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NCT05758558

Cognitive, Psychological, and Physical Functioning in Long-COVID Patients With Different Levels of Fatigue.

Completed Last updated 12 February 2026
What this trial tests

trial in Post-Acute COVID-19 Syndrome in 69 participants. Completed in 1 June 2024.

Timeline
5 May 2023
Primary endpoint
1 June 2024
1 June 2024

Quick facts

Lead sponsorHasselt University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment69
Start date5 May 2023
Primary completion1 June 2024
Estimated completion1 June 2024
Sites1 location across Belgium

Conditions studied

Sponsor

Hasselt University

Who can join

18 and older, any sex, with Post-Acute COVID-19 Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Post COVID-19 usually occurs 3 months from the onset of COVID-19 with symptoms that last for at least 2 months and cannot be explained by an alternative diagnosis. Patients report a range of disabling symptoms such as fatigue, shortness of breath, cognitive impairment, memory loss and mental health and employment issues. This clinical heterogeneity complicates the identification of the appropriate needs and care. The aim of this cross-sectional study is to identify subgroups (clusters) of post COVID patients based on clinical symptoms, demographic characteristics, levels of fatigue and physical, cognitive and psychological functioning of the individuals.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Post-Acute COVID-19 Syndrome

Currently open trials in the same condition.

Other Hasselt University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05758558.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing