Understanding cognitive, psychological, and physical functioning in long-COVID patients with fatigue.
Cognitive, Psychological, and Physical Functioning in Long-COVID Patients With Different Levels of Fatigue.
Hasselt University · NCT05758558
This study looks at how fatigue affects people with long-COVID by checking their thinking, mood, and physical abilities to better understand their different experiences and needs.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Hasselt University (other) |
| Locations | 1 site (Diepenbeek) |
| Trial ID | NCT05758558 on ClinicalTrials.gov |
What this trial studies
This observational study aims to identify subgroups of patients suffering from post-acute COVID-19 syndrome, focusing on their clinical symptoms, demographic characteristics, and levels of fatigue. By assessing cognitive, psychological, and physical functioning, the study seeks to better understand the diverse experiences of long-COVID patients. Participants will be evaluated based on their reported symptoms and functional status, allowing for a comprehensive analysis of their needs and care requirements.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old who have experienced persistent symptoms of COVID-19 for more than two months and report significant fatigue.
Not a fit: Patients who are pregnant, have certain medical devices, or specific neurological disorders may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and tailored interventions for long-COVID patients, enhancing their quality of life.
How similar studies have performed: While there is ongoing research into long-COVID, this specific approach to categorizing patients based on fatigue and functioning is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: The participant must report current persisting symptoms (such as brain fog, anxiety, shortness of breath, headaches but also others) and indicate on the Post COVID-19 Functional Status Scale that these have an impact on everyday functioning (grade 2, 3, and 4). These symptoms need to be present for more than two months. Further inclusion criteria are: * Fatigue Severity Scale (FSS) score \> 4 * Aged over 18 years old * Willing to sign the digital informed consent * Dutch speaking and Dutch understanding * Be tested positive for COVID-19, i.e. by reverse transcription polymerase chain reaction (RT-PCR), computed tomography (CT) of the lungs, or symptom-based diagnosis by the general practitioner. Exclusion Criteria: * Pregnant women * Pacemaker, defibrillator * Brain or nerve disorders * Epilepsy * A copper spiral or recent bone fracture
Where this trial is running
Diepenbeek
- Hasselt University — Diepenbeek, Belgium (RECRUITING)
Study contacts
- Study coordinator: Stef Feijen, Dr
- Email: stef.feijen@uhasselt.be
- Phone: +32494044431
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Post-Acute COVID-19 Syndrome