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Tests treatment safety and results for Post COVID-19 Syndrome
Official title Effectiveness of Functional Respiratory Muscle Training in Post-COVID-19 Syndrome
ClinicalTrials.gov ID: NCT07051954
What this study is testing
- What it's testing
- This study aims to investigate the effects of core stabilization exercises and functional inspiratory muscle training (IMT) on various physiological and psychological parameters in individuals with post-COVID-19 syndrome. Participants diagnosed with post-COVID-19 syndrome will be randomly assigned to two groups using stratified computer-assisted randomization.
- Time commitment: about 8 weeks
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 65
You may be able to join if
- Diagnosed with Post-COVID-19 Syndrome.
- Literate and able to understand study procedures.
- Aged between 18 and 65 years.
- Willing to voluntarily participate in the study.
- Classified as functional class 2-3 according to the Post-COVID-19 Functional Status Scale (PCFS).
You likely can't join if
- History of recent myocardial infarction or pulmonary embolism.
- Presence of uncontrolled chronic diseases.
- Any orthopedic or neurological disorders that limit mobility.
- Neurological impairments (e.g., cerebrovascular disease) or psychiatric disorders that impair cooperation or compliance with exercise testing.
See the full eligibility criteria
- Diagnosed with Post-COVID-19 Syndrome.
- Literate and able to understand study procedures.
- Aged between 18 and 65 years.
- Willing to voluntarily participate in the study.
- Classified as functional class 2-3 according to the Post-COVID-19 Functional Status Scale (PCFS).
- Clinically stable; comorbid conditions such as hypertension or diabetes must be controlled.
- No orthopedic or neurological conditions that would prevent assessment of peripheral muscle strength, balance, or exercise capacity.
- History of recent myocardial infarction or pulmonary embolism.
- Presence of uncontrolled chronic diseases.
- Any orthopedic or neurological disorders that limit mobility.
- Neurological impairments (e.g., cerebrovascular disease) or psychiatric disorders that impair cooperation or compliance with exercise testing.
The study team makes the final eligibility decision.
Where it's taking place
- Ankara, Çankaya, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The study runs about 8 weeks per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 65 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Ankara, Çankaya, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.