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COVID-19 Follow up Intensive Care Studies

COVID-19 Follow up Intensive Care Studies

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04460170
Acronym
COFICS
Enrollment
122
Registered
2020-07-07
Start date
2020-07-01
Completion date
2022-02-01
Last updated
2026-05-26

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

Conditions

COVID-19, Quality of Life

Keywords

Critical Care, Family Members, Patients, Follow-Up Studies, Quality of Life, COVID-19

Brief summary

Since the SARS-CoV-2 infection is relatively new, the long term attributable burden related to COVID19 has not been investigated yet. To date, in patients with COVID-19 and their family members, there is little information on the functional status, cognitive ability, pattern of return to work, and health related quality of life after the ICU admission. This study aims to describe the psychological wellbeing, physical - and social functioning of COVID-19 ICU survivors and their family members up to 12 months following ICU discharge.

Detailed description

Study design The COVID-19 Follow up Intensive Care Study (COFICS) is a single center, prospective cohort study performed at a University Medical Center in The Netherlands. Study population The study population consists of all admitted critically ill COVID-19 patients with a \> 48 hours ICU admission at the ICU of a University Medical Center and a family member of the patient. Family members in this study can be partners, other family members, or friends who are identified by the patient as important. Sample size All consecutive patients admitted to the ICU of the University Hospital for respiratory distress due to COVID-19 between March 19th 2020 and September 30th 2020 will be enrolled. With consent of the patient, family member(s) of participating patients will be enrolled.

Interventions

None listed

Sponsors

University Medical Center Groningen
Lead SponsorOTHER
Hanze University of Applied Sciences Groningen
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* ≥ 18 years old * Ability to speak and write Dutch * Ability to conduct a telephone call * Diagnosed with COVID-19 infection (only in patients) * 48 hours ICU admission (only in patients)

Exclusion criteria

* Refuse to participate * Serious language barrier * Cognitive impairment * Severe psychiatric disorder * Chronic ventilator dependency (only in patients)

Design outcomes

Primary

MeasureTime frameDescription
General Health3 months post ICU dischargeMOS Short-Form General Health Survey (SF-20). The SF-20 contains 20 items and has six dimensions; physical functioning (min. score 6, max. score 12) rolefunctioning (min. score 2, max. score 4) social functioning (min. score 1, max. score 6) mental health (min. score 5, max. score 30) general health (min. score 5, max. score 25) pain (min. score 1, max score 5) All endscores will be transformed to a 100 points scale where a higher score means better functioning. Except for pain where a higher score means more pain. The five mental health questions will be excluded from our questionnaire because the questions are comparable with the HADS.
Anxiety and Depression3 months post ICU dischargeHospital Anxiety and Depression Scale (HADS). The HADS contains two subscale of 7 items each. Minimal score is 0, maximal score 21 for each subscale where a higher score means a higher burden.
Long function6 months post ICU discharge (only in patients)Spirometry test
Frailty3 months post ICU discharge (only in patients)Clinical Frailty Scale with a single outcome measure summarizing the overall level of fitness.
Family functioning6 months post ICU dischargeMcMaster Family Assessment Device (FAD-GF6+). The FAD-GF6+ contains 6 items (min. score 6, max. score 24) where a higher scores indicate a lower caregiver burden.
Effect of an ICU admission on return to work3 months post ICU discharge (only in family members)Return to work knowing; possible job loss, change of work activities and worsening employment status

Secondary

MeasureTime frameDescription
age24 hours (patient) / 3 months post ICU discharge (family member)age (years)
Gender24 hours (patient) / 3 months post ICU discharge (family member)Gender (male/female)
Social status3 months post ICU dischargeSocial status (married/living together/ single)
APACHE IV24 hours (only in patients)Acute Physiology And Chronic Health Evaluation (APACHE IV). It is applied within 24 hours of admission of a patient to an intensive care unit (ICU): based on several measurements; higher scores correspond to more severe disease and a higher risk of death
Comorbidity3 months post ICU discharge (only in patients)Comorbidity ( free text)
Body mass index3 months post ICU discharge (only in patients)Body mass index (kg/m2)
ICU stayhospital discharge, an average of 4 weeks (only in patients)ICU stay (days)
Mechanical ventilationhospital discharge, an average of 4 weeks (only in patients)Mechanical ventilation (days)
Deleriumhospital discharge, an average of 4 weeks (only in patients)Delerium (no / yes --\> CAM-ICU / DOS score)
Hospital stayhospital discharge, an average of 4 weeks (only in patients)Hospital stay (days)
Discharge locationnhospital discharge, an average of 4 weeks (only in patients)Discharge location (home, other hospital, nursing home, revelidation center)
Mortality3 months post ICU discharge (only in patients)Mortality (no / yes --\> date)
Relationship with the patient3 months post ICU discharge (only in family members)Relationship with the patient (Partner, sibling, child, other)
Educational level3 months post ICU dischargeEducational level (low, middle, high)
Readmission3 months post ICU discharge (only in patients)Readmission (no / yes --\> free text)
Health care consumption3 months post ICU dischargeHealth care consumption (general practicionar, home care, physiotherapist, lung specialist, psychologist, onther (free text))
Weight3 months post ICU dischargeWeight (kg)
Hypertensive3 months post ICU dischargeHypertensive (RR)
Thrombosis3 months post ICU dischargeThrombosis (no / yes --\> anticoagulant, DVT or PE)
Diabetes3 months post ICU dischargeDiabetes (no /yes --\> current insulin level, metformin/ insulin use)

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 27, 2026