Prognostic of Dysfunctional Breathing in Long Covid: a Follow up Study
1 other identifier
observational
50
1 country
1
Brief Summary
Dysfunctional breathing might participate to dyspnoea in long COVID-19. This study investigate the prognosis of patients diagnosed with dysfunctional breathing after SARS-CoV-2 infection in our center.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Nov 2021
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2021
CompletedFirst Submitted
Initial submission to the registry
January 31, 2022
CompletedFirst Posted
Study publicly available on registry
February 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2022
CompletedFebruary 1, 2022
December 1, 2021
7 months
January 31, 2022
January 31, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Persistence/resolution of dysfunctional breathing at follow-up visit
defined by persistence/resolution of dyspnea, as compared with patient's baseline (equivalent level of dyspnea as before COVID-19).
6 to 9 monts from diagnosis
Secondary Outcomes (9)
Change in ventilatory patterns (tidal volume [VT], breathing frequency [BF] at isowork as compared with baseline
6 to 9 monts from diagnosis
Dispersion of VT and BF during the CPET
6 to 9 monts from diagnosis
Change in ETCO2 and PaCO2
6 to 9 monts from diagnosis
Qualitative changes (increase/decrease/no change of DB pattern of CPET)
6 to 9 monts from diagnosis
Score HADS changes
6 to 9 monts from diagnosis
- +4 more secondary outcomes
Eligibility Criteria
\- Patients of 14 years or more diagnosed with DB after COVID-19 using a combined approach of symptoms and CPET in the Hospitals of Sion, of Martigny or Rennaz
You may qualify if:
- patients 14 years or more
- diagnosis of DB after SARS-CoV-2 at our long covid clinic using a combined approach of symptoms and CPET analysis in the hospitals of Sion, Martigny or Rennaz
You may not qualify if:
- Refusal to participate
- comorbidities preventing the CPET or PFT to be carried out
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Centre hospitalier du valais romand
Martigny-Ville, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 31, 2022
First Posted
February 1, 2022
Study Start
November 1, 2021
Primary Completion
June 1, 2022
Study Completion
August 1, 2022
Last Updated
February 1, 2022
Record last verified: 2021-12