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Prognostic of Dysfunctional Breathing in Long Covid: a Follow up Study

Prognostic of Dysfunctional Breathing in Long Covid: a Follow up Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05217875
Enrollment
50
Registered
2022-02-01
Start date
2021-11-01
Completion date
2022-08-31
Last updated
2022-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19, Dysfunctional Breathing

Keywords

COVID-19, Dysfunctional breathing, Hyperventilation syndrome, Sighs, erratic breathing

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.

Detailed description

Dysfunctional breathing (DB) with or without hyperventilation syndrome (HVS) as diagnosed using cardiopulmonary exercise test (CPET) was recently demonstrated as an important physiopathological mechanism of persistent dyspnoea in long COVID patients \[1\]. DB is characterized by specific ventilation pattern on CPET accompanied by respiratory discomfort and/or dyspnea at exercise \[2\]. Most patients with DB will have undergone some sort a specific physiotherapy retraining \[3\]. However the prognostic and the predictors of persistence/resolution of DB after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are unknown. The aim of the study is to determine the prognostic of patients diagnosed with DB after SARS-CoV-2 infection, as well as prognosis factors and predictors of persistence/resolution of DB during a prospective follow up visit.

Interventions

None listed

Sponsors

Hôpital du Valais
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
14 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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 * Inclusion between November 2020 and until the end of October 2021

Exclusion criteria

* Refusal to participate * comorbidities preventing the CPET or PFT to be carried out

Design outcomes

Primary

MeasureTime frameDescription
Persistence/resolution of dysfunctional breathing at follow-up visit6 to 9 monts from diagnosisdefined by persistence/resolution of dyspnea, as compared with patient's baseline (equivalent level of dyspnea as before COVID-19).

Secondary

MeasureTime frame
Dispersion of VT and BF during the CPET6 to 9 monts from diagnosis
Change in ETCO2 and PaCO26 to 9 monts from diagnosis
Qualitative changes (increase/decrease/no change of DB pattern of CPET)6 to 9 monts from diagnosis
Score HADS changes6 to 9 monts from diagnosis
Change in ventilatory patterns (tidal volume [VT], breathing frequency [BF] at isowork as compared with baseline6 to 9 monts from diagnosis
Specific symptom scale changes6 to 9 monts from diagnosis
Specific work capacity changes questions6 to 9 monts from diagnosis
Post-COVID Functional Status (PCFS) changes6 to 9 monts from diagnosis
Score SF-36 changes6 to 9 monts from diagnosis

Countries

Switzerland

Contacts

Primary ContactPierre-Olivier v Bridevaux
pierre-olivier.bridevaux@hopitalvs.ch+41792079069
Backup ContactLéon Genecand
leon.genecand@hcuge.ch+41799372687

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026