Dysfunctional Breathing in Post COVID-19 Condition.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorKarolinska Institutet

About this trial

The goal of this observational study with a cross-sectional design is to investigate what signs, symptoms and assessment which can describe and explain dysfunctional breathing in patients with post COVID-19 condition. The main question aims to answer which measurements can identify and asses dysfunctional breathing in patients with post COVID-19 condition?

Participants for this study will be recruited from the ReCov cohort will be evaluated with diffrent measurments and questionnaires.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

Not able to perform the measurements because of cognitive or physical impairments, ongoing intervention of breathing exercises.

Trial population

Patients (approximately n=200) for this study will be recruited from the ReCov cohort. All patients will be \> 18 years old. Patients that state that they have persistent respiratory problems and abnormal clinical respiratory findings will be included. Patients will also be recruited from primary care if they have suspected dysfunctional breathing pattern (unable to breathe with a normal breathing pattern in standing)

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

200 Participants
are grouped into 1 trial group
Group A: Patients with post COVID-19 condition.

Trial outcomes

Primary outcomes

1

Breathing pattern by Respiratory Movement Measuring Instrument (RMMI) and Health-related Quality of Life (EQ-5D-5L)

Will be assesed in a supine position, using the RMMI. First, during 30 seconds of tidal volume breathing. Second, during 60 seconds of performing maximal breathing manoeuvres interspaced by tidal volume breathing and then during 60 seconds after performing activity that triggers dyspnea. The RMMI records bilateral changes in the anterior posterior diameter, including both upper and lower thoracic and abdominal movements. Health-related Quality of Life is measured with EuroQualityOf Life 5 dimensions questionnaire (EQ-5D-5L), which is an instrument that evaluates the generic quality of life. EQ-5D includes a descriptive system, which comprises 5 dimensions of health: mobility, selfcare, usual activities, pain/discomfort, and anxiety/depression. A descriptive index-score between 0-1, higher score indicates higher HRQoL. EQ-5D also includes a visual analog scale (VAS), which records self-rated health status on a graduated (0-100) scale, with higher scores for higher HRQoL

Time frame
Assessment will be applied only once and takes about 5-10 minutes to be completed.

Secondary outcomes

1

Maximal Inspiratory Pressure (MIP)

Maximal Inspiratory muscle strength (MIP) will be measured with Micro RPM in cmH2O

Time frame
Assessment will be applied only once and takes about 5-10 minutes to be completed.
2

Maximal Expiratory Pressure ( MEP)

Maximal expiratory muscle strength (MEP) will be measured with Micro-RPM in cm H20

Time frame
Assessment will be applied only once and takes about 5-10 minutes to be completed.
3

Chest mobility

Chest mobility will be measured with a tape measure at the xiphoid process and the 4th rib

Time frame
Assessment will be applied only once and takes about 5 minutes to be completed.
4

Six-minute walk test (6MWT)

Six-minute walk to measure endurance (in meters)

Time frame
Assessment will be applied only once and takes about 15 minutes to be completed.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Karolinska Institutet

Lead sponsor

Karolinska University Hospital

Collaborator