Physical function and cardiorespiratory fitness recovery in ICU survivors
- Conditions
- criticall ilness, multi-orgaanfalencriticall ilnesspost-ICU patient
- Registration Number
- NL-OMON49541
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 72
- * 18 years
- having received between * 48 hours of mechanical ventilation
- conscious and adequate (Richmond Agitation and Sedation Scale (RASS) score *
2)
- cooperative (Standard 5 Questions * 3)
- free from delirium for at least 24 hours (i.e. being eligible to test)
- pre-existing orthopaedic or neuromuscular comorbidity that affects adequate
physical function assessment
- central neurologic or spinal cord pathology
- non-ambulatory prior to ICU admission
- receiving palliative care
- Insufficient understanding of the Dutch language
- Unable to give written informed consent to participate in the study
- Not eligible to perform maximal exercise testing at 3-6 months post-ICU
discharge using the American College of Sports Medicine screening form (ACSM,
1998)
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>1] Performance-based physical function; </p><br>
- Secondary Outcome Measures
Name Time Method <p>2] Cardiorespiratory fitness; 3] Self-reported physical function pre-ICU<br /><br>admission; 4] (Health Related) Quality of life; 5] Psychological distress; 6]<br /><br>Self-reported daily physical activity; 7] Self-reported use of healthcare<br /><br>resources; 8] Participation in work and/or study; 9] Global perceived recovery<br /><br>in comparison to pre-ICU status; 10] Proportion of included patients who<br /><br>completed entire follow-up per protocol</p><br>