Stopped: The study was cancelled due to a change in the thesis topic before any participants were enrolled.
The aim of this study was to investigate the effects of postoperative early mobilization and Bottle-P.E.P. application on respiratory parameters and functional capacity in patients undergoing heart valve surgery.
Age range
25 Years – 75 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
European System for Cardiac Operative Risk Evaluation (EuroSCORE):
Timeframe: Preoperative period
New York Heart Association (NHYA) Functional Class Assessment:
Timeframe: Preoperative period
Respiratory function test:
Timeframe: Preoperative 1st and 7th days
Baseline transthoracic echocardiography:
Timeframe: Preoperative 1st and 7th days
NT-ProBNP measurement:
Timeframe: Preoperative 1st and 7th days
Functional capacity assessment:
Timeframe: Preoperative 1st and 7th days
The Borg Category-Ratio scale (Borg CR-10) and The Modified Borg Dyspnea Scale (MBS):
Timeframe: Preoperative 1st and 7th days
Functional Independence Measurement (FIM):
Timeframe: Preoperative 1st and 7th days]
Visual Analog Scale - Pain Assessment:
Timeframe: Preoperative 1st and 7th days