The Feasibility of Measuring Energy Expenditure During Physical Rehabilitation In Critically Ill Patients (ENERGY-ICU)

February 20, 2017 updated by: Guy's and St Thomas' NHS Foundation Trust

A Pilot Observational Cohort Study Examining the Feasibility of Measuring Energy Expenditure During Physical Rehabilitation In Critically Ill Patients

Many patients who are admitted to the intensive care unit (ICU) experience muscle weakness. This muscle weakness occurs whilst patients are unconscious, immobile in bed and on a breathing machine (ventilator). It can develop very quickly, as soon as they become unwell. The investigators know that this weakness can make it harder for patients to regain their normal level of functional ability, such as standing and walking independently. Physical rehabilitation, delivered by physiotherapists, is important for patients as they recover from their critical illness to help them regain strength and to practice the ability to perform physical activities. These activities include sitting on the edge of the bed, standing, stepping on the spot and walking.

However it is difficult to know how hard it is for patients who are recovering from critical illness to perform these types of activities - in other words, how much energy is required. Some patients may find certain activities harder or easier than others. By knowing the energy requirements of patients whilst they take part in different physical rehabilitation activities, physiotherapists may be able to be more accurate with prescribing exercises and designing rehabilitation sessions for patients to practice achieving those activities.

In this study, the investigators will measure the energy requirements of the patients when they take part in physiotherapy-led physical rehabilitation they will have during their admission. To do this, the investigators will use a different ventilator to the one normally used to help their breathing. This ventilator works in exactly the same way, but has an extra component built into it to measure energy requirements. After the rehabilitation session, the patient will return to using their normal ventilator.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Admission to the intensive care unit (ICU) with critical illness is typically associated with profound physical impairments including peripheral skeletal muscle wasting and dysfunction. These effects demonstrate a rapid onset from the point of ICU admission, affect those with higher illness acuity to greater levels, and contribute to the development of intensive care unit-acquired weakness (ICU-AW) defined as severe upper and lower limb muscle weakness. Clinically patients present with significant limitations in exercise capacity and performance of physical functional activities, with deficits persisting for many years following resolution of the original illness.

Physical rehabilitation is recommended to address the physical and functional deficits associated with ICU-AW, and delivery is advocated across the continuum of the patient recovery pathway, commencing whilst in the ICU, following transfer to the ward and beyond hospital discharge. Physical rehabilitation within the ICU typically incorporates early mobilisation (EM), characterised by a hierarchical progression of increasingly functional activities such as active-assisted bed exercises, sitting-on-the-edge-of-the-bed (SOEOB), standing, marching-on-the-spot and walking. These activities are summarised in the ICU Mobility Scale. In recent years, adjunctive technologies including electrical muscle stimulation, interactive video-games and passive cycle ergometry have also been utilised.

Delivery of early mobilisation is feasible, safe and effective in improving both short and long-term outcomes in critically ill patients even in the early stages of recovery whilst patients remain ventilated and receiving other forms of organ support. However, the optimum 'dose' of physical rehabilitation to deliver to patients whilst in the ICU remains undetermined. Early mobilisation reflects a clinically pragmatic approach to patient management, but there are few data to support the intensity, frequency and timing of interventions.

Furthermore, there is little known of the acute physiological response to undertaking this type of exercise in this patient population. Metabolic monitoring can provide information on the energy expenditure of patients. However, direct methods of data acquisition such as use of pulmonary artery catheters to measure whole-body oxygen consumption can be unreliable and their use in clinical practice has diminished in recent years. The non-invasive technique of indirect calorimetry (IC) has therefore emerged as a potential alternative that may be more practically applicable in the clinical setting. Indirect calorimetry measures total gas exchange, oxygen consumption and carbon dioxide production which can in turn determine energy expenditure. However the widespread clinical utility of the IC technique, can be offset by the number of clinical factors that may preclude its use across all patients e.g. those with cardiovascular or ventilator instability, those with open chest drainage or receiving renal haemofiltration.

Two studies to date have used IC to examine the response to physical rehabilitation activities performed by patients in the ICU. Collings et al conducted a randomised cross-over study in which 10 ICU patients completed either a passive chair transfer or an active sit-over-the-edge-of-the-bed (SOEOB) on one day, followed by the alternative activity on the consecutive day. The 'active' SOEOB activity elicited a significantly greater increase in oxygen consumption than the passive activity (90.69 ml/min (95% CI 44.04 to 137.34) vs 14.43 ml/min (95% CI -27.28 to 56.14), p = 0.007). Hickmann et al examined active or passive cycling in critically ill patients and healthy controls, demonstrating increased oxygen consumption during the active exercise compared to passive in patients with differing energy requirements compared to healthy individuals.

