Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
ID07394998

Comparison of Exercise Capacity, Muscle Oxygenation and Aortic Stiffness in Patients With a History of Mitral Valve Intervention for Mitral Stenosis With Healthy Subjects

Led by Gazi University · Updated on 2026-02-06

40

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Heart valve diseases are a leading cause of illness and death after coronary artery disease, hypertension, and heart failure. Mitral stenosis narrows the heart's mitral valve, limiting blood flow and causing symptoms like shortness of breath, fatigue, and difficulty with physical activity. This condition also reduces exercise capacity, worsens quality of life, and impairs respiratory function. Research groups studying these effects often lack uniformity, and most focus on patients who have undergone a specific procedure called percutaneous mitral balloon valvuloplasty. The study compares patients who have had surgery for mitral stenosis to healthy individuals. It evaluates exercise capacity using a cardiopulmonary exercise test, muscle oxygenation with near-infrared spectroscopy, respiratory functions with spirometry, respiratory muscle strength and endurance with specialized devices, aortic stiffness with an arteriograph, physical activity with a multisensor monitor, and quality of life using the SF-36 questionnaire. Participants include a patient group and a healthy control group, with assessments done over about one year. Participants will undergo various tests to measure exercise capacity, muscle oxygenation, aortic stiffness, respiratory muscle strength and endurance, lung function, physical activity, and quality of life. These tests include exercise testing, respiratory measurements, and monitoring of daily activity levels. The study tracks these outcomes continuously through one year to understand differences between those who had mitral valve surgery and healthy people. This helps researchers learn how surgery affects heart and lung function as well as overall well-being.

CONDITIONS

Brief Title

Assessment of Exercise Capacity, Muscle Oxygenation and Aortic Stiffness in Patients With Mitral Stenosis

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 80 years
  • Patients who have undergone mitral valve intervention due to mitral stenosis
  • At least 3 months have passed since the intervention
  • Healthy controls aged between 18 and 80 years
  • Healthy controls agree to participate voluntarily
Not Eligible

You will not qualify if you...

  • Patients who have had aortic valve intervention other than mitral valve intervention
  • Acute infection
  • Orthopedic, neurological, or psychological disorders affecting functional capacity
  • Healthy controls with diagnosed chronic disease
  • Healthy controls with acute infection
  • Healthy controls with a smoking history of at least 10 packs×years or more

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Through study completion, an average of 1 year

Participants undergo assessments of exercise capacity, muscle oxygenation, aortic stiffness, respiratory muscle strength and endurance, pulmonary function, physical activity levels, and quality of life.

Initial evaluation and subsequent periodic assessments over 1 year

Long-term Monitoring

Duration - Through study completion, an average of 1 year

Participants are monitored over time to observe changes in exercise capacity, muscle oxygenation, aortic stiffness, respiratory function, physical activity, and quality of life.

Follow-up visits as scheduled throughout the study period

Trial Site Locations

Total: 1 location

1

Gazi University Faculty of Health Sciences Department of Physiotherapy and Rehabilitation, Cardiopulmonary Rehabilitation Unit

Ankara, Çankaya, Turkey (Türkiye), 06490

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Research Team

M

Meral BOŞNAK GÜÇLÜ, Prof. Dr.

E

Ebrar TÜLÜMENOĞLU, Pt

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Frequently Asked Questions

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