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临床试验/NCT03328767
NCT03328767已完成不适用

A Pilot Randomised Controlled Trial in Extracorporeal Membrane Oxygenation Physical Training (ECMO-PT)

Australian and New Zealand Intensive Care Research Centre10 个研究点 分布在 2 个国家目标入组 20 人开始时间: 2018年2月19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
20
试验地点
10
主要终点
Feasibility of delivering the intervention in the first 7 days after randomisation and the separation between the groups

研究概览

简要总结

Critically ill patients who require extracorporeal membrane oxygenation (ECMO) are the sickest in the hospital. More patients are surviving but survivors have compromised functional recovery for months or years. This trial aims to determine if early, physical training commenced within 48 hours of ECMO is feasible and improves muscle strength and functional status in patients compared to standard practice in a randomised controlled trial of 30 ICU patients.

详细描述

The use of extracorporeal membrane oxygenation (ECMO) has expanded dramatically in Australia and globally. While life-saving in the short-term, it is typically associated with prolonged immobility and inflammation, which contributes to severe muscle weakness and wasting. Standard care delivers minimal physical training while patients remain on ECMO because standard care prioritises concerns about catheter dislodgement and cardio-respiratory strain. However, in other intensive care unit (ICU) conditions, techniques have been developed to allow early physical training in patients previously thought too unstable to be exercised, with important patient-centred and long-term cost-saving benefits. Our preliminary work shows that early individualised physical training is safe in ICU patients. A multicentre pilot study to establish feasibility in ECMO patients is urgently needed.

The primary aim is to test the hypothesis that early, individualised, physical training (commenced within first 48 hours of ECMO) is feasible and improves functional recovery (the highest level of activity and duration). This has previously been reported to be associated with improved independent function at hospital discharge and discharge to home.1 The secondary aims are to test the hypothesis that early individualised physical training is (i) safe; (ii) improves muscle strength at day 7 and 10 and 20; and (iii) improves functional status (IMS) at day 7, 10 and 20 in ECMO patients relative to standard care.

We are also aiming to describe the acute physiological effects of early physical training (commenced within 48hours of ECMO initiation) Respiratory and haemodynamic parameters, along with ECMO settings, will be recorded 30 minutes prior to each physical training session, during the session and 30 minutes post the training session. In addition, the range of values (min to max) for these parameters will be recorded for each 24hour period over the 7 days.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • adults ≥ 18 years of age
  • were physically independent prior to the current admission;
  • receiving ECMO (veno-arterial or veno-venous) for at least 24 hours;
  • clinician in charge of patient care has no objection to randomisation

排除标准

  • have been in ICU > 5 days prior to the commencement of ECMO;
  • have received ECMO for more than 48 hours;
  • in the opinion of the treating clinician, is not expected to recover in 90 days (e.g. intracerebral haemorrhage);
  • whom death is expected within 24 hours;
  • are unable to communicate in English

结局指标

主要结局

Feasibility of delivering the intervention in the first 7 days after randomisation and the separation between the groups

时间窗: 7 days

Feasibility of delivering the intervention in the first 7 days after randomisation and the separation between the groups using the ICU mobility scale to report the highest level of activity. It is reported as median (IQR) over 7 days.

次要结局

  • ICU and hospital length of stay(Time from ICU admission to ICU and hospital discharge respectively censored at day 90)
  • Time to first stand out of bed(Within the first 28 days)
  • Incidence of Treatment-Emergent Adverse Events, Safety events (including decannulation of ventilator or ECMO cannula, fall to the floor during mobilization, desaturation SpO2 < 85%) at anytime during the first 7 days(During the first 7 days)
  • Strength at day 7 and 10(Days 7 & 10)
  • Function (reported as ICU mobility scale) measured at days 7, 10 and 20(Days 7, 10 & 20)
  • ICU and in-hospital mortality(Time from ICU admission to ICU and hospital discharge respectively censored at day 90)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (10)

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