This limited existing evidence-base demonstrates the potential for use of IC to characterise physical rehabilitation in critically ill patients, but is restricted to particular types of activities and fails to capture sequential assessments of patients as their rehabilitation progresses through increasingly functional levels. Acknowledging the potential clinical limitations of applying the IC measurement technique to all critically ill patients, the aim of this study is to examine the feasibility of measuring energy expenditure of critically ill patients completing a range of physical rehabilitation activities (as characterised on the ICU Mobility Scale) performed sequentially during their ICU or ventilator weaning unit (Lane Fox Respiratory Unit, LFU) admission using indirect calorimetry.

Study Type

Observational

Enrollment (Actual)

4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • London, United Kingdom, SE1 7EH
        • Guys and St Thomas NHS Foundation

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Adult critically ill patients undergoing physical rehabilitation in either the Intensive Care Units or the Lane Fox Unit at Guys and St Thomas' NHS Foundation Trust.

Description

Inclusion Criteria:

  • Adult, ≥18years
  • Receiving physical rehabilitation as part of routine physiotherapy management
  • Invasively mechanically ventilated for ≥48hours
  • Receiving invasive mechanical ventilation with stable settings

Exclusion Criteria:

  • Endotracheal or tracheal leak >10%
  • Burns
  • Open chest drainage
  • Inspired oxygen (FiO2) ≥0.6
  • Extra-corporeal membrane oxygenation (ECMO)
  • Pregnancy
  • Cardiorespiratory instability requiring frequent adjustment of ventilator settings or FiO2, inotropic or sedative dosage, or positive end-expiratory pressure (PEEP) >10cmH2O
  • Any neurological, orthopaedic or other factor contraindicating mobilisation
  • Medical diagnosis mandating a specialist rehabilitation pathway e.g. amputee, acute neurological injury
  • Palliative management

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Observational Group
  • 2hours before planned physical rehabilitation patients will have their regular ventilator changed to the study ventilator by an ICU Consultant and patients will be clinical stable for 30mins prior to the start of the planned physical rehabilitation.
  • Intended physical rehabilitation as planned will continue without change. This session will be observed by a member of the research team to ensure accurate documentation of the exact timing of performance of the physical rehabilitation activity.
  • Patients will also undergo an assessment by the Medical Research Council Sum-score and maximal inspiratory pressure (all part of routine physiotherapy assessment).
  • Following the physical rehabilitation session, the patient to rate their perceived exertion then patients will also undergo ultrasound assessment of peripheral skeletal muscle architecture.
  • Patients return to their original ventilator after 30mins by an ICU Consultant.
Indirect calorimetry measurement during Physical Rehabilitation. Observing planned physical rehabilitation session to determine the rehabilitation activity achieved with IC utilised to determine the number of calories used per session

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Oxygen consumption during different physical rehabilitation activities.
Time Frame: Through Critical Care stay, an average of 1 per day
Measurements of oxygen consumption during physical rehabilitation activities whilst on ICU
Through Critical Care stay, an average of 1 per day
Carbon dioxide production during different physical rehabilitation activities.
Time Frame: Through Critical Care stay, an average of 1 per day
Measurements of carbon dioxide production during physical rehabilitation activities whilst on ICU
Through Critical Care stay, an average of 1 per day
Minute ventilation during different physical rehabilitation activities.
Time Frame: Through Critical Care stay, an average of 1 per day
Measurements of minute ventilation during physical rehabilitation activities whilst on ICU
Through Critical Care stay, an average of 1 per day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Limitations of data acquisition using the indirect calorietry
Time Frame: Through Critical Care stay, an average of 9 days
Measuring the quality of data acquired to identify technical issues, pragmatic factors, number of rehabilitation sessions by eligible patients and limiting factors to use of the indirect calorimetry.
Through Critical Care stay, an average of 9 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Bronwen Connolly, Guys and St Thomas Nhs Foundation Trust

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2016

Primary Completion (ACTUAL)

December 1, 2016

Study Completion (ACTUAL)

December 1, 2016

Study Registration Dates

First Submitted

April 7, 2016

First Submitted That Met QC Criteria

April 25, 2016

First Posted (ESTIMATE)

April 28, 2016

Study Record Updates

Last Update Posted (ACTUAL)

February 23, 2017

Last Update Submitted That Met QC Criteria

February 20, 2017

Last Verified

February 1, 2017

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 16/LO/0076

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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