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IMT for Post-CABG Recovery
N/A
Waitlist Available
Led By Cemal Ozemek, Assoc. Prof.
Research Sponsored by University of Illinois at Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Had coronary artery bypass graft (CABG) surgery
Be able to walk independently
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 weeks
Awards & highlights
Study Summary
This trial will investigate if high-intensity inspiratory muscle training after CABG surgery can improve endothelial function and reduce arterial stiffness.
Who is the study for?
This trial is for adults over 18 who can walk on their own and have had coronary artery bypass graft (CABG) surgery. They must understand English well enough to consent and follow the study's instructions. People with recent pneumonia, other cardiothoracic surgeries, current smokers, unstable angina, certain chronic diseases, cognitive impairments or those on antipsychotic meds cannot join.Check my eligibility
What is being tested?
The trial tests if high-intensity inspiratory muscle training (IMT) improves heart and artery function after CABG surgery compared to a sham-IMT. Participants are randomly assigned to either real IMT at 60% of their max breathing power or a fake version for four weeks while cardiovascular functions are monitored.See study design
What are the potential side effects?
Potential side effects may include discomfort from intense breathing exercises and possible strain on respiratory muscles due to high-intensity training. However, specific side effects will be closely monitored throughout the study.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have had heart bypass surgery.
Select...
I can walk on my own without help.
Select...
I am older than 18 years.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
arterial stiffness
endothelial function
inspiratory muscle function
Secondary outcome measures
dyspnea
functional exercise capacity
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Study GroupExperimental Treatment1 Intervention
Patients who will perform inspiratory muscle training (IMT) with %60 of MIP intensity
Group II: Sham GroupPlacebo Group1 Intervention
Patients who will perform Sham-IMT
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
IMT
2015
N/A
~60
Find a Location
Who is running the clinical trial?
University of Illinois at ChicagoLead Sponsor
610 Previous Clinical Trials
1,559,415 Total Patients Enrolled
TUBİTAKUNKNOWN
6 Previous Clinical Trials
615 Total Patients Enrolled
The Scientific and Technological Research Council of TurkeyOTHER
127 Previous Clinical Trials
17,556 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there still opportunities to partake in this clinical venture?
"Unfortunately, this clinical trial is not currently accepting participants. Despite being initially posted on November 20th of 2021 and updated in mid-November of the same year, there are no current openings for patients. However, 119 other trials actively recruiting at this time can be found online."
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