
  • •Moribund patients

研究组 & 干预措施

Intervention group

Experimental

Providing patient-reported outcome: patients receive personalized information on expected quality of life one year after ICU during ICU admission (during a family meeting)

干预措施: Providing patient-reported outcome (Behavioral)

Control group

No Intervention

Family meetings take place as usual.

结局指标

主要结局

Patient reported experience measure (PREM)

时间窗: Within 3 months of family meeting

Patient and/or relative's experience (measured using the CollaboRATE)

次要结局

  • Patient reported outcome measure (PROM)(After 3 months and after 1 year)
  • ICU professionals' experiences(Two months before inclusion first patient and two months after inclusion last patient)

研究者

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

Marieke Zegers

PhD and Principal Investigator

Radboud University Medical Center

研究点 (2)

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