Actively Recruiting
Dysfunctional Breathing in Patients With Post COVID-19 Condition
Led by Karolinska Institutet · Updated on 2025-02-14
200
Participants Needed
2
Research Sites
25 weeks
Total Duration
On this page
Sponsors
K
Karolinska Institutet
Lead Sponsor
K
Karolinska University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating dysfunctional breathing in patients with post COVID-19 condition to understand what signs, symptoms, and assessments can describe and explain this issue. The study aims to identify measurements that can detect dysfunctional breathing and to evaluate methods for measuring it regarding validity, reliability, and sensitivity. The research is part of a larger project called ReCOV, which looks at the long-term effects of COVID-19 on patients, their families, and healthcare staff. This observational study has a cross-sectional design and will recruit about 200 patients from the ReCOV cohort and primary care. Participants will be adults over 18 years old who report persistent respiratory problems or suspected dysfunctional breathing patterns. Evaluations include physical and psychological function assessments, questionnaires, and various measurements such as breathing pattern analysis with a Respiratory Movement Measuring Instrument, muscle strength tests, chest mobility, walking endurance, spirometry, diaphragmatic ultrasound, and carbon dioxide levels during exercise. Participants will undergo a one-time assessment using multiple tools to measure breathing patterns, physical activity, symptoms, and health-related quality of life. Questionnaires will evaluate breathing dysfunction, respiratory symptoms, anxiety, depression, and overall health status. The study will also collect data on diaphragm thickness and movement. The primary outcomes focus on breathing pattern and quality of life, with secondary outcomes covering muscle strength, chest mobility, endurance, and other respiratory functions. The study helps to better understand breathing difficulties after COVID-19 and to develop tailored interventions for rehabilitation.
CONDITIONS
Brief Title
Dysfunctional Breathing in Post COVID-19 Condition.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who report persistent respiratory problems
- Patients with a score of 2 or higher on the mMRC scale
- Patients with a score of 23 or over on the Nijmegen scale
- Patients aged 18 years or older
- Patients able to perform physical and breathing measurements
You will not qualify if you...
- Patients unable to perform measurements due to cognitive or physical impairments
- Patients currently undergoing breathing exercise interventions
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single assessment visit
Participants undergo assessments to evaluate dysfunctional breathing, physical and psychological function, symptoms, and quality of life.
1 visit (in-person)
Duration - Ongoing throughout the study period
Participants are observed to understand the experience of living with dysfunctional breathing and recovery after COVID-19 condition.
Assessments occur once; no repeated visits specified
Trial Site Locations
Total: 2 locations
1
Karolinska University Hospital
Stockholm, Solna, Sweden, 17176
Not Yet Recruiting
2
Karolinska Institutet
Huddinge, Sweden, 14183
Actively Recruiting
Research Team
M
Malin Nygren-Bonnier, Associate professor, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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