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Quality of Life and Functional Capacity in Post Intensive Care Unit

NCT05149430 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 101

Last updated 2022-02-23

No results posted yet for this study

Summary

BACKGROUND. Staying in an intensive care unit can lead to physical and cognitive complications and post-traumatic stress. Currently, the aim is to find out the level of quality of life, functional capacity and cognitive status post intensive care unit. Describe the evolution of the quality of life, functional capacity and cognitive status of a cohort of patients admitted to the ward room after discharge from the intensive care unit, with subsequent follow-up at 3, 6 and 12 months of his discharge.

METHODS. Prospective, observational, analytical cohort study. Subjects over 18 years of age with at least 48 hours of confinement in a closed area were included. Demographic variables, quality of life, functional capacity and cognitive status were recorded. A telephone follow-up was carried out three, six and twelve months after institutional discharge. For the evaluation of the primary variables, Euroqol 5d-5L (Eq5d - Eq5d-VAS), Barthel Index and Fototest were used.

Conditions

  • Post-intensive Care Syndrome

Interventions

OTHER

Observational Quality of life and functional capacity

Observational Quality of life and functional capacity

Sponsors & Collaborators

  • Cagide Sabrina

    collaborator UNKNOWN

  • Di giorgio Victoria

    collaborator UNKNOWN

  • Villalba Dario

    collaborator UNKNOWN

  • Accoce Matias

    collaborator UNKNOWN

  • Sanatorio Anchorena San Martin

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-01
Primary Completion
2019-09-30
Completion
2020-03-31

Countries

  • Argentina

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05149430 on ClinicalTrials.gov