A Two Year Longitudinal Clinical Study of Neurocognitive and Psychiatric Symptoms in Post COVID-19 Patients
- Disease/Condition
- COVID-19
- Drug/Device/Intervention
- Follow-up
- Study type
- Observational
- Intervention type
- other
- Primary sponsor
- Region Örebro County
- Location
- Örebro, Sweden
- Phase
- N/A
- Start date
- Feb 22, 2022
- End date
- Jun 30, 2027
- Enrollment
- 100 participants
Change in cognitive functions measured with Mindmore and change in cognitive profile in Mindmore.,Symptom improvement in depression,Self-reported symptom improvement in depression,Grade of self-reported mental fatigue,Rate of self-reported symptoms suggestive of post-traumatic stress disorder (PTSD),Grade of self-reported stress,Grade of self-reported cognitive failures in everyday life
The prospective, longitudinal, open observational study monitors patients with cognitive and
 neuropsychological symptoms after COVID-19 infection, in a longitudinal manner to see how the
 disease has affected their physical, psychological and cognitive function, their ability to
 be active, return to work, their health-related quality of life in correlation with potential
 diagnostic and prognostic markers.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06298006
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06298006 through Pure Global AI's free database. This phase not specified trial is sponsored by Region Örebro County and is currently Recruiting. The study focuses on COVID-19. Target enrollment is 100 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.