NCT05224830

Brief Summary

Following an acute COVID-19 infection, many patients suffer from long lasting physical symptoms that may greatly impair quality of life. Persisting dyspnea and other functional respiratory complaints could evoke Hyperventilation Syndrome (HVS) as a putative contributor of the long-COVID presentation in COVID-19 survivors. We aimed to assess the possible relationship between a HVS and previous acute SARS-CoV-2 infection.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,846

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2021

Geographic Reach
1 country

1 active site

Status
completed

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

January 1, 2021

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

February 3, 2022

Completed
1 day until next milestone

First Posted

Study publicly available on registry

February 4, 2022

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2022

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2022

Completed
Last Updated

September 7, 2022

Status Verified

February 1, 2022

Enrollment Period

1.3 years

First QC Date

February 3, 2022

Last Update Submit

September 6, 2022

Conditions

Keywords

covid-19dyspneaHyperventilation Syndrome

Outcome Measures

Primary Outcomes (1)

  • Assess the relationship between a hyperventilation syndrome and previous acute SARS-CoV-2 infection.

    Nijmegen questionnaire during 15 minutes (cross-sectional monocentric study)

Secondary Outcomes (1)

  • Assess the relationship between a hyperventilation syndrome and dyspnea

    Nijmegen questionnaire during 15 minutes (cross-sectional monocentric study)

Study Arms (2)

Presence of Hyperventilation Syndrome (HVS+)

Study population was divided into two groups according to the diagnosis of Hyperventilation Syndrome HVS +- : Nijmegen questionnaire score \> 23/64

Other: Nijmegen questionnaire score

No presence of Hyperventilation Syndrome (HVS-).

Study population was divided into two groups according to the diagnosis of Hyperventilation Syndrome HVS - : Nijmegen questionnaire score \< 24/64

Other: Nijmegen questionnaire score

Interventions

We collected the Nijmegen Questionnaire in order to diagnosis of Hyperventilation Syndrome

No presence of Hyperventilation Syndrome (HVS-).Presence of Hyperventilation Syndrome (HVS+)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The inclusion criteria were age greater than 18 years old, with the ability to perform a pulmonary function test in our Lung Function and Exercise Testing Department. Eligible patients were able to read and speak French in order to correctly answer to the self-reported questionnaire. The exclusion criteria were incomplete questionnaire or inability to obtain an interpretable lung function assessment.

You may qualify if:

  • Read and speak French
  • Perform a pulmonary function test

You may not qualify if:

  • \- incomplete questionnaire or inability to obtain an interpretable lung function assessment

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre Hospitalier Régional Universitaire de Nancy.

Vandœuvre-lès-Nancy, 54500, France

Location

MeSH Terms

Conditions

COVID-19Dyspnea

Condition Hierarchy (Ancestors)

Pneumonia, ViralPneumoniaRespiratory Tract InfectionsInfectionsVirus DiseasesCoronavirus InfectionsCoronaviridae InfectionsNidovirales InfectionsRNA Virus InfectionsLung DiseasesRespiratory Tract DiseasesRespiration DisordersSigns and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 3, 2022

First Posted

February 4, 2022

Study Start

January 1, 2021

Primary Completion

May 1, 2022

Study Completion

July 1, 2022

Last Updated

September 7, 2022

Record last verified: 2022-02

Locations