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临床试验/NCT02917694
NCT02917694已完成不适用

A Feasibility Study to Assess Pre Admission Status and Six Month Outcomes of Major Trauma Patients Admitted to an Intensive Care Unit, Using the WHO DAS 2.0.

Oxford University Hospitals NHS Trust1 个研究点 分布在 1 个国家目标入组 57 人开始时间: 2016年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
57
试验地点
1
主要终点
WHODAS 2.0 completion rate

研究概览

简要总结

This study aims to assess the feasibility of obtaining details about a patients previous level of function from the patient of friend/relative, after they have been admitted an intensive care unit (ICU). It will also assess the feasibility of re-assessing level of function at 6 months after the patient has been discharged from ICU.

详细描述

Currently there is no standardised way of obtaining details about a patients pre-admission level of function. the process of gaining this history is often done by several different people with no standard questions asked.

There is also a need to be able to measure what happens to patients after they leave ICU, and compare their abilities to preadmission status.

This feasibility study will aim to investigate:

  • the time taken to train the physiotherapy team in the use of the outcome measure
  • the ability to obtain pre admission functional status from patients/friend/relative on admission to ICU
  • the ability to follow patients up at 6 months post discharge with re-assessment of the outcome measure

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Participant is willing and able to give informed consent for participation in the study
  • Participants relative or friend (consultee) is willing and able to give informed consent for participation in the study (where the patient is unable to give informed consent)
  • Male or Female, aged 18 years or above
  • Injury Severity Score greater than 9
  • Admitted as an emergency to AICU
  • Experienced at least 24 hours level three care during their admission

排除标准

  • Non UK resident (due to potential loss to follow up)
  • Unwilling to consent
  • No GP details available
  • Patients with a palliative diagnosis or established on a palliative treatment pathway

结局指标

主要结局

WHODAS 2.0 completion rate

时间窗: 2 days

Number of questionnaires completed/returned on admission to ICU

次要结局

  • Time to questionnaire completion rate(2 days)
  • WHODAS 2.0 completion rate(6 months post ICU discharge)

研究者

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

Rebekah Haylett

Physiotherapist

Oxford University Hospitals NHS Trust

研究点 (1)

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