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A Novel Electronic Method of Collecting Pain Scores in the Emergency Department (PIMPERNEL)

2020年1月29日 更新者:University of Leicester

Patient Input Monitoring of Pain in the Emergency Room: Novel Electronic Log (PIMPERNEL). A Randomised Controlled Trial of an Electronic Pain Score Display in Adults in the Emergency Department

Can a novel electronic display of pain be successfully used in the emergency department and does it (1) change analgesic prescription and (2) change amount of pain experienced? Pain is a common symptom in emergency care. As patients are seldom reassessed, staff may not be aware of pain. Currently, members of nursing or medical staff need to ask patients about their pain and record it manually using a visual analogue scale from 0-10.

The new electronic display uses buttons to represent a pain scale from 0 (no pain) to 10 (worst pain). Patients will select the number that best corresponds to their pain every 15 minutes. In the experimental group, the score will be displayed on a screen. In the control group, the score will not be displayed. The investigators will compare the overall amount of pain in both groups, and will look at their pain management (painkillers prescribed). The investigators will also ask patients and staff for their opinions on the display.

The study will include adult patients in the emergency department at Leicester Royal Infirmary with an initial pain score of 5 or more who are able to make a decision about whether to participate. Participants will also need to be likely to stay in the hospital for more than 2 hours to allow the investigators to gather enough useful data. The study will recruit 200 participants. If the study can demonstrate that the monitor is acceptable to patients and staff and results in improved pain management, it is a low cost intervention which could be widely implemented within the NHS. It also has the potential for being used in other areas such as surgical wards. The investigators have previously found that 300-400 patients per week in the department have moderate to severe pain and might therefore benefit from this monitor.

研究概览

研究类型

介入性

注册 (实际的)

105

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Leicestershire
      • Leicester、Leicestershire、英国、LE1 5WW
        • Leicester Royal Infirmary

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • adult (18 years and over)
  • underlying condition giving rise to significant pain (initial VAS pain score of 5 or more)
  • likely to be staying in the hospital for at least 2 hours
  • willing and able to give informed consent
  • able to understand and speak a good level of English

Exclusion Criteria:

  • children (under 18 years)
  • patients not willing to undergo routine care (analgesic treatment)
  • patients who do not have capacity to consent
  • patients who are unwilling or unable to give informed consent
  • prisoners
  • patients who cannot understand the study information in English
  • currently participating in another clinical trial as far as can be determined from information available at the time of assessment
  • patients who have a physical or visual disability which will prevent them from holding or using the pain display

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:PIMPERNEL Novel Electronic Log - intervention

The display is an electronic version of the 11 point NRS. An audible 'beep' every 15 minutes prompts the patient to record their pain level.

The display measures 122mm x 30mm x 15mm. Through a wireless connection, the data from the display are transmitted to a display unit (a Nexus tablet).

Pain scores are displayed on the screen when the participant presses the corresponding button
其他:PIMPERNEL Novel Electronic Log - control

The display is an electronic version of the 11 point NRS. An audible 'beep' every 15 minutes prompts the patient to record their pain level.

The display measures 122mm x 30mm x 15mm. Through a wireless connection, the data from the display are transmitted to a display unit (a Nexus tablet).

Participants press the buttons to record their pain score but the score is not on display (the screen is turned backwards).

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Pain reported by the patient:11 point numerical pain scale
大体时间:Up to 6 hours
Data collected from the display using the 11 point numerical pain scale. The area under the curve will be compared between the intervention and control groups. The Numerical Rating Scale is a scale from 0-10 (whole numbers only, where 0 represents 'no pain' and 10 represents 'worst pain ever').
Up to 6 hours

次要结果测量

结果测量
措施说明
大体时间
Proportion of possible scores recorded by patients
大体时间:Up to 6 hours
Up to 6 hours
Comparison of pain recorded on the display (closest minute) with verbal pain assessment at 2 and 4 hours
大体时间:Up to 6 hours
The scores recorded by the participants at 2 and 4 hours into their hospital stay will be compared with the scores recorded by nursing staff in the electronic record. The 11 point numerical rating scale is used for both measurements. The Numerical Rating Scale is a scale from 0-10 (whole numbers only, where 0 represents 'no pain' and 10 represents 'worst pain ever').
Up to 6 hours
Understanding the pattern of pain (shape of the curve of pain scores) over the time of the ED stay
大体时间:Up to 6 hours
Up to 6 hours
Recording time to second dose of analgesia and whether there is a pattern to this
大体时间:Up to 6 hours
Up to 6 hours
Use of analgesia in intervention and control groups (dose, time prescribed, time administered and name)
大体时间:Up to 6 hours
The dose, time prescribed, time administered and name of analgesia given pre-hospital and whilst in hospital will be recorded and a comparison made between the groups. This is a feasibility study only so exact outcome depends upon what data can be collected.
Up to 6 hours
Opinion of patients
大体时间:Up to 6 hours

Uses a short (4 question) questionnaire designed for this study. Questions on ease of use, whether the monitor is a good idea, whether participants would use it again in the future and whether it improved their experience as a patient, plus a comments box.

Questions: 1) How easy was it to use the pain monitor? (very easy, easy, no opinion, difficult, very difficult) 2) I think that the pain monitor is a good idea (strongly agree, agree, no opinion, disagree, strongly disagree) 3) I would use the monitor again in the future (strongly agree, agree, no opinion, disagree, strongly disagree) 4) The pain monitor improved my experience as a patient (strongly agree, agree, no opinion, disagree, strongly disagree)

Up to 6 hours
Opinion of staff (including their opinion of whether patients press the button for reasons other than pain)
大体时间:Up to 6 hours

Short (4 question) questionnaire designed for the study. Questions on whether the display is practical to use in the Emergency Department, whether they think it is a good idea, whether it is likely to improve the patient experience and whether a patient used the display to get their attention for a reason other than pain. Also has a comments box.

Questions: 1) The pain display is practical to use in the Emergency Department (strongly agree, agree, no opinion, disagree, strongly disagree) 2) I think that the pain display is a good idea (strongly agree, agree, no opinion, disagree, strongly disagree) 3) The pain display is likely to improve the patient experience (strongly agree, agree, no opinion, disagree, strongly disagree) 4) A patient used the pain display to get my attention for a reason other than pain (yes, not sure, no)

Up to 6 hours
Opinion of researchers regarding any likely stratification needs
大体时间:Up to 6 hours
Subjective opinion of researchers having completed the study on whether stratification would be required in future studies. No specific measurement used.
Up to 6 hours

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Timothy J Coats, Prof、University of Leicester

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2017年8月3日

初级完成 (实际的)

2019年7月31日

研究完成 (实际的)

2019年7月31日

研究注册日期

首次提交

2019年1月28日

首先提交符合 QC 标准的

2019年3月15日

首次发布 (实际的)

2019年3月20日

研究记录更新

最后更新发布 (实际的)

2020年1月30日

上次提交的符合 QC 标准的更新

2020年1月29日

最后验证

2019年1月1日

更多信息

与本研究相关的术语

其他研究编号

  • 0588
  • IRAS 210798 (其他标识符:IRAS)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

We are collecting feasibility data only in this trial.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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