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CORona (COVID-19) Follow Up Study: Epidemiology, Pathophysiology, Prediction, and Communication (CORFU)

Maastricht University Medical Centre (MUMC) logo

Maastricht University Medical Centre (MUMC)

Status

Invitation-only

Conditions

COVID-19
Post COVID-19 Condition
Long COVID

Treatments

Other: no intervention, the CORFU study conducts analyses based on data which has been prospectively collected (and aggregated when possible) in 7 existing cohorts

Study type

Observational

Funder types

Other

Identifiers

NCT05240742
METC2021-2990

Details and patient eligibility

About

The CORFU study, funded by ZonMW, is a prospective, multiple, cohort study with a maximum follow-up of 24 months after COVID-19. Dutch COVID-19 patients from 7 existing prospective cohorts, aiming and designed to conduct COVID-19 research, will be included in this study.

The CORFU study has 5 aims, divided into 4 work packages (WPs):

  1. To describe the nature, severity, pattern and duration of long COVID complaints up to a maximum of two years after infection and its relationship with quality of life (WP1);
  2. To describe the rehabilitation and corresponding activities for the treatment and improvement of complaints and quality of life (WP1);
  3. To describe the pathophysiological processes that cause long COVID complaints, and the role of vulnerability/resilience factors (WP2);
  4. To develop a prediction model for the persistence of complaints, with distinction between patients with and without pre-existing morbidity (WP3);
  5. To develop a patient platform prototype in which patients can digitally consult their answers and compare their answers with reference populations (WP4, in collaboration with the EuroQol foundation).

The 7 cohorts participating in the CORFU study are: POPCOrn, COVAS, ELVIS, MaastrICCht, DC&TC, CAPACITY-COVID, and Adelante cohort.

(Clinical) baseline and follow-up data has been collected in these cohorts and will be used/aggregated to investigate CORFU study aims. In addition, questionnaires will be send to the (former) patients of the existing cohorts and patients will be asked about several domains such as persisting complaints and quality of life, at several moments, depending on when the patients have experienced COVID-19. Within this study a patient platform prototype will be developed, together with the EuroQol foundation, to be able to inform patients about the individual situation and course of disease.

Enrollment

5,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

All 7 existing cohorts have specific inclusion and exclusion criteria.

For the CORFU study, in general, the criteria are:

Patients with proven or suspected COVID-19:

  • Confirmed (or suspected) COVID-19 - both home-isolated patients and patients who were admitted to the hospital ward and/or ICU;
  • Included in one of the seven cohorts from March 2020 onwards;
  • Aged 18 years or older;
  • Mastering the Dutch language sufficiently to answer the questionnaires;
  • Informed consent.

Controls who did not experience COVID-19:

  • Aged 18 years or older;
  • Mastering the Dutch language sufficiently to answer the questionnaires;
  • Informed consent.

There were no exclusion criteria.

Trial design

5,000 participants in 2 patient groups

Dutch COVID-19 patients
Description:
The study population consists of Dutch (former) COVID-19 patients who have been included in one of the cohorts and categorized in various subgroups: * Patients who suffered from (confirmed) COVID-19 and were admitted to the hospital ward. * Patient who suffered from (confirmed) COVID-19 and were admitted to the ICU. * Patients who suffered from (confirmed or suspected) COVID-19 at home. * Patients who suffered from (confirmed) COVID-19 and were in need of inpatient or outpatient rehabilitation after infection at home or in the hospital (ward and/or ICU).
Treatment:
Other: no intervention, the CORFU study conducts analyses based on data which has been prospectively collected (and aggregated when possible) in 7 existing cohorts
Dutch controls who did not experience COVID-19
Description:
One of the cohorts, the POPCOrn cohort, is a community-based cohort which partly consists of controls who did not experience COVID-19
Treatment:
Other: no intervention, the CORFU study conducts analyses based on data which has been prospectively collected (and aggregated when possible) in 7 existing cohorts

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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