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Heart Rate Variability for Practitioner Stimulated Reflection and Decision-making Optimisation (HRV-PRO)

2026年9月15日 更新者:Papworth Hospital NHS Foundation Trust

At the heart of healthcare is the interaction between healthcare practitioners and patients. It is believed that optimisation of this interaction can improve patient relevant outcomes, safety and patient experience. Through utilisation of practitioner physiological data, heart rate variability (HRV), to help practitioners make better decisions and optimise practice, it is considered possible to improve decision making around patient care and improve outcomes and safety.

The modern intensive care unit (ICU) is a dynamic data rich environment requiring rapid and accurate decision making. Advances in ventilator technology, electronic patient monitoring and electronic health records (EHR) have provided exponential growth in data produced for patients and the need for complex decision making. However, data overload and alarm fatigue can result in poor understanding and a delayed response from the practitioner in addressing the patient's needs.

The aim of this study is to present and evaluate a psychophysiology training approach for practitioners derived from their cardiovascular response through the course of the working day, this will be measured using heart rate variability (HRV). Practitioner HRV has been shown to be linked to work related stress and is considered a biomarker of decision-making.

研究概览

详细说明

A Critical Participatory Action Research learning model is proposed, whereby practitioners can explore the nature and consequences of their practice utilising their HRV during two intervention periods. The aim is to improve practitioner performance and develop a more context aware approach to patient care.

Impact will be measured through:

  • improvement in HRV of the practitioners
  • measurement of response times to ventilator related events (decreased response times)
  • improvement of time spent at bedside
  • improvement in ventilation related outcomes for the patients.
  • Reduction in bedside noise (reduced response time to alarms and reduction in inappropriate alarms)

研究类型

介入性

注册 (估计的)

20

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。

学习联系方式

学习地点

    • Cambridgeshire
      • Cambridge、Cambridgeshire、英国、CB2 0AY
        • 招聘中
        • Royal Papworth Hospital NHS Foundation Trust
        • 接触:
        • 首席研究员:
          • Robert Gatherer, MBBS

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

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • Nurse working in Enhanced Recovery Unit at Royal Papworth Hospital NHS Foundation Trust
  • Willingness to participate in the trial

Exclusion Criteria:

  • Staff with permanent pacemakers
  • Staff on medication that could affect HRV (e.g. b-blockers)

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:卫生服务研究
  • 分配:不适用
  • 介入模型:单组作业
  • 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:Bedside nurses in Enhanced Recovery Unit
Baseline collection will consist of data from 20 bedside nurses over 10 shifts (12 hours +/- 3 hrs) each. 5 shifts post first intervention (1st workshop) and 5 shifts post second intervention (2nd workshop).
The intervention is based on a Critical Participatory Action Research learning model, using the participant's heart rate variability data collected during clinical shifts. Before the intervention, participants will complete repeated HRV monitoring and use a diary to record clinical events and reflections. The intervention includes facilitated workshops introducing reflective practice, cognitive bandwidth, and related educational concepts. Participants will receive individual coaching to review their HRV data and identify patterns and triggers in their clinical work, followed by group discussions to share experiences and develop strategies to adapt practice. A second workshop builds on this process with further reflection, additional HRV analysis, and collaborative strategy development. Between and after sessions, participants continue data collection and apply insights in practice, aiming to enhance clinical performance and develop a more context-aware approach to patient care.

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
Reduction in response time to ventilator patient physiological alarms
大体时间:At completion of 20th clinical shift (each shift is 12 hours)
Practitioner response time (in seconds) to ventilator-related physiological alarm events measured using ventilator event logs and bedside monitoring system records.
At completion of 20th clinical shift (each shift is 12 hours)
Adherence to bedside noise level targets
大体时间:At completion of 20th clinical shift (each shift is 12 hours)
Duration of time (seconds) bedside noise levels remain outside predefined acceptable clinical thresholds, measured using bedside environmental noise monitoring during clinical shifts.
At completion of 20th clinical shift (each shift is 12 hours)

次要结果测量

结果测量
措施说明
大体时间
Improvement in practitioner heart rate variability during clinical practice
大体时间:At completion of 20th clinical shift (each shift is 12 hours)
Can practitioners improve their HRV through the iterative stimulated reflection intervention.
At completion of 20th clinical shift (each shift is 12 hours)
Participant-reported work effectiveness, job satisfaction, and stress levels
大体时间:At completion of 20th clinical shift (each shift is 12 hours)
Participant-reported perceptions of work effectiveness, job satisfaction, and stress levels measured using study questionnaires
At completion of 20th clinical shift (each shift is 12 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:Robert Gatherer, MBBS、Papworth Hospital NHS Foundation Trust

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)

2026年7月14日

初级完成 (估计的)

2027年6月1日

研究完成 (估计的)

2027年6月1日

研究注册日期

首次提交

2026年5月19日

首先提交符合 QC 标准的

2026年7月13日

首次发布 (实际的)

2026年7月16日

研究记录更新

最后更新发布 (实际的)

2026年9月18日

上次提交的符合 QC 标准的更新

2026年9月15日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • P03174
  • 25/HRA/2201 (其他标识符:Health Research Authority)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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