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Precision Medicine for more Oxygen - COVID-19 extensio

Recruiting
Conditions
COVID-19
Registration Number
NL-OMON28553
Lead Sponsor
Amsterdam UMC, location AMC
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

Age: 40-65 years.
-Proven ex-COVID-19: Positive PCR/serology for SARS-CoV2 or CORADS score 4/5.
-Able to provide informed consent.
-Access to internet (either at home or via relatives/friends).
-Understanding of Dutch language.

Exclusion Criteria

-Inability to provide informed consent.
-History or suspicion of inability to cooperate adequately.
-Participation in any other study involving investigational or marketed products concomitantly or within four weeks prior to entry into the study or during the study.
-Investigator’s uncertainty about the willingness or ability of the patient to comply with the protocol requirements.
-Patients with terminal illness.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
A.To assess pulmonary and extra-pulmonary damage (with imaging techniques), complaints (e.g. fatigue and Quality of Life) and other signs of disease (both clinical signs and multi-omics biomarkers) in the year after infection in ex-COVID-19 patients.<br>B.To assess whether a personalized counselling intervention on quality of dietary intake and level of physical activity can improve general health and decrease complaints and signs of disease (both pulmonary and extrapulmonary).
Secondary Outcome Measures
NameTimeMethod
-To determine the course of lung damage and complaints due to SARS-COV2 infection.<br>-To identify different phenotypes in ex-COVID-19 patients.<br>-To determine the influence of the exposome (environmental exposure) to lung damage and complaints in ex-COVID-19 patients one year post infection.<br>-To define different exposome-based groups at risk to develop lung damage after SARS-COV2 infection and subsequent hospitalisation.<br>-To assess the ability to use imaging techniques to detect lung damage in ex-COVID-19 patients without clear complaints. <br>-To determine whether SARS-CoV-2 infection triggers the onset of ME/CSF.<br>-To assess what risk factors are associated with the development of ME/CSF in ex-COVID-19 patients.<br>
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