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Physical function and cardiorespiratory fitness recovery in ICU survivors

Physical function and cardiorespiratory fitness recovery in ICU survivors - Functional recovery after IC

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON49541
Enrollment
72
Registered
2019-07-29
Start date
2019-10-18
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

criticall ilness, multi-orgaanfalen criticall ilness

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - * 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)

Exclusion criteria

Exclusion criteria: - 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)

Design outcomes

Primary

MeasureTime frame
1] Performance-based physical function;

Secondary

MeasureTime frame
2] Cardiorespiratory fitness; 3] Self-reported physical function pre-ICU admission; 4] (Health Related) Quality of life; 5] Psychological distress; 6] Self-reported daily physical activity; 7] Self-reported use of healthcare resources; 8] Participation in work and/or study; 9] Global perceived recovery in comparison to pre-ICU status; 10] Proportion of included patients who completed entire follow-up per protocol

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)