Investigating dysfunctional breathing in patients with post COVID-19 condition
Dysfunctional Breathing in Patients With Post COVID-19 Condition
This study is trying to see how breathing problems affect people who are dealing with long-term symptoms after having COVID-19.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Karolinska Institutet Academic / other |
| Locations | 2 sites (Stockholm, Solna and 1 other locations) |
| Trial ID | NCT06776263 on ClinicalTrials.gov |
What this trial studies
This observational study aims to explore the signs and symptoms of dysfunctional breathing in patients suffering from post COVID-19 condition. It will utilize various measurements and questionnaires to identify and assess dysfunctional breathing, focusing on the underlying mechanisms and patient experiences. The study is part of a larger project, ReCOV, which takes a holistic approach to understanding the consequences of COVID-19. Participants will be recruited from the ReCov cohort and evaluated for their physical and psychological recovery over time.
Who should consider this trial
Good fit: Ideal candidates are patients reporting persistent respiratory problems with specific scores on the mMRC or Nijmegen scales.
Not a fit: Patients unable to perform the required measurements due to cognitive or physical impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved assessment and management strategies for patients experiencing dysfunctional breathing after COVID-19.
How similar studies have performed: While this approach is part of a larger multi-disciplinary project, similar studies have shown promise in understanding post-viral syndromes, though this specific focus on dysfunctional breathing is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients that state that they have persistent respiratory problems, have 2 or higher on mMRC scale or 23 and over on the Nijmegen scale will be included. Exclusion Criteria: * Not able to perform the measurements because of cognitive or physical impairments, ongoing intervention of breathing exercises.
Where this trial is running
Stockholm, Solna and 1 other locations
- Karolinska University Hospital — Stockholm, Solna, Sweden (Not_yet_recruiting)
- Karolinska Institutet — Huddinge, Sweden (Recruiting)
Study contacts
- Study coordinator: Malin Nygren-Bonnier, Associate professor, PhD
- Email: malin.nygren-bonnier@ki.se
- Phone: +46852488831
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.