Actively Recruiting

Age: 18Years +
All Genders
ID03753412

Prospective Observational Study on Functional Disability and Quality of Life in Patients Recovering From Severe Cardiac or Respiratory Failure Using Mechanical Cardiorespiratory Support

Led by Barts & The London NHS Trust · Updated on 2026-01-07

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

B

Barts & The London NHS Trust

Lead Sponsor

Q

Queen Mary University of London

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying patients who have experienced severe cardiac or respiratory failure requiring life support with extracorporeal membrane oxygenation (ECMO) to understand recovery from intensive care unit-acquired weakness (ICUAW). This condition includes muscle and nerve damage that occurs in critically ill patients and can affect physical function and quality of life after hospital treatment. The study aims to identify factors influencing recovery and the impact of ICUAW on health-related quality of life (HRQoL) following critical illness. The study observes physical and psychological effects of ICUAW in patients receiving ECMO. Researchers will use ultrasound to measure the size of a leg muscle (Rectus Femoris cross-sectional area) during the first week of admission and at set times later. Muscle strength, physical performance tests, and quality of life questionnaires will be used to see how muscle size relates to recovery. Blood and urine samples will be collected to study molecular and genomic markers, and muscle biopsies may be taken when patients have surgery to start ECMO. Participants will be monitored up to about one year after their illness. Measurements include muscle strength tests, lung function, body composition, and questionnaires assessing anxiety, depression, and daily living reintegration. Biological samples will help understand molecular changes. This comprehensive approach aims to connect physical recovery with patient-reported outcomes and biological markers to better understand ICUAW after severe cardiorespiratory failure.

CONDITIONS

Brief Title

Recovery From ICUAW Following Severe Respiratory and Cardiac Failure

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Above the age of 18
  • Adults with severe cardio-respiratory failure requiring ECMO
  • Adults with personal and professional consultee agreement for enrollment
Not Eligible

You will not qualify if you...

  • Previous stroke
  • Neuromuscular disease
  • Malignancy
  • Underlying neuromuscular disease
  • Pediatric patients

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to approximately 1 year

Participants recovering from severe cardiorespiratory failure supported by mechanical cardio-respiratory support are observed to assess muscle size, strength, physical function, and quality of life over time.

Multiple visits during admission and follow-up up to 1 year

Trial Site Locations

Total: 1 location

1

St Bartholomew's hospital (Barts NHS trust)

London, United Kingdom, EC1A 7BE

Actively Recruiting

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Research Team

M

Mark Griffiths, PhD FRCP

A

Ashley Thomas, MSc

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

MiR-181a: a potential biomarker of acute muscle wasting following elective high-risk cardiothoracic surgery.

Susannah A A Bloch, Anna V J Donaldson, Amy Lewis...

https://pubmed.ncbi.nlm.nih.gov/25888214