Testing the reliability of mobility assessments in adults with long COVID
Reliability of 30 Seconds Sit-to-stand and Timed Up and Go in Adults With Long Covid
This study is testing if two mobility tests are reliable for adults with long COVID by having them do the tests on the same day and again three days later.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 19 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | European University Cyprus Academic / other |
| Locations | 1 site (Larnaca) |
| Trial ID | NCT05886842 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the reliability of two functional mobility tests, the 30 seconds Sit-to-Stand and Timed Up and Go, in adults suffering from long COVID. Conducted in a rehabilitation center, the study will involve 19 participants who will perform both tests on the same day and again three days later without any intervening physical therapy. The results will be analyzed using statistical methods to determine the consistency of the test outcomes, which are crucial for assessing the functional status of long COVID patients.
Who should consider this trial
Good fit: Ideal candidates for this study are adults diagnosed with long COVID who were infected with the COVID-19 virus within the last six months.
Not a fit: Patients under 18 years of age or those with significant cognitive and psychiatric impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide reliable assessment tools for evaluating mobility and endurance in long COVID patients, aiding in their rehabilitation.
How similar studies have performed: While the reliability of these tests has been established in other populations, this specific application in long COVID patients is novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults who were infected with COVID-19 virus in the last 6 months and were diagnosed with long-covid * Patients must be willing to give written consent for participation in the study * Negative rapid test for COVID-19 Exclusion Criteria: * People under 18 years of age * Significant cognitive and psychiatric impairments (inability to follow simple commands or give consent) * Refuse to give consent
Where this trial is running
Larnaca
- Eden resort wellness rehabilitation — Larnaca, Cyprus (Recruiting)
Study contacts
- Principal investigator: Marina E Kloni — European University Cyprus
- Study coordinator: Marina E Kloni
- Email: marina.eleni@gmail.com
- Phone: 00357 99007245
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.