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A Feasibility Study of Early Mobilisation Programmes in Critical Care (EMPRESS)

U

University Hospital Southampton NHS Foundation Trust

Status

Completed

Conditions

Critical Illness

Treatments

Other: Early mobility

Study type

Interventional

Funder types

Other

Identifiers

NCT03771014
UHSEmpress

Details and patient eligibility

About

The objective of this study is to determine the feasibility of delivering a very early mobility rehabilitation program in Intensive Care Units (ICU), within the context of a randomised controlled trial (RCT). This will inform the design of a future RCT investigating very early ICU rehabilitation in the UK National Health Service.

Full description

Early ICU-based physical rehabilitation may benefit patients with acute severe respiratory failure by attenuating the development of severe and persistent weakness and impaired physical function seen in these patients.

Muscle wasting occurs early (within 12 hours) and progresses rapidly after ICU admission. Patients may suffer from consequent physical impairment for months or years following their discharge.

ICU based rehabilitation has the potential to improve physical function outcomes, through mitigating muscle wasting.

The investigators have successfully introduced a very early ICU mobility program in their institution, which results in increased ventilator free days and reduced length of ICU stay.

The primary aim is to investigate whether this method will work in other ICUs. EMPRESS will test the feasibility of running this intervention as an RCT. The results and a concurrent process evaluation will inform the design of a future, multi-centre randomised controlled trial.

Enrollment

46 patients

Sex

All

Ages

42+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Acute/unplanned medical admissions to the ICU.
  • > 42 years old.
  • Functionally independent prior to ICU admission (Barthel >80).
  • In hospital for <5 days prior to intubation and ventilation.
  • Intubated and ventilated for <72 hrs.
  • Expected to remain ventilated for a further 48 hours.

Exclusion criteria

  • In hospital for 5 days or more prior to ITU admission.
  • Patients with acute brain or spinal cord injury.
  • Known or suspected neurological / muscular impairment.
  • Condition limiting use of cycle ergometer e.g. lower limb fracture / amputation.
  • Not expected to survive >48hrs.
  • Persistent therapy exemptions in first 3 days of mechanical ventilation.
  • Body habitus such as unable to use cycle ergometer.
  • Consultant clinician view that patient not suitable or not expected to survive admission.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

46 participants in 2 patient groups

Early mobility
Experimental group
Description:
Patients will receive standard physiotherapy regimen plus 2 x 30 minute rehabilitation sessions 5 days per week.
Treatment:
Other: Early mobility
Standard care
No Intervention group
Description:
Patients will receive standard physiotherapy regimen

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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