Active — Not RecruitingNot Applicable

MONITOR-IC Post ICU Care Study

Netherlands2,250 participantsStarted 2022-02-01

Plain-language summary

* OBJECTIVE To evaluate the clinical effectiveness and cost effectiveness of structured, multidisciplinary and personalized post-ICU care versus usual care on physical and psychological functioning, and quality of life (QoL) of ICU survivors one and two years post-ICU. * RESEARCH QUESTION What is the clinical- and cost effectiveness of structured, personalized post-ICU care versus usual care on physical and psychological functioning, and QoL of ICU survivors? * HYPOTHESIS Structured, multidisciplinary, and personalized post-ICU care results in improved QoL of ICU survivors and is more cost effective compared to usual care.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * ICU patients at high risk of critical illness-associated morbidity post-ICU * 18 years or older * Patient or legal representative understands the Dutch language Exclusion Criteria: * Patients discharged from ICU/hospital direct to a nursing home * Patients discharged from ICU/hospital direct to a medical or geriatric rehabilitation clinic * Patients discharged for palliative care

What they're measuring

Individual's perception of their position in life assessed by the EuroQol-5 dimension (EQ5D) .

Timeframe: 1 year post-ICU

Mental impairments assessed by the Hospital Anxiety and Depression Scale (HADS)

Timeframe: 1 year post-ICU

Trial details

NCT IDNCT05066984

SponsorRadboud University Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-07-01

View on ClinicalTrials.gov More Post ICU Syndrome trials