Evaluating fatigue in COVID-19 survivors
Profile of COVID-19 Patients Related to Fatigue
This study is trying to understand how fatigue affects people who have recovered from COVID-19 by comparing those who feel tired to those who don’t.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 398 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Universidad de Granada Academic / other |
| Locations | 1 site (Granada) |
| Trial ID | NCT05731817 on ClinicalTrials.gov |
What this trial studies
This observational study aims to evaluate the profile of patients who have recovered from COVID-19, specifically focusing on those who experience fatigue. Participants will be divided into two groups based on the presence or absence of fatigue, and their profiles will be assessed using various evaluation methods, including online surveys and face-to-face assessments. The study will take place at the Virgen de las Nieves University Hospital in Granada, where patients will be recruited and evaluated for their symptoms and physical performance related to fatigue.
Who should consider this trial
Good fit: Ideal candidates for this study are adults over 18 years old who have been diagnosed with COVID-19 and have basic internet access.
Not a fit: Patients with severe comorbidities or those with mental, physical, or organic problems that may pose a risk are unlikely to benefit from this study.
Why it matters
Potential benefit: If successful, this study could help identify the characteristics of COVID-19 survivors who experience fatigue, leading to better management and support for these patients.
How similar studies have performed: Other studies have indicated that fatigue is a common issue among COVID-19 survivors, suggesting that this approach to understanding patient profiles is relevant and necessary.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * diagnosis of COVID-19 * adults (\>18 years) * basic knowledge and access to the internet * wish to participate in the study and sign the informed consent Exclusion Criteria: * patients with severe comorbidities that interfere with the ability to perform the study, and those with mental, physical or organic problems that under medical criteria may pose a risk to the patient
Where this trial is running
Granada
- University of Granada — Granada, Spain (Recruiting)
Study contacts
- Principal investigator: Irene Torres Sánchez, PhD — Universidad de Granada
- Study coordinator: Irene Torres Sánchez, PhD
- Email: irenetorres@ugr.es
- Phone: 0034958249591
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.